Deposition parameters and properties of n‐doped a‐/μc‐Si:H thin films.
High‐quality and low‐cost fabrication of Si‐based materials, in which many fundamental and technology problems still remain, have attracted tremendous interests due to their wide applications in solar cell area. Low‐frequency inductively coupled plasma (LFICP) provides a new and competitive solution, thanks to its inherent advantages of high‐density plasma, low sheath potential, and low electron temperature, etc. The plasma characteristic‐dependent microstructures, optical and electronic properties of the LFICP CVD‐based hydrogenated amorphous/microcrystalline silicon and silicon oxides are systematically studied. Remote‐LFICP combing the high‐density plasma nature of ICP and mild ion bombardment on growing surface in remote plasma allows the deposition of high‐quality Si‐based materials providing excellent c‐Si surface passivation. The mechanism of surface passivation by LFICP CVD Si‐based materials, interaction between plasma species and growing surface are analyzed in terms of the plasma properties. These results pave the way for LFICP CVD utilization in Si‐based high‐efficiency and low‐cost solar cell fabrication.
- LFICP CVD
- Si‐based materials
- solar cells
Plasma‐enhanced chemical vapor deposition (PECVD) is an excellent alternative for depositing thin films at lower temperature than those utilized in a conventional CVD process. Plasma generated by a glow discharge absorbs the electrical energy, and hence the neutral gases were dissociated into reactive radicals, ion, neutral atoms and molecules, and other highly excited species through the electron impact instead of conventional thermal energy. These atomic and molecular fragments interact with a substrate and, depending on the nature of these interactions, either etching or deposition processes occur at the substrate. Therefore, the substrate can be maintained at a lower temperature keeping the reactions for the thin‐film deposition. These salient advantages of PECVD, i.e., low temperature nature, together with the high quality of the deposited films make PECVD be an important route for the fabrication of Si‐based materials, which have been the dominant material system for the present solar cell research and commercial market. PECVD‐based silicon nitride (SiNx:H) with the feedstock gases of SiH4 and NH3 act as the passivation and antireflection layer of the bulk Si solar cells. Fabrication of Si thin‐film solar cells consisting of the stack of p‐, i‐, and n‐type hydrogenated amorphous/microcrystalline Si (a‐/μc‐Si:H) films also relies on PECVD technology. The interface quality and energy conversion efficiency of HIT (heterojunction with intrinsic thin layer) solar cell with the record efficiency of 25.6%  closely depends on the PECVD process because the symmetric intrinsic passivation layers and doped layers (front emitter and back surface field layers) are also prepared by PECVD technology .
Although PECVD‐associated Si‐based materials are dominant over other materials in present solar cell market, there are a variety of challenges due to the nature of the utilized PECVD method. The common PECVD uses the capacitively coupled plasma (CCP) between parallel plates driven by a 13.56 MHz RF power generator. The ionization degree of the neutral gas is at a low level of ∼10−6–10−4 because of the low electron density of ∼109–1010/cm3 in a CCP discharge mode. In principle, this means a low deposition rate of the targeted materials. As a consequence, the deposition rate of PECVD‐based a‐/μc‐Si:H is about 0.5 nm/s , which is not desirable for cost‐efficient, thin‐film solar cell productions. Furthermore, the intensive coupling of the plasma density and ion energy in CCP complicates the deposition of high‐quality thin films and the achievement of high‐efficiency solar cells because strong ion bombardment would result in excessive defect formation in the films and on the growing surface/interface, and hence significant deterioration of the energy conversion efficiency of the solar cells . These disadvantages of PECVD can be partially remedied by using very high‐frequency (VHF) PECVD, which can effectively decouple the plasma density and electron density due to the increasing electron input power fraction of the total input power with frequency [5, 6] and enhance the deposition rate. However, there is not any report on the higher efficiency of the VHF‐PECVD‐based solar cells .
High‐density plasma represented by inductively‐coupled plasma (ICP) has increasingly attracted more interests due to its wide application areas such as microelectronics, display, and solar cells, etc. The prominent advantage of high density of ICP makes it very appropriate for the deposition of Si‐based materials (a‐/μc‐Si:H, silicon carbide, silicon oxide, and silicon nitride), which are widely used in solar cells. Although there are numerous reports on the ICP‐based deposition of these materials, the as‐deposited Si‐based materials with low defect density and excellent interface features are few, not to mention the involved high‐efficiency solar cells. We have been making many efforts on low‐frequency (460 kHz) ICP (LFICP) excitation, characterization, and application in nano‐fabrication  and a wide range of thin films’ synthesis [9, 10]. A discharging photograph of the LFICP facility and its schematic structure are shown in Figure 1(a) and 1(b), respectively. The power of the low‐frequency power generator is coupled into the reactive chamber sealed by a quartz window via a matching/tuning unit to sustain the reactive gases discharge.
In comparison with the conventional CCP source, the LFICP source has several prominent merits as follows [11, 12]: (i) high densities of the plasma species; in particular, the electron number density
High‐quality Si‐based materials have been attained by means of remote‐LFICP:
As‐deposited a‐Si:H exhibits competitive surface passivation ability on crystalline silicon, thanks to the minimized inner and interface defect density ;
Silicon nitride with controlled bandgap due to the excellent dissociation ability of LFICP facility was realized . Meanwhile, the remote‐LFICP‐deposited silicon‐rich a‐SiNx:H displays excellent Si surface passivation (surface recombination velocity of 36 cm/s for low resistivity n‐type Si wafer) .
Remote‐LFICP‐based a‐SiOx:H provides effective surface passivation of low resistivity Si wafer (surface recombination of 70 cm/s obtained) .
The aim of this work is to systematically report the high‐density plasma‐enhanced chemical vapor deposition of device‐grade Si‐based materials by means of LFICP and its solar cell applications. The as‐deposited Si‐based materials will be studied in combination with the LFICP characteristics. Their soar cell applications mainly focus on the Si surface passivation using remote‐LFICP‐CVD‐based Si‐based materials. This article is organized as follows. Section 2 makes a brief introduction on a‐/μc‐Si:H and then focuses on the processing parameters dependent microstructures and properties of the LFICP‐CVD intrinsic and doped a‐/μc‐Si:H thin films. Section 3 focuses on the applications of LFICP‐CVD a‐/μc‐Si:H for c‐Si surface passivation. The influence of the plasma characteristics on the properties of LFICP‐based materials and growing surface properties are intensively investigated.
2. a-/μc-Si:H thin films
Amorphous silicon (a‐Si) is a solid‐state material made of silicon atoms which are arranged in a short‐range order. With the absence of the constraints of periodicity in elemental amorphous silicon, it is difficult for each silicon atom to be linked up with four others. Compared with crystalline silicon (c‐Si), the average bond angles between nearest‐neighboring atoms are distorted. Some bonds are even broken and result in so‐called “dangling bonds”. These two main defects of the lattice of a‐Si:H, i.e., bond distortion and dangling bonds, create large densities of allowed states within the forbidden band gap in such a way that the material cannot be effectively doped N‐ or P‐type and is not electronically useful. However, if the substance is hydrogenated, the hydrogen atoms saturate the dangling bonds and reduce the density of states within the forbidden gap. The bond distortion results in band tails near the valence and conduction bands. In these band tails, the electrons (or holes) are localized in space and do not directly participate in the electronic transport. The deep states near the middle of the band gap results from the non‐passivated dangling bonds. These defect centers are “amphoteric”—there are three charge states, i.e., +e, 0, and –e charges, leading to two levels (transitions between the 0/+ and −/0 charge states). The dangling bonds act as recombination centers for free electrons and holes.
μc‐Si:H is known to be a complex material consisting of crystalline and amorphous silicon phase plus grain boundaries . Figure 2(a) shows a typical transmission electron microscopy (TEM) of μc‐Si:H. Apparent columnar grains are observed. The crystalline growth starts at nucleation centers near the interface between film and substrate. During the competitive growth between the nucleation centers, the diameter of the remaining crystalline increases leading to the cone‐shaped crystallites near the substrate surface . Figure 2(b) displays the microstructure evolution from highly crystal μc‐Si:H to amorphous a‐Si:H. The highly crystal and amorphous structure are described in the left and right margin, respectively. From left to right, the column size decreases and more amorphous phase is introduced between the crystalline grains. This interrupts the columnar crystalline structure in the lateral direction.
Practically, μc‐Si:H is closely related to a‐Si:H, as the deposition technique for both materials is the same. However, the deposition parameters, such as discharge power density, working pressure, substrate temperature, etc., in the RF discharge deposition method, collectively determine the ultimate microstructures of the obtained silicon thin films. CCP‐PECVD is the most widely studied technique for the deposition of a‐/μc‐Si:H films. In this technique, hydrogen‐diluted silane is dissociated by electron impact from the RF field between two parallel plate electrodes to form SiHx radicals and atomic hydrogen. The generated species diffuse/drift to the growing surface. The species and their reaction products are either incorporated into the growing film or are re‐emitted from the surface into the gas phase. The radicals then undergo various secondary reactions during their transport to the substrate.
2.3. a‐/μc‐Si:H by LFICP CVD
Although method of ICP has the advantages over the traditional CCP as demonstrated above, the reports on its applications in silicon thin‐film deposition are not abundant, not to mention the solar cell fabrication. For reference, some main progresses are summarized as follows. Li et al.  used the built‐in one‐turn coil inductance antenna driven by 13.56 MHz RF power to fabricate μc‐Si:H with tunable preferred orientation through controlling the hydrogen dilution. By the similar method with external conductance coil power by the same frequency generator, Shen et al. [26, 27] obtained low defect density ((3 x 1015/cm3) a‐Si:H films, from which a single‐junction a‐Si:H solar cell with energy conversion efficiency of 9.6% was successfully fabricated. The researchers from Hiroshima University realized the high‐rate deposition (up to 4 nm/s) of μc‐Si:H with a low‐level defect density in the year of 2001 [28, 29]. They systematically studied the films’ optoelectronic properties such as the optical band gap, dark and photo conductivity, defect density, crystalline fraction ratio, etc. It seems that as‐deposited silicon films are device grade and fulfill the common requirements for solar cell fabrications. Unfortunately, they have not reported their subsequent achievements in their research. The reports on the application of ICP‐grown silicon thin films in heterojunction solar cells are not available. The only related work on the surface passivation by ICP‐grown a‐Si:H was reported in Ref. , where minority carrier lifetime of 53 μs was obtained on a P‐type silicon substrate (resistivity 1–20 Ωcm) with a 15‐nm‐thick a‐Si:H passivation layer.
For ICP reactor, there are two types of antenna configurations, namely cylindrical and planar. The present LFICP driven by a low frequency of 460 kHz power generator belongs to a planar coil configuration. As mentioned above, high‐density ion region in ICP is not suitable for a‐Si:H thin‐film deposition for silicon surface passivation due to the severe ion bombardment. In order to decrease the ion bombardment, the distance
2.4. Discharge power effect
The a‐Si:H/μc‐Si:H thin films were deposited on the double‐side polished silicon and glass substrates cleaned by standard methods. The sample holder was heated to a temperature of 140 °C monitored by an internally equipped thermal couple. The flux of silane (H2) was kept constant at 5 sccm (20 sccm). The inductive RF discharge power was varied between 1.0–2.5 kW. The thicknesses of all the deposited thin films were measured directly from the cross‐sectional scanning electron microscopy (SEM) image by using a JEOL JSM‐6700F filed emission scanning electron microscope. The deposition rate can be calculated from the thickness divided by deposition duration. FTIR measurements were performed on a Perkin‐Elmer FTIR 1725X spectrometer in the mid‐infrared range from 400 to 4000 cm−1 with an increment of 1 cm−1. The Cary 510 Bio spectrometer (300–1100nm) was used to measure the UV‐VIS transmission spectra.
2.4.1. Optical band gap and deposition rate
The UV‐VIS transmission spectra (shown in Figure 3(a)) of the thin films deposited on glass at different RF powers were measured to extract the parameter of optical band gap
Another feature of the present films is the higher optical band gap
Although it was recognized that the Tauc method will lead to a larger value for
2.4.2. Raman scattering and crystallinity of the thin films
The micro‐Raman scattering experiments were performed to estimate the crystal phase information in the thin films. The obtained spectra are displayed in Figure 4(a). It was observed that the dominant peak gradually shifts from (480 to (520 cm−1 through a mixed phase state at the power of 1.8 kW. This change reflects phase evolution from completely amorphous to highly crystal with an applied RF power in the films. In fact, the crystallinity value can be estimated by using different methods described in Ref. . In this work, the method based on Gaussian line fitting  is used, where
2.4.3. FTIR and hydrogen content in the thin films
The FTIR spectra of the thin films deposited with various RF power are shown in Figure 5(a). Within a wavenumber range of 500–2300 cm−1, three Si‐H bond‐related bands were observed. The first one, located at around 640 cm−1 was unambiguously attributed to Si‐H rocking/wagging mode. Its exact location gradually changed from 644 to 630 cm−1 with increasing RF power as displayed in Figure 5(b) (the filled circles). This is also correlated to the phase evolution from amorphous to crystal silicon . The second one comprising of two sub‐peaks located at 845 and 890 cm−1 were identified as the bending mode of dihydrides SiH2 . The third one at the region of (2100 cm−1 is recognized as the SiH
where the oscillator strength
2.5. Hydrogen dilution effect
Hydrogen in the deposited films originates from the diluent hydrogen gas and hydrogen atom bonded in silane molecules. From the point view of the deposition process, hydrogen facilitates the dissociation of silane through increasing the ion/electron impact, influences the surface energy of the growing surface via terminating the surface silicon atom, and etches the growing surface. Therefore, the hydrogen dilution should have a substantial effect on the microstructures of the ultimate silicon thin films. In this set, the RF discharge power and substrate are fixed at 1.5 kW and 140 °C, respectively. The total flow rate of SiH4 and H2 is kept at 20 sccm. The respective flow rate of SiH4 and H2 are changed with varying dilution ratio [H2]/[SiH4] = 0, 0.25, 0.5, 1, 2, 3, and 4. The working pressure in the deposition chamber is kept at 7.2 Pa.
Figure 6 shows the average deposition rate and
Figure 7 shows the extract waging/rocking vibration mode. With a small amount of hydrogen introduction (H2/SiH4 = 0.25), the hydrogen content CH increases from 26.3 to 27.5% and the wagging/rocking mode location shifts from 649 to 644 cm−1. CH drastically drops to 24.4% at a dilution ratio of 0.5. The values of CH and the location of wagging/rocking mode are comparably steady in the dilution range of 0.5–2. Beyond 2, CH decreases drastically to 12.2% and the mode location shifts to 631 cm−1 at a ratio of 4. The location shift to the small wavenumber side with increasing dilution ratios implies the phase evolution to the crystalline orientation.
In view of the above experimental results, hydrogen dilution in LFICP method is also a key parameter influencing the hydrogen content CH in the films. However, its effect on the crystallinity of the films is less pronounced than that of the discharge power.
2.6. Working pressure effect
One of the inherent features of LFICP is low working pressure up to several tens of Pa. In this section, the working pressure is altered in the range (1–19Pa) enabling a stable discharge. The discharged power was kept at 2.5 kW. No external heating was applied to the substrate. The flow rate of SiH4 and H2 are 12.5 sccm. The Raman scattering experiments revealed the amorphous structure of these films. Figure 8 displays the working pressure‐dependent
Figure 9(a) shows the FTIR absorbance spectra of these films. The intensity of the waging/rocking mode becomes weaker with increasing work pressure, indicating the effusion of the bonded hydrogen with increase in the working pressure. The detailed hydrogen content as a function of working pressure is shown in Figure 9(b). The hydrogen content was reduced about 20% when the working pressure is increased from 1 to 19 Pa. The location of this mode experiences a slight shift to higher wavenumbers with working pressure, which implies an amorphous phase change. It is well known that an increase in the gas pressure enhances the collisions in the plasma and reduces the electron and ion energies, and hence decreases the crystallinity.
It is worth noting that the stretching mode also decreases considerably with increasing working pressure. Assuming the stretching mode corresponds to SiH‐associated peak at 2000 cm−1 and the SiH2‐associated peak at 2100 cm−1, we will note the severe decrease of SiH2 fraction in this mode. This should be responsible for the reduced hydrogen content in the a‐Si:H films.
In summary, the working pressure substantially influences the optical band gap
2.7. Effect of substrate temperature
The substrate temperature substantially affects the plasma species diffusion on the surface and nucleation process, and hence the properties of the resulting a‐/μc‐Si:H thin films. In this set, the feed gas flow rate ratio is SiH4/H2 =5:20 (in sccm) and the discharge power is 2.0 kW. The substrate temperature is varied in the range of 27–150 °C. Figure 10 shows the temperature‐dependent deposition rate and
Figure 11 shows the substrate temperature‐dependent Raman spectra. The obtained films are highly crystalline under the present deposition conditions. The elevated substrate temperature results in the enhanced intensity of the 520 cm−1 peak, and thus more order structure in the films.
The wagging/rocking mode in FTIR transmission spectra provides the bonded hydrogen numbers information which is displayed in Figure 12. The bonded hydrogen content CH is very sensitive to the substrate temperature, decreasing by about 21% with substrate temperature from room temperature to 150 °C.
2.8. Effect of antenna‐substrate distance
In the axial direction, the plasma properties should be dependent on the antenna‐substrate distance
Figure 15 shows the evolution of FTIR absorbance spectra with respect to the distance
2.9. Doped a‐/μc‐Si:H films by LFICP CVD
In this section, the process parameters‐dependent microstructure and electrical properties of the n‐ and p‐doped a‐/μc‐Si:H films are studied to evaluate the doping ability of LFICP. Doping of a‐Si:H by PECVD was first demonstrated by Spear and Le Comber in Ref. . The disordered structure of a‐Si:H was supposed to allow the incorporation of dopant into the amorphous network, thus impeding the doping of the material. Subsequently, the underlying doping mechanism of a‐Si:H was further clarified by Street . Nevertheless, the doping efficiency of a‐Si:H (<1%) as a disordered material is much lower than in crystalline silicon .
Here, the feed gas silane is pure without hydrogen pre‐dilution. The n‐type dopant resource gas phosphine (PH3) and p‐type dopant resource gas diborane (B2H6) both were H2‐diluted to a 15% concentration. In the following discussions, the gas consumptions are directly denoted as the nominal flow rate. It was found that the antenna‐substrate distance
Different‐flux phosphine gas was introduced into the feed gases of SiH4:H2 = 6:60 (in sccm) discharged by RF power of 3 kW with substrate temperature of 100 °C. Figure 17(a) shows the electrical parameters (from Hall effect measurement using the Ecopia HMS‐3000 system) of as‐deposited p‐doped a‐/μc‐Si:H films. The hole density
It is found that the doping is strongly dependent on the deposition temperature. Increasing substrate temperature improves the conductivity of the deposited films. Figure 18(a) shows the electrical properties of the doped a‐/μc‐Si:H films deposited in the substrate temperature range of 100–200 °C. The flux of B2H6 is kept at 0.4 sccm. The increased temperature facilitates the activation of the dopant in the film leading to the improvement in the hole density and degraded mobility. The resulting conductivity
It seems that the n‐doping is more difficult than p‐doping in the case of higher antenna‐substrate distance. Herein, the substrate temperature ranges from 100–200 °C, PH3 flux covers the range of 0.5–1.0 sccm, and the feed gas ratio SiH4:H2 is changed from 5:40 to 5:60 (in sccm). The discharge power is set at 2.75 kW. Figure 19 shows the Raman scattering spectra of the a‐/μc‐Si:H films n‐doped by different PH3 flux. The microstructure change with the PH3 introduction is not as monotonic as shown in Figure 17 associated with the case of B2H6. Table 1 presents the deposition parameters and associated electrical properties of the obtained n‐doped a‐/μc‐Si films. At PH3 flux of 0.5 and 0.62 sccm (100 °C), the electron density
Figure 20 shows the n‐doped a‐/μc‐Si:H films deposited with different hydrogen dilution ratio. Up to the ratio of SiH4/H2 = 5:50, the film is a completely amorphous network impeding the doping behavior. The structure turns into microcrystalline at the ratio of SiH4/H2 = 5:60, where the better conductivity can be obtained in present experiments.
Figure 21 shows a typical top view (a) and cross‐sectional (b) SEM image of a n‐doped μc‐Si:H film deposited at a temperature of 200 °C and dilution ratio of H2:SiH4 = 60:5. Nanostructured Si particles are uniformly distributed on the surface in Figure 21(a). There are no any observable voids or apparent defects. The apparent column growth is observed in Figure 21(b). The interface between the film and the Si substrate is clear and free of incubation layer.
3. c‐Si surface passivation by LFICP CVD a‐/μc‐Si:H
In Sections 1–2, the intrinsic and doped a‐/μc‐Si:H films based on LFICP‐CVD method are studied in terms of the plasma parameters. The optical band gap, bond configuration, microstructure, and hydrogen content in the films are dependent on the deposition parameters of RF power, gas ratio, working pressure, and substrate temperature. In particular, the properties of the LFICP‐grown a‐/μc‐Si:H films are sensitive to the antenna‐substrate distance
In this section, the crystalline silicon surface passivation by LFICP‐CVD a‐/μc‐Si:H is investigated. In terms of the antenna‐substrate distance
3.1. Recombination and passivation in Si‐based solar cells
Usually, the loss in photovoltaic solar cell comprises surface light loss, the transmitted light loss, thermalization loss (thermal electron loss). In a practical heterojunction (HJ) silicon solar cell, the a‐/μc‐Si:H layer is of several nanometers thick, which marginally absorbs sunlight. The photogeneration of excess charge carrier pairs mainly occur in the bulk c‐Si. In order to efficiently collect the photogenerated carriers which can be extracted and thus contribute to the externally retrievable current, reducing the carrier recombination in silicon, especially on the surface, is particularly important.
The carrier recombination originating from bulk silicon primarily comprises two types, i.e., the intrinsic and extrinsic ones. The intrinsic recombination, which mainly includes radiative  and Auger recombination , occurs in a pure and defect‐free semiconductor, while the extrinsic recombination stems from contaminants and defects which act as recombination centers.
Total bulk recombination is the sum of the above three terms and is expressed as
Surface recombination is a special case of SRH recombination due to the localized states appearing at the surface. Different from the bulk SRH centers, these states usually form a set of states across the band gap instead of a single energy level. Surface recombination is usually evaluated in terms of surface recombination velocity (SRV) instead of lifetime. However, the principles are same to bulk SRH recombination. It mainly originates from the surface dangling bond, i.e., the missing of crystalline network. The chemically and mechanically created defect can also result in surface recombination. In a simple condition with a constant bulk lifetime
High carrier lifetime is a critical issue in achieving high‐energy conversion efficiency in solar cells. There are many techniques that have been developed over the past two decades with the objective of measuring minority carrier lifetime in Si . Two techniques, namely the transient photoconductance decay (TPCD) and the more recent quasi‐steady‐state photoconductance method (QSSPC), are the basis of the WCT‐120 tester, which are widely used in this work to characterize the solar cell precursors.
Compared with the optical management by conventional methods like an antireflection layer, the minimization of electronic losses at the crystal silicon surface is a more delicate challenge for high‐efficiency solar cell . Recombination losses at silicon interface or surface can be minimized by using two passivation schemes, namely, via chemical passivation or filed passivation. The former aims to reduce the interface defects that originate from the dangling bonds by H atom, a thin dielectric, or semiconductor film. The latter is based on the fact that the electron/hole density at the interface will be significantly reduced by formation of a built‐in potential from the introduction of a passivation layer. Based on these two strategies, various Si‐based materials, such as hydrogenated amorphous silicon (a‐Si:H) , silicon nitride (SiN) , thermal oxygenated silicon dioxide (SiO2) , and amorphous silicon carbide (a‐SiCx)  have been investigated for passivation purposes. Among these materials, a‐Si:H is still the best candidate for silicon heterojunction solar cells [56, 57] due to its excellent passivation properties obtained at low deposition temperatures, and also simple processing without the introduction of any atoms other than silicon and hydrogen.
The a‐Si:H (including SiOx, SiNx and SiCx) passivation layers were mainly deposited by using conventional CCP‐PECVD or hot wire chemical vapor deposition (HWCVD) in literatures. A detailed review of c‐Si surface passivation can be found in Refs.  and , where the millisecond level lifetime and below tens cm/s surface recombination velocity prevails. Schmidt et al.  used a‐Si1−
However, the ICP‐grown a‐Si:H for c‐Si surface passivation is rarely reported , not to mention that grown by LFICP.
3.2. c‐Si surface passivation by semi‐remote LFICP CVD a‐/μc‐Si:H
It was found that a‐/μc‐Si films deposited at direct LFICP region (with an antenna‐substrate distance
3.2.1. Passivation effect of a‐/μc‐Si:H deposited from hydrogen‐diluted silane
In this subsection, a‐/μc‐Si:H films deposited from only hydrogen‐diluted silane at the antenna‐substrate distance of
The a‐/μc‐Si:H thin films of thickness of 50 nm were deposited on the double‐side polished, p‐type CZ Si (comparatively higher resistivity of 8 Ωcm, thickness of 600 μm, (100) orientation, and area of about 3 × 3 cm2). The pre‐deposition hydrogen plasma treatment on the substrates was applied for various durations to investigate the effect of hydrogen plasma exposure on the surface recombination. The microstructures and properties of the thicker counterpart of the thin passivation layer were studied in Section 2.1. The effective minority carrier lifetime of the symmetrically passivated wafer was measured by using the quasi‐steady state photoconductance decay (QSSPCD) technique on the facility of WCT‐120.
220.127.116.11. Effect of pre‐deposition H2 plasma treatment on surface passivation
Prior to the passivation layer deposition, the substrates were treated by H2 plasma for different durations (0–90 s) to improve the interface properties. The final structure for the minority carrier lifetime measurement is shown in inset of Figure 22. All the specific minority carrier lifetimes were recorded at an excess carrier of 1015/cm3.
τeff values are plotted in Figure 23 as a function of H2 plasma treatment time. τeff is 127 μs without H2 plasma treatment. An intermediate treatment time (30–60 s) is beneficial to silicon surface passivation, which is evidenced by the improved lifetime value. However, overlong treatment (>60 s) is detrimental to the surface quality, resulting in a less lifetime value of 73 μs. The maximum value of carrier lifetime ∼230 μs was obtained at a time of 30 s.
18.104.22.168. Influence of RF power on surface passivation
The RF power‐dependent effective lifetime τeff is shown in Figure 22 (filled squares). This curve can be separated into three stages: In the first stage (1.0–1.5 kW), τeff decreases from 67 to 42 μs; in the second stage (1.5–2.0 kW), τeff rapidly increases from 42 μs to its maximum of 234 μs; in the third stage (2.0–2.5 kW) τeff drops down to 129 μs. The observed pattern of τeff will be explained in terms of the properties of the thin films and the interface between the thin film and silicon substrate.
The passivation effect described by τeff is not only related to the deposited thin films itself but also the a‐Si:H/c‐Si interface quality. The low defect density in the thin films is presumably a consequence of hydrogen passivation. As mentioned above, the hydrogen content in these thin films is comparatively larger. However, in the current experiments, the maximum value of τeff is obtained at RF power of 2.0 kW, where the corresponding thin film contains the least hydrogen as shown in Figure 5. Therefore, the change of lifetime τeff should not simply be attributed to the change of hydrogen content with the RF power.
Another crucial mechanism to determine the passivation effect is the interface defect between the passivation layer and the substrate. It has been observed that during the deposition of a μc‐Si:H layer on top of a substrate, a 30–50 nm thick interlayer referred as incubation zone  is produced. Its crystallinity and thickness strongly depend on the deposition condition and the substrate material. In our experiments, the incubation layer was directly observed in the high‐magnification cross‐sectional SEM images of the deposited thin films on double‐side‐polished Si substrate. Figure 24 shows the high‐magnification cross‐sectional SEM images of the thin films deposited at the power of 1.2 (a), 1.5 (b), 1.8 (c) and 2.0 kW (d). The clear scratches and cracks come from the cross‐section preparation process. Except the sample deposited at 2.0 kW, evident incubation layers were observed between the crystal Si and the films. Furthermore, the thickness of the incubation layers can be determined from the SEM measurement tool by making measurement multiple times at different locations and the results as a function of RF power are plotted in Figure 22 (the open squares). The error bars shown in Figure 22 represent the standard deviations from the mean thickness values from the multiple metering. At a power of 1.5 kW, the thickness has a maximum of 80 ′ 7 nm (>the standard passivation layer thickness of 50 nm), while the lifetime has a minimum of 42 μs. No evident incubation layer was observed at the power of 2.0 kW, at which the greatest minority lifetime value was obtained. Linking the curve of incubation layer thickness with that of the lifetime, one will find that the incubation layer thickness changes with the RF power in an opposite way to the minority carrier lifetime τeff dose. This observation suggests the fact that the incubation layer on the interface between the passivation layer and the crystal Si will worsen the passivation effect of the a‐/μc‐Si:H thin films.
The CVD deposition of Si thin films involves a complex combination of several processes including the arrival and removal of gas molecules or precursors at the substrate surface, the decomposition into reactive species, and the migration of these species on the surface where they can lead to nucleation and continued deposition . The adsorbed reactive species are likely to come to rest when a position of minimum energy position is found. The minimum energy position can be a defect at the substrate surface, which will result in a new nucleus, or an existing nucleus . At certain process conditions, the formation of nuclei will be delayed for some time known as the incubation time . From the point view of the growth mechanism, the incubation layer (initial growth) will be rich of defects, which will lead to the intense recombination of the photon‐induced carriers and thus a decreasing lifetime value observed in Figure 22.
22.214.171.124. Influence of thermal annealing on surface passivation
In order to investigate the influence of the post‐deposition annealing on the silicon surface, the samples were thermally annealed in vacuum and H2 flow atmosphere. For simplicity, one sample with an as‐deposited lifetime value of 196 μs was annealed just in vacuum in the temperature range of 230–500 °C. Figure 25(a) shows the evolution of lifetime τeff with annealing temperatures. The annealing duration at each temperature point is 30 min. One can see that the lifetime increases almost linearly in the range of 230–420 °C. Further increasing of temperature to 500 °C results in a significant decrease in lifetime value. The relatively low temperature (<500 °C) annealing in vacuum leads to the lifetime improvement by a factor of about 2.5. The corresponding FTIR transmission spectra of the sample before and after thermal annealing were measured in the wavenumber range of 550–950 cm−1 to clarify the H role in the surface passivation. The spectra of the as-deposited and the 420 and 500 °C annealed samples are shown in Figure 25(b). The Si‐H wagging/rocking mode at about 630 cm−1 slightly changes with temperature increasing from 230 to 420 °C. In comparison, this mode considerably recedes when temperature is increased from 420 to 500 °C, which is indicative of lower hydrogen content after annealing. The mode around 850–900 cm−1 also becomes weak after annealing at a temperature of 420 and 500 °C.
The vacuum annealing results discussed above represent the important role of the hydrogen atom in the Si surface passivation. Low‐temperature (<420 °C) annealing enables the diffusion of hydrogen in the thin film towards the Si substrate, which effectively reduces the dangling bond density at the interface and enhances the minority carrier lifetime. At higher temperatures (>420 °C), hydrogen atom effuses leading to the re‐generation of the dangling bonds and thus a decrease in the lifetime value. Systematic annealing experiments were performed on the samples deposited at different RF powers, and the ultimate lifetime values (not shown here) presented the same trend with that of the as‐deposited samples shown in Figure 22 (filled squares). These results show that the as‐deposited interface features, especially the incubation layer properties discussed above, are the crucial factors in determining the ultimate lifetime values in our case. Therefore, we will focus on the sample with the highest as‐deposited lifetime value. It is worth stressing that the ultimate lifetime value is dependent on the annealing circumstance. Figure 26 exhibits the lifetime value evolution with annealing time at 420 °C in vacuum (filled squares), H2 flow (filled circles), and N2 flow. In the case of vacuum annealing, the lifetime value increases sharply in the 95 min and saturates at the value of 421 μs at about 185 min. On the contrary, the lifetime reaches the maximum of 524 μs in a short time of 11 min in the case of H2 flow. It seems that the presence of hydrogen in the annealing circumstance is essential to improve surface passivation by present a‐Si:H/μc‐Si:H thin films, despite the presence of rich hydrogen in the film as evidenced by the FTIR result. With N2 flow, lifetime reaches its maximum value of 425 μs in 5 min, followed by a drastic drop for time longer than 5 mins. The H2 preference is confirmed by multiple annealing experiments. It is well known that N2 is the commonly used protective gas for post‐deposition annealing of passivation layer a‐Si. But H2 circumstance annealing is indeed better than N2 in our experiments. The underlying mechanism needs a further study to clarify.
126.96.36.199. Injection level‐dependent surface recombination
The effective minority carrier lifetime τeff is related to the effective surface recombination velocity
188.8.131.52. The high as‐deposited lifetime values in the case of semi‐remote LFICP
The present as‐deposited lifetime value of 234 μs is much higher than that reported in literatures, where PECVD or HWCD methods were used to deposit the passivation a‐/μc‐Si‐H layer. Jan‐Willem et al.  summarized the passivation effects of a‐Si:H deposited by various methods: 34 μs for PECVD, 43 μs for VHF PECVD, and 87 μs for HWCVD. In principle, passivation can be physically divided into two types, i.e., hydrogen‐related chemical passivation and built‐in potential related field passivation. In the former, defect density can be remarkably lowered due to the reduced number of dangling bonds which is terminated by hydrogen atoms. With regard to the filed passivation, a‐/μc‐Si:H has a wider band gap than crystal silicon substrate, which results in a barrier on the interface preventing the recombination of photogenerated carrier pairs through the surface/interface defects.
It has been shown that the pre‐deposition hydrogen plasma exposure significantly influences the surface passivation (see Figure 23). In the post‐deposition annealing, the interaction between hydrogen atom from the passivation layer and the c‐Si substrate is crucial to the surface passivation. Mitchell et al.  studied the thermal activation of the hydrogen‐related chemical passivation on silicon substrate and determined the thermal activation energy of
184.108.40.206. Incubation layer and its thickness control
Figure 28(a) [(b)] shows a low‐ (high‐) magnification cross‐sectional TEM micrograph of LFICP‐grown μc‐Si:H on silicon substrate. In Figure 28(a), a clear incubation layer (dark area) between the film and substrate is discriminated like in SEM images. Figure 28(b) exhibits more details of the interface. The grey area in the film corresponds to the microcrystalline Si fractions, which are conical conglomerates of microcrystals. As observed above, the incubation layer is detrimental for the improvement of lifetime and its thickness is highly dependent on the process parameters, e.g., the applied RF power in present experiments. Therefore, a deep understanding on the mechanism to control the formation of incubation layer is extremely important. It was recognized that the ion bombardment played a crucial role in the formation of incubation layer . The ion beam works in two possible ways, namely (i) a surface effect: very small grains do not survive the high dose of ion irradiation, thereby reducing the nucleation rate, (ii) a bulk effect: the ion beam induces defect‐related grains growth. Accordingly, two strategies  to control the ion beam were proposed: the choice of the frequency of the power source generating the plasma, and the design of the electrode configuration to avoid its formation. In present antenna‐substrate distance
From the point of view of a growth mechanism, the key to diminish the initial growth of incubation layer seems to be the rapid nucleation without retard on the interface. In present experiment, this occurs at the power of 2.0 kW, near the transition point (1.8 kW) from a‐Si:H to μc‐Si:H. This is consistent with some authors’ findings that the good passivation effect is obtained with microcrystalline‐oriented passivation layers, where the depletion fraction of SiH4 is comparatively higher than that of amorphous regimes [52, 68]. In the current study, although the silane depletion was not experimentally measured at certain RF power, the high depletion fraction at the power of 2.0 kW is expected. The detailed relation between the depletion fraction and the incubation time in the growth of a‐/μc‐Si:H needs to be further clarified.
220.127.116.11. Passivation of low resistivity c‐Si
It is more difficult to passivate a lower‐resistivity Si surface due to the defect associated with more recombination. However, the lower‐resistivity wafer is more meaningful in practical solar cell application. In this part, two types of wafers have been investigated: p‐type (100), 2 Ωcm, and n‐type (100), 3 Ωcm wafers. The process parameters such as discharge power, substrate temperature, dilution ratio, and post‐deposition annealing have been widely explored to improve their surface passivation. Figure 29 shows the effective minority carrier lifetime τeff in the n‐type 3 Ωcm c‐Si passivated with a‐Si:H deposited at different substrate temperatures. τeff drastically drops from 164 μs to 25 μs with increasing substrate temperature from room temperature to 140 °C. This is possibly originated from the local epitaxial growth or reduced hydrogen content with increasing temperature.
Figure 30 displays τeff in both types c‐Si passivated by a‐Si:H deposited from hydrogen‐diluted silane with different dilution ratios (H2/SiH4). The discharge power and substrate temperature were kept at 2.0 kW and room temperature, respectively. The flow rate of SiH4 and H2 is 20:0, 12.5:12.5, 8.3:16.7, 5:20, corresponding to the hydrogen dilution ratio of 0, 1, 2, and 4, respectively. τeff reaches its maximum values at the dilution ratio of 1 in both p‐ and n‐type c‐Si. Based on the above analysis on passivation, the higher depletion of silane and reduced incubation layer are expected. Figure 31 shows the discharge power‐dependent lifetime values, which reached its maximum at RF power of 2.5 kW. Above 2.5 kW, τeff begins to drop again.
The optimized lifetime results of these two types of low‐resistivity c‐Si have been shown in Figure 32. At the specific excess carrier density of 1015/cm3, the lifetime value is 305 and 150 μs for the n‐type 3 Ωcm and p‐type 2 Ωcm c‐Si, respectively. It should be noted that these results are as‐deposited values without post‐deposition annealing. Unfortunately, post‐deposition annealing cannot improve the lifetime values anymore in the present low‐resistivity c‐Si substrates. The hydrogen chemical annealing mentioned above has already raised the lifetime values to its maximum during the deposition process.
Although the as‐deposited values without post‐deposition long time annealing are much bigger than that reported in references, the present lifetime values are still lower than the ms level results in the literatures. The plasma density in the growth region has already been reduced a lot by increasing the antenna‐substrate distance
3.2.2. Introduction of CO2 into the reactive gas
a‐Si:H is easy for (partially) epitaxial growth on c‐Si even at low deposition temperatures, which will severely reduce the carrier lifetime values and thus the photovoltaic performance of HJ solar cell . Incorporation of O into the amorphous silicon network can effectively suppress the epitaxial growth . In the aspect of optics, the inherent blue light loss in a‐Si:H layer also restricts the solar cell optimization. As a consequence, wide‐banded Si‐based materials become a promising candidate. Thermally grown SiO2 provides a state‐of‐art level of surface passivation with a reduced surface recombination velocity as low as 2 cm/s . However, the thermally grown SiO2 suffers from the inherent disadvantages such as extremely high process temperature ((1000 °C) and low deposition rate. As a consequence, non‐stoichiometric silicon oxide (SiO
In this section, CO2 is introduced into the reactive gases of SiH4+H2 and efficiently dissociated in the LFICP system. The discharge power is set at 1.8 kW, flow rate of both SiH4 and H2 are 12.5 sccm, and no external heating is applied to the substrate. Various flow rates of CO2 are introduced into the deposition chamber. The microstructure evolution with the introduction of CO2 in the obtained films is investigated. Two types of c‐Si wafers: n‐type, 3 Ωcm and p‐type, 2 Ωcm, are passivated by these films. The underlying passivation mechanism is analyzed.
Figure 33 shows
Figure 34 shows the FTIR absorbance spectra of the corresponding films. Besides the Si‐H waging/rocking signal ((640 cm−1) and Si‐H stretching signal ((2100 cm−1) usually observed in a‐Si:H, some oxygen and carbon‐associated modes appear. The Si‐C stretching mode, which couples with the doublet signal of (SiH2)
About 60 nm thick SiC1−
In order to clarify the passivation mechanism for the LFICP‐grown SiC1−
3.3. c‐Si surface passivation by remote LFICP CVD a‐Si:H
In subsection 3.2.2, reactive gas CO2 was introduced into SiH4+H2 to improve the c‐Si surface passivation. The introduction of CO2 can widen the optical band gap of the passivation layer, and simultaneously suppress the partial epitaxial growth of the passivation layer on c‐Si. The passivated sample exhibits high as‐deposited lifetime values, whereas the lifetime values cannot be enhanced effectively after post‐deposition annealing. It is believed that the frequent ion bombardment from the high‐density plasma should be responsible for these two effects: it conveys energy to the growing surface acting as plasma annealing, and possibly results in damages to the interface. The damaged interface will define the hydrogen diffusion to the interface when annealing and results in a limited enhancement in lifetime. One possible solution is to keep the substrate away from the plasma generation space. In this section, the antenna‐substrate distance
Figure 38 shows the lifetime τeff curves before and after the thermal annealing in 275 °C for different durations. In Figure 38(a), the as‐deposited τeff value is 3 μs, and τeff surges upon annealing. The similar behavior is observed in the case of the n‐type 4 Ωcm c‐Si. The saturation values of 295 and 716 μs are achieved in p‐type 1 Ωcm and p‐type 4 Ωcm c‐Si, respectively. The lifetime values τeff reaches their maximums at annealing duration of 45 min. The present annealing behavior is different from that in the case of antenna‐substrate distance
In a narrow tunable working pressure range, we have compared the lifetime curve of the passivated samples under different pressures. Figure 39 shows the comparison between the two discharge pressures of 0.2 and 1.0 Pa. The lifetime values are measured in the passivated c‐Si substrates (n‐type 4 Ωcm) before and after the thermal annealing treatment. The as‐deposited lifetime values at 0.2 Pa are much greater than that at 1.0 Pa. Nevertheless, the vice verse is true after the thermal annealing. As mentioned above, a higher pressure means a smaller mean free path of the particles and a higher deposition rate. A faster growth can minimize the partial epitaxial growth of a‐Si:H on c‐Si surface. In addition, the lower‐pressure mode possibly still causes some surface defects which limit the beneficial effect of thermal annealing.
Figure 40 shows the lifetime curves in two types of c‐Si substrates passivated by a‐Si:H deposited under two temperature points of RT and 140 °C. For the p‐type 2 Ωcm c‐Si substrate, substrate temperature does not strongly influence the lifetime curve. In comparison, increasing temperature from RT to 140 °C deteriorates the lifetime value severely in n‐type 4 Ωcm c‐Si substrate. This difference is possibly from the different conductivity values which strongly influence temperature‐dependent hydrogen diffusion on the surface or at the interface. The detailed mechanism needs further study to clarify.
Figure 41 shows the best lifetime results we obtained in three types of c‐Si substrates. At the excess carrier density of 1015/cm3, the best lifetime values are 1.3 ms, 620 μs, and 290 μs for the n‐type 4 Ωcm, p‐type 2 Ωcm, and p‐type 1 Ωcm c‐Si substrates, respectively.
3.4. c‐Si passivation by stack configuration and implied
It is well known that the passivation effect is strongly dependent on the passivation layer thickness. In a practical HIT solar cell, the total thickness of deposited functional layer on one side is several tens of nanometers, less than the commonly used thickness of 50 nm in passivation studies. In addition, in a practical HIT solar cell, the passivation configuration is a stack of intrinsic and doped a‐Si:H layers instead of above only intrinsic layer. Therefore, it is important to study the stack layer passivation configuration for the HIT solar cell applications. The passivation effect associated open‐circuit voltage, namely, the implied
Intrinsic and doped a‐Si:H films were symmetrically deposited on the p‐type 1 Ωcm c‐Si substrates to form the passivation configurations of n/i/P‐c‐Si/i/n or p/i/P‐c‐Si/i/p. This stack passivation scheme combines the chemical passivation (by intrinsic a‐Si:H) and the field passivation (by doped a‐Si:H). As an example, Figure 42 shows the field passivation by p‐a‐Si:H in (a) and the combination of both passivation mechanisms in (b). Addition of a p‐doped layer introduces an additional electrical filed to hinder the minority diffusion to the surface. The barrier ФBSF exponentially reduces the concentration of minority at the interface and thus the surface recombination. In Figure 42(b), the interface defect density is reduced by the chemical passivation of addition of an intrinsic layer. Then, the solar cell precursor with the structure of n/i/P/i/p was fabricated to estimate the lifetime values. In these structures, the intrinsic and doped layer thicknesses are about 5 and 15 nm, respectively, estimated from the average deposition rate at corresponding deposition conditions. Figure 43 shows the lifetime curves in different passivation configurations. Lifetime value τeff in p/i/P/i/p is much lower than that in n/i/P/i/n. It is reported that B dopant is prone to react with Si atom to form complex, increasing the interface defect density .
The relation between
As a low‐temperature plasma source, LFICP has the inherent advantages of high‐density plasma, low sheath potential, and low electron temperature, etc., which deserves an excellent CVD route. In LFICP CVD, the parameters of the RF power, hydrogen dilution, working pressure, and substrate temperature significantly influence the microstructures and properties of the films. The ion bombardment on the growing surface in LFICP CVD can be effectively controlled by the parameter of antenna‐substrate distance
The passivation effects of LFICP CVD Si‐based materials are strongly dependent on the plasma configuration. In a region not far away the plasma generation area (semi‐remote LFICP), the passivated c‐Si shows a high as‐deposited carrier lifetime due to the hydrogen‐related chemical annealing during the deposition process. However, the additional thermal annealing does not lead to a considerable increase in the lifetime value. The addition of CO2 into the reactive gases substantially influences the microstructure of the obtained thin films and improves the interface quality. In the region far away from plasma generation region (with a high antenna‐substrate distance, remote‐LFICP), a‐Si:H passivated c‐Si shows a low as‐deposited and a high post‐deposition annealing lifetime value. The highest lifetime value of 1.3 ms after thermal annealing is obtained in passivated 4 Ωcm c‐Si substrate. After being passivated by the device‐like scheme of undoped/doped silicon film stack, p‐type substrate (1 Ωcm, 300 μm) shows an implied open voltage of 670 mV.
This work was jointly supported by AcRF Tier1 (No. RP 6/13 XS), A*STAR, Singapore, and the National Science Foundation of China (Grant No. 51302028 and 61404061).
Panasonic HIT Solar Cell Achieves World's Highest Energy Conversion Efficiency of 25.6% at Research Level Internet] 2014. Available from: http://news.panasonic.com/press/news/official.data/data.dir/2014/04/en140410‐4/en140410‐4.html
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