1. Introduction
Graphene exhibits unique electrical properties and offers substantial potential as building blocks of nanodevices owing to its unique two-dimensional structure (Geim et al., 2007; Geim et al., 2009; Ihn et al., 2010). Besides being a promising candidate for high performance electronic devices, graphene may also be used in the field of quantum computation, which involves exploration of the extra degrees of freedom provided by electron spin, in addition to those due to electron charge. During the past few years, significant progress has been achieved in implementation of electron spin qubits in semiconductor quantum dots (Hanson et al., 2007; Hanson et al., 2008). To realize quantum computation, the effects of interactions between qubits and their environment must be minimized (Fischer et al., 2009). Because of the weak spin-orbit coupling and largely eliminated hyperfine interaction in graphene, it is highly desirable to coherently control the spin degree of freedom in graphene nanostructures for quantum computation (Trauzettel et al., 2007; Guo et al., 2009). However, the low energy quasiparticles in single layer grapheme behave as massless Dirac fermions (Geim et al., 2007; Geim et al., 2009), and the relativistic Klein tunneling effect leads to the fact that it is hard to confine electrons within a small region to form quantum dot in graphene using traditional electrostatical gates (Ihn et al., 2010; Trauzettel et al., 2007). It is now possible to etch a grapheme flake into nano-constrictions in size, which can obtain electron bound states and thus act as quantum dots. As a result, usually a diamond-like characteristic of suppressed conductance consisting of a number of sub-diamonds is clearly seen (Stampfer et al., 2009; Gallagher et al., 2010), indicating that charge transport in the single graphene quantum dot device may be described by the model of multiple graphene quantum dots in series along the nanoribbon. The formation of multiple quantum dot structures in the nanoribbons may be attributed to edge roughness or local potential. The rough edges also lift the valley degeneracy, which could suppress the exchange coupling between spins in the grapheme quantum dots (Trauzettel et al., 2007; Ponomarenko et al., 2008). Recently, there was a striking advance on experimental production of graphene single (Ponomarenko et al., 2008; Stampfer et al., 2008a; Stampfer et al., 2008 b; Schenz et al., 2009; Wang et al., 2010; Guttinger et al., 2011) or double quantum dots (Molitor et al., 2009; Molitor et al., 2010; Liu et al., 2010; Wang et al., 2011a; Volk et al., 2011; Wang et al., 2012;) which is an important first step towards such promise.
In this chapter, we introduce the design and fabrication of etched gate tunable single and double quantum dots in single-layer and bilayer graphene and present several important quantum transport measurements in these systems. A quantum dot with an integrated charge sensor is becoming a common architecture for a spin or charge based solid state qubit. To implement such a structure in graphene, we have fabricated a twin-dot structure in which the larger QD serves as a single electron transistor (SET) to read out the charge state of the nearby gate controlled small QD. A high SET sensitivity allowed us to probe Coulomb charging as well as excited state spectra of the QD, even in the regime where the current through the QD is too small to be measured by conventional transport means (Wang et al., 2010; Wang et al., 2011b). We also have measured quantum transport properties of gates controlled parallel-coupled double quantum dots (PDQD) and series-coupled double quantum dots (SDQD) device on both single layer and bilayer graphene (Wang et al., 2011a; Wang et al., 2012). The inter-dot coupling strength can be effectively tuned from weak to strong by in-plane plunger gates. All the relevant energy scales and parameters can be extracted from the honeycomb charge stability diagrams. We precisely extract a large inter-dot tunnel coupling strength for the series-coupled quantum dots (SDQD) allowing for the observation of tunnel-coupled molecular states extending over the whole double dot. The present method of designing and fabricating graphene QD is demonstrated to be general and reliable and will enhance the realization of graphene nanodevice and desirable study of rich QD physical phenomena in grapheme. These results demonstrate that both single and double quantum dots in single-layer and bilayer graphene bode well for future quantum transport study and quantum computing applications. The clean, highly controllable systems serves as an essential building block for quantum devices in a nuclear-spin-free world.
2. A graphene quantum dot with a single electron transistor as an integrated charge sensor
The measurement of individual electrons or its spins in GaAs quantum dots (QDs) has been realized by so-called charge detection via a nearby quantum point contact (QPC) or single electron transistor (SET) (Lu et al., 2003; Elzerman et al., 2004a). In particular, the combination of high speed and high charge sensitivity has made SET useful in studying a wide range of physical phenomena such as discrete electron transport (Lu et al., 2003; Bylander et al., 2005; Gotz et al., 2008), qubit read out (Lehnert et al., 2003; Duty et al., 2004; Vijay et al., 2009) and nanomechanical oscillators (Knobel et al., 2003; Lahaye et al., 2004). So far, most SETs have been using
In this section, we realize an all graphene nanocircuit integration with a SET as charge read out for a QD. In conventional semiconductor systems, the gate-defined structure limits the distance between the QD and the detector. However, in our device reported here, the QD and the SET in the same material are defined in a single etching step, and the distance between the graphene nanostructures is determined by the etched area, which enables optimized coupling and sensing ability. The SET is placed in close proximity to the QD giving rise to a strong capacitive coupling between the two systems. Once an additional electron occupies the QD, the potential in the neighboring SET is modified by capacitive interaction that gives rise to a measurable conductance change. Even if charge transport through the QD is too small to be measured by conventional transport means, the SET charge sensor also allows measurements. These devices demonstrated here provide robust building blocks in a practical quantum information processor.
The graphene flakes were produced by mechanical cleaving of graphite crystallites by Scotch tape and then were transferred to a highly doped Si substrate with a 100 nm SiO2 top layer. Thin flakes were found by optical microscopy, and single layer graphene flakes were selected by the Raman spectroscopy measurement. We used the standard electron beam lithography and lift off technique to make the Ohmic contact (Ti/Au) on the present graphene devices. Next, a new layer of polymethyl methacrylate is exposed by electron beam to form a designed pattern. Then, the unprotected areas are removed by oxygen reactive ion etching. One of our defined sample structures with a quantum dot and proximity SET is shown in Fig. 1. The quantum dot is an isolated central island of diameter 90 nm, connected by 30nm wide tunneling barriers to source and drain contacts. Here, the Si wafer was used as the back gate and there is also a graphene side gate near the small dot. The SET has a similar pattern while the conducting island has a much larger diameter (180nm). Electronic transport through both the devices exhibits Coulomb blockade (CB) characteristics with back/side gate voltage. The distance between the CB peaks is determined by the sum of charging and quantum confinement energies, and the former contribution becomes dominant for our devices with diameter >100nm (Kouwenhoven et al., 1997). Accordingly, we refer to it as a SET rather than a QD. The device was first immersed into a liquid helium storage Dewar at 4.2K to test the functionality of the gates. The experiment was carried out in a top-loading dilution refrigerator equipped with filtered wiring and low-noise electronics at the base temperature of 10 mK. In the measurement, we employed the standard ac lock-in technique.
Fig. 2(a) shows the conductance through the dot Al/AlOx/Al for applied side gate voltage Vsg. Clear CB peaks are observed related to charging of the tunable dot on the graphene. The dashed green lines in the range of 0.2-0.7V for side gate voltages show that the current through the dot becomes too small to be seen clearly. Fig. 2(b) shows the conductance through the SET versus side gate voltage Vsg. The SET is as close as possible to the QD and in this way charging signals of the dot were detected by tracking the change in the SET current. The addition of one electron to the QD leads to a pronounced change of the conductance of the charge detector by typically 30%. The slope of the SET conductance is the steepest at both sides of its CB resonances giving the best charge read-out signal. To offset the large current background, we used a lock-in detection method developed earlier for GaAs dot (Elzerman et al., 2004b). A square shaped pulse was superimposed on the dc bias on side gate voltage Vsg. A lock-in detector in sync with the pulse frequency measured the change of SET current due to the pulse modulation. Fig. 2(c) shows a typical trace of the lock-in signal of the transconductance through the SET
More quantitative information on the system can be obtained from the measurement of the height response of the peak at 0.152 V in Fig. 2(c) as a function of the modulating pulse frequency on the side gate. The resulting diagram for the SET
The information contained in the signal goes beyond simple charge counting. For instance, the stability diagram measurement can reveal excited states, which is crucial to get information of the spin state of electrons on a quantum dot (Hanson et al., 2003). Fig. 4(a) shows Coulomb diamonds for the conductance through the dot GQD versus bias voltage Vsd and side gate voltage Vsg. For comparison, Fig. 4(b) shows the transconductance of the SET
In summary, we have presented a simple fabrication process that produces a quantum dot and highly sensitive single electron transistor charge detector with the same material, graphene. Typically the addition of a single electron in QD would result in a change in the SET conductance of about 30%. The charging events measured by both the charge detector and direct transport through the dot perfectly match and more excited states information beyond the conventional transport means is also obtained. The devices demonstrated here represent a fascinating avenue towards realizing a more complex and highly controllable electronic nanostructure formed from molecular conductors such as graphene.
3. Controllable tunnel coupling and molecular states in a graphene double quantum dot
Previously, the charge stability diagram in coupled quantum-dot systems has been studied by the classical capacitance model (van der Wiel et al., 2003). However the quantum effect should also manifest itself (Yang et al., 2011). In particular, the tunnel coupling
In this Section, we report an experimental demonstration and electrical transport measurement in a tunable graphene double quantum dot device. Depending on the strength of the inter-dot coupling, the device can form atomic like states on the individual dots (weak tunnel coupling) or molecular like states of the two dots (strong tunnel coupling). We also extract the inter-dot tunnel coupling t by identifying and characterizing the molecule states with wave functions extending over the whole graphene double dot. The result implies that this artificial grapheme device may be useful for implementing two-electron spin manipulation.
A scanning electron microscope image of our defined sample structure with double quantum dot is shown in Fig. 5(a) and
Fig. 5(b). The double quantum dot has two isolated central island of diameter 100 nm in series, connected by 20
Fig. 6(a) displays the differential conductance through the graphene double quantum dot circuit as a function of gate voltages VGL and VGR. Here the measurement was recorded at Vsd= 20
More quantitative information such as double dot capacitances can be extracted using a electrostatic model as shown in Fig. 6(b) (van der Wiel et al., 2003). First, the capacitance of the dot to the side gate can be determined from measuring the size of the honeycomb in Fig. 6(c) as
It has been expected that opening the interdot constriction by gate voltage will cause the tunnel coupling to increase exponentially faster than the capacitive coupling (Kouwenhoven et al., 1997). Fig. 7(a)-(c) represent a selection of such measurements by holding the same VGR and Vbg and scanning different ranges of VGL between -0.5 V to 0.35 V. An evolution of conductance pattern indicates that the stability diagram changes from weak to strong tunneling regimes (van der Wiel et al., 2003; Mason et al., 2004). The conductance near the vertices depends on the relative contributions of the capacitive coupling and tunnel coupling. For the former, the vertices become a sharpened point, while for the latter, the vertices become blurred along the edges of the honeycomb cell (Graber et al., 2007). In Fig. 7(b), the vertices is not obvious as those in Fig. 7(a), which indicates a stronger tunnel coupling. The results suggest that two graphene dots are interacting with each other through the large quantum mechanical tunnel coupling, which is analogous to covalent bonding. We will analyze it in details below. An increase in inter-dot coupling also leads to much larger separation of vertices in Fig. 7(b) (Mason et al., 2004), and finally, to a smearing of honeycomb features in Fig. 7(c). In this case, the double dots behave like a single dot, as illustrated in Fig. 7(g). We note that a similar evolution is observed for four different values of Vbg from 2.5 V to 2.0 V at the same VGL and VGR regimes as shown in Fig. 7(d)-(f). Thus the inter-dot tunnel coupling could also be changed by VGL or Vbg. This can be explained by the fact that the side gates and back gate may influence the central barrier through the existing capacitances between the gates and the central barrier.
Similar to the definitions in Ref. (Livermore et al., 1996), we define
Having understood the qualitative behavior of the graphene device in the strong coupling regime, we extract the quantitative properties based on a quantum model of graphene artificial molecule states (Yang et al., 2003; Graber et al., 2007; Hatano et al., 2005). Here we only take into account the topmost occupied state in each dot and treat the other electrons as an inert core (van der Wiel et al., 2003; Golovach et al., 2004). In the case of neglected tunnel coupling, the nonzero conductance can only occur right at the vertices which are energy degenerate points as
Where
Here
Provided that the graphene double-dot molecule eigenstate
Finally, we discuss the relevance of graphene double dot device for implementing a quantum gate and quantum entanglement of coupled electron spins. A
In summary, we have measured a graphene double quantum dot with multiple lectrostatic gates and observed the transport pattern evolution in different gate configurations. This way offers us a method to identify the molecular states as a quantum-mechanical superposition of double dot and measure the contribution of the interdot tunneling to the splitting of the differential conductance vertex. The precisely extracted values of inter-dot tunnel coupling t for this system is much larger than those in previously reported semiconductor device. These short operation times due to large tunneling strength together with the predicted very long coherence times suggest that the requirements for implementing quantum information processing in graphene nanodevice are within reach.
4. Gates controlled parallel-coupled double quantum dot on both single layer and bilayer grapheme
In contrast to DQD in series, where the applied current passes through the double dot in serial, the parallel-coupled double quantum dot (PDQD) requires two sets of entrances and exits, one for each dot. In addition, the source and drain must maintain coherence of the electron waves through both dots, in a manner analogous to a Young’s double slit. Thus PDQD is an ideal artificial system for investigating the interaction and interference. Rich physical phenomena, such as Aharonov- Bohm (AB) effect, Kondo regimes and Fano effect, have been predicted to be observed in parallel DQD (Holleitner et al., 2001; Lo´pez et al., 2002; Ladro´n de Guevara et al., 2003; Orellana et al., 2004; Chen et al., 2004). Particularly excitement is the prospect of accessing theoretically predicted quantum critical points in quantum phase transitions (Dias da Silva et al., 2008). The grapheme PDQD is an attractive system for investigating the quantum phase transitions due to its intrinsically large energy separation between on-dot quantum levels, thus offering a significant advantage over conventional systems as GaAs or silicon based quantum dots.
In this section, we present the design, fabrication, and quantum transport measurement of double dot structure coupled in parallel, on both bilayer and single layer grapheme flakes, which may open a door to study the rich PDQD physical phenomena in this material the parallel graphene structure can be tuned from a strong-coupling resulted artificial molecule state to a weak-coupling resulted two-dot state by adjusting in plane plunger gates. The tuning is found to be very reliable and reproducible, with good long-term stability on the order of days.
Graphene flakes are produced by mechanical cleaving of bulk graphite crystallites by Scotch tape (Novoselov et al., 2004). For this kind of exfoliated graphene flakes on SiO2 substrate, the mobility is normally about 15000 cm2/(Vs) (Geim et al., 2007). By using heavily doped Si substrate with 100 nm thick SiO2 on top, we can identify monolayer, bilayer, and few layer graphenes through optical microscope. Monolayer and bilayer graphenes were further checked by Raman spectrum. Firstly, graphene flakes are transferred to the substrate with gold markers. Then, a layer of 50nm thick polymethyl methacrylate (PMMA) is spun on the substrate for electron beam lithography (EBL) to form a designed pattern. After that, O2/Ar (50:50) plasma is used to remove unprotected parts of graphene. Next, an area of over exposed PMMA is used to separate a bridge plunger gate from the drain part of graphene (Chen et al., 2004; Huard et al., 2007). The final step is to make the metal contacts, which are defined by the standardized EBL process, followed by the E-beam evaporation of Ti/Au (2 nm/50 nm).
Fig. 9(a) shows a scanning electron microscope (SEM) image of one sample with the same structure as the bilayer device we measured. Two central islands with diameter of 100 nm connect through 30 nm wide narrow constrictions to the source and the drain regions. Another narrow constriction (35nm in both width and length) connects the two central islands. Seven in-plane plunger gates labeled as GL, GR, GM, PSL, PDL, PSR, and PDR are integrated in close proximity to the dots. GL, GR, and GM are, respectively, designed to adjust the energy level of left dot, right dot, and inter-dot coupling strength. And PSL, PDL (PSR, PDR) are used for the tuning of the coupling of the left (right) dot to source and drain. The n-type heavily doped silicon substrate is used as a global back gate. The bridge plunger gate GM is separated from the drain part of graphene by a layer of over exposed PMMA. All the devices were primarily tested to check the functionality of all the gates in a liquid helium storage dewar at 4.2 K. Then the samples were mounted on a dilution refrigerator equipped with filtering wirings and low-noise electronics at the base temperature of 10 mK. To maintain consistency, we will use the data from one sample only in the following.
Fig. 10(a) shows color scale plot of the measured differential conductance of the double dot as a function of VGL and VGR detected in standard ac lock-in technique with anexcitation ac voltage 20
By applying voltage to the middle plunger gate GM, the interdot coupling can be tuned efficiently. Fig.11(a), 11(b),and 11(c) show the charge stability diagrams of the PDQD in three different coupling regimes. [(a) weak, (b) medium, and (c) strong]. In these measurements, back gate voltage VBG =3V, Source-Drain DC bias Vbias is set to-1.0mV, the scan regions of GL and GR are the same. Only the voltage applied to the gate GM is adjusted as (a) VGM= -0.15 V, (b) VGM=0.2 V, and (c) VGM=0.45 V. By using the same model as in Figure 2, we can calculate the corresponding coupling energy between the dots: (a) ECM=0.58 meV, (b) ECM=1.34 meV, and (c) ECM=4.07 meV. The honeycomb diagrams of the parallel and serial DQD look similar except for the weak coupling regime, as shown in Figure3(a). In this case, the lines delimiting the hexagons are more visible in comparison with serial DQD, because the leads have two parallel accesses to the dots in parallel DQD, which also enables correlated tunneling of two valence electrons simultaneously (Holleitner et al., 2002). Fig. 11(d) indicates the coupling energy changes with the gate voltage VGM. As in the previous reports of graphene DQD in series (Molitor et al., 2010; Liu et al., 2010), the inter-dot coupling is non-monotonically depended on the applied gate voltage. Although the detailed reasons for this non-monotony are undetermined, we assumed that one key factor will be the disorders in graphene introduced by either fabrication steps or substrate (Todd et al., 2009). Many more efforts are still needed to address this issue for the realization of practical graphene based nanodevices.
We have designed and fabricated an alternative structure of a PDQD integrated with two quantum point contact sensors (QPCs) in single layer graphene, as shown in Figure 4(a). The integrated QPCs can be used as a non-invasive charge detector which may have various applications (van der Wiel et al., 2003; Hanson et al., 2007; Guo et al., 2001; Zhang et al., 2007). As primary tests of the present structure, we can get similar charge stability diagram of the PDQD as in Fig.12 (b) by the direct quantum transport tests at 4.2 K. Although the non-invasive measurements by QPC are still under processing, no remarkable difference is founded between PDQD in bilayer and monolayer graphenes from direct transport measurement. Making tunable coupling double dot is the first step towards the quantum dot based quantum computation bits, the architectonics with integrated charge detector around double quantum dot demonstrated here offers the chance to achieve the charge or spin reading out, which is essential for the quantum computation device. Therefore, a lot of extended and follow-up works can be done on this basis in the future. Both bilayer and single layer graphenes can be exploited in this application.
In summary, we have discussed low temperature quantum transport measurement of gate-controlled parallel coupled double quantum dot on both bilayer and single layer graphenes. The inter-dot coupling strength can be largely tuned by graphene in-plane gates. With the quantum transport honeycomb charge stability diagrams, a common model of purely capacitively coupled double dot is used to extract all the relevant energy scales and parameters of grapheme PDQD. Although many more effects are still needed to further upgrade and exploit the present designed grapheme quantum dot system, the results have intensively demonstrated the promise of the realization of graphene nanodevice and desirable study of rich PDQD physical phenomena in graphene.
5. Conclusion
To conclude, we have discussed the design and fabrication of etched gate tunable single and double quantum dots in single-layer and bilayer graphene and present several important quantum transport measurements in these systems. A quantum dot with an integrated charge sensor is becoming a common architecture for a spin or charge based solid state qubit. To implement such a structure in graphene, we have fabricated a twin-dot structure in which the larger QD serves as a single electron transistor (SET) to read out the charge state of the nearby gate controlled small QD. A high SET sensitivity of
and parameters can be extracted from the honeycomb charge stability diagrams. The present method of designing and fabricating graphene DQD is demonstrated to be general and reliable and will enhance the realization of graphene nanodevice and desirable study of rich DQD physical phenomena in graphene, and highly controllable system serves as an essential building block for quantum devices in a nuclear-spin-free world.
Acknowledgments
This work was supported by the National Basic Research Program of China (Grants No. 2011CBA00200 and 2011CB921200), and the National Natural Science Foundation of China (Grants No. 10934006, 11074243, 11174267, 91121014, and 60921091)
References
- 1.
Berman D, Zhitenev N. B, Ashoori R. C, and Shayegan M, Phys. Rev. Lett. 82, 161 (1999). - 2.
Bylander J, Duty T, and Delsing P, Nature London 434, 361 (2005). - 3.
Chen J. C, Chang A. M, and Melloch M. R., Phys. Rev. Lett. 92, 176801 (2004). - 4.
Dias da Silva L. G. G. V, Ingersent K, Sandler N, and Ulloa S. E, Phy. Rev. B 78, 153304 (2008). - 5.
Duty T, Gunnarsson D, Bladh K, and Delsing P, Phys. Rev. B 69, 40503(R) (2004). - 6.
Elzerman J. M, Hanson R, L. van Beveren H. W, L. Vandersypen M. K, and Kouwenhoven L. P, Appl. Phys. Lett. 84, 4617 (2004b). - 7.
Elzerman J. M, Hanson R, van Beveren L. H. Witkamp W, B, Vandersypen L. M. K, and L. P. Kouwenhoven, Nature London 430, 431 (2004a). - 8.
Fischer J, Trauzettel B, and Loss D, Phys. Rev. B 80, 155401 (2009). - 9.
Fischer J. and Loss D, Science 324, 1277 (2009). - 10.
Foletti S, Bluhm H, Mahalu D, Umansky V, and Yacoby A, Nat. Phys. 5, 903 (2009). - 11.
Gallagher P., Todd K., and Goldhaber-Gordon D., Phys. Rev. B 81, 115409 (2010). - 12.
Geim A. K and Novoselov K. S, Nature Mater. 6, 183 (2007). - 13.
Geim A. K., Science 324, 1530 (2009). - 14.
Golovach V. N, and Loss D, Phys. Rev. B 69, 245327 (2004). - 15.
Gotz G, Steele G. A, Vos W. J, and Kouwenhoven L. P, Nano Lett. 8, 4039 (2008). - 16.
Graber M. R, Coish W. A, Hoffmann C, Weiss M, Furer J, Oberholzer S, Loss D, and Scho°nenberger C, Phys. Rev. B 74, 075427 (2007). - 17.
Guo G. P, Li C. F, and Guo G. C, Phys. Lett. A 286, 401 (2001). - 18.
Guo G. P, Lin Z. R, Tu T, Cao G, Li X. P, and Guo G. C, New J. Phys.11, 123005 (2009). - 19.
Güttinger J, Seif J, Stampfer C, Capelli A, Ensslin K, and Ihn T, Phys. Rev. B 83, 165445 (2011). - 20.
Güttinger J, Stampfer C, Hellmüller S, Molitor F, Ihn T, and Ensslin K, Appl. Phys. Lett. 93, 212102 (2008). - 21.
Hanson R, Kouwenhoven L. P, Petta J. R, Tarucha S, and Vandersypen L. M. K, Rev. Mod. Phys. 79, 1217 (2007). - 22.
Hanson R, Witkamp B, Vandersypen L. M. K, van Beveren L. H. W, Elzerman J. M, and Kouwenhoven L. P, Phys. Rev. Lett. 91, 196802 (2003). - 23.
Hanson R. and Awschalom D, Nature 453, 1043 (2008) - 24.
Hatano T, Stopa M, and Tarucha S, Science 309, 268 (2005). - 25.
Holleitner A. W, Blick R. H, Hu° ttel A. K, Eberl K, and Kotthaus J. P, Science 297, 70 (2002). - 26.
Holleitner A. W, Decker C. R, Qin H, Eberl K, and Blick R. H, Phys. Rev. Lett. 87, 256802 (2001). - 27.
Huard B, Sulpizio J. Stander A, Todd N. K, Yang B, and Goldhaber Gordon D, Phys. Rev. Lett. 98, 236803 (2007). - 28.
Ihn T., Guttinger J, Molitor F, Schnez S. Schurtenberger E, Jacobsen A, Hellmu°ller S, Frey T, Droscher S, Stampfer C. et al., Mater. Today 13, 44 (2010). - 29.
Knobel G. and Cleland A. N., Nature London 424, 291 (2003). - 30.
Kouwenhoven L. P, Marcus C, McEuen P. L, Tarucha S, Westervelt R. M, and N. S. Wingreen, in Mesoscopic Electron Transport, Series E:Applied Sciences Vol. 345, edited by Sohn L. L, Kouwenhoven L. P, and Schon G, Dordrecht Kluwer, 1997, pp. 105–214. - 31.
L. Ponomarenko, F. Schedin, Katsnelson M, Yang R, Hill E, Novoselov K, and Geim A, Science 320, 356 (2008). - 32.
Ladro´n de Guevara M. L, Claro F, and Orellanal P. A, Phys. Rev. B 67, 195335 (2003). - 33.
LaHaye D, Buu O, Camarota B, and Schwab K. C, Science 304, 74 (2004). - 34.
Lehnert K. W, Bladh K, Spietz L. F, Gunnarsson D, Schuster D. I, Delsing P, and Schoelkopf R. J, Phys. Rev. Lett. 90, 027002 (2003). - 35.
Liu X. L, Hug D, and L. Vandersypen M. K. Nano Lett. 10, 1623 (2010). - 36.
Livermore C, Crouch C. H, Westervelt R. M, Campman K. L, and A. Gossard C, Science 274, 1332 (1996). - 37.
Lo´pez R, Aguado R, and Platero G, Phys. Rev. Lett. 89, 136802 (2002). - 38.
Lu W, Ji Z. Q, Pfeiffer L, K. W. West, and A. J. Rimberg, Nature London 423, 422 (2003). - 39.
Mason N, Biercuk M. J, and Marcus C. M, Science 303, 655 (2004). - 40.
Molitor F, Droscher S, Guttinger J, Jacobson A, Stampfer C, Ihn T, and Ensslin K, Appl. Phys. Lett. 94, 222107 (2009). - 41.
Molitor F, Knowles H, Droscher S, Gasser U, Choi T, Roulleau P, Guttinger J, Jacobsen A, Stampfer C, Ensslin K. et al., Europhys. Lett. 89, 67005 (2010). - 42.
Moriyama S, Tsuya D, Watanabe E, Uji S, Shimizu M, T. Mori, T. Yamaguchi, and Ishibashi K, Nano Lett. 9, 2891 (2009). - 43.
Novoselov K. S, Geim A. K, Morozov S. V, Jiang D, Zhang Y, Dubonos S. V, Grigorieva I. V, and Firsov A. A, Science 306, 666 (2004). - 44.
Orellana P. A, Ladron de Guevara M. L, and Claro F, Phys. Rev. B 70, 233315 (2004). - 45.
Petta J. R, Johnson A. C, Taylor J. M, Laird E. A, Yacoby A, Lukin M. D , Marcus C. M, Hanson M. P, and Gossard A. C, Science 309, 2180 (2005). - 46.
Ponomarenko L, Schedin F, Katsnelson M, Yang R. Hill E, Novoselov K, and Geim A. K, Science 320, 356 (2008). - 47.
Schnez S, Molitor F, Stampfer C, Guttinger J, Shorubalko I, Ihn T, and Ensslin K, Appl. Phys. Lett. 94, 012107 (2009). - 48.
Stampfer C, Guttinger J, F. Molitor, D. Graf, T. Ihn, and K. Ensslin, Appl. Phys. Lett. 92, 012102 (2008a). - 49.
Stampfer C, Schurtenberger E, Molitor F, Guettinger J, Ihn T, and Ensslin K, Nano Lett. 8, 2378 (2008b). - 50.
Stampfer C., Güttinger J., Hellmüller S., Molitor F., Ensslin K., and Ihn T., Phys. Rev. Lett. 102, 056403 (2009). - 51.
Todd K, Chou H. Amasha T, S, and Goldhaber-Gordon D, Nano Lett. 9, 416 (2009). - 52.
Trauzettel B, Bulaev D. V, Loss D, and Burkard G, Nat. Phys. 3, 192 (2007). - 53.
van der Wiel W. de Francheschi G, S, Elzermann J. M, Fujisawa T, Tarucha S, and Kouwenhoven L P, Rev. Mod. Phys. 75, 1 (2003). - 54.
Vijay R, M. H. Devoret, and I. Siddiqi, Rev. Sci. Instrum. 80, 111101 (2009). - 55.
Vink I. T, Nooitgedagt T, Schouten R. N, and Vandersypen L. M. K, Appl. Phys. Lett. 91, 123512 (2007). - 56.
Volk C, Fringes S, Terres B, Dauber J, Engels S, Trellenkamp S, and Stampfer C,.Nano Lett. 11, 3581 (2011). - 57.
Wang L. J, Cao G, Li H. O, Tu T, Zhou C, Hao X. J, Guo G. C, and Guo G. P, Chinese .Physics. Letters. 28, 067301 (2011b). - 58.
Wang L. J, Cao G, Tu T, Li H. O, Zhou C, Hao X. J, Su Z, Guo G. C, Jiang H. W, and Guo G. P, Appl. Phys. Lett. 97, 262113 (2010). - 59.
Wang L. J, Guo G. P, Wei D, Cao G, Tu T, Xiao M, Guo G. C, and Chang A.M, Appl. Phys. Lett. 99, 112117 (2011a). - 60.
Wang L. J, Li H. O, Tu T, Cao G, Zhou C, Hao X. J, Su Z, Xiao M, Guo G. C, Chang A.M, and Guo G. P, Appl. Phys. Lett. 100, 022106(2012). - 61.
Yang S, Wang X, and Das Sarma S, Phys. Rev. B 83, 161301(R) (2011). - 62.
Zhang H, Guo G. P, Tu T, and Guo G. C, Phys. Rev. A 76, 012335 (2007). - 63.
Ziegler R, Bruder C, and Schoeller H, Phys. Rev. B 62, 1961 (2000).