Open access peer-reviewed chapter

Hydrogen Storage Properties and Structure of Magnesium-Based Alloys Prepared with Melt-Spinning Technique

By Kazuhide Tanaka

Submitted: December 10th 2011Reviewed: May 25th 2012Published: September 5th 2012

DOI: 10.5772/50170

Downloaded: 2301

1. Introduction

Magnesium is known to have a relatively high hydrogen storage capacity of 7.6 wt. % by forming a non-metallic hydride MgH2, and has long been a target of many research works for developing excellent hydrogen storage materials. However, owing to very small hydrogen solubility and diffusivity in metallic Mg, together with very low chemical reactivity of its surface with hydrogen gas, the hydrogenation (and dehydrogenation) rate of Mg is generally quite slow, and temperatures above ~400ºC and gas pressures exceeding ~10 MPa are required to cause the reaction. Several techniques have been developed to overcome this drawback of Mg without significantly reducing its hydrogen capacity. Among them, ball-milling and melt-spinning techniques appear to be most important. In the former, commercially available MgH2 powder is mixed with a small amount of transition metal powder (Ti, V, Mn, Fe, Ni, Nb, Pd, etc., and their oxides or fluorides) and ball-milled for appropriate time periods. The mechanically milled powder exhibits an excellent reactivity with hydrogen, absorbing H2 gas even at ~100°C or lower temperatures, and desorbing it above ~200ºC. Here, the transition metal additives play crucially important roles by working as chemical catalysts for the abs/des reactions on the surface of micron-size Mg powder (Barkhordarian et al., 2004; Liang et al., 1999; Zaluska et al., 1999). On the other hand, in the latter, Mg alloyed with small amounts of transition metal (Ni, Pd, etc.) and/or rare earth (La, Ce, Nd, etc.) is melt-spun to form a thin metallic ribbon of normally amorphous structure. Upon crystallization, it changes into a stable multi-phase nanostructure where nano-sized grains of the alloying elements or their compounds are homogeneously precipitated in a nano-crystalline Mg matrix. The ribbon thus produced also exhibits an excellent reactivity with hydrogen. Here, nano-sized precipitates promote the chemisorption of H2 molecules on the ribbon surface and enhance the flow of H atoms into the interior to form alloy hydrides (Spassov & Köster, 1999; Tanaka et al., 1999).

We have studied the hydrogen storage properties and structures of melt-spun and crystallized Mg-(Ni, Pd)-(La, Nd) alloys using several experimental and analytical techniques, and have made clear the absorption and desorption processes of hydrogen in the alloys (Tanaka, 2008; Tanaka et al., 2009; Yamada et al., 2001; Yin & Tanaka, 2002). In this chapter, some of our results specifically on Mg-Ni-La alloy, in comparison with Mg-Ni alloy, are reviewed and desorption mechanisms of hydrogen in these alloys are discussed. This chapter is composed of the following sections. In section 2, experimental procedures for the sample preparation with melt-spinning technique and for hydriding/dehydriding (H/D) measurements are described, and phase structures of hydrogenated/dehydrogenated samples characterized by X-ray diffraction (XRD) are shown. In section 3, equilibrium properties and kinetic behavior of hydrogen in the alloys as revealed by pressure-composition isotherms (PCT) and H/D rates, respectively, are described. In section 4, thermal desorption spectra (TDS) of samples subjected to various H/D treatments are provided, where component TDS peaks are related with existing hydride phases in the alloy. Section 5 is devoted to transmission electron microscope (TEM) observation of nanostructures of hydrogenated and dehydrogenated samples. High-resolution TEM (HRTEM) combined with electron energy-loss spectroscopy (EELS) is used to identify the metallic and hydride phases in the samples. An EELS plasmon peak (H-plasmon) of MgH2 is successfully used to visualize the formation and destruction of the hydride phase in the sample. In section 6, the H-plasmon peak is applied to an in situ observation of the desorption process of the MgH2 phase during heating. Finally, in section 7, concluding remarks are given, where the importance of the role of nano-grain boundaries as pathways of hydrogen flowing into and out of the nanostructured alloy is emphasized.

2. Sample preparation and phase-structure characterization

Magnesium-rich alloys with nominal compositions, Mg85Ni10La5 and Mg90Ni10 (in at.%), have been prepared in this study. Appropriate amounts of raw materials (99.9% pure Mg and 99.9% pure La) and a mother alloy (Mg70Ni30) are mixed together, melted at 900ºC in sealed steel crucibles under high purity Ar atmosphere and slowly cooled. The chemical compositions of the ingots obtained by SEM-EDX analyses are Mg89.2Ni7.6La3.2 and Mg89.5Ni10.5. Amorphous ribbons (~20 μm thick and ~1 mm wide) are prepared from these ingots with a melt-spinning technique using a single Cu roll under Ar atmosphere. They are cut into small pieces, slightly ground and subjected to H/D measurements using a Sieverts-type PCT apparatus. The crystallization temperature Tx for these amorphous alloys as determined by DSC measurements is 162±5ºC, which is well below the initial activation temperature 300ºC adopted for hydrogenation in this study, hence all the H/D measurements have been performed for the crystallized alloys.

The SEM photographs for the as-cast Mg90Ni10 and Mg85Ni10La5 alloys shown in Fig. 1 indicate that a primary dendritic phase of Mg (α) is coexistent with Mg (α)/Mg2Ni (γ) eutectic phases in the former, whereas a primary equiaxial phase of Mg2Ni (γ) is coexistent with both the Mg/Mg2Ni eutectic phases and a Mg17La2 compound phase in the latter. These phase structures are consistent with the equilibrium phase diagrams of Mg-Ni (Massalski, 1986) and Mg-Ni-La (De Negri at al.., 2005) systems. Since the grains of all the constituent phases are so coarse that the initial activation and subsequent H/D processes of the as-cast alloys inevitably become sluggish. However, this difficulty is overcome substantially by refining the microstructure employing higher cooling rates of casting (Yamada et al., 2001; Yin et al., 2002). The melt-spinning technique combined with the crystallization treatment employed here is a quite efficient method for attaining the grain refining. An equal channel angular pressing (ECAP) treatment has also been applied for the grain refining in a Mg-Ni-Mm alloy (Lϕken et al., 2006), and a high hydrogen absorbency exceeding 5 wt%H with moderate H/D kinetics has been attained.

Figure 1.

SEM photographs of as-cast Mg90Ni10 and Mg85Ni10La5 alloys.

The phase structures of melt-spun Mg90Ni10 and Mg85Ni10La5 alloys have been examined for the samples subjected to crystallization annealing, hydriding and dehydriding treatments at 300ºC using X-ray diffraction with Cu Kα radiation, as shown in Fig. 2. After crystallization, the Mg90Ni10 alloy is composed of Mg + Mg2Ni phases similarly to the as-cast alloy. After hydriding to 4.8 wt%H, β-MgH2 + Mg2NiH4 phases appear, with a part of the Mg2Ni phase left unchanged. The Mg2NiH4 phase is separated to the low-temperature (LT) and high-temperature (HT) phases. The γ-MgH2 phase, which commonly exists in ball-milled MgH2 (Liang et al., 1999), is not formed in the melt-spun alloy. After dehydriding, the alloy recovers to the original Mg + Mg2Ni phases. In the subsequent H/D processes, the alloy phases cyclically change as:

Mg + Mg2Ni + H2 ↔ MgH2 + Mg2NiH4 (Mg90Ni10 alloy)

Figure 2.

X-ray diffraction patterns (Cu Kα) of melt-spun Mg90Ni10 and Mg85Ni10La5 alloys subjected to crystallization annealing, hydriding and dehydriding at 300ºC.

On the other hand, the Mg85Ni10La5 alloy is composed of Mg + Mg2Ni + Mg17La2 phases after crystallization similarly to the as-cast alloy. Upon hydriding to 4.0 wt%H, these metallic phases transform into β-MgH2 + Mg2NiH4 (HT) + LaH3 hydride phases. In this process, the Mg17La2 phase is decomposed to MgH2 + LaH3 through a disproportionation reaction. A part of the Mg2Ni phase is remaining. After dehydriding, Mg + Mg2Ni metallic phases recover whereas the thermally stable LaH3 hydride remains unchanged. Thus, the H/D processes for this alloy are simply written as:

Mg + Mg2Ni + Mg17La2 + H2 → Mg + Mg2Ni + LaH3 + H2

MgH2 + Mg2NiH4 + LaH3 (Mg85Ni10La5 alloy)

The metallic and hydride phases described above provide stable nano-grain structures in these alloys, as shown later (Section 5 and 6).

3. Pressure-composition isotherms and H/D kinetics

Pressure (p) – composition (c) isotherms are measured for the crystallized and activated samples (~1.0 g) with a volumetric method using a Sieverts–type apparatus. Figure 3 shows a result on Mg85Ni10La5 alloy for temperatures (T) between 240º and 330ºC, where the absorption and desorption isotherms are displayed with dashed and solid lines, respectively. Here, the H-content c is given by c (wt%) = (weight of H)/(weight of alloy + weight of H) × 100. All the isotherms clearly show two-stage plateaus. The first (lower pressure) stage corresponds to Mg – MgH2, and the second (higher pressure) one to Mg2Ni – Mg2NiH4 equilibria. The H-capacity (c ~ 4.6 wt%) and the ratio of the widths of the two stages, ~ 3.8/0.8, are consistent with those expected for the alloy assuming a complete hydride formation. It can be seen from the figure that the first stage is flat and exhibits only a small hysteresis except for the initial parts of the isotherms, whereas the second one is slightly inclined and exhibits a definite hysteresis which is more emphasized at lower temperatures.

Figure 3.

Pressure – composition isotherms for the melt-spun Mg85Ni10La5 alloy. (Tanaka, 2008)

Relationships between the pressure and inverse temperature for the first and second plateaus in the absorption and desorption processes are shown in Fig. 4. The formation enthalpy ΔHf and standard formation entropy ΔSf0 for MgH2 and Mg2NiH4 are related with the plateau pressure p and temperature T as

ln(pp0)=ΔHfRTΔSf0R,E1

where p 0 = 0.1 MPa and R is the gas constant. They can be evaluated from the linear relationships shown in the figure. Values of ΔHf and ΔSf0 are listed in Table 1 and compared with those for an ordinary coarse-grained material (Wiswall, 1978). The values for MgH2 are comparable between the melt-spun and ordinary alloys. However, those for Mg2NiH4 are definitely different between the two. Namely, the formation enthalpy and entropy for Mg2NiH4 are closer to those for MgH2 in the melt-spun alloy than in the ordinary alloys.

Figure 4.

Relationships between plateau pressures p and inverse temperatures T-1 for hydrogen absorption (broken lines) and desorption (solid lines) in Mg85Ni10La5 alloy. (Tanaka, 2008)

HydridesProcessΔHf /(kJ/molH2)ΔSf0 /(J/K/molH2)
MgH2abs-75.9-136
des-76.2 (-74.8)-136 (-136)
Mg2NiH4abs-52.0-105
des-73.3 (-64.7)-135 (-122)

Table 1.

Thermodynamic parameters ΔHf and ΔSf0 for the formation of MgH2 and Mg2NiH4 in Mg85Ni10La5 alloy. The values in the parentheses are for an ordinary alloy.

Figure 5 shows PCT curves for the as-cast Mg85Ni10La5 alloy. Although the gross features of the isotherms are similar, the as-cast alloy provides more inclined plateaus than the melt-spun alloy. Furthermore, the boundary between the first and second plateaus is less clearly defined in the former than the latter. These unfavorable features of the PCT characteristics of the as-cast alloy are possibly due to the presence of structural and compositional inhomogeneities such as coarse grains and Mg/Mg2Ni eutectics. The PCT Measurements for the melt-spun Mg90Ni10 alloy have also been carried out, and isotherms qualitatively similar to those of melt-spun Mg85Ni10La5 alloy (Fig. 3) have been obtained. However, the measured H-capacity (c ~ 4.6 wt%) is substantially smaller than that expected for the alloy (~ 6.1 wt%). The isotherms show that the magnitude of the second plateau (formation of Mg2NiH4) is far smaller than that expected. A much slower reaction rate for the Mg2NiH4 formation in the Mg90Ni10 alloy than in the Mg85Ni10La5 alloy might have caused this apparent loss of H-capacity in the binary Mg90Ni10 alloy.

Figure 5.

Pressure-composition isotherms for the as-cast Mg85Ni10La5 alloy. (Tanaka, 2008)

Figure 6.

Hydrogen absorption characteristics of melt-spun Mg85Ni10La5 alloy. (Tanaka et al., 2009)

Figure 6 shows hydrogen absorption rates of a melt-spun Mg85Ni10La5 alloy (~150 mg) at temperatures between 51º and 274ºC under H2 pressures well above the corresponding plateau pressures of Mg2NiH4 and MgH2. In the measurements of H/D kinetics, the H-content is defined, for convenience, as c (wt%) = (weight of H)/(weight of alloy) × 100. At temperatures above 200ºC, a maximum H-content of c ~ 5 wt% is readily reached within ~0.5 h, although the absorption rate is drastically reduced at lower temperatures. This behavior is qualitatively similar to those of ball-milled MgH2 added with transition metals (Liang et al., 1999) or transition metal-oxides (Hanada et al. 2006; Oelerich, 2001). These absorption curves reflect complex underlying processes depending on T and p, for which simple analytical expressions are unavailable at present except for the initial parts of absorption (Hanada et al., 2007).

Figure 7.

Hydrogen desorption characteristics of melt-spun Mg85Ni10La5 alloy. (Tanaka et al., 2009)

Figure 7 shows hydrogen desorption rates of the same sample as above at temperatures between 201º and 270ºC. For these measurements, the sample is initially saturated with hydrogen (~ 5 wt%H) by equilibrating with H2 gas above the plateau pressure of Mg2NiH4 at the measuring temperature. The chamber is then instantly evacuated to lower than 0.001 MPa, well below the plateau pressure of MgH2, and the subsequent increment in pressure due to desorption from the sample is recorded. It can be seen from this figure that the absorbed hydrogen is almost wholly desorbed in a reasonable time period in the measured temperature range. The desorption appears to take place according to an equation

c=c0rt,E2

where c 0 is the initial H-content, t the desorbing time and r is a rate constant that depends on the temperature. Assuming that r is given by an Arrhenius-type equation

r=r0exp(EdRT),E3

Ed (apparent activation energy for desorption) is calculated as 98.1 kJ/mol H2, as shown in Fig. 8. This value is definitely larger than the enthalpies of decomposition of MgH2 (76.2 kJ/mol H2) and Mg2NiH4 (73.3 kJ/mol H2). The linear time dependence given by eq. (2) may reflect a rate-controlling process at the powder surface of the alloy. Namely, hydrogen is desorbed from the surface at a constasnt rate irrespective of the H-content. The activation energy Ed for this alloy is intermediate between those for undoped MgH2 (~120 kJ/mol H2) and for Nb2O5-doped MgH2 prepared by ball milling (62 kJ/mol H2) (Barkhordarian, 2004). The desorption process of hydrogen will be discussed in conjunction with TDS measurements later (Section 4).

Figure 8.

The desorption rate r for melt-spun Mg85Ni10La5 plotted against T-1. (Tanaka et al., 2009)

4. Thermal desorption spectroscopy for hydrogen

The thermal desorption spectroscopy (TDS) is a technique in which a small piece of hydrogenated sample is heated at a constant rate in high vacuum, and the H-desorption rate is measured by monitoring the partial gas pressure of hydrogen as a function of temperature. In the present experiment, a powder specimen (~10 mg) is measured at a heating rate between 0.5º and 4ºC/min in a vacuum of ~10-6 Pa using an apparatus equipped with a turbo-molecular pumping system and a quadrupole mass spectrometer, as shown in Fig. 9. A sample cell compatible with the PCT measurement is used. With this cell, a hydrogenated sample is transferred from the PCT to TDS apparatus for measuring a desorption spectrum, or vice versa for loading the specimen with hydrogen, without exposing to the air. This process is repeated several times for a single specimen in a series of measurements to examine the heating-rate dependence of a TDS spectrum or to examine the effect of thermal cycles on the spectrum.

Figure 9.

Apparatus used for TDS measurements. 

Figure 10.

TDS spectrum of a hydrogenated melt-spun Mg85Ni10La5 alloy compared with that of commercial MgH2 powder.

Figure 10 shows an example of TDS spectrum of a hydrogenated Mg85Ni10La5 alloy stabilized by exposing to a few hydrogenation/thermal desorption cycles at 300ºC, compared with that of commercial MgH2 powder. In this figure, a hydrogen partial pressure derived from a measured ion current of the mass spectrometer is plotted against a specimen temperature. The partial pressure can be used as a measure of hydrogen desorption rate if the pumping speed of the apparatus is assumed to be constant irrespective of the pressure. Clearly, a prominent peak with a few substructures occurs around 200ºC in the Mg85Ni10La5 alloy, while a single peak is caused around 400ºC in MgH2, indicating that the desorption temperature is significantly reduced in the melt-spun alloy. Although the nature of the TDS spectrum of the alloy is not clear solely from this figure, it will be shown in the following that the main peak as well as the substructures is related with thermal decomposition of hydride phases present in the alloy.

Figure 11 shows TDS spectra, measured at 1ºC/min (left) and 2ºC/min (right), of melt-spun Mg85Ni10La5 alloy subjected to hydrogenation/thermal desorption cycles (1st to 4th). Prior to each desorption measurement, the sample has been fully hydrogenated at ~300℃ under ~1 MPaH2. Each spectrum is optionally shifted vertically for the sake of clarity. Except for apparent upward shifts of peak temperatures for the higher heating rate, the two sets of spectra provide common features with increasing cycles. In the 1st cycle, a broad peak c is dominantly seen together with a shoulder associated with peak b. In the 2nd cycle, peak b develops while peak c diminishes without altering the total peak area appreciably. In the 3rd and 4th cycles, peak b further develops and becomes narrower while peak c changes less. Throughout these processes, peak d changes little. Beyond the 4th cycle, the spectral change almost ceases and all the peaks remain stable if the measuring temperature is not increased beyond ~400ºC. A substructure, a, is occasionally observable as a shoulder on the lower-temperature tail of peak b, but it is not always reproducible in these measurements.

Figure 11.

Evolution of TDS peaks of melt-spun Mg85Ni10La5 alloys subjected to 1st to 4th hydrogenation/thermal desorption cycles measured with heating rates of 1ºC/min (left) and 2ºC/min (right). (Tanaka, 2008)

Figure 12.

Heating-rate dependence of the TDS profiles of Mg85Ni10La5 subjected to 4th hydrogenation/desorption cycle. (Tanaka, 2008)

In Fig. 12, TDS spectra of Mg85Ni10La5 measured at different heating rates (0.5, 1, 2, and 4ºC/min) are compared, where a spectrum stabilized by subjecting at least four hydrogenation/thermal desorption cycles is chosen as a representative for each heating rate. It can be seen from the figure that, with increasing heating rate, peaks b to d systematically shift toward higher temperatures, although peak a is not well defined in these spectra. Furthermore, the integrated strength of each peak tends to increase with increasing heating rate. The latter feature is a natural effect of the TDS technique. The observed peak shifts are analyzed according to Kissinger’s method below.

The relation between the heating rate β and peak temperature Tm is shown in Fig. 13, where β/Tm2 is plotted against Tm-1 in a semi-log scale for the peaks b to d. Nearly linear relations can be seen, indicating that Kissinger’s equation,

ln (β/Tm2)=Edes/RTm+lnk0,E4

holds for these peaks. Here, Edes denotes an apparent activation energy for desorption and k0 is a reaction constant. Values of Edes obtained in this way are also given in the figure.

Figure 13.

Kissinger’s plots for the TDS peaks b ~ d of Fig.12. Values of Edes are given. (Tanaka, 2008)

To examine further the evolution of TDS spectra due to heating up to higher temperatures (~380ºC), measurements have been done for a single specimen of melt-spun Mg85Ni10La5 alloy using D2 gas, instead of H2 gas, as shown in Fig. 14. The specimen is fully pre-charged at 300ºC under 1 MPa of D2 pressure in every cyclic measurement, and heated from room temperature up to 300ºC for the 1st to 5th cycles, and up to ~380℃ for the 6th to 10th cycles at a rate of 1℃/min. The spectral feature and its variation up to the 6th cycle are similar to those shown in Fig. 11. A sharp prominent peak b at ~210ºC is stabilized if the specimen temperature is kept below 300ºC. However, if the temperature is raised to ~380℃ in the 7th to 10th cycles, a drastic change takes place; the main peak b undergoes significant broadening and shifts toward higher temperatures, causing a single peak at ~280℃ in the 10th cycle. In this cycle, both the amount of pre-charged hydrogen and its absorption rate are markedly reduced. This result shows that the internal structure of the specimen is altered to some extent by heating up to ~380ºC repeatedly.

Figure 14.

Evolution of TDS spectra of melt-spun Mg85Ni10La5-D2 system from 1st to 5th cycles (a) and from 6th to 10th cycles (b). (Tanaka et al., 2009)

Figure 15 shows TDS spectra, measured at 1ºC/min, of a melt-spun Mg90Ni10 alloy subjected to the hydrogenation/thermal desorption cycle as mentioned above. We find that, in contrast to Mg85Ni10La5, peak d is absent in Mg80Ni10, indicating that this peak is exclusively derived from LaH3 hydride present only in the Mg85Ni10La5 alloy. We also find that peak b and peak c really exist in the 1st cycle, but peak c is much smaller than peak b even in the 1st cycle. The peak c quickly decays with increasing number of cycle, leaving only the peak b beyond the 4th cycle. These spectral features of Mg90Ni10 are somewhat different from those of Mg85Ni10La5 shown in Fig. 11. This difference of TDS spectra is possibly associated with the difference in the thermal stability of the structures formed in these alloys. The behavior of peak b of Mg90Ni10 at different heating rates has also been examined and a result analogous to that of Mg85Ni10La5 (Fig. 12) has been obtained.

In the following, we discuss the origins of TDS peaks a ~ d of melt-spun Mg85Ni10La5 alloy and their behavior with the thermal cycles. It seems to be reasonable to assume that when a hydrogenated sample is slowly heated in vacuum, the thermal desorption, or the decomposition of hydrides, takes place according to a reaction process as manifested by the PCT desorption isotherms of the sample. Referring to Fig. 3, the main peak b at ~200ºC and its lower-temperature shoulder a in Figs. 11 and 14 are attributable to the decompositions of MgH2 and Mg2NiH4, respectively. The plateau pressure for the decomposition of Mg2NiH4 becomes closer to that of MgH2 as the temperature decreases. This might be a reason why the shoulder a is not clearly defined as a single peak in the TDS spectra. Now, peak c at ~250ºC, which is broad but well defined in the 1st cycle, progressively shrinks with increase in the number of cycle; peak b develops at the expense of peak c instead. This peak might be attributable to desorption of hydrogen dissolved in unstable grain boundaries (nano-boundaries) existing in high density after the crystallization. Most of these boundary regions are expected to transform to nano-crystalline Mg grains to form MgH2 in the following 2nd to 6th cycles. The fact that the main peak b is broadened and shifts toward higher temperatures when the alloy is heated up to ~380℃ (7th to 10th cycles) suggests that the nanostructure is altered to some extent allowing redistribution and coarsening of the nano-grains. In this temperature range, the stable LaH3 hydrides are also decomposed to form coarse grains of metallic La, resulting in destabilizing the nano-grain structure of the alloy. This structural change will necessarily lead to retarding the decomposition reaction of hydrides and the subsequent hydrogen transport toward the alloy surfaces. Indeed, a much longer time is required for hydrogenating the sample at 300℃ in the 10th cycle in comparison with those in the 2nd to 6th ones. The structural change suggested above has been really confirmed by TEM observation, as shown later (Section 5 and 6).

Figure 15.

Evolution of TDS peaks of a melt-spun Mg90Ni10 alloy subjected to 1st to 4th hydrogenation/thermal desorption cycles. (Tanaka, 2008)

We next discuss the hydrogen desorption process in melt-spun Mg85Ni10La5 alloy. As mentioned in connection with eq. (2), the linear time dependence of H-desorption at a fixed temperature suggests that the surface reaction is a rate-controlling step for the process. Namely, the decomposition of hydrides and subsequent diffusion of hydrogen toward external surfaces of powder grains occur quickly enough to establish a homogeneous hydrogen distribution within the grains. Thus, hydrogen in a grain may be assumed to be in a quasi-equilibrium state during the desorption. Although data for H-diffusion in Mg-rich nano-crystalline alloys are unavailable at present, the H-diffusivity along grain boundaries may be higher than those in Mg and Mg2Ni grains, or in MgH2 and Mg2NiH4 hydrides (Spassov & Köster, 1999). Hydrogen atoms released from the hydrides inside a grain (diameter < ~5μm) might quickly diffuse through nano-boundaries toward the surface of the grain and be chemisorbed on some surface sites such as Mg2Ni nano-grains (Yamaga et al., 2008). Hydrogen molecules are desorbed from the chemisorbed sites into vacuum via a recombination reaction.

Now, we consider a thermal desorption spectrum for a simple isolated system of hydrogen atoms adsorbed on an Mg2Ni grain surface. The peak temperature of the TDS spectrum is just given by eq. (4) with Edes = Ead, adsorption energy of a hydrogen molecule. In a real system, where hydrogen is continuously supplied from an interior hydride to the surface sites, a modified relation, Edes = Ead + Ebind, may hold, where Ebind is an effective binding energy of hydrogen of the hydride relative to the surface sites. The effective binding energy may be evaluated from the formation enthalpy ΔHf of the hydride, as shown below.

Figure 16.

Hydrogen potential energy diagram in melt-spun Mg85Ni10La5 alloy, showing interrelations between the formation enthalpies of hydrides, ΔHf, and the activation energy of desorption, Edes. (Tanaka, 2008)

Figure 15 displays a potential energy diagram of hydrogen existing in the hydrides or nano-boundaries in melt-spun Mg85Ni10La5 relative to that of the gas phase at standard state. Here, the formation enthalpy ΔHf is taken as the potential energy E in a hydride, and values given in Table 1 (desorption process) are used for the MgH2 and Mg2NiH4 hydrides. The potential energies for hydrogen in the nano-boundaries and LaH3 are estimated and given in the parentheses. Now, we set an energy barrier of Ead = 50 kJ/mol H2 above the potential of Mg2NiH4 hydride for the desorption of hydrogen. (In the real system, desorption from Mg2Ni grain surface will occur, for which an alternate value of Ead must be used. In the present model, direct desorption from Mg2NiH4 hydride surface is tentatively assumed.) Then the net activation energy for desorption is given by Edes = Ead + Ebind, where Ebind means the potential depth referred to the Mg2NiH4 hydride. This value can be obtained from Edes measured by TDS (Fig. 13), as shown in the figure. In this way, ΔHf of nano-crystalline LaH3 is estimated at –131 kJ/mol H2, for which a value of –188 kJ/mol H2 is given in conventional material (Fukai, 1993). Furthermore, the potential energy of hydrogen dissolved in nano-boundaries (mean value) is estimated at –95 kJ/mol H2, indicating that hydrogen in the nano-boundary is more stable than in MgH2 hydride by about 20 kJ/mol H2. It should be argued here that the apparent energy for desorption, Ed = 98.1 kJ/mol H2, obtained by analyzing the desorption rates, r, at fixed temperatures for melt-spun Mg85Ni10La5 (eq. (3) and Fig. 8) is much larger than Edes = 53.1 kJ/mol H2 obtained from TDS for the decomposition of MgH2 in the same alloy. Reasons to explain this difference may not be simple. A big difference in the experimental conditions between the two measurements is that, while the TDS is always measured in a high vacuum of 10-6 to 10-5 Pa, the measurement of the desorption-rate is performed under pH2 ~ 103 Pa. In the latter case, a driving force correction is needed because the plateau pressure for the decomposition of the hydride becomes closer to pH2 especially at lower temperatures (Fernandez & Sanchez, 2002). This correction, however, has not been performed in the present study. Therefore, the present Ed value is expected to be lowered toward that of Edes if the correction is correctly applied.

5. High-resolution TEM and EELS studies of nanostructures

Nano-sized structures of melt-spun Mg90Ni10 and Mg85Ni10La5 alloy subjected to crystallization, hydrogenation and dehydrogenation have been investigated using a Hitachi H-9000 electron microscope operated at 300 kV. High-resolution TEM (HRTEM) and electron energy-loss spectroscopy (EELS) imaging techniques have been employed to reveal the structures in detail. Each sample has been ground in acetone into a fine powder with a diameter of ~1 to ~2 μm, dispersed on a carbon micro-grid, and inserted into the TEM sample chamber for observation. In the following, some results mainly on the Mg85Ni10La5 alloy are presented.

Figure 17 shows a TEM bright-field (BF) image and its electron diffraction (ED) pattern of melt-spun and crystallized Mg85Ni10La5 alloy. The ED pattern exhibits broad diffraction rings of Mg, Mg2Ni and Mg17La2 phases, consistently with the XRD pattern of the same alloy shown in Fig. 2. The alloy is composed of homogeneous distribution of nano-sized grains of these phases. Figure 18 shows a HRTEM image of the encircled region of Fig. 17. Lattice fringes of Mg, Mg2Ni and Mg17La2 nano-grains are evidently seen. Their sizes range between 5 and 10 nm. The outer regions of these grains are also composed of nano-grains of the same phases, although their lattice fringes are not observable in this figure. No evidence of the formation of Mg/Mg2Ni eutectics has been found in the crystallized alloy.

Figure 17.

TEM bright-field image and its electron diffraction pattern of melt-spun and crystallized Mg85Ni10La5 alloy.

Figure 18.

HRTEM image of the encircled region of the BF image shown in Fig. 17.

Figure 19.

BF image of hydrogenated Mg85Ni10La5 alloy and its ED pattern.

Fig. 19 shows a BF image and its ED pattern of hydrogenated Mg85Ni10La5 alloy. The ED pattern shows that MgH2, Mg2NiH4 and LaH3 hydrides are present together with remained Mg2Ni phase, in agreement with the XRD result shown in Fig. 2. The diffraction rings are not continuous but spotty, indicating that some grains of the hydride phases have undergone grain growth during the hydrogenation at 300ºC. In the BF image are seen spherical particles with dark-grey contrast dispersed in a matrix of light-grey contrast. The former are identified as nano-grains of Mg2NiH4 and LaH3 or their clusters and the latter as aggregates of MgH2 nano-grains by EELS and HRTEM micrographs shown below.

Figure 20 shows EELS mapping (Egerton, 1996) for the same sample area as in Fig. 19, where a plasmon loss (~10 eV), Mg-K (1305 eV), Ni-L2,3 (872, 855 eV) and La-M4,5 (849, 832 eV) absorption edges are employed. The plasmon-loss image, denoted as H-plasmon here, represents the distribution of MgH2 phase (bright region) present in the sample, as explained in detail later (Section 6).

Figure 20.

EELS mapping for the sample shown in Fig. 19, using H-plasmon, Mg-K, Ni-L2,3 and La-M4,5 absorption edges.

Figure 21.

HRTEM images of areas at the lower part of the sample shown in Fig. 19. (Tanaka et al., 2009)

Figure 22.

HRTEM image and its ED pattern of dehydrogenated Mg85Ni10La5 alloy.

The Mg-K edge image likewise represents the MgH2 phase, and it is clearly recognized that the MgH2 phase provides bright regions common to both the H-plasmon and the Mg-K edge in these pictures. Likewise, the Ni-L2,3 and La-M4,5 images should represent Mg2NiH4 and LaH3 phases, respectively. Both these phases, observed as bright particles of roughly ~10 nm in size, give rise to dark-grey or light-grey spots in the H-plasmon and Mg-K images. However, owing to a rather poor energy resolution employed in the present EELS mapping, the Ni-L2,3 and La-M4,5 absorption edges are not necessarily well discriminated from each other and certain overlapping generally occurs, resulting in providing nearly similar patterns of phase distribution in the present pictures. To avoid the confusion involved in specifying the Mg2NiH4 and LaH3 hydride nano-grains, a combined use of EELS and HRTEM techniques appears to be important.

Figure 21 shows HRTEM images of the same sample as shown in Fig. 19. The hydride phase of each nano-grain has been identified in such a way that a measured d-spacing of lattice planes is consistent with a calculated one of the hydride. In these figures, nano-boundaries formed between MgH2 and LaH3 nano-grains (left) and a small cluster composed of LaH3 and Mg2NiH4 nano-grains embedded in a matrix of MgH2 nano-grains (right) can be seen.

Figure 22 shows a HRTEM image and its ED pattern of a dehydrogenated Mg85Ni10La5 alloy. After the dehydrogenation at 300ºC, the alloy transforms into a structure composed of Mg and Mg2Ni metallic phases together with the LaH3 hydride phase remaining unchanged. This phase structure is consistent with the XRD result shown in Fig. 2. Although the grain growth of Mg nano-grains is suppressed during the dehydrogenation, coarsening of Mg2Ni nano-grains is often observed by HRTEM. It is reflected on the ED pattern as a continuous diffraction ring of Mg and a spotty one of Mg2Ni.

7. In situ TEM-EELS studies of dehydrogenation process

It is interesting to observe the hydrogen desorption process at elevated temperatures directly in the electron microscope. For this purpose, a hydrogenated sample is deposited on a tungsten wire of 25 μm in diameter and heated by passing an electric current under a vacuum of 10-5 Pa in the microscope. The temperature of the sample is determined from the current using a calibrated curve with an accuracy of about ± 20ºC. Since the sample has been exposed to the air for a few minutes before inserting into the microscope, it inevitably suffers from surface contamination. This may cause a substantial delay of the onset of hydrogen desorption in comparison with those found in the TDS measurements. The desorption process of a hydrogenated sample has been continuously video-recorded for TEM BF and EELS H-plasmon images at a fixed temperature of ~350º and ~450ºC.

Figure 23 shows a time evolution of a TEM BF image of a hydrogenated Mg85Ni10La5 alloy held at ~350ºC. It can be seen from the figure that, a few minutes later from the start, a bright spot appears at a central part of the sample, goes on extending outwards with the holding time, and covers almost the whole area at the final stage of the heating. This change of the BF image just corresponds to the thermal desorption of hydrogen from the observed area. In fact, the ED patterns taken before and after the heating indicate that, while the sample is composed of nano-grains of MgH2, Mg2NiH4 and LaH3 hydrides before heating, it changes into the structure consisting of metallic Mg and Mg2Ni nano-grains in addition to the LaH3 hydrides, as shown in Fig. 24. Although some grains appear to undergo coarsening during the heating, the others stay mostly in the nano-size range at this temperature.

The desorbing process has also been pursued by observing an EELS H-plasmon image at ~450ºC for the same alloy as above. Its change with the holding time is shown in Fig. 25. It can clearly be seen from the figure that the hydrogen desorption which is initiated on an edge side of the sample soon after the heating proceeds into the interior region, and finally covers the whole area of the sample. A bright region corresponding to an MgH2-enriched zone initially extends throughout the sample, but it tends to shrink with the progress of desorption, and is finally replaced by a dark region completely. This change indicates that the MgH2 matrix has been altered to a metallic Mg matrix by desorbing hydrogen.

Figure 23.

Time evolution of a BF image of a hydrogenated Mg85Ni10La5 alloy during heating at ~350ºC.

Figure 24.

ED patterns of the same sample as in Fig. 23 taken before and after heating at ~350ºC.

Figure 26 shows BF images and the corresponding ED patterns of the same sample as above before and after the heating at ~450ºC. Before heating, fine dark-grey particles corresponding to LaH3 and Mg2NiH4 hydrides are uniformly distributed in the matrix of MgH2 throughout the sample. This structure has changed drastically after heating. These fine particles have undergone redistribution and reconstruction forming coarse aggregates or precipitates of metallic Mg2Ni and La in the metallic Mg matrix. The ED pattern taken after heating exhibits strong diffraction spots lying along weak continuous rings of Mg, Mg2Ni and La, indicating that a majority of these metallic nano-grains has undergone the grain growth at the end of the heating. All these features have also been well recognized in the corresponding EELS images (Tanaka et al., 2009).

Figure 25.

Evolution of EELS H-plasmon image of hydrogenated Mg85Ni10La5 alloy with holding time at ~450ºC. (Tanaka et al., 2009)

Figure 27 shows a HRTEM image of the sample subjected to the heating at ~450ºC, showing a spheroidal Mg grain grown to ~20 nm in size together with smaller Mg2Ni and La grains in the close vicinity of the Mg grain. A HRTEM image of a rod-shape La grain grown to ~50 nm in length has also been observed (Tanaka et al., 2009).

The TEM-EELS results presented above clearly show that the nano-crystalline hydrides are really formed by hydrogenation and are completely decomposed by heating up to ~450ºC in the melt-spun Mg85Ni10La5 alloy. These results are, however, in contradiction to recent TEM studies (Hanada et al., 2008; Porcu et al., 2008), which claim that MgH2 is readily decomposed to Mg even at room temperature by the electron beam irradiation during observation. In these studies, ball-milled MgH2 sample doped with Nb2O5, which exhibits excellent hydrogen reactivity, is used in contrast to our melt-spun ternary alloy. A difference in the hydride stability between the two samples may have caused these contradictive results. Another aspect of discriminating the ball-milled sample from the melt-spun alloy is that a thermally unstable hydride, γ-MgH2, is amply formed and mixed with the stable hydride, β-MgH2, by ball milling (Danaie, 2010). Such an unstable hydride is not formed in the melt-spun alloy. It must also be taken into account that our powder sample used for the TEM-EELS studies is inevitably contaminated with oxygen on the surface before it is inserted into the electron microscope. This may have prevented the desorption of hydrogen from the sample and hence the decomposition of hydrides during the observation. Further studies are necessary to clarify these points.

Figure 26.

BF images and ED patterns of the same sample as in Fig. 25 taken before heating (upper) and after heating (lower) at ~450ºC. (Tanaka et al., 2009)

Figure 27.

Fig. 26. HRTEM image of the same sample as in Figs. 25 and 26 observed after heating at ~450ºC. (Tanaka et al., 2009)

Finally, we discuss the nature of an EELS plasmon peak in a hydrogenated sample. The EELS plasmon (or H-plasmon) peak observed in this study is considered to be associated with an excitation of bulk plasmons by an incident electron beam in the MgH2 nano-grains. This is justified from the similarity between the EELS H-plasmon and Mg-K images of the hydrogenated Mg85Ni10La5 sample shown in Fig. 20. The bright region of the Mg-K image reflects the MgH2 phase, which just corresponds to the bright region of the H-plasmon image. This bright region of H-plasmon image has been confirmed to disappear completely after the in situ hydrogen desorption, as shown in Fig. 25, although the Mg-K image still provides a bright region for the metallic Mg phase formed (Tanaka et al., 2009).

To prove the interrelation between the EELS plasmon spectrum and the H-plasmon image more closely, we reexamine

the EELS spectrum and the corresponding image of MgH2 using a commercially pure sample, as shown in Fig. 28, where the measured EELS spectra and the corresponding images are compared between the as-received sample (MgH2) and the dehydrogenated one (Mg) prepared by in situ heating at ~450ºC. The H-plasmon peak (indicated by arrow) can be clearly seen at an energy-loss E~11eV in MgH2, whereas it is almost diminished in Mg. The H-plasmon peak causes a bright image of the MgH2 phase throughout the sample in the former, whereas a dark-grey image of metallic Mg is left in the latter. Another small peak at E~22eV, which is detected in every sample studied, is attributable to a plasmon excitation in a thin MgO layer which covers the sample surface. In the free-electron model, the plasmon energy Ep is given by (Egerton, 1996),

Figure 28.

EELS spectra in the low energy-loss region and the corresponding H-plasmon images for MgH2 (upper) and Mg (lower) for a sample prepared from a commercially pure MgH2 powder. The H-plasmon peak is indicated by an arrow. The encircled area of the sample shows a spot where the EELS spectra have been taken. (Tanaka et al., 2009)

Ep=h2πωp=h2π(ne2ε0m)12,E5

where ωp is the plasmon angular frequency, n is the electron density, and other quantities have their usual meaning. Taking n = 129.8 nm-3 (MgH2) and 428.4 nm-3 (MgO), Ep is calculated as 13.3 eV and 24.2 eV, respectively. These calculated energies approximately agree with the observed ones of the EELS spectra shown in Fig. 28. Now, the plasmon energy for metallic Mg is calculated as Ep = 10.8 eV taking n = 86.1 nm-3, which falls in the close vicinity of MgH2. However, owing to the lack of energy resolution of the present EELS experiment and/or to the lack of the spectral intensity of the plasmon peak of metallic Mg in comparison with that of MgH2, this peak has not been clearly detected in the present study. In this respect, it is worthwhile to note that both peaks have been detected in a partially dehydrogenated MgH2 sample subjected to ball milling (Danaie, 2010). An H-plasmon peak similar to our study has also been observed in a ball-milled NbB5-doped MgH2 sample (Kim et al., 2010).

7. Summary and conclusions

(1) A magnesium-based Mg-Ni-La alloy, specifically Mg85Ni10La5 alloy, prepared by melt-spinning and subsequent crystallization annealing exhibits favorable reaction kinetics and PCT characteristics for hydrogen absorption and desorption. The p-c isotherms at 240-330ºC manifest a flat two-stage plateau with small hysteresis and a maximum H-capacity of ~4.6 wt.%. A temperature as low as ~200ºC is enough for hydriding and dehydridng the alloy entirely in a moderate time period. XRD results show that a mixed phase structure of Mg and Mg2Ni before hydrogenation, or MgH2 and Mg2NiH4 after hydrogenation, together with a thermally stable hydride LaH3, is the main source of these excellent hydrogen storage characteristics.

(2) The fully hydrogenated alloy exhibits, in general, four TDS peaks (a~d). The magnitude and temperature of each peak depend on the specimen history and the heating rate (0.5~4ºC/min) for the TDS measurement. Assuming that a quasi-equilibrium condition is established in the specimen, these peaks are attributed to decomposition of Mg2NiH4 (peak a), decomposition of MgH2 (peak b), release from nano-grain boundaries (peak c), and decomposition of LaH3 (peak d). The heating-rate dependence of the TDS peak temperature is successfully analyzed on the basis of Kissinger’s equation, from which the activation energy for desorption Edes is obtained for each peak. Assuming that the desorption is a surface-controlled process and that Edes is the sum of an adsoption energy Ead and an effective binding energy Ebind of hydrogen in the alloy, a relationship between Ebind and the formation enthalpy ΔHf of a hydride is proposed. From this relationship, the hydrogen dissolved in the nano-boundaries appears to be ~20 kJ/mol H2 more stable than in MgH2.

(3) The role of Ni and La for facilitating the hydrogen storage properties of the Mg-based alloy is multifold. Both elements act to promote the amorphization of the alloy by melt-spinning and to produce a homogeneous nano-grain structure by crystallization. Nickel forms stable Mg2Ni nano-grains, which act as dissociation and recombination catalysts for hydrogen molecules on the surface of the alloy and contribute to enhance the absorption and desorption kinetics of hydrogen. On the other hand, La forms thermally stable LaH3 nano-hydrides, which work to stabilize the whole nanostructure during the hydriding and dehydriding cycles at temperatures below ~350ºC.

(4) The improved kinetics of hydrogen absorption and desorption of the alloy is partly due to faster diffusion of hydrogen along the nano-boundaries than through inside the Mg/MgH2 or Mg2Ni/Mg2NiH4 grains. The relatively fast diffusivity and high solubility of hydrogen in the nano-boundaries will facilitate the hydrogen transport inside the alloy and hence enhance its absorption and desorption rates.

(5) It has been confirmed by TEM and HRTEM studies that, after hydrogenation at 300ºC, this alloy exhibits a nanostructure consisting of Mg2NiH4 and LaH3 nano-particles (~10 nm) imbedded uniformly in MgH2 nano-grain (3~5 nm) matrices. After dehydrogenation at 300ºC, this alloy exhibits Mg2Ni and LaH3 nano-particles imbedded uniformly in the Mg nano-grain matrix. This nanostructure is almost maintained if the hydrogenation and dehydrogenation treatments are performed at temperatures below ~350ºC.

(6) If the temperature is raised beyond ~400ºC,the desorbing as well as the absorbing characteristics of the alloy are significantly degraded. The in situ TEM observation during heating at ~450ºC indicates that the original nanostructure undergoes remarkable redistribution and reconstruction of the alloy phases, in parallel with the decomposition of the hydrides. Instead of a uniform distribution of the hydride particles, segregations of coarse precipitates of Mg2Ni and La, together with the grain growth of Mg matrix, take place. These coarsening of the alloy phases and their inhomogeneous redistribution must have retarded the reaction kinetics for hydrogen.

(7) We have succeeded in clearly visualizing a global hydrogen distribution in the alloy sample by imaging the EELS plasmon peak (H-plasmon) arising from the MgH2 phase. By using this technique, the thermal desorption process has been directly observed in the microscope. Melt-spun and nano-crystallized Mg-based alloys are quite favorable materials for this kind of studies.

Acknowledgement

The author is grateful to Prof. H. Inokuchi, Prof. A. Ikushima and Prof. Y. Ishibashi of Toyota Physical & Chemical Research Institute for stimulating discussions and comments. He is also grateful to Dr. S. Towata of Toyota Central R/D Laboratories for the collaboration in the PCT measurements and useful advices, to Mr. T. Miwa, Dr. K. Sasaki and Prof. K. Kuroda of Nagoya University for the cooperation in the TEM-EELS studies, and to Dr. M. Yamada and Mr. K. Hibino of Nagoya Institute of Technology for the collaboration in the sample preparation.

© 2012 The Author(s). Licensee IntechOpen. This chapter is distributed under the terms of the Creative Commons Attribution 3.0 License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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Kazuhide Tanaka (September 5th 2012). Hydrogen Storage Properties and Structure of Magnesium-Based Alloys Prepared with Melt-Spinning Technique, Hydrogen Storage, Jianjun Liu, IntechOpen, DOI: 10.5772/50170. Available from:

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