Boosting low-temperature de/re-hydrogenation performances of MgH2 with Pd-Ni bimetallic nanoparticles supported by mesoporous carbon |
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Affiliation: | 3. Guangdong Provincial Key Laboratory of Advance Energy Storage Materials, South China University of Technology, Guangzhou 510640, Guangdong, China |
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Abstract: | Bimetallic Pd-Ni nano-particles supported by a mesoporous carbon material CMK-3 (denoted as Pd30Ni70/CMK-3) were synthesized through solution impregnation and hydrogen reduction methods. Among those hierarchical Ni-Pd nano-particles, majorly large ones (>10 nm) are dispersed over the surface of CMK-3, while a litter small ones (<10 nm) are embedded into the pores. It significantly improves the de/re-hydrogenation performances of MgH2 at low temperature. The onset desorption temperature of MgH2-Pd30Ni70/CMK-3 is lowered by 150 K from that of pristine MgH2 (above 593 K). About 6 wt% hydrogen could be released during its decomposition below 561 K. Noticeably, MgH2-Pd30Ni70/CMK-3 is capable of releasing 1.3 wt% H2 even at 373 K. 4 wt% hydrogen can be absorbed at 343 K under a hydrogen pressure of 3 MPa within 18000 s. Activation energy values of both hydrogen decomposition (65.9 kJ mol?1) and absorption (78.9 kJ mol?1) for MgH2-Pd30Ni70/CMK-3 are greatly improved from those of as-milled MgH2. Thermal stability of the composite system is remarkably destabilized by 4.3 kJ mol H2?1 from pristine MgH2 according to pressure-composition isotherm curves and van't Hoff plots. The enhanced performances can be ascribed to the synergistic effects of both destabilization and catalysis from nano-dispersed Pd and Ni particles, respectively. |
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Keywords: | Nano-dispersion Bimetallic Pd-Ni particles Hydrogen storage Magnesium hydride |
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