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REVERSIBLE HYDROGEN STORAGE IN COMPLEX METAL HYDRIDES NANOCONFINED IN METAL ORGANIC FRAMEWORKS

机译:在金属有机框架中纳米中的复合金属氢化物中可逆储氢

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Significant efforts have been recently devoted to the design and synthesis of new materials for solid-state hydrogen storage. Complex metal hydrides are attractive hydrogen storage media due to their high gravimetric and volumetric hydrogen densities and possible reversibility. However, most bulk complex metal hydrides suffer from unfavorable thermodynamics and slow kinetics. Nano-confinement and catalysis are promising strategies to both enhance the reversibility and decrease the H2 desoprtion temperatures of complex metal hydrides.For example, it has been shown that at nanoscale, the thermodynamic properties of metal hydride particles can be altered by controlling their surface energy.Nanostructuring is also explored to improve the kinetics of H2 release, arguably through the increase in the surface area and the number of grain boundaries, which accelerate the diffusion rate through the solid.
机译:最近致力于设计和合成固态储氢的设计和合成的重大努力。复杂金属氢化物由于其高重量和体积氢密度以及可能的可逆性,是有吸引力的储氢介质。然而,大多数散装复合物氢化物患有不利的热力学和缓慢的动力学。纳米限制和催化是增强复合金属氢化物的可逆性和降低的可逆性和降低的策略。如图所示,在纳米尺度下,可以通过控制它们的表面能来改变金属氢化物颗粒的热力学性质。还探讨了脑结构,以改善H2释放的动力学,可以通过表面积的增加和晶界的数量来改善通过固体加速扩散速率。

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