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包覆有碳的过渡金属(钴、镍)纳米颗粒及其对氢化镁可逆储氢的优异催化活性。

Transition metal (Co, Ni) nanoparticles wrapped with carbon and their superior catalytic activities for the reversible hydrogen storage of magnesium hydride.

作者信息

Huang Xu, Xiao Xuezhang, Zhang Wei, Fan Xiulin, Zhang Liuting, Cheng Changjun, Li Shouquan, Ge Hongwei, Wang Qidong, Chen Lixin

机构信息

State Key Laboratory of Silicon Materials, Key Laboratory of Advanced Materials and Applications for Batteries of Zhejiang Province, School of Materials Science and Engineering, Zhejiang University, Hangzhou 310027, P. R. China.

出版信息

Phys Chem Chem Phys. 2017 Feb 1;19(5):4019-4029. doi: 10.1039/c6cp07852d.

Abstract

Magnesium hydride (MgH) exhibits long-term stability and has recently been developed as a safe alternative to store hydrogen in the solid state, due to its high capacity of 7.6 wt% H and low cost compared to other metal hydrides. However, the high activation energy and poor kinetics of MgH lead to inadequate hydrogen storage properties, resulting in low energy efficiency. Nano-catalysis is deemed to be the most effective strategy in improving the kinetics performance of hydrogen storage materials. In this work, robust and efficient architectures of carbon-wrapped transition metal (Co/C, Ni/C) nanoparticles (8-16 nm) were prepared and used as catalysts in the MgH system via ball milling to improve its de/rehydrogenation kinetics. Between the two kinds of nano-catalysts, the Ni/C nanoparticles exhibit a better catalytic efficiency. MgH doped with 6% Ni/C (MgH-6%Ni/C) exhibits a peak dehydrogenation temperature of 275.7 °C, which is 142.7, 54.2 and 32.5 °C lower than that of commercial MgH, milled MgH and MgH doped with 6% Co/C (MgH-6%Co/C), respectively. MgH doped with 6% Ni/C can release about 6.1 wt% H at 250 °C. More importantly, the dehydrogenated MgH-6%Ni/C is even able to uptake 5.0 wt% H at 100 °C within 20 s. Moreover, a cycling test of MgH doped with 8% Ni/C demonstrates its excellent hydrogen absorption/desorption stability with respect to both capacity (up to 6.5 wt%) and kinetics (within 8 min at 275 °C for dehydrogenation and within 10 s at 200 °C for rehydrogenation). Mechanistic research reveals that the in situ formed MgNi and MgNiH nanoparticles can be regarded as advanced catalytically active species in the MgH-Ni/C system. Meanwhile, the carbon attached around the surface of transition metal nanoparticles can successfully inhibit the aggregation of the catalysts and achieve the steadily, prompting de/rehydrogenation during the subsequent cycling process. The intrinsic catalytic effects and the uniform distributions of MgNi and MgNiH result in a favorable catalytic efficiency and cycling stability. Nano-catalysts with this kind of morphology can also be applied to other metal hydrides to improve their kinetics performance and cycling stability.

摘要

氢化镁(MgH)具有长期稳定性,由于其7.6 wt%的高储氢容量以及与其他金属氢化物相比成本较低,最近已被开发为一种安全的固态储氢替代品。然而,MgH的高活化能和较差的动力学导致储氢性能不足,从而使能量效率较低。纳米催化被认为是提高储氢材料动力学性能最有效的策略。在这项工作中,制备了坚固且高效的碳包覆过渡金属(Co/C、Ni/C)纳米颗粒(8 - 16 nm)结构,并通过球磨将其用作MgH体系中的催化剂,以改善其脱氢/加氢动力学。在这两种纳米催化剂中,Ni/C纳米颗粒表现出更好的催化效率。掺杂6% Ni/C的MgH(MgH - 6%Ni/C)的脱氢峰值温度为275.7 °C,分别比商业MgH、球磨MgH和掺杂6% Co/C的MgH(MgH - 6%Co/C)低142.7、54.2和32.5 °C。掺杂6% Ni/C的MgH在250 °C时可释放约6.1 wt%的氢。更重要的是,脱氢后的MgH - 6%Ni/C甚至能够在100 °C下20 s内吸收5.0 wt%的氢。此外,对掺杂8% Ni/C的MgH进行的循环测试表明,其在容量(高达6.5 wt%)和动力学(275 °C脱氢8分钟内,200 °C加氢10秒内)方面都具有出色的吸氢/脱氢稳定性。机理研究表明,原位形成的MgNi和MgNiH纳米颗粒可被视为MgH - Ni/C体系中先进的催化活性物种。同时,附着在过渡金属纳米颗粒表面的碳能够成功抑制催化剂的聚集,并在随后的循环过程中实现稳定的脱氢/加氢。MgNi和MgNiH的固有催化作用以及均匀分布导致了良好的催化效率和循环稳定性。这种形态的纳米催化剂也可应用于其他金属氢化物,以改善其动力学性能和循环稳定性。

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