Guo Yusang, Liu Yafei, Feng Lizhuang, An Cuihua, Wang Yijing
Key Laboratory of Advanced Energy Materials Chemistry (Ministry of Education), Renewable Energy Conversion and Storage Center (RECAST), College of Chemistry, Nankai University, Tianjin, 300071, P.R. China.
Key Laboratory of Hebei Province on Scale-span Intelligent Equipment Technology, and School of Mechanical Engineering, Hebei University of Technology, Tianjin, 300401, P.R. China.
Chem Asian J. 2023 Apr 3;18(7):e202300009. doi: 10.1002/asia.202300009. Epub 2023 Mar 3.
Catalysts combined with nanoconfinement can improve the sluggish desorption kinetics and poor reversibility of LiBH . However, at high LiBH loading, their hydrogen storage performance is significantly reduced. Herein, a porous carbon-sphere scaffold decorated with Ni nanoparticles (NPs) was synthesised by calcining a Ni metal-organic framework precursor, followed by partial etching of the Ni NPs to fabricate an optimised scaffold with a high surface area and large porosity that accommodates high LiBH loading (up to 60 wt.%) and exhibits remarkable catalyst/nanoconfinement synergy. Owing to the catalytic effect of Ni B (formed in situ during dehydrogenation) and the reduced hydrogen diffusion distances, the 60 wt.% LiBH confined system exhibited enhanced dehydrogenation kinetics with >87% of the total hydrogen storage capacity released within 30 min at 375 °C. The apparent activation energies were significantly reduced to 110.5 and 98.3 kJ/mol, compared to that of pure LiBH (149.6 kJ/mol). Moreover, partial reversibility was achieved under moderate conditions (75 bar H , 300 °C) with rapid dehydrogenation during cycling.
催化剂与纳米限域相结合可改善LiBH缓慢的解吸动力学和较差的可逆性。然而,在高LiBH负载量下,它们的储氢性能会显著降低。在此,通过煅烧镍金属有机框架前驱体,然后对镍纳米颗粒进行部分蚀刻,合成了一种装饰有镍纳米颗粒(NPs)的多孔碳球支架,以制备具有高表面积和大孔隙率的优化支架,该支架可容纳高LiBH负载量(高达60 wt.%)并表现出显著的催化剂/纳米限域协同效应。由于脱氢过程中原位形成的NiB的催化作用以及氢扩散距离的缩短,60 wt.% LiBH受限体系在375℃下30分钟内释放了超过87%的总储氢容量,表现出增强的脱氢动力学。与纯LiBH(149.6 kJ/mol)相比,表观活化能显著降低至110.5和98.3 kJ/mol。此外,在中等条件(75 bar H₂,300℃)下实现了部分可逆性,且循环过程中脱氢迅速。