High-loading LiBH4 Confined in Structurally Tunable Ni Catalyst-decorated Porous Carbon Scaffold for Fast Hydrogen
Yusang Guo1, Yafei Liu1, Lizhuang Feng1
1Key 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.
Abstract:
Catalysts combined with nanoconfinement can improve the sluggish desorption kinetics and poor reversibility of LiBH4 . However, at high LiBH4 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 LiBH4 loading (up to 60 wt.%) and exhibits remarkable catalyst/nanoconfinement synergy. Owing to the catalytic effect of Ni2 B (formed in situ during dehydrogenation) and the reduced hydrogen diffusion distances, the 60 wt.% LiBH4 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 LiBH4 (149.6 kJ/mol). Moreover, partial reversibility was achieved under moderate conditions (75 bar H2 , 300 °C) with rapid dehydrogenation during cycling.
More Related Videos
06:32A Simple, Low-cost, and Robust System to Measure the Volume of Hydrogen Evolved by Chemical Reactions with Aqueous Solutions
Published on: August 17, 2016
10:57Synthesis and Performance Characterizations of Transition Metal Single Atom Catalyst for Electrochemical CO2 Reduction
Published on: April 10, 2018
Related Concept Videos
Catalysis
Reduction of Alkenes: Asymmetric Catalytic Hydrogenation
The metal catalyst used can be either heterogeneous or homogeneous. When hydrogenation of an alkene generates a chiral center, a pair of enantiomeric products is expected to form. However, an enantiomeric excess of one of the products can be facilitated using an enantioselective reaction or an...
Reduction of Alkenes: Catalytic Hydrogenation
Metals like palladium, platinum, and nickel are commonly used in their solid forms — fine powder on an inert surface. As these catalysts remain insoluble in the reaction mixture, they are referred to as heterogeneous catalysts.
The hydrogenation process takes place on the...
