Functional Group Regulated Ni/Ti₃C₂T_<i>x</i> (T_<i>x</i> = F, −OH) Holding Bimolecular Activation Tunnel for Enhanced Ammonia Borane Hydrolysis

Abstract

Developing economical and efficient catalyst for hydrogen generation from ammonia borane (AB) hydrolysis is still a huge challenge. As an alternative strategy, the functional group regulation of metal nanoparticles (NPs)-based catalysts is believed to be capable of improving the catalytic activity. Herein, a series of Ni/Ti₃C₂T_<i>x</i>-Y (T_<i>x</i> = F, -OH; Y denotes etching time (d)) catalysts are synthesized and show remarkably enhanced catalytic activity on the hydrolysis of AB in contrast to the corresponding without regulating. The optimized Ni/Ti₃C₂T_<i>x</i>-4 with a turnover frequency (TOF) value of 161.0 min^-1 exhibits the highest catalytic activity among the non-noble monometallic-based catalyst. Experimental results and theory calculations demonstrate that the excellent catalytic activity benefits from the bimolecular activation channels formed by Ni NPs and Ti₃C₂T_<i>x</i>-Y. H₂O and AB molecules are activated simultaneously in the bimolecular activation tunnel. Bimolecular activation reduces the activation energy of AB hydrolysis, and hydrogen generation rate is promoted. This article provides a new approach to design effective catalysts and further supports the bimolecular activation model for the hydrolysis of AB.