Efficient Hydrogen Generation from Ammonia Borane Hydrolysis on a Tandem Ruthenium–Platinum–Titanium Catalyst

Author:

Guan Shuyan12,Yuan Zhenluo1,Zhao Shiqian1,Zhuang Zechao2,Zhang Huanhuan1,Shen Ruofan3,Fan Yanping1,Li Baojun3,Wang Dingsheng2ORCID,Liu Baozhong1

Affiliation:

1. College of Chemistry and Chemical Engineering Henan Polytechnic University 2001 Century Avenue Jiaozuo 454000 P. R. China

2. Department of Chemistry Tsinghua University Beijing 100084 P.R. China

3. Research Center of Green Catalysis College of Chemistry Zhengzhou University 100 Science Road Zhengzhou 450001 P. R. China

Abstract

AbstractHydrolysis of ammonia borane (NH3BH3, AB) involves multiple undefined steps and complex adsorption and activation, so single or dual sites are not enough to rapidly achieve the multi‐step catalytic processes. Designing multi‐site catalysts is necessary to enhance the catalytic performance of AB hydrolysis reactions but revealing the matching reaction mechanisms of AB hydrolysis is a great challenge. In this work, we propose to construct RuPt−Ti multi‐site catalysts to clarify the multi‐site tandem activation mechanism of AB hydrolysis. Experimental and theoretical studies reveal that the multi‐site tandem mode can respectively promote the activation of NH3BH3 and H2O molecules on the Ru and Pt sites as well as facilitate the fast transfer of *H and the desorption of H2 on Ti sites at the same time. RuPt−Ti multi‐site catalysts exhibit the highest turnover frequency (TOF) of 1293 min−1 for AB hydrolysis reaction, outperforming the single‐site Ru, dual‐site RuPt and Ru−Ti catalysts. This study proposes a multi‐site tandem concept for accelerating the dehydrogenation of hydrogen storage material, aiming to contribute to the development of cleaner, low‐carbon, and high‐performance hydrogen production systems.

Funder

National Key Research and Development Program of China

National Natural Science Foundation of China

Publisher

Wiley

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