Issue 11, 2023

Ultrafine Pt nanoparticles anchored on core–shell structured zeolite–carbon for efficient catalysis of hydrogen generation

Abstract

Ammonia borane (AB) is a potential hydrogen storage material with high-efficiency hydrolytic dehydrogenation under a suitable catalyst. Noble metal catalysts have drawn a lot of attention. In this study, a carbon-coated zeolite was obtained by calcination at high temperatures using glucose as a carbon source. Pt nanoparticles were fixed on a core–shell composite support by a simple chemical reduction method. A series of catalysts were prepared with different synthesis parameters. The results show that PSC-2 has excellent catalytic performance for hydrolytic dehydrogenation of AB in alkaline solution at room temperature, and the turnover frequency (TOF) is 593 min−1. The excellent catalytic performance is attributed to the carbon layer on the zeolite surface which inhibits the aggregation or deformation of metals in the catalytic reaction. The metal-support interaction activates the water and accelerates the rate-limiting step of hydrolysis. The activation energy (Ea = 44 kJ mol−1) was calculated based on the reaction temperature. In addition, the kinetics of AB hydrolysis was studied, and the effects of catalyst concentration, AB concentration and NaOH concentration on AB hydrolysis rate were further investigated. The high-efficiency catalyst prepared in this work provides a new strategy for the development of chemical hydrogen production in the field of catalysis.

Graphical abstract: Ultrafine Pt nanoparticles anchored on core–shell structured zeolite–carbon for efficient catalysis of hydrogen generation

Supplementary files

Article information

Article type
Paper
Submitted
17 Jan 2023
Accepted
07 Feb 2023
First published
08 Mar 2023
This article is Open Access
Creative Commons BY-NC license

RSC Adv., 2023,13, 7673-7681

Ultrafine Pt nanoparticles anchored on core–shell structured zeolite–carbon for efficient catalysis of hydrogen generation

Y. Wei, G. Yang, X. Xu, Y. Liu, B. Li, Y. Wang and Y. Zhao, RSC Adv., 2023, 13, 7673 DOI: 10.1039/D3RA00358B

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