期刊
INTERNATIONAL JOURNAL OF HYDROGEN ENERGY
卷 46, 期 49, 页码 25081-25091出版社
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.ijhydene.2021.05.062
关键词
Platinum nanoparticles; Modified silica spheres; Hydrogen generation; Ammonia borane; Catalytic hydrolysis
资金
- National Key R&D Program of China [2017YFA0206801]
- National Natural Science Foundation of China [22078017]
Poly(N-vinyl-2-pyrrolidone) (PVP)-protected platinum nanoparticles supported on gamma-methacryloxypropyltrimethoxysilane (gamma-MPS) modified silica spheres (Pt-PVP/SiO2(M)) exhibit high catalytic activity for the hydrolysis of ammonia borane (AB), with small size, uniform dispersion, and low activation energy. The synergistic effect between the modifier of silica spheres and the capping agent of metal nanoparticles contributes to the higher loading amount and turnover frequency (TOF) values compared to counterparts without gamma-MPS and PVP.
Ammonia borane (AB) is considered to be a promising solid hydrogen carrier. In this work, poly(N-vinyl-2-pyrrolidone) (PVP)-protected platinum nanoparticles are supported on gamma-methacryloxypropyltrimethoxysilane (gamma-MPS) modified silica spheres (Pt-PVP/SiO2(M)), which are firstly used as highly efficient catalysts for hydrolysis of AB. Platinum nanoparticles possess a tiny size of 2-3 nm and are uniformly dispersed over modified silica spheres. Pt-PVP/SiO2(M) catalysts with a Pt loading amount of 1.30 wt% show the highest catalytic activity with a turnover frequency (TOF) value of 371 mol(H2) mol(Pt)(-1) min(-1) (866 mol(H2) mol(Pt)(-1) min(-1) corrected for the surface atoms) at 25 degrees C. The activation energy is calculated to be 46.2 kJ/mol. Furthermore, owing to the synergistic effect between the modifier of silica spheres and the capping agent of metal nanoparticles, Pt-PVP/SiO2(M) catalysts have a higher loading amount (8.7 and 6.5 times) and TOF value (4.8 and 5.5 times) than the counterparts prepared without gamma-MPS and PVP, respectively. (C) 2021 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
作者
我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。
推荐
暂无数据