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Carbon nanotubes-supported Pt catalysts for decalin dehydrogenation to release hydrogen: A comparison between nitrogen- and oxygen-surface modification  ( SCI-EXPANDED收录 EI收录)  

文献类型:期刊文献

英文题名:Carbon nanotubes-supported Pt catalysts for decalin dehydrogenation to release hydrogen: A comparison between nitrogen- and oxygen-surface modification

作者:Tuo, Yongxiao[1,2];Yang, Liu[1];Ma, Xuefei[1];Ma, Zhejie[1];Gong, Shan[1];Li, Ping[1]

机构:[1]East China Univ Sci & Technol, State Key Lab Chem Engn, 130 Meilong Rd, Shanghai 200237, Peoples R China;[2]China Univ Petr East China, Sch Mat Sci & Engn, Qingdao 266580, Peoples R China

年份:2021

卷号:46

期号:1

起止页码:930

外文期刊名:INTERNATIONAL JOURNAL OF HYDROGEN ENERGY

收录:;EI(收录号:20204309393635);WOS:【SCI-EXPANDED(收录号:WOS:000605110100075)】;

基金:The authors are grateful for the financial support of National Key Research and Development Program of China (No. 2018YFB0105603) and the Postdoctoral Research Program of Qingdao, China (No. ZX20190140).

语种:英文

外文关键词:Decalin dehydrogenation; Carbon nanotubes; Nitrogen and oxygen groups; Pt catalyst; Metal-support interaction

摘要:The effect of carbon nanotubes (CNT) surface chemistry on supported Pt catalytic performance in decalin dehydrogenation to release hydrogen was investigated through modifying CNT surface with nitrogen and oxygen functional groups. The results indicate that the mechanism of improving Pt dispersion is different for nitrogen and oxygen groups. Although oxygen groups can improve Pt dispersion, their electron donating feature inhibits the electron transfer from Pt to carbon support. DFT calculations have clarified the negative effect of oxygen group on decalin dehydrogenation in aspect of adsorption energy. Moreover, the abundant oxygen species on catalyst surface lead to a bad wettability of catalyst in non-polar reaction liquid, which significantly weaken the approaching of reactant onto catalyst. Therefore, the introduction of oxygen groups is unfavorable to the catalyst activity. In contrast, the highly dispersed Pt nanoparticles anchored by nitrogen groups may be one reason for the high activity of Pt supported on CNT modified with nitrogen groups. Furthermore, nitrogen groups promote the electron transfer from Pt to CNT, leading to lower Pt d-band and weaker naphthalene adsorption. Meanwhile little change happened on the non-polar characteristics of CNT during nitrogen doping treatment. Therefore, the introduction of nitrogen functional groups is conducive to the catalytic dehydrogenation. (C) 2020 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.

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