电解
甲醇
兴奋剂
等离子体
材料科学
化学工程
纳米技术
工程物理
光电子学
化学
物理化学
工程类
物理
有机化学
电极
量子力学
电解质
作者
Yubin Kuang,Wei Qiao,Shuli Wang,Fulin Yang,Ligang Feng
出处
期刊:ACS materials letters
[American Chemical Society]
日期:2024-03-29
卷期号:: 1722-1731
被引量:2
标识
DOI:10.1021/acsmaterialslett.4c00244
摘要
The electrochemical methanol–hydrogen transformation as a significant technique for hydrogen generation is limited by a low Pt catalytic efficiency. Herein, the doping and interfacial support engineering of MoSe2 nanosheets by NH3 plasma confined in mesoporous hollow-carbon-spheres-supported Pt nanoparticles (Pt/N-MoSe2@MHCS) were demonstrated as a novel platform for catalyzing methanol electrolysis. Experiments and density functional theory (DFT) calculations confirm that the band structure of the Pt species is downshifted to weaken the adsorption energy of COad/Had, resulting in improved CO-poisoning resistance and accelerated electrocatalytic kinetics. As a result, Pt/N-MoSe2@MHCS shows the highest current density of 99.2 mA cm–2 for methanol oxidation and a low overpotential of 26 mV@10 mA cm–2 for hydrogen evolution. The methanol-assisted water electrolyzer assembled by Pt/N-MoSe2@MHCS showed a low cell voltage of 1070 mV to reach 10 mA cm–2. This work provides novel guidance for the design of reasonable noble-metal catalysts in methanol electrolysis for hydrogen production.
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