Electronic regulation over Pd nanoparticles: One-pot synthesis of B, N Co-doping MXene-supported Pd catalyst for efficient ethanol oxidation

被引:11
|
作者
Cao, Jiajie [1 ,2 ]
Wu, Xiaohui [1 ,2 ]
Chen, Yongyin [2 ]
Chen, Zhangxin [2 ]
Jiang, Ruoruo [2 ]
Zhao, Yanying [1 ]
Tian, Qinghua [1 ]
Chen, Dan [2 ]
Xiao, Shengwei [2 ]
Yu, Binbin [2 ]
Jin, Yanxian [2 ]
机构
[1] Zhejiang Sci Tech Univ, Sch Sci, Hangzhou 310018, Zhejiang, Peoples R China
[2] Taizhou Univ, Sch Pharmaceut, Jiaojiang 318000, Zhejiang, Peoples R China
基金
中国国家自然科学基金;
关键词
One-step codoping; Electronic regulation; Pd catalyst; Electrocatalytic properties; Ethanol oxidation; TOTAL-ENERGY CALCULATIONS; NITROGEN;
D O I
10.1016/j.jallcom.2023.170240
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Multi-element doping support is considered an effective method to improve the electrocatalytic performance of catalysts, but there is a lack of simple and mild methods to prepare catalysts. In this article, dimethylamine borane is used as a heteroatom dopant and a metal-reducing agent at the same time, realizing the co-doping of B and N atoms and the deposition of metal Pd on Ti3C2 through a rapid, one-step hydrothermal method. By exploring the electrocatalytic properties of ethanol oxidation, the Pd/DMAB-Ti3C2 exhibits much higher electrochemically active surface areas, ethanol-oxidated current densities, and electrochemical stability than those of the single-doped and undoped catalysts. And the current densities after 350 redox cycles of Pd/DMAB-Ti3C2 can retain 74.6 % of the maximum capacity. Such different properties can be attributed to the synergy of B and N species in the Ti3C2 introduced by dimethylamine borane, which significantly affects the electron transfer and d band center of supported metal Pd, thus facilitating the progress of the EOR along a favorable pathway. This work provides a new insight into synthesizing the highperformance B and N co-doped supported metal catalyst through a rapid one-step synthesis. (c) 2023 Published by Elsevier B.V.
引用
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页数:8
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