Suppressing Dissolution of Pt-Based Electrocatalysts through the Electronic Metal-Support Interaction

被引:79
作者
Lin, Gaoxin [1 ,2 ]
Ju, Qiangjian [1 ,2 ]
Jin, Yan [1 ,3 ]
Qi, Xiaohuan [1 ,2 ]
Liu, Weijing [4 ]
Huang, Fuqiang [1 ,2 ,5 ]
Wang, Jiacheng [1 ,2 ]
机构
[1] Chinese Acad Sci, Shanghai Inst Ceram, State Key Lab High Performance Ceram & Superfine, Shanghai 201899, Peoples R China
[2] Univ Chinese Acad Sci, Ctr Mat Sci & Optoelect Engn, Beijing 100049, Peoples R China
[3] ShanghaiTech Univ, Sch Phys Sci & Technol, Shanghai 200031, Peoples R China
[4] Jiangsu Prov Key Lab Environm Engn, Nanjing 210036, Jiangsu, Peoples R China
[5] Peking Univ, Coll Chem & Mol Engn, State Key Lab Rare Earth Mat Chem & Applicat, Beijing 100871, Peoples R China
基金
中国国家自然科学基金;
关键词
electronic metal-support interaction; graphitic-N doping; oxygen reduction reaction; platinum; stability; MEMBRANE FUEL-CELLS; PLATINUM DISSOLUTION; CARBON CORROSION; ATOMIC OXYGEN; MECHANISM; CATALYSTS; INSIGHTS;
D O I
10.1002/aenm.202101050
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
Suppressing the Pt dissolution still remains a big challenge in improving the long-term stability of Pt-based catalysts in electrochemical energy conversion. In this work, the degradation of Pt nanoparticles is successfully suppressed via weakening the Pt-O dipole effect by adjusting the electronic structure of surface Pt atoms. The specially designed graphitic-N-doped carbon nanosheets with balanced N content and graphitization degree as well as fewer defects are prepared for anchoring Pt nanoparticles to enhance the electronic metal-support interaction. This can accelerate the electron transfer from Pt to substrate, decrease the surface electron density of Pt, and attenuate the Pt-O interaction. As a result, the rate of Pt dissolution decreases by 95% compared to that of commercial Pt/C toward the oxygen reduction reaction and thus the catalytic stability is significantly improved in the electrochemical accelerated durability test. The theoretical simulation shows that the inhibition of surface Pt dissolution is attributed to the enhanced energy barrier in the initial relaxation process.
引用
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页数:7
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