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李箐

教授    博士生导师    硕士生导师

个人信息 更多+
  • 教师英文名称: Qing Li
  • 性别: 男
  • 在职信息: 在职
  • 所在单位: 材料科学与工程学院
  • 学历: 研究生(博士)毕业
  • 学位: 理学博士学位

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论文成果

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Interstitial B-Doping in Pt Lattice to Upgrade Oxygen Electroreduction Performance

发布时间:2024-12-29
点击次数:
论文类型:
Research Article
第一作者:
Mao,Zijie
通讯作者:
Cai,Wen-Bin,Zhang,Xia-Guang,Li,Qing
合写作者:
Junliang,Yang,Fan,Li,Hong,Qin,Xianxian,Zhang,Qing,Ding,Chen
发表刊物:
ACS Catalysis
所属单位:
华中科技大学
刊物所在地:
美国
文献类型:
Article
卷号:
12
期号:
15
页面范围:
8848-8856
关键字:
Oxygen Reduction Reaction; Pt catalyst; Interstitial B Doping; Durability Dimethylamine Borane
DOI码:
10.1021/acscatal.2c01052
发表时间:
2022-07-08
影响因子:
11.3
摘要:
The dissolution of M in currently popular Pt–M alloy catalysts (M = Co, Ni, and Fe) during the oxygen reduction reaction (ORR) may deter their wide application in proton exchange membrane fuel cells (PEMFCs). In this work, interstitial B-doping in the Pt lattice is instead used to design a durable and active ORR catalyst, by taking advantage of its unique regulation of the electronic structure of surface Pt sites. 3 nm Pt–B nanoparticles on carbon black (Pt–B/C) are obtained using dimethylamine borane (DMAB) as a reductant and the B source in a mixed H2O–ethylene glycol precursor solution. The formation of the B-doped Pt catalyst is verified by inductively coupled plasma-atomic emission spectrometry, X-ray diffractometry, and spherical aberration-corrected scanning transmission electron microscopy. Both half-cell and single-cell tests indicate that the as-synthesized Pt–B/C catalyst outperforms the commercial Pt/C(com) in terms of activity and durability. In particular, the Pt–B/C-based PEMFC exhibits an initial maximum power density 1.24 times as high as the Pt/C(com)-based one under otherwise same conditions, with a 15% decay for the former versus a 45% decay for the latter after 30 000 cycles of the accelerated degradation test (ADT). Comparative DFT calculations on B-doped and undoped Pt(111) surfaces reveal that the lowered Pt d-band center and the strong interaction of Pt–B bonding weaken the binding of OH and O species to surface Pt sites and lessen oxidative disruption of surface Pt atoms. This interstitial metalloid doping in conjunction with the simple and scalable synthesis protocol enables the Pt–B/C to be a competitive ORR catalyst for the PEMFCs.