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Diluted silicon promoting Pd/Pt catalysts for oxygen reduction reaction with strong anti-poisoning effect.

Authors :
Ma, Mengjie
Zhang, Yi
Ji, Yujin
Shao, Qi
Yin, Kui
Zhu, Wenxiang
Yang, Junjun
Liao, Fan
Fan, Zhenglong
Liu, Yang
Li, Youyong
Shao, Mingwang
Kang, Zhenhui
Source :
Applied Catalysis B: Environmental. Oct2022, Vol. 315, pN.PAG-N.PAG. 1p.
Publication Year :
2022

Abstract

Poisoning species, such as methanol and air pollutants, degrade the electrocatalytic activity for oxygen reduction reaction (ORR). Here, via taking advantage of the varied electronic property of nano-silicon, a versatile strategy is reported for enhancing the catalytic activity and anti-poisoning ability toward ORR by decorating noble metal catalysts with the size-controlled silicon nanoclusters (DS). Consequently, DS-Pd exhibits the enhanced ORR performance with a large halfwave potential of 0.892 V and an onset potential of 1.010 V. More importantly, it also shows enhanced anti-poisoning performance in methanol, NaNO 2 and NaHSO 3 electrolytes, compared to those of commercial Pt/C and Pd/C catalysts. Mechanism studies reveal that the synergistic effect between Pd and more oxygen-philic and less poison-philic Si nanoclusters largely abbreviate the absorption of poisoning species on the active sites. This strategy also improves the methanol-tolerant performance of Pt based catalysts, providing a versatile strategy for the fabrication of methanol-tolerant ORR catalysts. [Display omitted] • Diluted silicon nanoclusters reduce the d band center of Pd atoms. • A lower d band center of Pd further weakens the adsorption of poisons. • Diluted silicon nanoclusters increase the catalytic activity of Pd or Pt toward ORR. • Diluted silicon nanoclusters enhance the anti-poisoning performance of Pd or Pt. • DS-Pd exhibits improved ORR performance with a halfwave potential of 0.892 V. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
09263373
Volume :
315
Database :
Academic Search Index
Journal :
Applied Catalysis B: Environmental
Publication Type :
Academic Journal
Accession number :
157498116
Full Text :
https://doi.org/10.1016/j.apcatb.2022.121549