Local Structural Disorder Enhances the Oxygen Reduction Reaction Activity of Carbon-Supported Low Pt Loading CoPt Nanocatalysts

Dinesh Bhalothia, Yu Jui Fan, Tzu Hsi Huang, Zi Jun Lin, Ya Tang Yang, Kuan Wen Wang, Tsan Yao Chen

研究成果: 雜誌貢獻文章同行評審

8 引文 斯高帕斯(Scopus)

摘要

A facile strategy for preparing carbon-supported Co95Pt5 nanocatalysts (NCs) with low platinum (Pt) loading and high Pt utilization via thermal reduction treatment in a carbon monoxide (CO) atmosphere is reported. By cross-referencing results of microscopy, X-ray spectroscopy, and electrochemical analysis, we demonstrate that the Pt atoms tend to form disordered atomic clusters capping on the Co nanoparticle surface. The values of unfilled d-states (hTs) extracted from X-ray absorption near-edge spectroscopy were used to calculate the d-band vacancies of Pt. Accordingly, CoPt-CO570 (reduced in CO at 570 K) possesses the lowest hTs value (0.302) (i.e., the lowest Pt d-band vacancies) among experimental samples, indicating a strong electron relocation from Co atoms. Such electron relocations are attributed to the high extent of the heteroatomic intermix between Pt and Co atoms and thus improves the oxygen reduction reaction activity of CoPt-CO570. For providing further evidence, structural and electrochemical properties for H2 and NaBH4 reduction-prepared CoPt NCs are compared as the control. This work may represent an appealing step toward the structural design of low Pt and high activity catalysts for fuel cell cathode catalysts.

原文英語
頁(從 - 到)19013-19021
頁數9
期刊Journal of Physical Chemistry C
123
發行號31
DOIs
出版狀態已發佈 - 八月 8 2019

ASJC Scopus subject areas

  • Electronic, Optical and Magnetic Materials
  • Energy(all)
  • Physical and Theoretical Chemistry
  • Surfaces, Coatings and Films

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