Effect of Acid Treatment on Electrocatalytic Performance of PtNi Catalyst

I n this paper, we describe the synthesis of the AC-PtNi/G catalysts with graphene as the carrier, via the alcohol reduction and the sulfuric acid treatment. The prepared catalysts were microscopically characterized by X-ray diffractometry(XRD), X-ray photoelectron spectroscopy(XPS), scanning electr...

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Bibliographic Details
Published in:Chemical research in Chinese universities Vol. 37; no. 3; pp. 686 - 695
Main Authors: Guo, Ruihua, Qian, Fei, An, Shengli, Zhang, Jieyu, Chou, Kuo-chih, Ye, Jinyu, Zhou, Zhiyou
Format: Journal Article
Language:English
Published: Changchun Jilin University and The Editorial Department of Chemical Research in Chinese Universities 01-06-2021
Springer Nature B.V
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Summary:I n this paper, we describe the synthesis of the AC-PtNi/G catalysts with graphene as the carrier, via the alcohol reduction and the sulfuric acid treatment. The prepared catalysts were microscopically characterized by X-ray diffractometry(XRD), X-ray photoelectron spectroscopy(XPS), scanning electron microscopy(SEM), electron spectroscopy(EDAX), and transmission electron micros-copy(TEM). We tested the electrochemical performance of the prepared catalysts using an electrochemical workstation and in situ infrared spectroscopy(FTIR). The results showed that the acid-treated AC-PtNi/G catalysts had a more uniform dispersion and with the increased of treatment time, the particle size of the catalyst became smaller. And the electrocatalytic performance of the AC-PtNi/G-48h catalyst treated with sulfuric acid for 48 h was significantly better than that of the untreated PtNi/G catalyst. Its electrochemically active surface area was 76.63 m 2 /g, and the peak current density value for catalytic oxidation of ethanol was 1218.83 A/g, which was 10 times that of ordinary commercial Pt/C catalyst. The steady-state current density value of 1100 s was 358.77 A/g, and it has excellent anti-CO toxicity performance. It was determined that a sulfuric acid treatment controlled catalyst particle size and increased the electrocatalytic activity of the catalytic oxidation of ethanol.
ISSN:1005-9040
2210-3171
DOI:10.1007/s40242-020-0207-y