In Situ Synthesis of Nano PtRuW/WC Hydrogen Evolution Reaction Catalyst for Acid Hydrogen Evolution by a Microwave MethodSource: Journal of Electrochemical Energy Conversion and Storage:;2024:;volume( 022 ):;issue: 004::page 41003-1Author:Sun, Liangliang
,
Chen, Zihao
,
Huang, Zitong
,
Liu, Xiang
,
Yang, Yang
,
Wu, Yongxin
,
Han, Zhaoyan
,
Liang, Fengbo
DOI: 10.1115/1.4066938Publisher: The American Society of Mechanical Engineers (ASME)
Abstract: One of the primary challenges in electrocatalysis for the hydrogen evolution reaction (HER) lies in the development of highly efficient catalysts suitable in acidic environments. Tungsten carbide-based materials have long been proposed as potential substitutes for Pt due to their “Pt-like” electronic properties in the HER process. However, tungsten carbide still falls short of the performance exhibited by commercial precious-metal catalysts. Herein, PtRuW/WC was prepared by a microwave heating method and acted as a HER electrocatalyst. The microwave method not only enhances the diffraction peaks of the substrate tungsten carbide but also facilitates the growth of metal ions at specific sites. The PtRuW/WC catalyst demonstrates outstanding performance in acidic HER, characterized by a minimal overpotential of 40.7 mV at 10 mA/cm2 (ɳ10). Furthermore, it exhibits exceptional stability in acidic solutions, showing no substantial degradation during 20 h at 1000 mA/cm2. The catalyst-assembled polymer electrolyte membrane (PEM) electrolytic water electrode further proves that PtRuW/WC has excellent electrolytic water performance and makes some efforts for the development of commercial PEM electrolytic water.
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contributor author | Sun, Liangliang | |
contributor author | Chen, Zihao | |
contributor author | Huang, Zitong | |
contributor author | Liu, Xiang | |
contributor author | Yang, Yang | |
contributor author | Wu, Yongxin | |
contributor author | Han, Zhaoyan | |
contributor author | Liang, Fengbo | |
date accessioned | 2025-04-21T10:19:07Z | |
date available | 2025-04-21T10:19:07Z | |
date copyright | 11/25/2024 12:00:00 AM | |
date issued | 2024 | |
identifier issn | 2381-6872 | |
identifier other | jeecs_22_4_041003.pdf | |
identifier uri | http://yetl.yabesh.ir/yetl1/handle/yetl/4305930 | |
description abstract | One of the primary challenges in electrocatalysis for the hydrogen evolution reaction (HER) lies in the development of highly efficient catalysts suitable in acidic environments. Tungsten carbide-based materials have long been proposed as potential substitutes for Pt due to their “Pt-like” electronic properties in the HER process. However, tungsten carbide still falls short of the performance exhibited by commercial precious-metal catalysts. Herein, PtRuW/WC was prepared by a microwave heating method and acted as a HER electrocatalyst. The microwave method not only enhances the diffraction peaks of the substrate tungsten carbide but also facilitates the growth of metal ions at specific sites. The PtRuW/WC catalyst demonstrates outstanding performance in acidic HER, characterized by a minimal overpotential of 40.7 mV at 10 mA/cm2 (ɳ10). Furthermore, it exhibits exceptional stability in acidic solutions, showing no substantial degradation during 20 h at 1000 mA/cm2. The catalyst-assembled polymer electrolyte membrane (PEM) electrolytic water electrode further proves that PtRuW/WC has excellent electrolytic water performance and makes some efforts for the development of commercial PEM electrolytic water. | |
publisher | The American Society of Mechanical Engineers (ASME) | |
title | In Situ Synthesis of Nano PtRuW/WC Hydrogen Evolution Reaction Catalyst for Acid Hydrogen Evolution by a Microwave Method | |
type | Journal Paper | |
journal volume | 22 | |
journal issue | 4 | |
journal title | Journal of Electrochemical Energy Conversion and Storage | |
identifier doi | 10.1115/1.4066938 | |
journal fristpage | 41003-1 | |
journal lastpage | 41003-9 | |
page | 9 | |
tree | Journal of Electrochemical Energy Conversion and Storage:;2024:;volume( 022 ):;issue: 004 | |
contenttype | Fulltext |