Multistage structural self-supported electrode via structural engineering on carbon nanofibers for efficient hydrogen evolution reaction at high current density

被引:1
|
作者
Guan, Jibiao [1 ]
Xiao, Yuanxiang [1 ]
Zhu, Yingjing [1 ]
Wang, Lina [1 ]
Guo, Baochun [2 ]
Fu, Yaqin [1 ]
Zhang, Ming [1 ]
机构
[1] Zhejiang Sci Tech Univ, Natl Engn Lab Texile Fiber Mat & Proc Technol, Hangzhou 310018, Peoples R China
[2] South China Univ Technol, Dept Polymer Mat & Engn, Guangzhou 510640, Peoples R China
关键词
Multi -level structured; Morphological evolution; Superaerophobicity; Synergistic effects; Hydrogen evolution reaction;
D O I
10.1016/j.seppur.2024.127628
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
Pt -based catalysts suffered from the wastage of active sites, resulting in unsatisfactory actual catalytic performance and poor durability as non -self-supporting catalysts for alkaline hydrogen evolution reaction (HER). In this work, we designed a self-supporting electrode material with multi -level structure that utilized carbon nanofibers anchored with cobalt to load and stabilize Pt nanoparticles (Pt@Co/CNFs) for achieving high activity and stability in alkaline HER. The carbon nanofibers served as a framework, with cobalt nanoparticles as an electron donor that can transfer electrons to the metal Pt to accelerating water splitting. In addition, the morphology of the multi -level structure surface was controlled by the content of the reducing agent to giving the material excellent superhydrophilic/underwater superaerophobic properties with ultra -low Pt load (0.29 mg cm -2 ), which was beneficial for HER. HER test results showed that Pt@Co/CNFs exhibited great catalytic activity, with 1 10 = 15 mV and 1 100 = 101 mV. Besides, the stable mechanical structure and the stability of the designed catalytic surface and electron donor in the multi -level structure gave the material exceptional stability. During the 100 -hour stability test at 100 mA cm -2 , the voltage change was only 50 mV. Besides, utilizing the Pt@Co/CNFs self-supporting electrode directly in the AEM water electrolysis system, a cell voltage as low as 2.18 V was achieved at 500 mA cm -2 . Impressively, it demonstrated operational stability for over 200 h without noticeable decay. This work provides a promising approach for the development of advanced self-supporting electrode catalysts.
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页数:10
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