异质结
氯
碳纤维
材料科学
涂层
化学工程
电流(流体)
纳米技术
化学
光电子学
复合数
复合材料
物理
冶金
热力学
工程类
作者
Yuhao Duan,Liuxu Wei,Chenyu Cai,Junbao Mi,Fuyuan Cao,Jiaze Chen,Xiaolong Li,Xiujiang Pang,Bin Li,Lei Wang
出处
期刊:Nano Research
[Springer Nature]
日期:2024-02-02
卷期号:17 (6): 4764-4772
被引量:22
标识
DOI:10.1007/s12274-024-6419-6
摘要
The chlorine evolution reaction (CER) is a crucial step in the production of chlorine gas and active chlorine by chlor-alkali electrolysis. Currently, the endeavor to fabricate electrodes capable of yielding high current density at minimal overpotential remains a central challenge in advancing the realm of chlorine evolution reactions. Here, we grow TiO2 and RuO2 on MXene@carbon cloth (CC) through the favorable affinity and induced deposition effect between the surface functional groups of MXene and the metal. A self-supported electrode (RuTiO2/MXene@CC) with strong binding at the electrocatalyst–support interface and weak adhesion at electrocatalyst–bubble interface is constructed. The RuTiO2/MXene@CC can reduce the electron density of RuO2 by regulating the electron redistribution at the heterogeneous interface, thus enhancing the adsorption of Cl−. RuTiO2/MXene@CC could achieve a high current density of 1000 mA·cm−2 at a small overpotential of 220 mV, superior to commercial dimensionally stable anodes (DSA). This study provides a new strategy for constructing efficient CER catalysts at high current density.
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