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Coupling interface engineering with electronic interaction toward high-efficiency H2 evolution in pH-universal electrolytes
Journal of Energy Chemistry ( IF 14.0 ) Pub Date : 2023-02-14 , DOI: 10.1016/j.jechem.2023.01.060
Jinli Chen , Tianqi Yu , Zhixiang Zhai , Guangfu Qian , Shibin Yin

Herein, the merits of heterojunction, CeO2, and W are employed to design and prepare the PtCoW@CeO2 heterojunction catalyst, which can accelerate water dissociation and improve the desorption of OHad, displaying efficient hydrogen evolution reaction (HER) performance in pH-universal conditions. Density functional theory calculation results reveal that the electronic structure of Pt is regulated by CeO2 and W, which tunes the Pt–Had bond strength to boost HER intrinsic activity. Consequently, electrochemical results display that it has low potentials of −26, −25, and −23 mV at −10 mA cm−2 in alkaline, neutral, and acidic solutions, respectively, and it can stably cycle for 50,000 cycles. Thus, this work provides the guidance for developing high-performance Pt-based catalysts in pH-universal environments.



中文翻译:

将界面工程与电子相互作用耦合到 pH 通用电解质中的高效 H2 释放

在此,利用异质结、CeO 2和W的优点设计和制备了PtCoW@CeO 2异质结催化剂,该催化剂可以加速水离解并改善OH ad的解吸,在pH条件下表现出高效的析氢反应(HER)性能- 通用条件。密度泛函理论计算结果表明,Pt 的电子结构受 CeO 2和 W 的调节,从而调节 Pt-H 的合强度以提高 HER 的内在活性。因此,电化学结果显示它在 -10 mA cm -2时具有 -26、-25 和 -23 mV 的低电位分别在碱性、中性和酸性溶液中稳定循环5万次。因此,这项工作为在 pH 通用环境中开发高性能 Pt 基催化剂提供了指导。

更新日期:2023-02-14
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