Engineering High-Entropy Duel-Functional nanocatalysts with regulative oxygen vacancies for efficient overall water splitting

被引:45
作者
Liao, Shuangxiong [1 ]
Huang, Tieqi [1 ]
Wu, Weiying [1 ]
Yang, Ting [2 ]
Hou, Qianqian [1 ]
Sang, Shangbin [1 ]
Liu, Kaiyu [1 ]
Yang, Yahui [2 ]
Liu, Hongtao [1 ]
机构
[1] Cent South Univ, Coll Chem & Chem Engn, Hunan Prov Key Lab Chem Power Sources, Changsha 410083, Peoples R China
[2] Hunan Normal Univ, Coll Chem & Chem Engn, Changsha 410081, Peoples R China
基金
中国国家自然科学基金;
关键词
High-entropy oxides; Oxygen evolution reaction; Hydrogen evolution reaction; Oxygen vacancies; Overall water splitting; EVOLUTION; HYDROGEN; ALLOYS; NI; PERFORMANCE; CARBON; OXIDE; CO;
D O I
10.1016/j.cej.2023.144506
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
High-entropy materials (HEMs) have attracted growing attention in catalysis fields owing to their multielement synergy and tunable electronic configuration. As one of the commonest HEMs, high-entropy oxides (HEOs), however, are far from satisfactory in terms of their high crystallization with insufficient active sites. Herein, a surface activation strategy is proposed to engineer high-activity HEOs electrocatalysts in which ample surface oxygen vacancies (OVs) are imported by means of resin templating and temperature regulation. As a result, the modulated (Fe0.27Ni0.35Co0.24Cr0.10Mn0.04)2O3-& delta; HEO with stable structure as well as large electrochemical surface area (ECSA) exhibits robust electrocatalytic activity towards both oxygen evolution reaction (OER, & eta;10 = 174 mV) and hydrogen evolution reaction (HER, & eta;10 = 60 mV). Correspondingly, as-assembled water splitting cell only requires a low voltage of 1.55 V to achieve 10 mA cm-2 current density, far superior to that of 1.72 V using the commercial noble metal electrocatalysts. This work opens up a new avenue in designing structurestable HEOs for efficient electrocatalytic applications.
引用
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页数:8
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