Highly active and stable amorphous IrOx/CeO2 nanowires for acidic oxygen evolution

被引:72
|
作者
Gou, Wangyan [1 ]
Xia, Zhaoming [2 ]
Tan, Xiaohe [1 ]
Xue, Qingyu [1 ]
Ye, Fan [3 ]
Dai, Sheng [3 ]
Zhang, Mingkai [4 ]
Si, Rui [5 ]
Zou, Yong [1 ]
Ma, Yuanyuan [1 ]
Ho, Johnny C. [6 ]
Qu, Yongquan [1 ]
机构
[1] Northwestern Polytech Univ, Sch Chem & Chem Engn, Key Lab Special Funct, Smart Polymer Mat Minist Ind & Informat Technol, Xian 710072, Peoples R China
[2] Tsinghua Univ, Dept Chem, Beijing 100084, Peoples R China
[3] East China Univ Sci & Technol, State Key Lab Chem Engn, Shanghai 200237, Peoples R China
[4] Xi An Jiao Tong Univ, Frontier Inst Sci & Technol, Xian 710049, Peoples R China
[5] Shanghai Synchrotron Radiat Facil, Zhangjiang Lab, Shanghai 201204, Peoples R China
[6] City Univ Hong Kong, Dept Mat Sci & Engn, Kowloon, Peoples R China
基金
中国博士后科学基金;
关键词
Acidic oxygen evolution; Amorphous structure; Iridium oxide; Ceria; Electron buffer; TRANSMISSION ELECTRON-MICROSCOPY; REACTION ELECTROCATALYSTS; EVOLVING CATALYSTS; SURFACE-CHEMISTRY; IRIDIUM; IR; OXIDATION; RU; NANOCATALYSTS; NANOPARTICLES;
D O I
10.1016/j.nanoen.2022.107960
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Development of highly active and durable electrocatalysts for acidic oxygen evolution reaction (OER) remains an unresolved grand challenge. Here, we reported the amorphous IrOx/CeO2 nanowires as highly active and acidstable OER catalysts through a facile electro-spinning/calcination approach. The amorphous catalysts delivered a high mass activity of 167 A(gIr)(-1) at 1.51 V, a low overpotential of 220 mV at 10 mA cm(-2), and a stable performance for 300 h of continuous operation in acid. As revealed by complementary experimental and theoretical calculation results, the intimate nanoscale feature of IrOx/CeO2 creates abundant binary interfaces, at which CeO2 as an electron buffer regulates the adsorption of oxygen intermediates, lowers the activation barrier of OER, and suppresses the over-oxidation and dissolution of Ir, thereby significantly enhancing the OER activity and stability. This work provides a new strategy for designing highly active and acid-resistant OER catalysts.
引用
收藏
页数:11
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