Boron-incorporated IrO 2-Ta 2 O 5 coating as an efficient electrocatalyst for acidic oxygen evolution reaction

被引:7
作者
Huang, Quanbo [1 ]
Zhuang, Shaojie [1 ]
Zheng, Yuexi [1 ]
Peng, Xinyuan [1 ]
Ye, Zhiguo [1 ]
Li, Duosheng [1 ]
机构
[1] Nanchang Hangkong Univ, Sch Mat Sci & Engn, 696 Fenghenan Rd, Nanchang 330063, Peoples R China
基金
中国国家自然科学基金;
关键词
IrO2; Oxygen evolution reaction; Electrocatalytic activity; Durability; OXIDATION; WATER; ALLOY; REDOX; ANODE;
D O I
10.1016/j.cej.2024.152040
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The Ir-based electrocatalysts for the acidic oxygen evolution reaction (OER) have demonstrated remarkable durability. Enhancing the Ir-based electrocatalytic activity still remains crucial owing to the scarcity of iridium. Here, a high -temperature sintering technique is employed to fabricate a boron (B) -incorporated IrO 2 -Ta 2 O 5 coating with an almost perfect rutile-type crystal structure on a corrosion -resistant titanium substrate, ensuring exceptional stability for the acidic OER. The B -incorporated IrO 2 -Ta 2 O 5 electrode fabricated in a mixed solution of 0.6 M H 3 BO 3 , exhibits an overpotential of 210 mV at a current density of 10 mA cm -2 and a lower Tafel slope of 34.2 mV dec - 1 in a 0.5 M H 2 SO 4 solution, which is far lower than the 272 mV overpotential and the 45.3 mV dec - 1 of the IrO 2 -Ta 2 O 5 /Ti electrode. The electrode possesses a minimal potential increase even after undergoing continuous OER for 400 h at a high current density of 100 mA cm -2 in a 0.5 M H 2 SO 4 solution. The incorporation of B species into IrO 2 -Ta 2 O 5 effectively fine-tunes the electronic structure of Ir active sites, leading to a substantial enhancement of the intrinsic electrocatalytic activity. This study provides promising prospects for reducing the energy consumption of noble IrO 2 -based electrocatalysts in the practical application of electrochemical industry for the acidic OER.
引用
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页数:9
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