Ir-doped Co3O4 as efficient electrocatalyst for acidic oxygen evolution reaction

被引:21
|
作者
Xie, Yusheng [1 ]
Su, Yanyan [1 ]
Qin, Haoran [1 ]
Cao, Zhilin [1 ]
Wei, Hehe [3 ]
Wu, Fengchi [2 ]
Ou, Gang [1 ,4 ]
机构
[1] Jinan Univ, Coll Chem & Mat Sci, Guangzhou 511443, Peoples R China
[2] Guangdong Polytech Normal Univ, Sch Innovat & Entrepreneurship, Guangzhou 510665, Peoples R China
[3] East China Univ Sci & Technol, Ctr Computat Chem & Res Inst Ind Catalysis, Key Lab Adv Mat, 130 Meilong Rd, Shanghai 200237, Peoples R China
[4] Guangzhou Panyu Polytech, Inst Adv Mat & Technol, Guangzhou 511483, Peoples R China
关键词
Iridium doping; Acidic medium; WATER OXIDATION; COMPLEX; CARBON; CATALYST;
D O I
10.1016/j.ijhydene.2022.12.292
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
Oxygen evolution reaction (OER) is an important bottleneck for large-scale acidic water splitting applications due to its sluggish reaction kinetics. Therefore, the development of highly active, stable, and inexpensive electrocatalysts for OER remains a challenge. Herein, we develop the iridium doped Co3O4 (Ir-Co3O4) with low Ir content of 2.88 wt% for efficient acidic OER. Considering systemic characterizations, it is probably concluded that Ir can be uniformly doped into the lattice of Co3O4 and induce a certain distortion. The electrochemical results reveal that Ir-Co3O4 nanoparticles demonstrate significantly enhanced electrocatalytic OER activity and stability in 0.5 M H2SO4 solution compared with pure Co3O4, in which the overpotential at the current density of 10 mA cm-2 decreases from 382 mV to 225 mV and the value of Tafel slope decreases from 101.7 mV dec-1 to 64.1 mV dec-1. Besides, Ir-Co3O4 exhibits excellent electrocatalytic durability for continuous 130 h's
引用
收藏
页码:14642 / 14649
页数:8
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