Laser assisted oxygen vacancy engineering on Fe doped CoO nanoparticles for oxygen evolution at large current density

被引:3
|
作者
Zhu, Min [1 ]
Sheng, Zongqiang [1 ]
Fu, Zhifen [1 ]
Li, Yang [1 ]
Gao, Juan [1 ]
Zhang, Chao [2 ]
机构
[1] Anhui Univ Sci & Technol, Sch Mech & Optoelect Phys, Huainan 232001, Peoples R China
[2] Univ Sci & Technol China, Sch Chem & Mat Sci, Hefei 230026, Peoples R China
关键词
Laser irradiation; Oxygen vacancy; Fe doped; Oxygen evolution reaction; Large current density; COBALT OXIDE; CO3O4; NANOSHEETS; WATER OXIDATION; PULSED-LASER; ELECTROCATALYSTS; NANOMATERIALS; ABLATION; LIQUID; NICKEL; ANODES;
D O I
10.1016/j.electacta.2024.143841
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
Exploring cost-effective non -noble metal-based catalysts with high activity and stability is of great significance for energy conversion and storage involving oxygen evolution reaction (OER). Here, we employed a laser irradiation technique to synthesis Fe doped CoO nanoparticles with ultrafine size (approximate to 5.4 nm) and abundant oxygen vacancies (Fe-Ov-CoO). The ultrafine size of Fe-Ov-CoO nanoparticles provides more active sites to be exposed. Fe doping and oxygen vacancy promote the intrinsic activity and electron transfer rates of Fe-Ov-CoO, giving rise to high activity and stability catalyst for OER. Fe-Ov-CoO delivers a large current density of 1000 mA cm -2 at an overpotential of 548 mV, which is much better than commercial RuO2. Moreover, Fe-Ov-CoO presents a remarkable long-term stability with negligible degeneration at a high current density of 500 mA cm -2 for 120 h. This work provides a new route to develop OER electrocatalyst with high activity and stability.
引用
收藏
页数:7
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