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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.
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页数:7
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