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Nitrogen-phosphorus co-doped carbon layer-confined cobalt phosphide-anchored nickel molybdate heterojunctions for efficient electrocatalytic overall water splitting
被引:3
|作者:
Dai, Ruijie
[1
]
Guan, Zhixi
[2
]
Guo, Daying
[2
]
Xi, Bin
[1
]
机构:
[1] Sun Yat Sen Univ, Sch Mat Sci & Engn, Guangzhou 510275, Peoples R China
[2] Wenzhou Univ, Coll Chem & Mat Engn, Key Lab Carbon Mat Zhejiang Prov, Wenzhou 325035, Peoples R China
关键词:
Nickel molybdate;
Cobalt phosphide;
Confined;
Electrocatalysis;
Overall water splitting;
D O I:
10.1016/j.cej.2024.154257
中图分类号:
X [环境科学、安全科学];
学科分类号:
08 ;
0830 ;
摘要:
Aiming at the problems of low catalytic activity and poor stability of nickel molybdate-based catalysts. Herein, we successfully prepared nitrogen and phosphorus co-doped carbon (NPC) layer-confined cobalt phosphide (CoP)-anchored nano-cuboid nickel molybdate (NNM) catalysts (NNM-CoP@NPC/NF) on nickel foam (NF) by hydrothermal and phosphating methods. The strong interaction between CoP and NNM is verified by experimental characterization and theoretical calculation, which improves the electronic structure of NNM and reduces the orbital energy of the central anti-bond, thus optimizing the adsorption and desorption of reaction intermediates/products. NiOOH and MoO42- formed by reforming the catalyst under the action of NPC-confined layer maintain catalytic activity and stability in cooperation with CoP and NPC, respectively. Accordingly, in the assembled two-electrode system NNM-CoP@NPC/NF, the cell voltage of only 1.51 V is needed to drive a current density of 10 mA cm- 2. More importantly, the current density remained at 100 mA cm- 2 for 100 h under the voltage of 1.66 V with almost no attenuation. This strategy of constructing interface regulation and confinement provides a new insight for improving the activity and stability of water splitting in alkaline media.
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页数:9
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