海水
电催化剂
催化作用
电解质
电流密度
分解水
析氧
氢
材料科学
化学
化学工程
无机化学
海洋学
电极
地质学
物理化学
电化学
有机化学
工程类
物理
量子力学
光催化
作者
Shipeng Geng,Limin Chen,Lianmei Kang,Ruchun Li,Haixin Chen,Cheng Luo,Dandan Cai,Yi Wang,Shuqin Song
标识
DOI:10.1016/j.apcatb.2023.123486
摘要
Developing efficient and durable non-precious metal electrocatalysts with industrial current density is urgent for hydrogen evolution reaction from alkaline water/seawater but remains challenging. Here, a heterostructured Co/W5N4 catalyst with porous structure is innovatively constructed. The theoretical calculations confirm the strong d-p hybridization between Co and N at the interface of Co/W5N4 with the modulation of d‐band center of Co sites. The synergistic effect between Co and W5N4 is disclosed that H2O can rapidly dissociate on the W sites to generate H* adsorbed at the Co sites for favorable H2 production. Consequently, the Co/W5N4 catalyst affords low overpotentials of 113 and 118 mV to drive current density of 100 mA cm−2 in alkaline water/seawater electrolytes, respectively, which are even superior to those of commercial Pt/C. More importantly, it can also present outstanding HER stability at large current density of 500 mA cm−2 for over two weeks (350 h) in alkaline water/seawater electrocatalysis.
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