电催化剂
过电位
双功能
材料科学
电化学
分解水
析氧
纳米技术
电子转移
电极
异质结
化学工程
催化作用
化学
光电子学
物理化学
有机化学
光催化
工程类
作者
Xin‐Yao Yu,Jing Mei,Yeshuang Du,Xiaohong Cheng,Xing Wang,Qi Wu
出处
期刊:Nano Research
[Springer Science+Business Media]
日期:2023-08-05
卷期号:17 (6): 4693-4701
被引量:27
标识
DOI:10.1007/s12274-023-5740-9
摘要
Heterojunction structures improve the intrinsic activity of electrocatalysts by enhancing the charge transfer between the catalyst and the electrode. In this paper, the NiS/FeS 2 heterostructured electrocatalyst is fabricated by a simple sulfidation method using an interface engineering strategy to adjust the surface electron density of the electrocatalyst. As expected, NiS/FeS 2 electrocatalyst exhibits superior activity and durable oxygen evolution reaction (OER) stability, requiring only a low overpotential of 183 mV to achieve a current density of 10 mA·cm −2 and can be stable for more than 80 h, superior to NiS, FeS 2 electrocatalyst individually, and precious RuO 2 . Notably, NiS/FeS 2 is also a good bifunctional electrocatalyst with good overall water splitting performance, and it only requires a voltage 1.56 V to obtain a current density of 10 mA·cm −2 for more than 12 h. Remarkably, the NiS/FeS 2 hybridization facilitates the formation of coral-like structures, increasing the electrochemical surface area (ECSA) and enhancing the charge transfer efficiency, thus leading to excellent electrocatalytic performance. This work proposes a constructive strategy for designing efficient electrocatalysts based on interface engineering, and lays a foundation for designing a new class of electrocatalysts.
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