Graphyne doped with transition-metal single atoms as effective bifunctional electrocatalysts for water splitting

分解水 过电位 双功能 电催化剂 催化作用 析氧 石墨 电化学 纳米片 过渡金属 材料科学 化学 电子转移 石墨烯 纳米技术 光化学 物理化学 光催化 电极 有机化学
作者
Xiaoping Gao,Yanan Zhou,Yujia Tan,Shiqiang Liu,Zhiwen Cheng,Zhemin Shen
出处
期刊:Applied Surface Science [Elsevier BV]
卷期号:492: 8-15 被引量:72
标识
DOI:10.1016/j.apsusc.2019.06.050
摘要

Developing highly active and non-precious-metal single-atom catalysts (SAC) for electrochemical water splitting is of great significance to the development of renewable energy technology in future. Herein, 10 first-row transition-metal (TM, from Sc to Zn) single atoms anchored on a graphyne (GY) nanosheet ([email protected]) as electrocatalysts for water splitting are explored through computational screening approach. It is found that the single atoms prefer to tightly bind at the acetylenic-ring center of GY. Meanwhile, these [email protected] catalysts show metallic properties or reduced band gap, favoring electron transfer during the electrochemical processes. Moreover, both [email protected] and [email protected] catalysts present good catalytic performance for hydrogen evolution reaction (HER) with both the acetylenic C and TM atoms being highly active sites. However, only the [email protected] catalyst shows good oxygen evolution reaction (OER) activity with an overpotential of 0.55 V. Thus, [email protected] could serve as a potential bifunctional electrocatalyst for water splitting. Besides, the d-band center of TM atoms on [email protected] can be turned through controlling TM atoms with different d-electron number and be used to predict the OER performance. This work highlights that GY doped with single non-precious-metals can be considered for designing high-active and low-cost bifunctional electrocatalysts for practical electrochemical reactions.
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