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
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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