反键分子轨道
催化作用
吸附
X射线光电子能谱
光催化
电子结构
密度泛函理论
材料科学
化学工程
纳米技术
光化学
化学
电子
物理化学
计算化学
有机化学
原子轨道
工程类
物理
量子力学
作者
Xidong Zhang,Duoduo Gao,Bicheng Zhu,Bei Cheng,Jiaguo Yu,Huogen Yu
标识
DOI:10.1038/s41467-024-47624-7
摘要
Abstract Gold-based co-catalysts are a promising class of materials with potential applications in photocatalytic H 2 O 2 production. However, current approaches with Au co-catalysts show limited H 2 O 2 production due to intrinsically weak O 2 adsorption at the Au site. We report an approach to strengthen O 2 adsorption at Au sites, and to improve H 2 O 2 production, through the formation of electron-deficient Au δ+ sites by modifying the electronic structure. In this case, we report the synthesis of TiO 2 /MoS x -Au, following selective deposition of Au onto a MoS x surface which is then further anchored onto TiO 2 . We further show that the catalyst achieves a significantly increased H 2 O 2 production rate of 30.44 mmol g −1 h −1 in O 2 -saturated solution containing ethanol. Density functional theory calculations and X-ray photoelectron spectroscopy analysis reveal that the MoS x mediator induces the formation of electron-deficient Au δ+ sites thereby decreasing the antibonding-orbital occupancy of Au-O ads and subsequently enhancing O 2 adsorption. This strategy may be useful for rationally designing the electronic structure of catalyst surfaces to facilitate artificial photosynthesis.
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