材料科学
光催化
硼酸
硼
氢键
吸附
光化学
选择性
电子转移
氢
兴奋剂
化学工程
纳米技术
化学物理
有机化学
催化作用
分子
光电子学
工程类
化学
作者
Yu-Chen Guo,Jiaming Sun,Zikang Geng,Junying Zhang,Xin Tan,Jinhua Ye,Tao Yu
标识
DOI:10.1002/aenm.202401285
摘要
Abstract Maximizing the utilization of photogenerated electrons and holes to drive the coupling reaction of hydrogen evolution with selective value‐added organic synthesis holds great potential for more efficient exploitation of solar energy. Herein, the interstitial boron‐doped CdS is synthesized by taking SiO 2 as a template as well as the adsorption sites of boric acid, which contributes to the boron doping and induces the reinforced Cd─Se bonding for enhancing the interfacial interaction with co‐catalyst MoSe 2 . Thus, the interfacial Cd─Se bond with more electron localization provides rapid channels at the atomic level for accelerating the charge transfer with a lower energy barrier, achieving the efficient hydrogen evolution and high selectivity pyruvic acid synthesis concurrently. This work provides a new perspective in avoiding the use of sacrificial agents uneconomically and producing green hydrogen with high‐value‐added chemicals simultaneously.
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