化学
选择性
人工光合作用
电场
光催化
分解水
化学物理
催化作用
制氢
化学能
化学反应
析氧
氢
纳米技术
太阳能
光化学
电化学
有机化学
物理化学
电极
材料科学
物理
生物
量子力学
生态学
作者
Kejian Li,Wenbo You,Yucheng Zhu,Wei Wang,Longqian Wang,Yangyang Liu,Qiuyue Ge,Tao Wang,Runbo Wang,Xuejun Ruan,Hanyun Cheng,Liwu Zhang
摘要
Selective conversion of solar energy to chemical bonds remains a grand challenge in artificial photosynthesis. Though H2O2 production via photocatalytic two-electron oxygen reduction (2e--ORR) offers a sustainable alternative to the energy-intensive anthraquinone process, competing hydrogen evolution reaction (HER) severely limits both efficiency and selectivity. Here, we reveal that the strong electric fields on water microdroplet surfaces serve as powerful selectivity switches, directing photogenerated electrons exclusively toward H2O2 synthesis while completely suppressing hydrogen evolution. This interfacial electric field control mechanism transforms ZnIn2S4-based photocatalysts─commonly dominated by HER─into H2O2 producers with near-unity selectivity and production rates 2 orders of magnitude higher than bulk reactions. Through spatially resolved spectroscopy characterizations and theoretical calculations, we elucidate that the high electric fields on water microdroplets simultaneously enhance charge carrier separation, lower energy barriers for 2e--ORR, and erect kinetic barriers against HER. Beyond providing an energy-efficient route to selective H2O2 photosynthesis, this study offers valuable insights into selectivity control in other solar-to-chemical transformations without the need for catalyst modification or system engineering.
科研通智能强力驱动
Strongly Powered by AbleSci AI