材料科学
氧化还原
异质结
碳纤维
氮化碳
过氧化氢
氮化物
吸附
量子产额
电化学
氢
石墨氮化碳
光化学
纳米技术
分解水
产量(工程)
化学工程
动力学
制氢
电催化剂
无机化学
分子工程
人工光合作用
光催化
催化作用
作者
Yuxin Yao,Teng Liang,Zhijun Li,Zhongyuan Wang,Pengze Wang,Tianwei Dou,Ziyu Chen,Zhuo Li,Ji Bian,Liqiang Jing,Ji Bian,Liqiang Jing
标识
DOI:10.1002/adfm.202515298
摘要
Abstract Carbon nitride (CN), a highly promising photocatalyst for hydrogen peroxide (H 2 O 2 ) production, still suffers from rapid electron‐hole recombination and sluggish kinetics in both the O 2 reduction reaction (ORR) and water oxidation reaction (WOR). Here, a molecular engineering strategy enables the controlled synthesis of carbon and Gd‐N 4 single‐atoms co‐incorporated CN nanotubes. Subsequently, a Z‐scheme heterojunction is constructed via electrostatic self‐assembly with Bi 2 WO 6 nanosheets (BWO). The optimized composite exhibits exceptional performance in visible‐light‐driven H 2 O 2 synthesis (749.5 µmol g −1 h −1 ) in pure water, achieving a 37‐fold enhancement compared to pristine CN. Moreover, the apparent quantum yield (AQY) reaches an impressive 11.13% at 420 nm. The enhanced activity is primarily attributed to the synergistic effects of C/Gd co‐incorporation and the Z‐scheme heterojunction, which collectively promote the separation of photogenerated charges in CN. Particularly, the unsaturated coordination Gd‐N 4 sites effectively facilitate O 2 adsorption and the 2e − ORR pathway, enabling efficient H 2 O 2 production. Meanwhile, BWO enhances the WOR, thus improving the matching efficiency of redox reactions in the system. This study establishes a facile molecular engineering strategy for single‐atoms anchoring with tailored coordination environments, while highlighting the critical role of redox dual‐regulation in achieving efficient H 2 O 2 photosynthesis.
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