异质结
光催化
材料科学
氧化还原
吸附
太阳能
化学工程
纳米技术
曙红Y
光电子学
化学能
载流子
可再生能源
分解水
电场
工作(物理)
可见光谱
有效核电荷
电荷(物理)
高能
表面电荷
作者
Rong Xia,Dapeng Dong,Zhenyang Wei,Xuedong Jing,Yongan Zhu,Q. Li,Jindou Huang,Dedi Liu,Zhenghua Li,Jinhai Niu,Zhenyi Zhang
出处
期刊:Small
[Wiley]
日期:2026-03-05
卷期号:22 (23): e73014-e73014
摘要
ABSTRACT Constructing metal‐organic framework (MOF) heterojunctions with effective photocatalytic activity, outstanding stability, and integrated redox centers remains challenging. Herein, a chiral [Cu I (IPEA)] 1) and an achiral [Cu II (IPEA)]·(H 2 O) 2) (IPEA = (E)‐3‐[4‐(imidazol‐1‐ylmethyl)phenyl]prop‐2‐enoic acid) were hydrothermally self‐assembled. Notably, [Cu II (IPEA)]·(H 2 O) vertically grew on the surface of [Cu I (IPEA)] to form a MOF‐on‐MOF S‐scheme heterojunction [Cu I Cu II (IPEA)] 3). Structural and interfacial charge transfer analyses (SEM/TEM/XRD/IR, XPS/UPS/KPFM, DFT) confirmed a built‐in electric field at the heterojunction interface, efficiently separating electrons/holes at redox terminals. Furthermore, Eosin Y (EY) chemical adsorption on [Cu I Cu II (IPEA)] sensitized it for photocatalytic H 2 evolution, achieving a high efficiency of 4800 µmol·g −1 ·h −1 . This work offers new insights for solar energy utilization and dye‐containing wastewater reutilization.
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