化学
人工光合作用
两亲性
细菌叶绿素
超分子化学
量子产额
光催化
光合作用
制氢
营业额
量子
光合反应中心
光化学
生物系统
光系统II
阳离子聚合
超分子组装
量子效率
纳米技术
氢
产量(工程)
染色质
分子
合理设计
自组装
组合化学
化学工程
纳米-
仿生合成
化学物理
生物物理学
工作(物理)
作者
Jiangshan Zhang,Danying Ma,Shunyi Ming,Yifei Lei,Yonghong Fu,Ru-Lei Zhang,Shixing Lei,Song-Hai Xie,Dan‐Wei Zhang,Zhan‐Ting Li,Jia Tian
摘要
The supramolecular architecture of light-harvesting complex 2 (LH2) and light-harvesting complex 1–reaction center (LH1–RC) complexes underpins the near-unity quantum efficiency of photosynthesis in purple bacteria. Constructing artificial photosynthetic systems that structurally and functionally mimic these natural assemblies remains a critical challenge. Here, we report a spherical chromatophore nanomicelle system that mimics both LH2 and LH1–RC in water. This system is constructed through hierarchical coassembly of an amphiphilic porphyrin-based bacteriochlorophyll analogue and a cationic molecular nickel catalyst. Cryogenic electron microscopy directly resolves high-resolution ring-like structures on the nanomicelle surface, providing the first visual confirmation of the biomimetic architecture. The system achieves photocatalytic hydrogen evolution with a turnover number exceeding 667,000 over 72 h and a turnover frequency of above 9000 h–1 with an absolute hydrogen yield of 1.34 μmol─40 times greater than the nonassembled free molecular system─along with an initial external quantum efficiency of 6.8% at 435 nm. This outstanding performance originates from the well-defined spatial organization of the photosensitizers and catalysts, which facilitates efficient light harvesting and directional energy/electron transfer. Our work establishes a promising strategy for constructing high-performance artificial photosynthetic systems through rational biomimetic design.
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