光催化
化学
纳米颗粒
超快激光光谱学
制氢
分子
电荷(物理)
化学工程
化学物理
光化学
有机分子
纳米技术
量子效率
吸收光谱法
吸收(声学)
载流子
氢
催化作用
光谱学
可再生能源
有效核电荷
化学稳定性
氢键
有机合成
生产率
光催化分解水
纳米晶
量子点
作者
Bin Cai,Andjela Brnovic,Mariia V. Pavliuk,Leif Hammarström,Lars Kloo,Sarah A. Barnett,Haining Tian
出处
期刊:Nature Chemistry
[Nature Portfolio]
日期:2026-01-20
卷期号:18 (4): 723-730
被引量:4
标识
DOI:10.1038/s41557-025-02035-z
摘要
Abstract Photocatalysis offers a promising approach for renewable energy conversion and storage, but short lifetimes of charge-separated states in photocatalysts due to charge recombination limit its utility. Here we report an organic molecule with an acceptor–donor–acceptor configuration that can self assemble into highly crystalline nanoparticles. Transient absorption spectroscopy reveals that these crystalline assemblies can induce an ultra-long-lived charge-separated state of up to 1.2 s, attributed to initial symmetry-breaking charge separation, followed by charge hopping across closely packed molecules. These self-assembled nanoparticles have an impressive photocatalytic H 2 evolution rate of 126 mmol g −1 h −1 with an external quantum efficiency of 12% at 550 nm under optimized conditions. This system shows a remarkable stability with 220 million turnover numbers (per particle) over the 77 h of operation. These findings suggest that rational design of organic molecules and their aggregates is vital for improving light-induced charge separation and for developing highly efficient, stable and scalable organic photocatalysts.
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