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
标识
DOI:10.1038/s41557-025-02035-z
摘要
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 H2 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.
科研通智能强力驱动
Strongly Powered by AbleSci AI