光催化
激子
半导体
有机半导体
光化学
材料科学
氢
化学物理
光电子学
化学
凝聚态物理
物理
有机化学
催化作用
作者
Yixiao Jia,Jiang Xin,Yuanxin Liang,Ying-Chen Peng,Songjie Fang,Ye Yang,Chunyang Miao,Yuze Lin,Shiming Zhang
标识
DOI:10.1016/j.dyepig.2024.111982
摘要
To achieve high performance organic photovoltaic hydrogen-evolution (OPH), it is crucial to extend the exciton lifetime of organic photovoltaic catalysis. This is primarily because it increases the exciton diffusion length. In this work, a new asymmetric organic photovoltaic catalysis (BTP-eC9-B4F) has been developed, which achieves a longer exciton lifetime of 1.25 ns and a higher fluorescence quantum yield of 9.4 % compared to symmetric structures. This has been made possible by using asymmetric end groups. Experimental results demonstrate that the photocatalyst with a longer exciton lifetime exhibits a more efficient average hydrogen evolution rate of 121.57 mmol h−1 g−1 under AM 1.5G, 100 mW cm−2 for 5 h. Therefore, extending the lifetime of excitons has been shown to be an effective approach to achieve high efficiency OPH.
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