异质结
材料科学
激子
光电子学
光伏系统
极化率
光催化
电场
极化子
化学物理
量子效率
有机半导体
离解(化学)
分子
纳米颗粒
纳米技术
接口(物质)
限制
制氢
二进制数
能量转换效率
载流子
有机太阳能电池
电荷(物理)
量子
Boosting(机器学习)
作者
T. J. Li,Wenqin Si,Ruijie Zheng,Wang Kh,Ye Yang,Yuze Lin
摘要
ABSTRACT Organic photovoltaic catalysts (OPCs) hold great potential for energy conversion and environmental purification yet often suffer from inefficient exciton dissociation and rapid charge recombination, particularly at disordered donor/acceptor (D/A) interfaces, limiting their photocatalytic performance. Herein, we propose an embedded interface strategy that involves a highly polarizable molecule named Y6CO‐S at the D/A interface within OPC bulk heterojunction (BHJ) to amplify the local electric field and enhance molecular ordering, improving hole transfer efficiency and prolonging hole polaron lifetime, and thereby boosting photocatalytic activity. Specifically, the optimized PM6:PYF‐T‐o:Y6CO‐S nanoparticles (NPs) achieve remarkable photocatalytic sacrificial average mass‐united/area‐united hydrogen evolution rates of 263.8‐1974.7 mmol h − 1 g − 1 and 42.7‐182.4 mmol h −1 m −2 at varied NP concentrations under simulated sunlight (AM 1.5G, 100 mW cm −2 ) for 10 h along with high external quantum efficiencies of >10% across the visible to near‐infrared region, 36%–47% exceeding those of the binary PM6:PYF‐T‐o system without Y6CO‐S embedded interface and representing one of the highest performances reported to date for photocatalysts. This work demonstrates the significant potential of embedded interface strategy in developing high‑performance heterojunction OPCs as well as other optoelectronic applications.
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