马库斯理论
超快激光光谱学
电荷(物理)
反应速率常数
量子点
化学物理
分子
化学
螺旋钻
俄歇效应
氧化还原
材料科学
分子线
原子物理学
吸收(声学)
分子物理学
二茂铁
光化学
量子
光谱学
吸收光谱法
电子转移
重组
部分电荷
基本电荷
有效核电荷
作者
Yan B. Vogel,Willemijn H. Boeije,Lotte van Steekelenburg,Demi Vollebregt,Reinout Ubbink,Hua Chen,Ali Tayefeh Younesi,Ronald Ulbricht,Wolter F. Jager,Ferdinand Grozema,Arjan J. Houtepen
出处
期刊:ACS Nano
[American Chemical Society]
日期:2026-01-15
卷期号:20 (4): 3487-3498
标识
DOI:10.1021/acsnano.5c13838
摘要
Charge transfer between quantum dots (QDs) and redox molecules is not well described by the Marcus theory, the hall-mark theory for charge transfer in molecular systems. The Marcus inverted region, where the rate decreases with increasing the free energy difference, has never been observed in QDs. The previously reported hypothesis for the absence of the Marcus inverted region in QDs is an Auger-assisted charge transfer pathway, which we refer to as the "Auger hypothesis". Here, we show that the Auger hypothesis does not hold to experimental tests. We measured the rate constants for two processes where Auger is either allowed or not: charge separation and charge recombination. We used ultrafast transient absorption spectroscopy to probe the rate of charge separation and recombination between PbS QDs and ferrocene derivatives ligands bound to their surface. We find that the rate constant for both charge separation and recombination increases by increasing the free energy difference, is temperature-independent, and increases with the number of molecular acceptors. All these results are against theoretical predictions for an Auger-assisted charge transfer pathway.
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