The effect of Cu(I)-doping on the photoinduced electron transfer from aqueous CdS quantum dots

被引:0
|
作者
Rana, Gourab [1 ]
Das, Sharmistha [1 ]
Singha, Prajit Kumar [1 ]
Ali, Fariyad [1 ]
Maji, Rohan [2 ]
Datta, Anindya [1 ]
机构
[1] Indian Inst Technol, Dept Chem, Powai, Mumbai 400076, India
[2] Indian Inst Sci Educ & Res Kolkata, Dept Chem, Mohanpur 741246, India
来源
JOURNAL OF CHEMICAL PHYSICS | 2024年 / 161卷 / 02期
关键词
CHARGE-CARRIER DYNAMICS; METHYL VIOLOGEN; PHOTOCATALYTIC REACTIONS; NANOCRYSTALS; SURFACE; ADSORPTION; EFFICIENCY;
D O I
10.1063/5.0218548
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The doping of CdS quantum dots (QDs) with Cu(I) disrupts electron-hole correlation due to hole trapping by the dopant ion, post-photoexcitation. The present paper examines the effect of such disruption on the rate of photoinduced electron transfer (PET) from the QDs to methyl viologen (MV2+), with implications in their photocatalytic activity. A significantly greater efficiency of PL quenching by MV2+ is observed for the doped QDs than for the undoped ones. Interestingly, the Stern-Volmer plots constructed using PL intensities exhibit an upward curvature for both the cases, while the PL lifetimes remain unaffected. This observation is rationalized by considering the adsorption of the quencher on the surface of the QDs and ultrafast PET post-photoexcitation. Ultrafast transient absorption experiments confirm a faster electron transfer for the doped QDs. It is also realized that the transient absorption experiment yields a more accurate estimate of the binding constant of the quencher with the QDs, than the PL experiment.
引用
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页数:9
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