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Layer-Dependent Photoinduced Electron Transfer in 0D–2D Lead Sulfide/Cadmium Sulfide–Layered Molybdenum Disulfide Hybrids
Author(s) -
JiaShiang Chen,
MingXing Li,
Qin Wu,
Eduard Fron,
Xiao Tong,
Mircea Cotlet
Publication year - 2019
Publication title -
acs nano
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.554
H-Index - 382
eISSN - 1936-086X
pISSN - 1936-0851
DOI - 10.1021/acsnano.9b04367
Subject(s) - molybdenum disulfide , lead sulfide , quantum dot , electron transfer , cadmium sulfide , acceptor , monolayer , materials science , electron acceptor , chemical physics , band gap , photoinduced electron transfer , electron , charge (physics) , sulfide , layer (electronics) , photochemistry , nanotechnology , optoelectronics , chemistry , condensed matter physics , physics , quantum mechanics , metallurgy
We demonstrate layer-dependent electron transfer between core/shell PbS/CdS quantum dots (QDs) and layered MoS 2 via energy band gap engineering of both the donor (QDs) and the acceptor (MoS 2 ) components. We do this by (i) changing the size of the QD or (ii) by changing the number of layers of MoS 2 , and each of these approaches alters the band gap and/or the donor-acceptor separation distance, thus providing a means of tuning the charge-transfer rate. We find the charge-transfer rate to be maximal for QDs of smallest size and for QDs combined with a 5-layer MoS 2 or thicker. We model this layer-dependent charge-transfer rate with a theoretical model derived from Marcus theory previously applied to nonadiabatic electron transfer in weakly coupled systems by considering the QD transferring photogenerated electrons to noninteracting monolayers within a few layers of MoS 2 .

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