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Unraveling the Emission Pathways in Copper Indium Sulfide Quantum Dots
被引:21
作者:
Xia, Chenghui
[1
,2
,3
]
Tamarat, Philippe
[1
,2
,3
]
Hou, Lei
[1
,2
,3
]
Busatto, Serena
[4
]
Meeldijk, Johannes D.
[5
]
Donega, Celso de Mello
[4
]
Lounis, Brahim
[1
,2
,3
]
机构:
[1] Univ Bordeaux, LP2N, F-33405 Talence, France
[2] Inst Opt, LP2N, F-33405 Talence, France
[3] CNRS, F-33405 Talence, France
[4] Univ Utrecht, Debye Inst Nanomat Sci, Condensed Matter & Interfaces, NL-3508 TA Utrecht, Netherlands
[5] Univ Utrecht, Debye Inst Nanomat Sci, Electron Microscopy Utrecht, NL-3584 CH Utrecht, Netherlands
来源:
关键词:
core-shell nanocrystals;
single dot spectroscopy;
exciton;
fine structure;
exciton-phonon coupling;
exciton self-trapping;
IN-ZN-S;
CUINS2;
NANOCRYSTALS;
SEMICONDUCTOR NANOCRYSTALS;
HIGHLY EFFICIENT;
BLINKING;
PHOTOLUMINESCENCE;
LUMINESCENCE;
EXCITON;
LIGHT;
D O I:
10.1021/acsnano.1c04909
中图分类号:
O6 [化学];
学科分类号:
0703 ;
摘要:
Semiconductor copper indium sulfide quantum dots are emerging as promising alternatives to cadmium- and lead-based chalcogenides in solar cells, luminescent solar concentrators, and deep-tissue bioimaging due to their inherently lower toxicity and outstanding photoluminescence properties. However, the nature of their emission pathways remains a subject of debate. Using low-temperature single quantum dot spectroscopy on core-shell copper indium sulfide nanocrystals, we observe two subpopulations of particles with distinct spectral features. The first class shows sharp resolution-limited emission lines that are attributed to zero-phonon recombination lines of a long-lived band-edge exciton. Such emission results from the perfect passivation of the copper indium sulfide core by the zinc sulfide shell and points to an inversion in the band-edge hole levels. The second class exhibits ultrabroad spectra regardless of the temperature, which is a signature of the extrinsic self-trapping of the hole assisted by defects in imperfectly passivated quantum dots.
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页码:17573 / 17581
页数:9
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