Ligand-Assisted Reconstruction of Colloidal Quantum Dots Decreases Trap State Density
Author(s) -
Bin Sun,
Maral Vafaie,
Larissa Levina,
Mingyang Wei,
Yitong Dong,
Yajun Gao,
Hao Ting Kung,
Margherita Biondi,
Andrew H. Proppe,
Bin Chen,
MinJae Choi,
Laxmi Kishore Sagar,
Oleksandr Voznyy,
Shana O. Kelley,
Frédéric Laquai,
ZhengHong Lu,
Sjoerd Hoogland,
F. Pelayo Garcı́a de Arquer,
Edward H. Sargent
Publication year - 2020
Publication title -
nano letters
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 4.853
H-Index - 488
eISSN - 1530-6992
pISSN - 1530-6984
DOI - 10.1021/acs.nanolett.0c00638
Subject(s) - passivation , quantum dot , nanocrystal , materials science , nanoparticle , colloid , diffusion , trap (plumbing) , nanotechnology , surface charge , potential well , optoelectronics , chemical physics , chemistry , physics , layer (electronics) , thermodynamics , environmental engineering , engineering
Increasing the power conversion efficiency (PCE) of colloidal quantum dot (CQD) solar cells has relied on improving the passivation of CQD surfaces, enhancing CQD coupling and charge transport, and advancing device architecture. The presence of hydroxyl groups on the nanoparticle surface, as well as dimers-fusion between CQDs-has been found to be the major source of trap states, detrimental to optoelectronic properties and device performance. Here, we introduce a CQD reconstruction step that decreases surface hydroxyl groups and dimers simultaneously. We explored the dynamic interaction of charge carriers between band-edge states and trap states in CQDs using time-resolved spectroscopy, showing that trap to ground-state recombination occurs mainly from surface defects in coupled CQD solids passivated using simple metal halides. Using CQD reconstruction, we demonstrate a 60% reduction in trap density and a 25% improvement in charge diffusion length. These translate into a PCE of 12.5% compared to 10.9% for control CQDs.
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