4.7 Article

Highly efficient A-site cation exchange in perovskite quantum dot for solar cells

期刊

JOURNAL OF CHEMICAL PHYSICS
卷 157, 期 3, 页码 -

出版社

AIP Publishing
DOI: 10.1063/5.0100258

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资金

  1. National Key Research and Development Program of China [2019YFE0108600]
  2. National Natural Science Foundation of China [52073198, 22161142003]
  3. Natural Science Foundation of Jiangsu Province [BK20211598]
  4. Science and Technology Program of Suzhou [SYG202037]
  5. 111 project
  6. Young Elite Scientist Sponsorship Program by CAST
  7. Collaborative Innovation Center of Suzhou Nano Science and Technology
  8. Soochow University

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In this study, the impact of various factors on the cation exchange process in mixed cation colloidal perovskite quantum dots (PQDs) was comprehensively investigated. The exchange process was monitored using photoluminescence spectroscopy. The results showed that extremely fast cation exchange can be achieved under specific conditions, and the solar cell devices fabricated using these mixed cation PQDs exhibited enhanced power conversion efficiency.
The mixed cation colloidal Cs(1-X)FA(X)PbI(3) perovskite quantum dots (PQDs) obtained by cation exchange between CsPbI3 and FAPbI(3) PQDs have been reported to exhibit enhanced photovoltaic performance. However, the cation exchange mechanism requires further in-depth investigation in terms of both material properties and device application. In this work, the impact of PQD weight ratio, PQD concentration, and host solvent polarity during cation exchange is comprehensively investigated for the first time. In addition, the whole exchange process under varying conditions is monitored by photoluminescence spectroscopy. As a result, we observe extremely fast cation exchange (& SIM;20 min) under a condition at a CsPbI3/FAPbI(3) PQD weight ratio of 1:1, a concentration of 70 mg/ml, and a host solvent using toluene. Moreover, we directly fabricate a PQD solar cell device using these obtained mixed cation Cs(0.5)FA(0.5)PbI(3) PQDs and achieved an enhanced power conversion efficiency of 14.58%. We believe that these results would provide more insights into the cation exchange in emerging PQDs toward efficient photovoltaic fabrication and application. Published under an exclusive license by AIP Publishing.

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