4.7 Article

Dual-Functional Quantum Dot Seeding Growth of High-Quality Air-Processed CsPbl2Br Film for Carbon-Based Perovskite Solar Cells

Journal

SOLAR RRL
Volume 6, Issue 4, Pages -

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/solr.202100989

Keywords

all-inorganic perovskites; carbon electrodes; ligands; quantum dot additives; solar cells

Funding

  1. Laboratory of Lingnan Modern Agriculture Project [NZ2021030]
  2. National Natural Science Foundation of China (NSFC) [51732004, 22122805, 22075090, 21975083]

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In this study, CdSe quantum dots were used as crystallization seeds for the first time to modulate the nucleation and crystal growth processes of CsPbl(2)Br perovskite film. The CdSe quantum dots as additives promoted the nucleation process and the surface ligands of the quantum dots influenced the subsequent crystal growth. The CsPbl(2)Br film prepared with the CdSe quantum dots capped with bifunctional organic ligands showed better crystallinity. The efficiency of the optimized carbon-based perovskite solar cells increased from 12.73% to 14.49%.
The high-quality perovskite film is a prerequisite for high-performance optoelectronic devices. Herein, CdSe colloidal quantum dots (QDs) serve as crystallization seeds for the first time to modulate the nucleation and crystal growth processes simultaneously of the CsPbl(2)Br film in the ambient environment. As additives, CdSe QDs help promote the nucleation process in the initial stage of perovskite formation. In addition, it is revealed that the surface ligands of QDs also have an essential influence on the subsequent crystal growth of the perovskite film. The bifunctional ligands on the surface of QDs are beneficial in delaying the growth process of perovskite due to the free functional groups at the ends. The CsPbl 2 Br film prepared with bifunctional organic ligand-capped CdSe QD additives shows better crystallinity than that of the inorganic ligand-based one due to the dual function of these kinds of QDs in not only promoting nucleation but also retarding crystal growth of CsPbl(2)Br crystals. As a result, the high-quality CsPbl(2)Br film with a low defect state density is prepared in the ambient environment. The optimized efficiency of the assembled hole-conductorfree carbon-based perovskite solar cells (C-PSCs) is increased from 12.73% to 14.49%, which is one of the best results for all-inorganic C-PSCs.

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