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Regulating crystallization dynamics and crystal orientation of methylammonium tin iodide enables high-efficiency lead-free perovskite solar cells

  • Long Ji
  • , Ting Zhang
  • , Yafei Wang
  • , Detao Liu
  • , Hao Chen
  • , Hualin Zheng
  • , Xuefeng Peng
  • , Shihao Yuan
  • , Zhi David Chen
  • , Shibin Li

Producción científica: Articlerevisión exhaustiva

32 Citas (Scopus)

Resumen

Tin (Sn)-based perovskite solar cells (PSCs) have attracted much attention because they are more environmentally friendly than lead-based PSCs. However, the fast crystallization of Sn-based perovskite films and the easy oxidation of Sn2+ to Sn4+ hinder the improvement of their efficiency and stability. In this work, ethylammonium bromide (EABr) was added to methylammonium tin iodide (MASnI3) perovskite precursor solution to regulate the crystallization dynamics and improve the film morphology. The results show that the large EA+ ions slow down the crystallization process of Sn-based perovskites and form a smooth perovskite film with high crystallinity, while the added Br- anions further improved the crystallinity and orientation of the perovskite film. Under the combined action of EA+ and Br- ions, the as-produced PSCs achieved a champion power conversion efficiency (PCE) of 9.59%. The EABr additive also retarded the oxidation of Sn2+, and the solar cell device maintained 93% of its initial efficiency after 30 days in a nitrogen-filled glove box without being encapsulated. This work provides a new strategy for the realization of high-efficiency Sn-based PSCs.

Idioma originalEnglish
Páginas (desde-hasta)1219-1225
Número de páginas7
PublicaciónNanoscale
Volumen14
N.º4
DOI
EstadoPublished - ene 28 2022

Nota bibliográfica

Publisher Copyright:
© The Royal Society of Chemistry.

Financiación

This work was supported by National Natural Science Foundation of China (62174021, 62104028, and 61874150), Sichuan Science and Technology Program (2020YJ0244) and China Postdoctoral Science Foundation (2021M700689). This work was partially supported by University of Kentucky. The authors also thank surface X-ray diffraction beamline at the SSRF for providing the beam time.

FinanciadoresNúmero del financiador
University of Kentucky
Sichuan Province Science and Technology Support Program2020YJ0244
Sichuan Province Science and Technology Support Program
National Natural Science Foundation of China (NSFC)62104028, 61874150, 62174021
National Natural Science Foundation of China (NSFC)
China Postdoctoral Science Foundation2021M700689
China Postdoctoral Science Foundation

    ASJC Scopus subject areas

    • General Materials Science

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