4.8 Article

Multifunctional Conjugated Ligand Engineering for Stable and Efficient Perovskite Solar Cells

期刊

ADVANCED MATERIALS
卷 33, 期 32, 页码 -

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/adma.202100791

关键词

charge transfer; organic semiconductors; perovskite solar cells; stability; surface passivation

资金

  1. US Office of Naval Research [N00014-19-1-2296]
  2. Davidson School of Chemical Engineering
  3. College of Engineering of Purdue University
  4. Lillian Gilbreth Postdoctoral Fellowship from College of Engineering of Purdue University
  5. US Department of Energy, Office of Basic Energy Sciences [DE-SC0016356]
  6. U.S. Department of Energy [DE-SC0018208]
  7. U.S. Department of Energy (DOE) [DE-SC0018208] Funding Source: U.S. Department of Energy (DOE)

向作者/读者索取更多资源

A novel multifunctional semiconducting organic ammonium cationic interface modifier is reported to boost the efficiency and stability of perovskite solar cells, achieving an excellent power conversion efficiency of 22.06%. By improving energy level alignment and stabilizing the interface, ion migration and halide phase segregation are suppressed, leading to long-term operational stability.
Surface passivation is an effective way to boost the efficiency and stability of perovskite solar cells (PSCs). However, a key challenge faced by most of the passivation strategies is reducing the interface charge recombination without imposing energy barriers to charge extraction. Here, a novel multifunctional semiconducting organic ammonium cationic interface modifier inserted between the light-harvesting perovskite film and the hole-transporting layer is reported. It is shown that the conjugated cations can directly extract holes from perovskite efficiently, and simultaneously reduce interface non-radiative recombination. Together with improved energy level alignment and the stabilized interface in the device, a triple-cation mixed-halide medium-bandgap PSC with an excellent power conversion efficiency of 22.06% (improved from 19.94%) and suppressed ion migration and halide phase segregation, which lead to a long-term operational stability, is demonstrated. This strategy provides a new practical method of interface engineering in PSCs toward improved efficiency and stability.

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