4.8 Article

Regulating off-centering distortion maximizes photoluminescence in halide perovskites

期刊

NATIONAL SCIENCE REVIEW
卷 8, 期 9, 页码 -

出版社

OXFORD UNIV PRESS
DOI: 10.1093/nsr/nwaa288

关键词

halide perovskites; high pressure; off-centering distortion; optical properties; lone-pair electrons; quantitative relationship

资金

  1. National Natural Science Foundation of China [51527801, U1930401, 17N1051-0213]
  2. US Department of Energy (DOE), Office of Science, Basic Energy Sciences [SC0012541]
  3. US Department of Energy, Office of Science, Basic Energy Sciences [DE-AC02-06CH11357]
  4. National Science Foundation (NSF)-Earth Sciences [EAR-1634415]
  5. Department of Energy GeoSciences [DE-FG02-94ER14466]
  6. COMPRES through NSF [EAR-1661511]
  7. DOE NationalNuclear Security Administration [DE-NA0001974]
  8. NSF
  9. DOE Office of Science [DE-AC02-06CH11357]
  10. Laboratory Directed Research and Development program of Los Alamos National Laboratory (LANL)
  11. TriadNational SecurityAdministration of theUSDepartment of Energy [89233218CNA000001]
  12. Tencent XPLORER Prize

向作者/读者索取更多资源

Pressure and chemical methods can regulate the metal off-centering distortion in metal halide perovskites, achieving giant tunability in photoluminescence properties and providing new insights for high-performance photovoltaics and optoelectronics.
Metal halide perovskites possess unique atomic and electronic configurations that endow them with high defect tolerance and enable high-performance photovoltaics and optoelectronics. Perovskite light-emitting diodes have achieved an external quantum efficiency of over 20%. Despite tremendous progress, fundamental questions remain, such as how structural distortion affects the optical properties. Addressing their relationships is considerably challenging due to the scarcity of effective diagnostic tools during structural and property tuning as well as the limited tunability achievable by conventional methods. Here, using pressure and chemical methods to regulate the metal off-centering distortion, we demonstrate the giant tunability of photoluminescence (PL) in both the intensity (>20 times) and wavelength (>180 nm/GPa) in the highly distorted halide perovskites [CH3NH3GeI3, HC(NH2)(2)GeI3, and CsGeI3]. Using advanced in situ high-pressure probes and first-principles calculations, we quantitatively reveal a universal relationship whereby regulating the level of off-centering distortion towards 0.2 leads to the best PL performance in the halide perovskites. By applying this principle, intense PL can still be induced by substituting CH3NH3+ with Cs+ to control the distortion in (CH3NH3)(1-x)CsxGeI3, where the chemical substitution plays a similar role as external pressure. The compression of a fully substituted sample of CsGeI3 further tunes the distortion to the optimal value at 0.7 GPa, which maximizes the emission with a 10-fold enhancement. This work not only demonstrates a quantitative relationship between structural distortion and PL property of the halide perovskites but also illustrates the use of knowledge gained from high-pressure research to achieve the desired properties by ambient methods.

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