One-dimensional organic lead halide perovskites with efficient bluish white-light emission

Zhao Yuan(Florida A&M University - Florida State University College of Engineering), Chenkun Zhou(Florida A&M University - Florida State University College of Engineering), Yu Tian(Florida State University), Yu Shu(Florida A&M University - Florida State University College of Engineering), Joshua Messier(Florida A&M University - Florida State University College of Engineering), Jamie C. Wang(Florida State University), Lambertus J. van de Burgt(Florida State University), Konstantinos Kountouriotis(Florida State University), Yan Xin(Florida State University), Ethan Holt(University of Florida), Kirk S. Schanze(University of Florida), Ronald J. Clark(Florida State University), Theo Siegrist(Florida State University), Biwu Ma(Florida State University)
Nature Communications
January 4, 2017
Cited by 780Open Access
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Abstract

Abstract Organic-inorganic hybrid metal halide perovskites, an emerging class of solution processable photoactive materials, welcome a new member with a one-dimensional structure. Herein we report the synthesis, crystal structure and photophysical properties of one-dimensional organic lead bromide perovskites, C 4 N 2 H 14 PbBr 4 , in which the edge sharing octahedral lead bromide chains [PbBr 4 2− ] ∞ are surrounded by the organic cations C 4 N 2 H 14 2+ to form the bulk assembly of core-shell quantum wires. This unique one-dimensional structure enables strong quantum confinement with the formation of self-trapped excited states that give efficient bluish white-light emissions with photoluminescence quantum efficiencies of approximately 20% for the bulk single crystals and 12% for the microscale crystals. This work verifies once again that one-dimensional systems are favourable for exciton self-trapping to produce highly efficient below-gap broadband luminescence, and opens up a new route towards superior light emitters based on bulk quantum materials.


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