Luminescent zero-dimensional organic metal halide hybrids with near-unity quantum efficiency

Chenkun Zhou(Florida A&M University - Florida State University College of Engineering), Haoran Lin(Florida A&M University - Florida State University College of Engineering), Yu Tian(Florida State University), Zhao Yuan(Florida A&M University - Florida State University College of Engineering), Ronald J. Clark(Florida State University), Banghao Chen(Florida State University), Lambertus J. van de Burgt(Florida State University), Jamie C. Wang(Florida State University), Yan Zhou(Florida State University), Kenneth Hanson(Florida State University), Quinton J. Meisner(Florida State University), Jennifer Neu(Florida State University), Tiglet Besara(Florida State University), Theo Siegrist(Florida State University), E. S. Lambers(University of Florida), Peter I. Djurovich(University of Southern California), Biwu Ma(Florida State University)
Chemical Science
November 21, 2017
Cited by 633Open Access
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Abstract

, respectively. The isolation of the photoactive metal halide species by the wide band gap organic ligands leads to no interaction or electronic band formation between the metal halide species, allowing the bulk materials to exhibit the intrinsic properties of the individual metal halide species. These 0D organic metal halide hybrids can also be considered as perfect host-guest systems, with the metal halide species periodically doped in the wide band gap matrix. Highly luminescent, strongly Stokes shifted broadband emissions with photoluminescence quantum efficiencies (PLQEs) of close to unity were realized, as a result of excited state structural reorganization of the individual metal halide species. Our discovery of highly luminescent single crystalline 0D organic-inorganic hybrid materials as perfect host-guest systems opens up a new paradigm in functional materials design.


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