Electron-Hole Diffusion Lengths Exceeding 1 Micrometer in an Organometal Trihalide Perovskite Absorber

Author:

Stranks Samuel D.1,Eperon Giles E.1,Grancini Giulia2,Menelaou Christopher1,Alcocer Marcelo J. P.2,Leijtens Tomas1,Herz Laura M.1,Petrozza Annamaria2,Snaith Henry J.1

Affiliation:

1. University of Oxford, Clarendon Laboratory, Parks Road, Oxford OX1 3PU, UK.

2. Center for Nano Science and Technology@PoliMi, Istituto Italiano di Tecnologia, Via Giovanni Pascoli 70/3, 20133, Milano, Italy.

Abstract

Unrestricted Travel in Solar Cells In the past 2 years, organolead halide perovskites have emerged as a promising class of light-harvesting media in experimental solar cells, but the physical basis for their efficiency has been unclear (see the Perspective by Hodes ). Two studies now show, using a variety of time-resolved absorption and emission spectroscopic techniques, that these materials manifest relatively long diffusion paths for charge carriers energized by light absorption. Xing et al. (p. 344 ) independently assessed (negative) electron and (positive) hole diffusion lengths and found them well-matched to one another to the ~100-nanometer optical absorption depth. Stranks et al. (p. 341 ) uncovered a 10-fold greater diffusion length in a chloride-doped material, which correlates with the material's particularly efficient overall performance. Both studies highlight effective carrier diffusion as a fruitful parameter for further optimization.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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