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Tuning the Excited-State Dynamics of CuI Films with Electrochemical Bias

[Image: see text] Owing to its high hole conductivity and ease of preparation, CuI was among the first inorganic hole-transporting materials that were introduced early on in metal halide perovskite solar cells, but its full potential as a semiconductor material is still to be realized. We have now p...

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Detalles Bibliográficos
Autores principales: Samu, Gergely F., Scheidt, Rebecca A., Balog, Ádám, Janáky, Csaba, Kamat, Prashant V.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2019
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6413481/
https://www.ncbi.nlm.nih.gov/pubmed/30882041
http://dx.doi.org/10.1021/acsenergylett.9b00182
Descripción
Sumario:[Image: see text] Owing to its high hole conductivity and ease of preparation, CuI was among the first inorganic hole-transporting materials that were introduced early on in metal halide perovskite solar cells, but its full potential as a semiconductor material is still to be realized. We have now performed ultrafast spectroelectrochemical experiments on ITO/CuI electrodes to show the effect of applied bias on the excited-state dynamics in CuI. Under operating conditions, the recombination of excitons is dependent on the applied bias, and it can be accelerated by decreasing the potential from +0.6 to −0.1 V vs Ag/AgCl. Prebiasing experiments show the persistent and reversible “memory” effect of electrochemical bias on charge carrier lifetimes. The excitation of CuI in a CuI/CsPbBr(3) film provides synergy between both CuI and CsPbBr(3) in dictating the charge separation and recombination.