| Literature DB >> 26942559 |
Alice Corani1, Ming-Hsien Li2, Po-Shen Shen2, Peter Chen2,3,4, Tzung-Fang Guo2,3,4, Amal El Nahhas1, Kaibo Zheng1, Arkady Yartsev1, Villy Sundström1, Carlito S Ponseca1.
Abstract
There is a mounting effort to use nickel oxide (NiO) as p-type selective electrode for organometal halide perovskite-based solar cells. Recently, an overall power conversion efficiency using this hole acceptor has reached 18%. However, ultrafast spectroscopic investigations on the mechanism of charge injection as well as recombination dynamics have yet to be studied and understood. Using time-resolved terahertz spectroscopy, we show that hole transfer is complete on the subpicosecond time scale, driven by the favorable band alignment between the valence bands of perovskite and NiO nanoparticles (NiO(np)). Recombination time between holes injected into NiO(np) and mobile electrons in the perovskite material is shown to be hundreds of picoseconds to a few nanoseconds. Because of the low conductivity of NiO(np), holes are pinned at the interface, and it is electrons that determine the recombination rate. This recombination competes with charge collection and therefore must be minimized. Doping NiO to promote higher mobility of holes is desirable in order to prevent back recombination.Entities:
Year: 2016 PMID: 26942559 DOI: 10.1021/acs.jpclett.6b00238
Source DB: PubMed Journal: J Phys Chem Lett ISSN: 1948-7185 Impact factor: 6.475