Abstract
The precise regulation of interfacial charge distribution highly determines the power conversion efficiency of perovskite solar cells (PSCs). Herein, inorganic (NiCo)1-y Fey Ox nanoparticle decorated graphene oxide (GO) is successfully demonstrated as a hole booster for all-inorganic CsPbIBr2 PSC free of precious metal electrode. Arising from the spontaneous electron transfer induced p-type doping of GO from edged oxygen-containing functional groups to (NiCo)1-y Fey Ox , the best all-inorganic CsPbIBr2 PSC achieves an efficiency of 10.95 % under one standard sun owing to the eliminated paradox between charge extraction and charge localization in GO surface. Furthermore, the champion device exhibits an excellent long-term stability at 10 % relative humidity without encapsulation over 70 days because of the suppressed ions migration.
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