Incorporating Potassium Citrate to Improve the Performance of Tin‐Lead Perovskite Solar Cells

Author:

Chen Lei1,Li Chongwen1,Xian Yeming1,Fu Sheng1,Abudulimu Abasi1,Li Deng‐Bing1,Friedl Jared D.1,Li You1,Neupane Sabin1,Tumusange Marie Solange1,Sun Nannan1,Wang Xiaoming1,Ellingson Randy J.1,Heben Michael J.1,Podraza Nikolas J.1,Song Zhaoning1ORCID,Yan Yanfa1

Affiliation:

1. Department of Physics and Astronomy and Wright Center for Photovoltaics Innovation and Commercialization The University of Toledo 2801 W. Bancroft Street Toledo OH 43606 USA

Abstract

AbstractEasy‐to‐form tin vacancies at the buried interface of tin‐lead perovskites hinder the performance of low‐bandgap perovskite solar cells (PSCs). Here, a synergistic strategy by incorporating potassium citrate (PC) into the poly(3,4‐ethylenedioxythiophene):poly(styrene sulfonate) (PEDOT:PSS) hole‐transport layer to passivate the buried interface of Sn‐Pb PSCs is reported. PC neutralizes the acidity of PEDOT:PSS and stabilizes the perovskite front surface, enhancing device stability. Citrate moieties coordinate with Sn2+ on the buried perovskite surface, preventing Sn2+ oxidation and suppressing defect formation. Additionally, potassium cations incorporate into Sn‐Pb perovskites, enhancing crystallinity and passivating halide defects. The combined benefits enable efficient low‐bandgap Sn‐Pb PSCs with a power conversion efficiency of 22.7% and a high open‐circuit voltage of 0.894 V. Using this method, 26.1% efficiency for all‐perovskite tandem solar cells is demonstrated. These results emphasize the significance of buried interface passivation in developing efficient and stable Sn‐Pb PSCs and all‐perovskite tandem solar cells.

Funder

U.S. Department of Energy

Office of Energy Efficiency and Renewable Energy

Solar Energy Technologies Office

Hydrogen and Fuel Cell Technologies Office

Air Force Research Laboratory

Publisher

Wiley

Subject

General Materials Science,Renewable Energy, Sustainability and the Environment

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