Enhancing the Efficiency and Stability of Tin‐Lead Perovskite Solar Cells via Sodium Hydroxide Dedoping of PEDOT:PSS

Author:

Wu Dong‐Tai1,Zhu Wen‐Xian1,Dong Yueyao2,Daboczi Matyas3,Ham Gayoung4,Hsieh Hsing‐Jung1,Huang Chi‐Jing1,Xu Weidong5,Henderson Charlie6,Kim Ji‐Seon6,Eslava Salvador3,Cha Hyojung47,Macdonald Thomas J.2,Lin Chieh‐Ting18ORCID

Affiliation:

1. Department of Chemical Engineering National Chung Hsing University 145 Xingda Road Taichung 402–27 Taiwan

2. School of Engineering and Materials Science Queen Mary University of London London E1 4NS UK

3. Department of Chemical Engineering and Centre for Processable Electronics Imperial College London London SW7 2AZ UK

4. Department of Energy Convergence and Climate Change Kyungpook National University Daegu 41566 Republic of Korea

5. Department of Chemical Engineering and Biotechnology University of Cambridge Philippa Fawcett Drive Cambridge CB3 0AS UK

6. Department of Physics and Centre for Processable Electronics Imperial College London London SW7 2AZ UK

7. Department of Hydrogen and Renewable Energy Kyungpook National University Daegu 41566 Republic of Korea

8. Innovation and Development Center of Sustainable Agriculture National Chung Hsing University Taichung City 402 Taiwan

Abstract

AbstractTin‐lead (Sn‐Pb) perovskite solar cells (PSCs) have gained interest as candidates for the bottom cell of all‐perovskite tandem solar cells due to their broad absorption of the solar spectrum. A notable challenge arises from the prevalent use of the hole transport layer, PEDOT:PSS, known for its inherently high doping level. This high doping level can lead to interfacial recombination, imposing a significant limitation on efficiency. Herein, NaOH is used to dedope PEDOT:PSS, with the aim of enhancing the efficiency of Sn‐Pb PSCs. Secondary ion mass spectrometer profiles indicate that sodium ions diffuse into the perovskite layer, improving its crystallinity and enlarging its grains. Comprehensive evaluations, including photoluminescence and nanosecond transient absorption spectroscopy, confirm that dedoping significantly reduces interfacial recombination, resulting in an open‐circuit voltage as high as 0.90 V. Additionally, dedoping PEDOT:PSS leads to increased shunt resistance and high fill factor up to 0.81. As a result of these improvements, the power conversion efficiency is enhanced from 19.7% to 22.6%. Utilizing NaOH to dedope PEDOT:PSS also transitions its nature from acidic to basic, enhancing stability and exhibiting less than a 7% power conversion efficiency loss after 1176 h of storage in N2 atmosphere.

Funder

National Science and Technology Council

National Research Foundation of Korea

Engineering and Physical Sciences Research Council

Royal Society

Royal Commission for the Exhibition of 1851

Ministry of Education

Publisher

Wiley

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