4.8 Article

Suppressing Nickel Oxide/Perovskite Interface Redox Reaction and Defects for Highly Performed and Stable Inverted Perovskite Solar Cells

Journal

SMALL METHODS
Volume 6, Issue 10, Pages -

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/smtd.202200787

Keywords

4-(2-Aminoethyl) benzoic acid bromide; interface modifications; NiOx redox reaction; stability

Funding

  1. University Grant Council of the University of Hong Kong [2019157209, 202011159254]
  2. General Research Fund from Hong Kong Special Administrative Region, China [17200518, 17201819, 17211220, 17200021]
  3. Collaboration Research Fund from Hong Kong Special Administrative Region, China [C5037-18G, C7035-20G]

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This study introduces ABABr as a solution to the redox reactions between NiOx and perovskites. Experimental and theoretical investigations show that ABABr chemically reacts with NiOx to reduce redox reactions and improves the performance of perovskite films.
The inorganic hole transport layer of nickel oxide (NiOx) has shown highly efficient, low-cost, and scalable in perovskite photovoltaics. However, redox reactions at the interface between NiOx and perovskites limit their commercialization. In this study, ABABr (4-(2-Aminoethyl) benzoic acid bromide) between the NiOx and different perovskite layers to address the issues has been introduced. How the ABABr interacts with NiOx and perovskites is experimentally and theoretically investigated. These results show that the ABABr molecule chemically reacts with the NiOx via electrostatic attraction on one side, whereas on the other side, it forms a strong hydrogen bond via the NH3+ group with perovskites layers, thus directly diminishing the redox reaction between the NiO, and perovskites layers and passivating the layer surfaces. Additionally, the ABABr interface modification leads to significant improvements in perovskite film morphology, crystallization, and band alignment. The perovskites solar cells (PSCs) based on an ABABr interface modification show power conversion efficiency (PCE) improvement by over 13% and maintain over 90% of its PCE after continuous operation at maximum power point for over 500 h. The work not only contributes to the development of novel interlayers for stable PSCs but also to the understanding of how to prevent interface redox reactions.

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