In Situ Reconstruction Post‐Treatment for Efficient Carbon‐Based Hole‐Conductor‐Free Printable Mesoscopic Perovskite Solar Cells

Author:

Han Chuanzhou1,Du Jiankang1,Liu Zhiyang2,Gao Qiaojiao1,Chen Xiayan1,Xiang Junwei1,Xiao Xufeng1,Cheng Yanjie1,Chen Kai1,Xia Minghao1,Liu Jiale1,Yang Li‐Ming3,Zhou Yang1,Mei Anyi1ORCID,Han Hongwei1ORCID

Affiliation:

1. Michael Grätzel Center for Mesoscopic Solar Cells Wuhan National Laboratory for Optoelectronics Huazhong University of Science and Technology Wuhan 430074 China

2. State Power Investment Corporation Hydrogen Energy Company Limited Beijing 102600 China

3. School of Chemistry and Chemical Engineering Huazhong University of Science and Technology Wuhan 430074 China

Abstract

AbstractPerovskite solar cells are regarded as the most promising and disruptive photovoltaic of the new generation. Carbon‐based hole‐conductor‐free printable mesoscopic perovskite solar cells (p‐MPSCs) with three mesoscopic layers have garnered considerable interest owing to their simple manufacturing process and cost‐effective raw materials, signaling the potential for commercialization. However, the energy level mismatch between the perovskite and the carbon electrode as well as defects at perovskite grain boundaries inevitably lead to additional non‐radiative carrier recombination and large voltage loss. In this study, a facile in situ reconstruction post‐treatment approach is employed to integrate lead sulfide (PbS) and the two‐dimensional (2D) perovskite K2PbI4 into the mesoporous scaffolds of p‐MPSCs. In this way, grain boundary defects are effectively passivated and the ion migration is suppressed by introducing 2D perovskite K2PbI4 at grain boundaries. Besides, the incorporation of PbS leads to the downward shift of the Fermi level for perovskite, which enhances hole collection within the device by optimizing band alignment at the perovskite/carbon interface. Consequently, an improved efficiency exceeding 20% is achieved for p‐MPSCs with no significant performance degradation observed over a storage period of 235 days. This strategy provides a facile and novel approach toward fabricating highly efficient and stable p‐MPSCs.

Funder

National Natural Science Foundation of China

Fundamental Research Funds for the Central Universities

Publisher

Wiley

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