Salt‐Based Catalyzer to Aid Heterogeneous Nucleation Enabling >23% Efficient Electron‐Transport‐Layer‐Free Perovskite Solar Cells

Author:

Deng Jidong12,Huang Xiaofeng34,Che Yuliang1,Wang Xiao1,Zhang Xiaoli5,Wu Binghui3,Yang Li12ORCID,Zhang Jinbao12

Affiliation:

1. College of Materials Fujian Key Laboratory of Advanced Materials Xiamen Key Laboratory of Electronic Ceramic Materials and Devices Xiamen University Xiamen 361005 China

2. Shenzhen Research Institute of Xiamen University Shenzhen 518000 China

3. College of Chemistry and Chemical Engineering Pen‐Tung Sah Institute of Micro‐Nano Science and Technology Xiamen University Xiamen 361005 China

4. Department of Chemistry Hong Kong Institute for Clean Energy City University of Hong Kong Kowloon Hong Kong 710119 China

5. School of Physics & Optoelectronic Engineering Guangdong University of Technology Guangzhou 510006 China

Abstract

AbstractCharge transport layers are critical components in perovskite solar cells (PSCs) for achieving satisfied power conversion efficiencies (PCEs) and device stability. However, these layers often bring incompatible interfaces and complex fabrication, limiting the stability and scalability of PSC technology. Here an alternative strategy of salt‐based catalyzer (SBC) is proposed to regulate the heterogeneous nucleation of perovskite, which enables uniform and well‐controlled perovskite coverage directly onto the salt‐treated substrate without electron transport layers (ETLs). By carefully adjusting the cations, anions, and the thickness of SBC, high‐quality perovskite films along with superior buried interfaces suppress the carrier recombination losses and strengthen the interfacial stability, promoting the resultant device to achieve a record PCE of 23.04%, which represents the highest reported efficiency for ETL‐free PSCs. Meanwhile, the SBC technique can be well extended to large‐area, flexible, and module‐based devices. More encouragingly, the SBC‐based unencapsulated devices exhibit remarkable operational stability by retaining over 90% of initial efficiency for 1540 h under illumination and for 6312 h in an air environment. This work provides an advisable way to fabricate efficient and stable ETL‐free PSCs toward reliable and cost‐effective production.

Funder

National Natural Science Foundation of China

Natural Science Foundation of Fujian Province

Shenzhen Science and Technology Innovation Program

Basic and Applied Basic Research Foundation of Guangdong Province

Publisher

Wiley

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