Bifunctional Dimethyldichlorosilane Assisted Air‐Processed Perovskite Solar Cell with Enhanced Stability and Low Voltage Loss

Author:

Zhou Peng1,Lu Shaojuan2,Mo Yanping1,Cheng Jiahao3,Jiao Chuanjia3,Zhang Xiao-Li4,Li Wangnan35ORCID,Liang Guijie35,Wang Jingyang35,Huang Fuzhi16ORCID,Cheng Yi-Bing16

Affiliation:

1. State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of Technology Wuhan 430070 P. R. China

2. Hubei Institute of Aerospace Chemotechnology Xiangyang 441003 P. R. China

3. Hubei Key Laboratory of Low Dimensional Optoelectronic Materials and Devices Hubei University of Arts and Science Xiangyang 441053 P. R. China

4. School of Materials Science and Engineering Zhengzhou University Zhengzhou Henan Province 450001 P. R. China

5. Hubei Longzhong laboratory Xiangyang 441000 P. R. China

6. Solar Hydrogen Production Lab Foshan Xianhu Laboratory of the Advanced Energy Science and Technology Guangdong Laboratory Foshan 528000 P. R. China

Abstract

As perovskite solar cells (PSCs) are sensitive to moisture, they cannot be prepared in the open air, which increases manufacturing costs. To address this issue, bifunctional dimethyldichlorosilane (DMDCS) is employed as both an additive and capping layer to passivate the grain boundaries and surfaces of MAPbI3 perovskite films, thus inhibiting water erosion. Accordingly, the preparation of highly efficient PSCs in an air atmosphere is realized. Herein, the passivation mechanism of DMDCS on the perovskite film and the interface is analyzed by investigating photoexcited carrier mobility and ultrafast transient adsorption spectroscopy (TAS). An improvement of charge‐carrier diffusion, featuring an enhanced lifetime from 7.62 to 11.22 ps by the precursor doping, is exhibited in the results of TAS. The charge‐carrier extraction at the interface is also greatly promoted, with the decreased decay time from 0.29 to 0.16 ns by surface passivation, consistent with the carrier mobility via space charge‐limited current. Finally, the modified devices achieve an exceptional efficiency of 20.69%, and demonstrate long‐term environmental stability, maintaining more than 80% of the initial efficiency after 1000 h in ambient at a relative humidity of 40% without encapsulation.

Funder

Natural Science Foundation of Hubei Province

National Natural Science Foundation of China

Publisher

Wiley

Subject

Electrical and Electronic Engineering,Energy Engineering and Power Technology,Atomic and Molecular Physics, and Optics,Electronic, Optical and Magnetic Materials

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