Interface Modification by Ammonium Sulfamate for High‐Efficiency and Stable Perovskite Solar Cells

Author:

Cao Yang1,Feng Jiangshan1,Wang Mingzi2,Yan Nan1,Lou Junjie3,Feng Xiaolong1,Xiao Fengwei1,Liu Yucheng1,Qi Danyang1,Yuan Yin1,Zhu Xuejie4,Liu Shengzhong (Frank)145ORCID

Affiliation:

1. Laboratory of Applied Surface and Colloid Chemistry Ministry of Education School of Materials Science and Engineering Shaanxi Key Laboratory for Advanced Energy Devices Shaanxi Engineering Lab for Advanced Energy Technology Institute for Advanced Energy Materials Shaanxi Normal University Xi'an Shaanxi 710119 P. R. China

2. School of Physics Northwest University Xi'an 710069 P. R. China

3. Institute of Nanoscience and Nanotechnology School of Materials and Energy Lanzhou University Lanzhou Gansu 730000 P. R. China

4. Dalian National Laboratory for Clean Energy iChEM Dalian Institute of Chemical Physics Chinese Academy of Sciences 457 Zhongshan Road Dalian 116023 P. R. China

5. University of Chinese Academy of Sciences Beijing 100049 P. R. China

Abstract

AbstractDefects in perovskite films are still the dominant destroyer of both power conversion efficiency (PCE) and long‐term stability in perovskite solar cells (PSCs). As the most popular electron transport layer (ETL), TiO2 film is used in many PSCs to achieve high PCE. However, pristine TiO2 by itself is not sufficient as an ETL due to lattice mismatch, poor alignment of the energy level gap, and hysteresis of the PSC. Herein, ammonium sulfamate (AS), with desired NH4+ and S═O functional groups, is designed to modify the TiO2 surface and interface to improve the PCE of PSCs. It is found that the AS works like a seed layer for the perovskite deposition, and, in addition, it effectively forms a bridge between the TiO2 surface and the perovskite. As a result, PSCs are successfully fabricated with a champion power conversion efficiency of 24.78% with smaller hysteresis. The PSCs prepared using the AS‐modified TiO2 also show excellent stability, and the bare device without any encapsulation retains 96% of its initial PCE after 1056 h of ambient exposure at 25 °C and 25% relative humidity.

Funder

Fundamental Research Funds for the Central Universities

National Natural Science Foundation of China

Higher Education Discipline Innovation Project

Publisher

Wiley

Subject

General Materials Science,Renewable Energy, Sustainability and the Environment

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