Crystallization regulation and defect suppression of CsPbI2Br perovskite using a dual-functional additive

Z Zhi Zhu (State Key Laboratory of Physical Chemistry of Solid Surfaces, Key Laboratory for Chemical Biology of Fujian Province, The MOE Key Laboratory of Spectrochemical Analysis and Instrumentation, Department of Chemical Biology, College of Chemistry and Chemical Engineering, State Key Laboratory of Vaccines for Infectious Diseases, Fujian Provincial Key Laboratory of Innovative Drug Target Research, School of Pharmaceutical Sciences, School of Life Sciences, Faculty of Medicine and Life Sciences) J Jing Xu Y Yuhan Zhou (Department of Chemistry) S Shisheng Ge (National Laboratory of Solid State Microstructures, Collaborative Innovation Center of Advanced Microstructures, School of Physics, Nanjing University 1 , Nanjing 210093,) T Tao Yu J Jie Yang C Chunxiong Bao (National Laboratory of Solid State Microstructures Collaborative Innovation Center of Advanced Microstructures School of Physics Nanjing University Nanjing China) Z Zhigang Zou (National Laboratory of Solid State Microstructures, College of Engineering and Applied Sciences, Nanjing University, 22 Hankou Road, Nanjing 210093, China)

Abstract

Inorganic CsPbI2Br perovskite solar cells have attracted widespread attention due to their outstanding performance and photo-thermal stability. However, the rapid crystallization of the solution-processed CsPbI2Br film often results in poor crystallinity and a high density of defects, which seriously restrict the improvement of the device performance. Here, we introduce a dual-functional additive, 4-amino-5-aminomethyl-2-methylpyrimidine (AMP), to regulate the crystallization and reduce the defect density of the CsPbI2Br film. The introduction of AMP notably improves the crystallinity and morphology of the CsPbI2Br film and promotes a preferred crystal orientation. The C=N and amino groups in AMP interact with Pb2+ and Br- in the perovskite, respectively, effectively passivating the defects and improving the carrier lifetime. As a result, the power conversion efficiency of the optimized carbon-based hole-transport layer-free device reaches 13.30%, which exceeds the 10.66% of the control device. The environmental and light stability of the device is also significantly improved. This work provides valuable insights into the development of high-performance all-inorganic perovskite solar cells via additive strategies.

Article Details

Volume / Issue Vol. 126, Issue 15
Published April 01, 2025
ISSN 0003-6951
Publisher American Institute of Physics

Journal Info

Applied Physics Letters

American Institute of Physics

ISSN: 0003-6951 Physical Sciences

Authors (8)

Z

Zhi Zhu

State Key Laboratory of Physical Chemistry of Solid Surfaces, Key Laboratory for Chemical Biology of Fujian Province, The MOE Key Laboratory of Spectrochemical Analysis and Instrumentation, Department of Chemical Biology, College of Chemistry and Chemical Engineering, State Key Laboratory of Vaccines for Infectious Diseases, Fujian Provincial Key Laboratory of Innovative Drug Target Research, School of Pharmaceutical Sciences, School of Life Sciences, Faculty of Medicine and Life Sciences

J

Jing Xu

Y

Yuhan Zhou

Department of Chemistry

S

Shisheng Ge

National Laboratory of Solid State Microstructures, Collaborative Innovation Center of Advanced Microstructures, School of Physics, Nanjing University 1 , Nanjing 210093,

T

Tao Yu

J

Jie Yang

C

Chunxiong Bao

National Laboratory of Solid State Microstructures Collaborative Innovation Center of Advanced Microstructures School of Physics Nanjing University Nanjing China

Z

Zhigang Zou

National Laboratory of Solid State Microstructures, College of Engineering and Applied Sciences, Nanjing University, 22 Hankou Road, Nanjing 210093, China