Broadband photoresponse enhancement in tin-based perovskites via CF3PEA <b>+</b> A-site doping

W Wenhao Zheng (Academy for Advanced Interdisciplinary Science and Technology, Beijing Key Laboratory for Advanced Energy Materials and Technologies, State Key Laboratory for Advanced Metals and Materials) G Guangyuan Li W Wenjing Zhai (National Laboratory of Solid-State Microstructures, School of Physics, and Collaborative Innovation Center of Advanced Microstructures, Nanjing University 1 , Nanjing 210093,) Y Yiran Ren (School of Physics, East China University of Science and Technology 1 , Shanghai 200237,) B Bingwen Su (National Laboratory of Solid-State Microstructures, School of Physics, and Collaborative Innovation Center of Advanced Microstructures, Nanjing University 1 , Nanjing 210093,) X Xiaomin Cui (National Laboratory of Solid-State Microstructures, School of Physics, and Collaborative Innovation Center of Advanced Microstructures, Nanjing University 1 , Nanjing 210093,) P Penghui Shi L Lin Lin Z Zhibo Yan J J.-M. Liu (National Laboratory of Solid-State Microstructures, School of Physics, and Collaborative Innovation Center of Advanced Microstructures, Nanjing University 1 , Nanjing 210093,)

Abstract

Eco-friendly tin-based perovskites have been promising lead-free alternatives for optoelectronic applications, yet their performance is limited by rapid crystallization and poor crystal quality. Here, we utilize 2-[4-(trifluoromethyl)phenyl]ethylammonium (CF3PEA+) doping at the A-site to simultaneously enhance the stability and optoelectronic properties of FASnI3 while preserving its three-dimensional structure. We demonstrate that optimal CF3PEA+ doping (6%) significantly slows down crystallization kinetics, suppresses Sn2+ oxidation, reduces deep-traps, and improves charge carrier mobility of the perovskite film. Compared to undoped films, the doped films exhibit significant improvements in charge transport and photoresponsivity (from 0.272 to 1.52 A/W at 637 nm) across 350–980 nm, outperforming phenethylammonium (PEA+)-doped counterparts. Spectroscopic studies reveal that these enhancements originate from strong chemical interactions between the CF3PEA+ and the perovskite cations. This work provides important insights into rational A-site engineering for high-performance tin-based optoelectronic devices.

Article Details

Volume / Issue Vol. 128, Issue 11
Published March 16, 2026
ISSN 0003-6951
Publisher American Institute of Physics

Journal Info

Applied Physics Letters

American Institute of Physics

ISSN: 0003-6951 Physical Sciences

Authors (10)

W

Wenhao Zheng

Academy for Advanced Interdisciplinary Science and Technology, Beijing Key Laboratory for Advanced Energy Materials and Technologies, State Key Laboratory for Advanced Metals and Materials

G

Guangyuan Li

W

Wenjing Zhai

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

Y

Yiran Ren

School of Physics, East China University of Science and Technology 1 , Shanghai 200237,

B

Bingwen Su

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

X

Xiaomin Cui

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

P

Penghui Shi

L

Lin Lin

Z

Zhibo Yan

J

J.-M. Liu

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