Synchronous defect passivation of all-inorganic perovskite solar cells enabled by fullerene interlayer

All-inorganic CsPbI3–xBrx perovskite solar cells (PSCs) are advantageous in terms of high thermal stability, while its efficiency lags behind those of organic-inorganic hybrid perovskite counterparts. Defect passivations have been extensively applied for enhancing efficiency of all-inorganic PSCs, w...

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Main Authors: Yanbo Shang, Pu Wang, Lingbo Jia, Xingcheng Li, Weitao Lian, Peisen Qian, Muqing Chen, Tao Chen, Yalin Lu, Shangfeng Yang
Format: Article
Language:English
Published: Tsinghua University Press 2023-09-01
Series:Nano Research Energy
Subjects:
Online Access:https://www.sciopen.com/article/10.26599/NRE.2023.9120073
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author Yanbo Shang
Pu Wang
Lingbo Jia
Xingcheng Li
Weitao Lian
Peisen Qian
Muqing Chen
Tao Chen
Yalin Lu
Shangfeng Yang
author_facet Yanbo Shang
Pu Wang
Lingbo Jia
Xingcheng Li
Weitao Lian
Peisen Qian
Muqing Chen
Tao Chen
Yalin Lu
Shangfeng Yang
author_sort Yanbo Shang
collection DOAJ
description All-inorganic CsPbI3–xBrx perovskite solar cells (PSCs) are advantageous in terms of high thermal stability, while its efficiency lags behind those of organic-inorganic hybrid perovskite counterparts. Defect passivations have been extensively applied for enhancing efficiency of all-inorganic PSCs, which are mainly based on univocal defect passivation of perovskite layer. Herein, we incorporated a bis-dimethylamino-functionalized fullerene derivative (abbreviated as PCBDMAM) as an interlayer between ZnO electron transport layer (ETL) and all-inorganic CsPbI2.25Br0.75 perovskite layer, accomplishing synchronous defect passivations of both layers and consequently dramatic enhancements of efficiency and thermal stability of PSC devices. Upon spin-coating PCBDMAM onto ZnO ETL, the surface defects of ZnO especially oxygen vacancies can be effectively passivated due to the formation of Zn−N ionic bonds. In addition, PCBDMAM incorporation affords effective passivation of PbI and IPb antisite defects within the atop perovskite layer as well via coordination bonding with Pb2+. As a result, the regular-structure planar CsPbI2.25Br0.75 PSC device delivers a champion power conversion efficiency (PCE) of 17.04%, which surpasses that of the control device (15.44%). Moreover, the PCBDMAM-incorporated PSC device maintains ~ 80% of its initial PCE after 600 h heating at 85 °C hot plate in N2 atmosphere, whereas PCE of the control device degrades rapidly to ~ 62% after 460 h heating under identical conditions. Hence, PCBDMAM incorporation benefited dramatic improvement of the thermal stability of PSC device.
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spelling doaj.art-95da8679ae7948c9922ba3825d32827b2023-06-21T06:25:21ZengTsinghua University PressNano Research Energy2791-00912790-81192023-09-0123e9120073e912007310.26599/NRE.2023.9120073Synchronous defect passivation of all-inorganic perovskite solar cells enabled by fullerene interlayerYanbo Shang0Pu Wang1Lingbo Jia2Xingcheng Li3Weitao Lian4Peisen Qian5Muqing Chen6Tao Chen7Yalin Lu8Shangfeng Yang9CAS Key Laboratory of Materials for Energy Conversion, Anhui Laboratory of Advanced Photon Science and Technology, Department of Materials Science and Engineering, University of Science and Technology of China, Hefei 230026, ChinaCAS Key Laboratory of Materials for Energy Conversion, Anhui Laboratory of Advanced Photon Science and Technology, Department of Materials Science and Engineering, University of Science and Technology of China, Hefei 230026, ChinaCAS Key Laboratory of Materials for Energy Conversion, Anhui Laboratory of Advanced Photon Science and Technology, Department of Materials Science and Engineering, University of Science and Technology of China, Hefei 230026, ChinaCAS Key Laboratory of Materials for Energy Conversion, Anhui Laboratory of Advanced Photon Science and Technology, Department of Materials Science and Engineering, University of Science and Technology of China, Hefei 230026, ChinaCAS Key Laboratory of Materials for Energy Conversion, Anhui Laboratory of Advanced Photon Science and Technology, Department of Materials Science and Engineering, University of Science and Technology of China, Hefei 230026, ChinaCAS Key Laboratory of Materials for Energy Conversion, Anhui Laboratory of Advanced Photon Science and Technology, Department of Materials Science and Engineering, University of Science and Technology of China, Hefei 230026, ChinaSchool of Environment and Civil Engineering, Dongguan University of Technology, Dongguan 523808, ChinaCAS Key Laboratory of Materials for Energy Conversion, Anhui Laboratory of Advanced Photon Science and Technology, Department of Materials Science and Engineering, University of Science and Technology of China, Hefei 230026, ChinaCAS Key Laboratory of Materials for Energy Conversion, Anhui Laboratory of Advanced Photon Science and Technology, Department of Materials Science and Engineering, University of Science and Technology of China, Hefei 230026, ChinaCAS Key Laboratory of Materials for Energy Conversion, Anhui Laboratory of Advanced Photon Science and Technology, Department of Materials Science and Engineering, University of Science and Technology of China, Hefei 230026, ChinaAll-inorganic CsPbI3–xBrx perovskite solar cells (PSCs) are advantageous in terms of high thermal stability, while its efficiency lags behind those of organic-inorganic hybrid perovskite counterparts. Defect passivations have been extensively applied for enhancing efficiency of all-inorganic PSCs, which are mainly based on univocal defect passivation of perovskite layer. Herein, we incorporated a bis-dimethylamino-functionalized fullerene derivative (abbreviated as PCBDMAM) as an interlayer between ZnO electron transport layer (ETL) and all-inorganic CsPbI2.25Br0.75 perovskite layer, accomplishing synchronous defect passivations of both layers and consequently dramatic enhancements of efficiency and thermal stability of PSC devices. Upon spin-coating PCBDMAM onto ZnO ETL, the surface defects of ZnO especially oxygen vacancies can be effectively passivated due to the formation of Zn−N ionic bonds. In addition, PCBDMAM incorporation affords effective passivation of PbI and IPb antisite defects within the atop perovskite layer as well via coordination bonding with Pb2+. As a result, the regular-structure planar CsPbI2.25Br0.75 PSC device delivers a champion power conversion efficiency (PCE) of 17.04%, which surpasses that of the control device (15.44%). Moreover, the PCBDMAM-incorporated PSC device maintains ~ 80% of its initial PCE after 600 h heating at 85 °C hot plate in N2 atmosphere, whereas PCE of the control device degrades rapidly to ~ 62% after 460 h heating under identical conditions. Hence, PCBDMAM incorporation benefited dramatic improvement of the thermal stability of PSC device.https://www.sciopen.com/article/10.26599/NRE.2023.9120073all-inorganic perovskite solar cellsfullerene derivativeelectron transport layerthermal stabilitydefect passivation
spellingShingle Yanbo Shang
Pu Wang
Lingbo Jia
Xingcheng Li
Weitao Lian
Peisen Qian
Muqing Chen
Tao Chen
Yalin Lu
Shangfeng Yang
Synchronous defect passivation of all-inorganic perovskite solar cells enabled by fullerene interlayer
Nano Research Energy
all-inorganic perovskite solar cells
fullerene derivative
electron transport layer
thermal stability
defect passivation
title Synchronous defect passivation of all-inorganic perovskite solar cells enabled by fullerene interlayer
title_full Synchronous defect passivation of all-inorganic perovskite solar cells enabled by fullerene interlayer
title_fullStr Synchronous defect passivation of all-inorganic perovskite solar cells enabled by fullerene interlayer
title_full_unstemmed Synchronous defect passivation of all-inorganic perovskite solar cells enabled by fullerene interlayer
title_short Synchronous defect passivation of all-inorganic perovskite solar cells enabled by fullerene interlayer
title_sort synchronous defect passivation of all inorganic perovskite solar cells enabled by fullerene interlayer
topic all-inorganic perovskite solar cells
fullerene derivative
electron transport layer
thermal stability
defect passivation
url https://www.sciopen.com/article/10.26599/NRE.2023.9120073
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