TY - JOUR
T1 - p-Type Carbon Dots for Effective Surface Optimization for Near-Record-Efficiency CsPbI2Br Solar Cells
AU - Guo, Xi
AU - Zhao, Biao
AU - Xu, Kunxiang
AU - Yang, Shaomin
AU - Liu, Zhike
AU - Han, Yu
AU - Xu, Jie
AU - Xu, Dongfang
AU - Tan, Zhanao
AU - Liu, Shengzhong
N1 - Generated from Scopus record by KAUST IRTS on 2023-09-21
PY - 2021/9/1
Y1 - 2021/9/1
N2 - Interface modification to minimize charge recombination and trapping for efficient charge transport is crucial for the performance of perovskite solar cells (PSCs). Herein, functionalized p-type blue carbon dots (B-CDs) are ventured as an interface passivation layer to enhance the efficiency and long-term stability of all-inorganic CsPbI2Br PSCs. It is found that first the blue carbon dots with abundant N-H, C-N, C-O, and C-O functional groups effectively passivate defects by reacting with I− and Pb2+ ions in the perovskite through hydrogen and coordinative bonds. Second, the p-type B-CDs modifiers form a P–N junction with the n-type perovskite to provide efficient pathways for hole transfer and electron blocking. Third, the B-CDs increase the hydrophobicity of the perovskite film to improve the stability of CsPbI2Br PSCs. With the above advantages, the CsPbI2Br PSC with B-CDs modification shows an efficiency as high as 16.76%, one of the highest for its type. In addition, the modification renders significant improvement of air and light stability, with 95.33% of the initial PCE retained after storage in the ambient environment for 1000 h. This work demonstrates the great potential of B-CDs application in perovskite-based optoelectronic devices.
AB - Interface modification to minimize charge recombination and trapping for efficient charge transport is crucial for the performance of perovskite solar cells (PSCs). Herein, functionalized p-type blue carbon dots (B-CDs) are ventured as an interface passivation layer to enhance the efficiency and long-term stability of all-inorganic CsPbI2Br PSCs. It is found that first the blue carbon dots with abundant N-H, C-N, C-O, and C-O functional groups effectively passivate defects by reacting with I− and Pb2+ ions in the perovskite through hydrogen and coordinative bonds. Second, the p-type B-CDs modifiers form a P–N junction with the n-type perovskite to provide efficient pathways for hole transfer and electron blocking. Third, the B-CDs increase the hydrophobicity of the perovskite film to improve the stability of CsPbI2Br PSCs. With the above advantages, the CsPbI2Br PSC with B-CDs modification shows an efficiency as high as 16.76%, one of the highest for its type. In addition, the modification renders significant improvement of air and light stability, with 95.33% of the initial PCE retained after storage in the ambient environment for 1000 h. This work demonstrates the great potential of B-CDs application in perovskite-based optoelectronic devices.
UR - https://onlinelibrary.wiley.com/doi/10.1002/smll.202102272
UR - http://www.scopus.com/inward/record.url?scp=85111881679&partnerID=8YFLogxK
U2 - 10.1002/smll.202102272
DO - 10.1002/smll.202102272
M3 - Article
SN - 1613-6829
VL - 17
JO - Small
JF - Small
IS - 37
ER -