TY - JOUR
T1 - Teaching an old anchoring group new tricks
T2 - Enabling low-cost, eco-friendly hole-transporting materials for efficient and stable perovskite solar cells
AU - Wang, Yang
AU - Liao, Qiaogan
AU - Chen, Jianhua
AU - Huang, Wei
AU - Zhuang, Xinming
AU - Tang, Yumin
AU - Li, Bolin
AU - Yao, Xiyu
AU - Feng, Xiyuan
AU - Zhang, Xianhe
AU - Su, Mengyao
AU - He, Zhubing
AU - Marks, Tobin J.
AU - Facchetti, Antonio
AU - Guo, Xugang
N1 - Funding Information:
We acknowledge the financial support by the National Natural Science Foundation of China (Nos. 21805128, 21774055, and 61804073) and the Shenzhen Science and Technology Innovation Commission (No. JCYJ20170817105905899). This work was also supported in part by the Center for Light Energy Activated Redox Processes (LEAP), an Energy Frontier Research Center funded by the U.S. Department of Energy, Office of Science, Office of Basic Energy Sciences under Award Number DE-SC0001059, by AFOSR grant FA9550-18-18-1-0320, and by ONR contract N00014-20-1-2116. We are grateful to the assistance of SUSTech Core Research Facilities.
Publisher Copyright:
© 2020 American Chemical Society
PY - 2020/9/30
Y1 - 2020/9/30
N2 - As a key component in perovskite solar cells (PVSCs), hole-transporting materials (HTMs) have been extensively explored and studied. Aiming to meet the requirements for future commercialization of PVSCs, HTMs which can enable excellent device performance with low cost and eco-friendly processability are urgently needed but rarely reported. In this work, a traditional anchoring group (2-cyanoacrylic acid) widely used in molecules for dye-sensitized solar cells is incorporated into donor−acceptor-type HTMs to afford MPA-BT-CA, which enables effective regulation of the frontier molecular orbital energy levels, interfacial modification of an ITO electrode, efficient defect passivation toward the perovskite layer, and more importantly alcohol solubility. Consequently, inverted PVSCs with this low-cost HTM exhibit excellent device performance with a remarkable power conversion efficiency (PCE) of 21.24% and good long-term stability in ambient conditions. More encouragingly, when processing MPA-BT-CA films with the green solvent ethanol, the corresponding PVSCs also deliver a substantial PCE as high as 20.52% with negligible hysteresis. Such molecular design of anchoring group-based materials represents great progress for developing efficient HTMs which combine the advantages of low cost, eco-friendly processability, and high performance. We believe that such design strategy will pave a new path for the exploration of highly efficient HTMs applicable to commercialization of PVSCs.
AB - As a key component in perovskite solar cells (PVSCs), hole-transporting materials (HTMs) have been extensively explored and studied. Aiming to meet the requirements for future commercialization of PVSCs, HTMs which can enable excellent device performance with low cost and eco-friendly processability are urgently needed but rarely reported. In this work, a traditional anchoring group (2-cyanoacrylic acid) widely used in molecules for dye-sensitized solar cells is incorporated into donor−acceptor-type HTMs to afford MPA-BT-CA, which enables effective regulation of the frontier molecular orbital energy levels, interfacial modification of an ITO electrode, efficient defect passivation toward the perovskite layer, and more importantly alcohol solubility. Consequently, inverted PVSCs with this low-cost HTM exhibit excellent device performance with a remarkable power conversion efficiency (PCE) of 21.24% and good long-term stability in ambient conditions. More encouragingly, when processing MPA-BT-CA films with the green solvent ethanol, the corresponding PVSCs also deliver a substantial PCE as high as 20.52% with negligible hysteresis. Such molecular design of anchoring group-based materials represents great progress for developing efficient HTMs which combine the advantages of low cost, eco-friendly processability, and high performance. We believe that such design strategy will pave a new path for the exploration of highly efficient HTMs applicable to commercialization of PVSCs.
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U2 - 10.1021/jacs.0c06373
DO - 10.1021/jacs.0c06373
M3 - Article
C2 - 32852200
AN - SCOPUS:85092332236
SN - 0002-7863
VL - 142
SP - 16632
EP - 16643
JO - Journal of the American Chemical Society
JF - Journal of the American Chemical Society
IS - 39
ER -