TY - JOUR
T1 - Dually Modified Wide-Bandgap Perovskites by Phenylethylammonium Acetate toward Highly Efficient Solar Cells with Low Photovoltage Loss
AU - Chen, Jiabang
AU - Wang, Deng
AU - Chen, Shi
AU - Hu, Hang
AU - Li, Yang
AU - Huang, Yulan
AU - Zhang, Zhuoqiong
AU - Jiang, Zhengyan
AU - Xu, Jiamin
AU - Sun, Xiyu
AU - So, Shu Kong
AU - Peng, Yuanjun
AU - Wang, Xingzhu
AU - Zhu, Xunjin
AU - Xu, Baomin
N1 - Funding Information:
This work was supported by the National Key Research and Development Program of China (2021YFB3800100 and 2021YFB3800101), the National Natural Science Foundation of China (62004089 and U19A2089), the Guangdong Basic and Applied Basic Research Foundation (2022A1515011218 and 2019B1515120083), the Shenzhen Science and Technology Program (JCYJ20190809150811504 and JCYJ20200109141014474), the Shenzhen Engineering Research and Development Center for Flexible Solar Cells Project funding from Shenzhen Development and Reform Committee (2019-126), the Innovation and Entrepreneurship Training program for College students (S202014325010), and the Guangdong-Hong Kong-Macao Joint Laboratory (2019B121205001). X.Z. thanks the financial support from the General Research Fund (HKBU 12304320) and Initiation Grant for Faculty Niche Research Areas (IG-FNRA) (2020/21)-RC-FNRA-IG/20-21/SCI/06. S.C. acknowledges the financial support from the Special Zone Support Program for Outstanding Talents of Henan University (CX3050A0970530).
Publisher Copyright:
© 2022 American Chemical Society.
PY - 2022/9/28
Y1 - 2022/9/28
N2 - Wide-bandgap perovskites as a class of promising top-cell materials have shown great promise in constructing efficient perovskite-based tandem solar cells, but their intrinsic relatively low radiative efficiency results in a large open-circuit voltage (VOC) deficit and thereby limits the whole device performance. Reducing film flaws or optimizing interfacial energy level alignments in wide-bandgap perovskite devices can efficiently inhibit nonradiative recombination to boost device VOC and efficiency. However, the simultaneous regulation on both sides and their underlying mechanism are less explored. Herein, a bifunctional modification approach is proposed to optimize the wide-bandgap perovskite surface with an ultrathin layer of phenylethylammonium acetate (PEAAc) to synchronously decrease the surface imperfection and mitigate the interfacial energy barrier. This treatment effectively heals under-coordinated surface defects through the formation of chemical interaction between the perovskite and PEAAc, bringing about a much slower charge trapping process and dramatically decreasing nonradiative recombination losses. Meanwhile, the passivation-induced upshifted Fermi level of the perovskite contributes to accelerated electron extraction and larger Fermi-level splitting under illumination. Consequently, the PEAAc-modified wide-bandgap (1.68 eV) device achieves an optimal efficiency of 20.66% with a high VOC of 1.25 V, among the highest reported VOC values for wide-bandgap perovskite devices, enormously outperforming that (18.86% and 1.18 V) of the device without passivation. In addition, the radiative limit of VOC for both cells is determined to be 1.42 V, delivering nonradiative recombination losses of 0.24 and 0.17 V for the control and PEAAc-modified devices, respectively. These results highlight the significance of the bifunctional modification strategy in achieving high-performance wide-bandgap perovskite devices.
AB - Wide-bandgap perovskites as a class of promising top-cell materials have shown great promise in constructing efficient perovskite-based tandem solar cells, but their intrinsic relatively low radiative efficiency results in a large open-circuit voltage (VOC) deficit and thereby limits the whole device performance. Reducing film flaws or optimizing interfacial energy level alignments in wide-bandgap perovskite devices can efficiently inhibit nonradiative recombination to boost device VOC and efficiency. However, the simultaneous regulation on both sides and their underlying mechanism are less explored. Herein, a bifunctional modification approach is proposed to optimize the wide-bandgap perovskite surface with an ultrathin layer of phenylethylammonium acetate (PEAAc) to synchronously decrease the surface imperfection and mitigate the interfacial energy barrier. This treatment effectively heals under-coordinated surface defects through the formation of chemical interaction between the perovskite and PEAAc, bringing about a much slower charge trapping process and dramatically decreasing nonradiative recombination losses. Meanwhile, the passivation-induced upshifted Fermi level of the perovskite contributes to accelerated electron extraction and larger Fermi-level splitting under illumination. Consequently, the PEAAc-modified wide-bandgap (1.68 eV) device achieves an optimal efficiency of 20.66% with a high VOC of 1.25 V, among the highest reported VOC values for wide-bandgap perovskite devices, enormously outperforming that (18.86% and 1.18 V) of the device without passivation. In addition, the radiative limit of VOC for both cells is determined to be 1.42 V, delivering nonradiative recombination losses of 0.24 and 0.17 V for the control and PEAAc-modified devices, respectively. These results highlight the significance of the bifunctional modification strategy in achieving high-performance wide-bandgap perovskite devices.
KW - wide-bandgap perovskite
KW - perovskite solar cells
KW - surface modification
KW - interfacial energy barrier
KW - nonradiative recombination
KW - low photovoltage loss
UR - http://www.scopus.com/inward/record.url?scp=85139106280&partnerID=8YFLogxK
U2 - 10.1021/acsami.2c10928
DO - 10.1021/acsami.2c10928
M3 - Journal article
C2 - 36112025
AN - SCOPUS:85139106280
SN - 1944-8244
VL - 14
SP - 43246
EP - 43256
JO - ACS Applied Materials and Interfaces
JF - ACS Applied Materials and Interfaces
IS - 38
ER -