TY - JOUR
T1 - Regulating Surface Termination for Efficient Inverted Perovskite Solar Cells with Greater Than 23% Efficiency
AU - LI, Fengzhu
AU - DENG, Xiang
AU - QI, Feng
AU - LI, Zhen
AU - LIU, Danjun
AU - SHEN, Dong
AU - QIN, Minchao
AU - WU, Shengfan
AU - LIN, Francis
AU - JANG, Sei Hum
AU - ZHANG, Jie
AU - LU, Xinhui
AU - LEI, Dangyuan
AU - LEE, Chun Sing
AU - ZHU, Zonglong
AU - JEN, Alex K.Y.
N1 - Publisher Copyright:
© 2020 American Chemical Society.
PY - 2020/11/25
Y1 - 2020/11/25
N2 - Passivating surface and bulk defects of perovskite films has been proven to be an effective way to minimize nonradiative recombination losses in perovskite solar cells (PVSCs). The lattice interference and perturbation of atomic periodicity at the perovskite surfaces often significantly affect the material properties and device efficiencies. By tailoring the terminal groups on the perovskite surface and modifying the surface chemical environment, the defects can be reduced to enhance the photovoltaic performance and stability of derived PVSCs. Here, we report a rationally designed bifunctional molecule, piperazinium iodide (PI), containing both R2NH and R2NH2+ groups on the same six-membered ring, behaving both as an electron donor and an electron acceptor to react with different surface-terminating ends on perovskite films. The resulting perovskite films after defect passivation show released surface residual stress, suppressed nonradiative recombination loss, and more n-type characteristics for sufficient energy transfer. Consequently, charge recombination is significantly suppressed to result in a high open-circuit voltage (VOC) of 1.17 V and a reduced VOC loss of 0.33 V. A very high power conversion efficiency (PCE) of 23.37% (with 22.75% certified) could be achieved, which is the highest value reported for inverted PVSCs. Our work reveals a very effective way of using rationally designed bifunctional molecules to simultaneously enhance the device performance and stability.
AB - Passivating surface and bulk defects of perovskite films has been proven to be an effective way to minimize nonradiative recombination losses in perovskite solar cells (PVSCs). The lattice interference and perturbation of atomic periodicity at the perovskite surfaces often significantly affect the material properties and device efficiencies. By tailoring the terminal groups on the perovskite surface and modifying the surface chemical environment, the defects can be reduced to enhance the photovoltaic performance and stability of derived PVSCs. Here, we report a rationally designed bifunctional molecule, piperazinium iodide (PI), containing both R2NH and R2NH2+ groups on the same six-membered ring, behaving both as an electron donor and an electron acceptor to react with different surface-terminating ends on perovskite films. The resulting perovskite films after defect passivation show released surface residual stress, suppressed nonradiative recombination loss, and more n-type characteristics for sufficient energy transfer. Consequently, charge recombination is significantly suppressed to result in a high open-circuit voltage (VOC) of 1.17 V and a reduced VOC loss of 0.33 V. A very high power conversion efficiency (PCE) of 23.37% (with 22.75% certified) could be achieved, which is the highest value reported for inverted PVSCs. Our work reveals a very effective way of using rationally designed bifunctional molecules to simultaneously enhance the device performance and stability.
UR - http://www.scopus.com/inward/record.url?scp=85096514877&partnerID=8YFLogxK
U2 - 10.1021/jacs.0c09845
DO - 10.1021/jacs.0c09845
M3 - Journal Article (refereed)
C2 - 33190487
SN - 0002-7863
VL - 142
SP - 20134
EP - 20142
JO - Journal of the American Chemical Society
JF - Journal of the American Chemical Society
IS - 47
ER -