Yuan L, Zhu W, Zhang Y, Li Y, Chan CCS, Qin M, Qiu J, Zhang K, Huang J, Wang J, Luo H, Zhang Z, Chen R, Liang W, Wei Q, Wong KS, Lu X, Li N, Brabec C, Ding L, Yan K (2023)
Publication Type: Journal article
Publication year: 2023
Book Volume: 16
Pages Range: 1597-1609
Journal Issue: 4
DOI: 10.1039/d2ee03565k
State-of-the-art n-i-p perovskite solar cells (PSCs) suffer from stability issues due to ionic interdiffusion. Herein, by enlarging the indacenodithiophene π-bridge donor (D′) to combine with the methoxy triphenylamine donor (D) and benzothiadiazole acceptor (A), three linear molecules termed L1, L2 and L3 with a D-A-D′-A-D structure are developed as dopant-free hole transport materials (HTMs). The π-bridge extension with active sites for coordination leverages the intramolecular dipole effect and intermolecular packing effect, resulting in a conformally bonded ultrathin interface with compact and uniform coverage (∼60 nm) to retard iodine migration and protect the buried perovskite. The unencapsulated L3-PSC (ITO/SnO
APA:
Yuan, L., Zhu, W., Zhang, Y., Li, Y., Chan, C.C.S., Qin, M.,... Yan, K. (2023). A conformally bonded molecular interface retarded iodine migration for durable perovskite solar cells. Energy and Environmental Science, 16(4), 1597-1609. https://doi.org/10.1039/d2ee03565k
MLA:
Yuan, Ligang, et al. "A conformally bonded molecular interface retarded iodine migration for durable perovskite solar cells." Energy and Environmental Science 16.4 (2023): 1597-1609.
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