A self-arranged metal–organic polyhedron/fullerene asymmetric structure improves the performance of inverted perovskite solar cells. Issue 39 (14th September 2022)

• Record Type: Journal Article
• Authors: Yu, Ming-Hsuan; Han, Po-Chun; Lee, Chia-Chen; Ni, I-Chih; Zhu, Zonglong; Kurmaev, Ernst Z.; Furukawa, Shuhei; Wu, Kevin C.-W.; Chueh, Chu-Chen
• Is Part Of: Journal of materials chemistry. Volume 10:Issue 39(2022)
• Page Start: 14542
• Page End: 14548
• Publication Date: 2022-09-14
• Subjects: Materials -- Periodicals; Chemistry, Analytic -- Periodicals; Optical materials -- Research -- Periodicals; Electronics -- Materials -- Research -- Periodicals; 543.0284
• DOI: 10.1039/d2tc02110b
• Languages: English
• ISSNs: 2050-7526

Abstract

Abstract : A hybrid dirhodium tetracarboxylate-based metal–organic polyhedron (MOP):PCBM electron transport layer is demonstrated to give rise to a 9% enhancement in power conversion efficiency for the derived inverted perovskite solar cell. Abstract : Developing new chemistry to passivate the defects in the perovskite layer is highly desired in researching high-performance and stable perovskite solar cells (PVSCs). We herein explore supramolecular chemistry to passivate the perovskite film by entailing the employment of robust metal–organic polyhedra (MOPs), [Rh2 (bdc)2 ]12 (HRhMOP; bdc = benzene-1, 3-dicarboxylate). HRhMOP is found to establish well-defined packing voids to well accommodate the filling of [6, 6]-phenyl-C61 -butyric acid methyl ester (PCBM) that is often used as an electron transport layer (ETL) in PVSCs. Detailed analysis suggests that HRhMOP forms an asymmetric distribution in the PCBM ETL, and the self-arranged HRhMOP at the ETL/perovskite interface considerably suppresses the Pb 0 formation and induces a larger band bending effect to facilitate interfacial charge transport. Synergetically combined effects give rise to a 9% enhancement in power conversion efficiency (PCE) of the derived inverted PVSCs. The successful utilization of MOPs could lead to the further development of supramolecular chemistry in state-of-the-art PVSCs.