Indeno[1,2-b]carbazole as Methoxy-Free Donor Group: Constructing Efficient and Stable Hole-Transporting Materials for Perovskite Solar Cells

Angew Chem Int Ed Engl. 2019 Oct 28;58(44):15721-15725. doi: 10.1002/anie.201909117. Epub 2019 Sep 16.

Abstract

With perovskite-based solar cells (PSCs) now reaching efficiencies of greater than 20 %, the stability of PSC devices has become a critical challenge for commercialization. However, most efficient hole-transporting materials (HTMs) thus far still rely on the state-of-the-art methoxy triphenylamine (MOTPA) donor unit in which methoxy groups usually reduce the device stability. Herein, a carbazole-fluorene hybrid has been employed as a methoxy-free donor to construct organic HTMs. The indeno[1,2-b]carbazole group not only inherits the characteristics of carbazole and fluorene, but also exhibits additional advantages arising from the bulky planar structure. Consequently, M129, endowed with indeno[1,2-b]carbazole simultaneously exhibits a promising efficiency of over 20 % and superior long-term stability. The hybrid strategy toward the methoxy-free donor opens a new avenue for developing efficient and stable HTMs.

Keywords: conjugation; energy conversion; fused-ring systems; materials science; solar cells.