Donor-Interacting Arylated Carbazole Self-Assembled Monolayer Enables Highly Efficient and Stable Organic Photovoltaics

Small. 2025 Jan 15:e2403233. doi: 10.1002/smll.202403233. Online ahead of print.

Abstract

Carbazole-derived self-assembled monolayers (SAMs) are promising materials for hole-extraction layer (HEL) in conventional organic photovoltaics (OPVs). Here, a SAM Cbz-2Ph derived from 3,6-diphenylcarbazole is demonstrated. The large molecular dipole moment of Cbz-2Ph allows the modulation of electrode work function to facilitate hole extraction and maximize photovoltage, thus improving the OPV performance. Additionally, the flanking aryls of Cbz-2Ph help establish CH-π interactions for forming a dense and well-organized SAM HEL and exhibit stronger van der Waals interactions with the donor PM6 than acceptor BTP-eC9. The stronger SAM-donor interactions modulate the PM6 distribution in PM6:BTP-eC9 bulk-heterojunction film, leading to PM6 enrichment near HEL to facilitate efficient hole extraction to the ITO anode in conventional p-i-n OPVs. Consequently, binary PM6:BTP-eC9-based devices incorporating the Cbz-2Ph HEL demonstrate an impressive efficiency of 19.18%. These cells also showcase excellent operational stability, with a T80 lifetime of ≈1260 h at the maximum power point, over 10 times longer than those using the traditional PEDOT:PSS HEL (T80 ≈96 h). Furthermore, the universal applicability of Cbz-2Ph as a HEL is evident through its successful implementation in PM6:BTP-eC9:L8-BO-F-based ternary devices and PM6:BTP-eC9-based printed OPV devices, achieving a PCE of 19.30% and 16.96%, respectively.

Keywords: charge extraction layer; molecular interaction; organic photovoltaics; photostability; self‐assembled monolayer.