Lite Version|Standard version

To gain access to this content please
Log in via your home Institution.
Log in with your member or subscriber username and password.
Download

Cathode interlayers (CILs) play crucial roles in boosting the performance of organic solar cells (OSCs). Herein, a class of novel electron-deficient electrolytes, namely BDOPV-1 and BDOPV-2, based on the benzodifurandione-based oligo(p-phenylene vinylene) (BDOPV) building block and different quaternary ammonium-type side chains, are presented as cathode interface materials (CIMs) for OSCs. The altering of alkyl chains on quaternary ammonium groups is found to effectively regulate the work function-amending abilities, self-doping interactions, film-forming properties, and compatibility with active layers of CIMs. Consequently, BDOPV-2 incorporating ethyl chains possesses superior electron-extracting/transporting, carrier recombination–restraining and device stability-improving capabilities in OSCs compared to BDOPV-1 with methyl groups. As a result, the D18:Y6-based non-fullerene OSCs modified by BDOPV-1 and BDOPV-2 output power conversion efficiencies (PCEs) of 15.74% and 17.49%, respectively. On the other hand, in the D18:L8-BO system, BDOPV-1- and BDOPV-2-decorated devices realize PCEs of 17.06% and up to 18.54%, respectively. In brief, this work provides a class of promising CILs with universality for fabricating high-performance OSCs, and a possible reference for developing efficient CIMs via side chain intervention.

Graphical abstract: Imide-free electron-deficient electrolytes with adjustable cathode-modifying capabilities achieved by side chain engineering for efficient organic solar cells

Page: ^ Top