Affiliation:
1. Department of Chemistry University of Calgary Calgary Alberta Canada
Abstract
AbstractTo achieve high‐performance indoor organic photovoltaics (OPVs), it is important to match the photoactive layer optical absorption with the light‐source emission. This can be accomplished by developing organic photoactive materials that can efficiently absorb visible light and thus minimize energy losses. While indoor OPVs have achieved efficiencies above 33% under low light intensities, the power output is limited by low open circuit voltages (VOC), often well below 1 V. In this study, we present a series of visible‐light absorbing (energy gap >1.90 eV) non‐fullerene acceptors (NFAs) based on perylene diimide dimers, which have been systematically modified with side chains of varying polarity and steric bulk (trimethyl benzyl, ethyl adamantane, trialkoxyl phenyl, and oligo ethylene glycol). Our results show that the incorporation of sterically bulky side chains such as ethyl adamantane and trimethyl benzyl, blended with the common widegap polymer PTQ10, provides photoactive layers with absorption greater than 2.0 eV, and consequently, VOCs higher than 1.2 V are achieved under AM 1.5 G illumination. Importantly, we found that the NFA with ethyl adamantane based side chains (tPDI2N‐ethyl adamantane, compound 4) exhibited the best performance, with minimized energy loss. As a result, devices using PTQ10:tPDI2N‐ethyl adamantane photoactive layers demonstrated excellent indoor efficiencies of over 16% and 18 μW cm−2 power output under a 2700 K LED lamp at 300 lux, and showed better repeatability compared to other systems. The PTQ10:tPDI2N‐ethyl adamantane based devices maintained a high VOC (>1.0 V) across a wide range of indoor lighting conditions, including 2700 K and 6500 K LED lamps. Overall, this work provides a sidechain engineering method to create NFAs for efficient indoor OPV devices.
Funder
Natural Sciences and Engineering Research Council of Canada
Canada First Research Excellence Fund
Cited by
1 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献