Since the ability of ionic liquid (IL) was demonstrated to act as a solvent or an electrolyte, IL-based electrolytes have been widely used as a potential candidate for renewable energy storage devices, like lithium ion batteries (LIBs) and supercapacitors (SCs). In this review, we aimed to present the state-of-the-art of IL-based electrolytes electrochemical, cycling, and physicochemical properties, which are crucial for LIBs and SCs. ILs can also be regarded as designer solvents to replace the more flammable organic carbonates and improve the green credentials and performance of energy storage devices, especially LIBs and SCs. This review affords an outline of the progress of ILs in energy-related applications and provides essential ideas on the emerging challenges and openings that may motivate the scientific communities to move towards IL-based energy devices. Finally, the challenges in design of the new type of ILs structures for energy and environmental applications are also highlighted.

We explore two small molecules containing arms of dicyano-n-hexylrhodanine and diathiafulvalene wings terminated with benzothiadiazole linker, denoted as BAF-4CN and BAF-2HDT, respectively, as small molecule non-fullerene acceptors (SMNFAs) in organic solar cells. The proposed materials are mixed with a low band gap polymer donor PTB7-Th having broad absorption in the range of 400–750 nm to form solution-processed bulk heterojunctions (BHJs). The photoluminescence (PL) measurements show that both donor and acceptor can quench each other’s PL effectively, implying that not only electrons are transferred from PTB7-Th → SMNFAs but also holes are transferred from SMNFAs → PTB7-Th for efficient photocurrent generation. Furthermore, solvent vapor annealing (SVA) processing is shown to yield a more balanced hole and electron mobility and thus suppresses the trap-assisted recombination significantly. With this dual charge transfer enabled via fine-tuning of end-groups and SVA treatment, power conversion efficiency of approximately 10% is achieved, demonstrating the feasibility of the proposed approach.

In bulk heterojunction organic solar cells (OSCs), nanomorphology of the photoactive layer plays a crucial role in determining photocurrent and fill factor (FF) of OSCs, and therefore it is essential to control the nanomorphology of the photoactive layer to fabricate devices with high power conversion efficiency (PCE). We demonstrate the combined effects of a ZnO nanorippled electron transport layer (ETL) and solvent additive (1,8-diiodooctane (DIO)) on the nanomorphology and performance of a model OSC in an inverted geometry. The photoactive layer in the model OSC is composed of Poly [4,8-bis (5-(2-ethylhexyl)thiophen-2-yl)benzo[1,2-b;4,5-b′]dithiophene-2,6-diyl-alt-(4-(2-ethylhexyl)-3-fluorothieno[3,4-b]thiophene-)-2-carboxylate-2-6-diyl] (PTB7-Th):phenyl-C71-butyric acid methyl ester (PC ₇₁ BM) blend. It is observed that the use of ZnO nanoripples as an ETL and DIO as a solvent additive facilitates the formation of near ideal nanomorphology of bi-continuous interpenetrating network of donor and acceptor. This is confirmed by morphological studies using atomic force microscopy, scanning electron microscopy and transmission electron microscopy. Photo-electrochemical impedance spectroscopy measurements confirm that obtained nanomorphology of bicontinuous interpenetrating network is contributing to the improved device performance. The device with 3 vol% DIO, with underneath ZnO nanoripples exhibited improved current density ( J _sc ), FF, open circuit voltage ( V _oc ) and PCE of 15.57 mA cm ⁻² , 64.50%, 0.81V and 8.20%, respectively.