Billy

In this work, polymer solar cells are fabricated based on the blend of PTB7-Th: PC₇₁BM by using a mixed solvent additive of 1,8-diiodooctane and N-methyl pyrrolidone to optimize the morphology of the blend. A high power conversion efficiency (PCE) of 10.8% has been achieved with a simple conventional device. In order to deeply investigate the influence of the mixed solvent additives on the morphology and device performance, the variations of the molecular packing and bulk morphology of the blend film cast from ortho-dichlorobenzene with single or binary solvent additives are measured. Although all the blend films exhibit similar domain size and nanoscale phase separation, the blend film processed with mixed solvent additive shows the highest domain purity, resulting in the least bimolecular recombination, relatively high J_sc and FF, and hence enhanced PCE. Therefore, the best photovoltaic performance with the V_oc of 0.82 V, J_sc of 19.1 mA cm⁻², FF of 69.1%, and PCE of 10.8% are obtained for the device based on the blend with binary solvent additive treatment.

For the PTB7-Th:PC₇₁BM blend system, the binary solvent additives of 1,8-diiodooctane and N-methyl pyrrolidone are used to enhance the domain purity, so that a power conversion efficiency of 10.8% is achieved with the conventional device structure, which is much higher than that of the devices without or with single solvent additive treatment.

An oxidation-resistant and elastic mesoporous carbon, graphene mesosponge (GMS), is prepared. GMS has a sponge-like mesoporous framework (mean pore size is 5.8 nm) consisting mostly of single-layer graphene walls, which realizes a high electric conductivity and a large surface area (1940 m² g⁻¹). Moreover, the graphene-based framework includes only a very small amount of edge sites, thereby achieving much higher stability against oxidation than conventional porous carbons such as carbon blacks and activated carbons. Thus, GMS can simultaneously possess seemingly incompatible properties; the advantages of graphitized carbon materials (high conductivity and high oxidation resistance) and porous carbons (large surface area). These unique features allow GMS to exhibit a sufficient capacitance (125 F g⁻¹), wide potential window (4 V), and good rate capability as an electrode material for electric double-layer capacitors utilizing an organic electrolyte. Hence, GMS achieves a high energy density of 59.3 Wh kg⁻¹ (material mass base), which is more than twice that of commercial materials. Moreover, the continuous graphene framework makes GMS mechanically tough and extremely elastic, and its mean pore size (5.8 nm) can be reversibly compressed down to 0.7 nm by simply applying mechanical force. The sponge-like elastic property enables an advanced force-induced adsorption control.

Oxidation-resistant and elastic mesoporous carbon consisting of single-layer graphene walls is prepared. The unique framework realizes a large surface area and minimal number of edge sites, thereby making the material promising for the application in electric double-layer capacitors. The framework is mechanically tough and greatly elastic, enabling an advanced force-induced adsorption control.

Three small molecules with different substituents on bithienyl-benzo[1,2-b:4,5-b′]dithiophene (BDTT) units, BDTT-TR (meta-alkyl side chain), BDTT-O-TR (meta-alkoxy), and BDTT-S-TR (meta-alkylthio), are designed and synthesized for systematically elucidating their structure–property relationship in solution-processed bulk heterojunction organic solar cells. Although all three molecules show similar molecular structures, thermal properties and optical band gaps, the introduction of meta-alkylthio-BDTT as the central unit in the molecular backbone substantially results in a higher absorption coefficient, slightly lower highest occupied molecular orbital level and significantly more efficient and balanced charge transport property. The bridging atom in the meta-position to the side chain is found to impact the microstructure formation which is a subtle but decisive way: carrier recombination is suppressed due to a more balanced carrier mobility and BDTT based devices with the meta-alkylthio side chain (BDTT-S-TR) show a higher power conversion efficiency (PCE of 9.20%) as compared to the meta-alkoxy (PCE of 7.44% for BDTT-TR) and meta-alkyl spacer (PCE of 6.50% for BDTT-O-TR). Density functional density calculations suggest only small variations in the torsion angle of the side chains, but the nature of the side chain linkage is further found to impact the thermal as well as the photostability of corresponding devices. The aim is to provide comprehensive insight into fine-tuning the structure–property interrelationship of the BDTT material class as a function of side chain engineering.

A comprehensive insight into fine-tuning the structure–property interrelationship (a trade-off beyond efficiency) of the bithienyl-benzo[1,2-b:4,5-b′]dithiophene material class as a function of side chain engineering is provided.

Layer-by-layer (LL) processes, i.e., sequential deposition of different active layers, are widely used in the fabrication of organic solar cells (OSCs). Recently, LL vacuum deposition and LL solution processes have attracted considerable attention. LL processing presents some advantages over the blend method: a) donor and acceptor layers can be easily and independently controlled and optimized; b) the charge carriers dissociated from excitons at the donor–acceptor interface are confined to each phase, so bimolecular recombination losses can be reduced; c) bilayer geometries enable an easier way for understanding the physical processes taking place at the donor–acceptor interface; d) desired vertical phase separation for charge extraction can be obtained through changing the sequence of donor and acceptor deposition. This report summarizes the recent developments of LL processed OSCs. The remaining problems and challenges, and the key research direction in near future are discussed.

Layer-by-layer (LL) processing techniques exhibit some advantages over the traditional blend-casting technique in organic solar cells. The recent developments of LL vacuum-deposited and solution-processed solar cells are summarized.

Highly efficient large-area organic solar cells (OSCs) with power conversion efficiency up to 7.09%, and device area of 4 cm² are demonstrated on flexible substrates. A conductance- or thickness-gradient ultra-thin Ag-based transparent electrode is developed to better balance the light trapping and energy loss, owing to the inhomogeneous energy-loss density on the large OSC sheet.