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A solvent-assisted methodology has been developed to synthesize CH3NH3PbI3 perovskite absorber layers. It involved the use of a mixed solvent of CH3NH3I, PbI2, γ-butyrolactone, and dimethyl sulfoxide (DMSO) followed by the addition of chlorobenzene (CB). The method produced ultra-flat and dense perovskite capping layers atop mesoporous TiO2 films, enabling a remarkable improvement in the performance of free hole transport material (HTM) carbon electrode-based perovskite solar cells (PSCs). Toluene (TO) was also studied as an additional solvent for comparison. At the annealing temperature of 100 °C, the fabricated HTM-free PSCs based on drop-casting CB demonstrated power conversion efficiency (PCE) of 9.73 %, which is 36 and 71 % higher than those fabricated from the perovskite films using TO or without adding an extra solvent, respectively. The interaction between the PbI2–DMSO–CH3NH3I intermediate phase and the additional solvent was discussed. Furthermore, the influence of the annealing temperature on the absorber film formation, morphology, and crystalline structure was investigated and correlated with the photovoltaic performance. Highly efficient, simple, and stable HTM-free solar cells with a PCE of 11.44 % were prepared utilizing the optimum perovskite absorbers annealed at 120 °C. Graphical Abstract

ZnO thin film was fabricated on tin-doped indium oxide electrode as an electron selective layer of inverted polymer solar cells using magnetron sputtering deposition. Ionic liquid-functionalized carbon nanoparticles (ILCNs) film was further deposited onto ZnO surfaces by drop-casting ILCNs solution to improve interface properties. The power conversion efficiency (PCE) of inverted polymer solar cells (PSCs) with only ZnO layer was quickly decreased from 2.7% to 2.2% when the thickness of ZnO layer was increased from 15 nm to 60 nm. However, the average PCE of inverted PSCs with ZnO layer modified with ILCNs only decreased from 3.5% to 3.4%, which is comparable to that of traditional PSCs with poly(3,4-ethylenedioxythiophene)/poly(styrenesulfonate) anode buffer layer. The results suggested that the contact barrier between ZnO layer and poly(3-hexylthiophene) and phenyl-C61-butyric acid methylester (P3HT:PCBM) blended film compared to ZnO bulk resistance can more significantly influence the performance of inverted PSCs with sputtered ZnO layer. The vanishment of negative capacitive behavior of inverted PSCs with ILCNs modified ZnO layer indicated ILCNs can greatly decrease the contact barrier of ZnO/P3HT:PCBM interface.

We explore a simple and eco-friendly approach for preparing CZTS powders and a screen-printing process for Cu2ZnSn(S,Se)4 (CZTSSe) counter electrodes (CEs) in dye-sensitized solar cells (DSCs). Cu2ZnSnS4 (CZTS) nanoparticles have been synthesized via a hydrazine-free solvothermal approach without the assistance of organic ligands. CZTS has been prepared by directly drop-casting the CZTS ink on the cleaned FTO glass, while CZTSSe CEs have been fabricated by screen-printing CZTS pastes, followed by post selenization using Se vapor obtained from elemental Se pellets. The crystal structure, composition and morphology of the as-deposited CZTS nanoparticles and CZTSSe electrodes are characterized by X-ray diffractometer, energy dispersive spectrometer, field emission scanning electron microscopy and transmission electron microscopy. The electrochemical properties of CZTS, CZTSSe and Pt CE based DSCs are examined and analyzed by electrochemical impedance spectroscopy. The prepared CZTS and CZTSSe CEs exhibit a cellular structure with high porosity. DSCs fabricated with CZTSSe CEs achieve a power conversion efficiency of 5.75% under AM 1.5 G illumination with an intensity of 100 mW/cm2, which is higher than that (3.22%) of the cell using the CZTS CE. The results demonstrate that the CZTSSe CE possesses good electrocatalytic activity for the reduction of charge carriers in electrolyte. The comprehensive CZTSSe CE process is cheap and scalable. It can make large-scale electro-catalytic film fabrication cost competitive for both energy harvesting and storage applications.

A flexible counter electrode (CE) for dye-sensitized solar cells (DSCs) has been fabricated using a micro-porous polyvinylidene fluoride membrane as support media and sputtered Pt as the catalytic material. Non-conventional structure DSCs have been developed by the fabricated CEs. The Pt metal was sputtered onto one surface of the membrane as the catalytic material. DSCs were assembled by attaching the TiO2 electrode to the membrane surface without Pt coating. The membrane was with cylindrical pore geometry. It served not only as a substrate for the CE but also as a spacer for the DSC. The fabricated DSC with the flexible membrane CE showed higher photocurrent density than the conventional sandwich devices based on chemically deposited Pt/FTO glass, achieving a photovoltaic conversion efficiency of 4.43%. The results provides useful information in investigation and development of stable, low-cost, simple-design, flexible and lightweight DSCs.