For an iron-chromium redox flow battery (ICRFB), sulfonated poly(ether ether ketone) (SPEEK) membranes with five various degrees of sulfonation (DSs) are studied. To select the SPEEK membrane with the ideal DS for ICRFB applications, the physicochemical characteristics and single-cell performance are taken into consideration. Following all the investigations, it has been determined that the SPEEK membrane, which has a DS of 57% and a thin thickness of 25 μm, is the best option for replacing commercial Nafion 212 in ICRFB. Firstly, it exhibits a better cell performance according to energy efficiency (EE) and coulombic efficiency (CE) at the current density range between 40 mA cm⁻² and 80 mA cm⁻². Additionally, it has a more stable EE (79.25–81.64%) and lower discharge capacity decay rate (50%) than the Nafion 212 (EE: 76.74–81.45%, discharge capacity decay: 76%) after 50 charge–discharge cycles, which proves its better oxidation stability as well. In addition, the longer self-discharge time during the open-circuit voltage test further demonstrates that this SPEEK membrane could be employed for large-scale ICRFB applications.

Poly[bis(4-phenyl) (2,5,6-trimethylphenyl) amine (PTAA), as a hole transfer material, has been widely used in perovskite solar cells (PSCs). However, the optimal solvent for preparing the PTAA solution and coating the PTAA layer is still uncertain. In this work, we investigated three types of organic solvents (toluene, chlorobenzene and dichlorobenzene) for processing PTAA layers as the hole transport layer in PSCs. Based on the experimental verification and molecular dynamics simulation results, all the evidence indicated that toluene performs best among the three candidates. This is attributed to the significant polarity difference between toluene and PTAA, which leads to the formation of a uniform surface morphology characterized by granular protuberances after spin coating. The contact area of the hole transfer layer with the surface aggregation is increased in reference to the rough surface, and the hydrophilicity of the PTAA layer is also increased. The improvement of these two aspects are conducive to the effective interfacial charge transfer. This leads to the generation of more photocurrent. The PSCs employing toluene-processed PTAA exhibit an average power conversion efficiency (PCE) of 19.1%, which is higher than that of PSCs using chlorobenzene- and dichlorobenzene-processed PTAA (17.3–17.9%). This work provides a direct optimization strategy for researchers aiming to fabricate PSCs based on PTAA as a hole transport layer and lays a solid foundation for the development of high-efficiency inverted PSCs.

Surface passivation, which has been intensively studied recently, is essential for the perovskite solar cells (PSCs), due to the intrinsic defects in perovskite crystal. A series of chemical or physical methods have been published for passivating the defects of perovskite, which effectively suppressed the charge recombination and enhanced the photovoltaic performance. In this study, the n-type semiconductor of [6,6]-phenyl-C61-butyric acid methyl ester (PCBM) is dissolved in chlorobenzene (CB) for the surface passivation during the spin-coating process for depositing the two-dimensional (2D) perovskite film. This approach simplifies the fabrication process of 2D PSCs and benefits the film quality. As a result, the defects of perovskite film are effectively passivated by this method. A better perovskite/PCBM heterojunction is generated, exhibiting an increased film coverage and improved film morphology of PCBM. It is found that this technology results in an improved electron transporting performance as well as suppressed charge recombination for electron transport layer. As a result, PSCs based on the one-step formed perovskite/PCBM heterojunctions exhibit the optimized power conversion efficiency of 15.69% which is about 37% higher than that of regular perovskite devices. The device environmental stability is also enhanced due to the quality-improved electron transport layer.