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Mixed-halide perovskites (MHPs) have attracted attention as suitable wide-band-gap candidate materials for tandem applications owing to their facile band-gap tuning. However, when smaller bromide ions are incorporated into iodides to tune the band gap, photoinduced halide segregation occurs, which leads to voltage deficit and photoinstability. Here, we propose an original post-hot pressing (PHP) treatment that suppresses halide segregation in MHPs with a band gap of 2.0 eV. The PHP treatment reconstructs open-structured grain boundaries (GBs) as compact GBs through constrained grain growth in the in-plane direction, resulting in the inhibition of defect-mediated ion migration in GBs. The PHP-treated wide-band-gap (2.0 eV) MHP solar cells showed a high efficiency of over 11%, achieving an open-circuit voltage (

Halide perovskites are currently intensively being investigated for applications in light-emitting diodes for next-generation lighting and display technology. A recent report shows that the control...

Interaction of conjugated polymers with liposomes is an attractive approach that benefits from both systems' characteristics such as electroactivity and enhanced interaction with cells. Conjugated polymer-liposome complexes have been investigated for bioimaging, drug delivery, and photothermal therapy. Their fabrication has largely been achieved by multistep procedures that require first the synthesis and processing of the conjugated polymer. Here, a new one step fabrication approach is reported based on in situ polymerization of a conjugated monomer precursor around liposomes. Polyaniline (PANI) doped with phytic acid is synthesized via oxidative polymerization in the presence of 1,2-dioleoyl-sn-glycero-3-phosphatidylcholine (DOPC) vesicles to produce a conductive aqueous suspension of Liposome-PANI complexes. PANI interacts with liposomes without disrupting the bilayer as shown using differential scanning calorimetry and fluorescence quenching studies of the hydrophobic Nile red probe. The electronic conductivity of the Liposome-PANI complexes, which stems from the doped PANI accessible on the liposome surface, is confirmed using conductive atomic force microscopy and electrochemical impedance spectroscopy. Further, short-term in vitro cell studies show that the complexes colocalize with the cell membrane without reducing cell proliferation. This study presents a novel fabrication route to conductive suspensions of conjugated polymer-liposome complexes suitable for potential applications at the biointerface.

In this work, we report on the design principles of high-power perovskite solar cells (PSCs) for low-intensity indoor light applications, with a particular focus on the electron transport layers (ETLs). It was found that the mechanism of power generation of PSCs under low-intensity LED and halogen lights is surprisingly different compared to the 1 Sun standard test condition (STC). Although a higher power conversion efficiency (PCE) was obtained from the PSC based on mesoporous-TiO2 (m-TiO2) under STC, compared to the compact-TiO2 (c-TiO2) PSC, c-TiO2 PSCs generated higher power than m-TiO2 PSCs under low-intensity (200–1600 Lux) conditions. This result indicates that high PCE at STC cannot guarantee a reliable high-power output of PSCs under low-intensity conditions. Based on the systemic characterization of the ideality factor, charge recombination, trap density, and charge-separation, it was revealed that interfacial charge traps or defects at the electron transport layer/perovskite have a critical impact on the resulting power density of PSC under weak light conditions. Based on Suns-VOC measurements with local ideality factor analyses, it was proved that the trap states cause non-ideal behavior of PSCs under low-intensity light conditions. This is due to the additional trap states that are present at the m-TiO2/perovskite interface, as confirmed by trap-density measurements. Based on Kelvin probe force microscopy (KPFM) measurements, it was confirmed that these traps prohibit efficient charge separation at the perovskite grain boundaries when the light intensity is weak. According to these observations, it is suggested that for the fabrication of high-power PSCs under low-intensity indoor light, the interface trap density should be lower than the excess carrier density to fill the traps at the perovskite's grain boundaries. Finally, using the suggested principle, we succeeded in demonstrating high-performance PSCs by employing an organic ETL, yielding maximum power densities up to 12.36 (56.43), 28.03 (100.97), 63.79 (187.67), and 147.74 (376.85) μW/cm2 under 200, 400, 800, and 1600 Lux LED (halogen) illumination which are among the highest values for indoor low-intensity-light solar cells.