Annealing-free alcohol-processable MoO_(X) anode interlayer enables efficient light utilization in organic photovoltaics

Molybdenum oxide(MoO_(x))is a commonly used hole extraction material in organic photovoltaics.The MoO_(x) interlayer is deposited typically via thermal evaporation in vacuum.To meet the need for rollto-roll manufacturing,solution processing of MoO_(x) without post-annealing treatment is essential.Herein,we demonstrate an effective approach to produce annealing-free,alcohol-processable MoO_(x) anode interlayers,namely S-MoO_(x),by utilizing the bis(catecholato)diboron(B_(2) Cat_(2))molecule to modify the surface oxygen sites in MoO_(x).The formation of surface diboron-oxygen complex enables the alcohol solubility of S-MoO_(x).An enhanced light utilization is realized in the S-MoO_(x)-based organic photovoltaics.This affords a superior short-circuit current density(Jsc)close to 26 mA cm^(-2) and ultimately a high power-conversion efficiency(PCE)of 15.2%in the representative PM6:Y6 based inverted OPVs,which is one of the highest values in the inverted OPVs using an as-cast S-MoO_(x) anode interlayer.

Dual‑Donor‑Induced Crystallinity Modulation Enables 19.23% Efficiency Organic Solar Cells

Trap-assisted charge recombination is one of the primary limitationsof restricting the performance of organic solar cells. However, effectivelyreducing the presence of traps in the photoactive layer remains challenging.Herein, wide bandgap polymer donor PTzBI-dF is demonstrated as an effectivemodulator for enhancing the crystallinity of the bulk heterojunction active layerscomposed of D18 derivatives blended with Y6, leading to dense and orderedmolecular packings, and thus, improves photoluminescence quenching properties.As a result, the photovoltaic devices exhibit reduced trap-assisted charge recombinationlosses, achieving an optimized power conversion efficiency of over 19%.Besides the efficiency enhancement, the devices comprised of PTzBI-dF as athird component simultaneously attain decreased current leakage, improved chargecarrier mobilities, and suppressed bimolecular charge recombination, leading toreduced energy losses. The advanced crystalline structures induced by PTzBI-dFand its characteristics, such as well-aligned energy level, and complementaryabsorption spectra, are ascribed to the promising performance improvements.Our findings suggest that donor phase engineering is a feasible approach to tuning the molecular packings in the active layer, providingguidelines for designing effective morphology modulators for high-performance organic solar cells.

Block copolymers as efficient cathode interlayer materials for organic solar cells

Emerging needs for the large-scale industrialization of organic solar cells require high performance cathode interlayers to facilitate the charge extraction from organic semiconductors.In addition to improving the efficiency,stability and processability issues are major challenges.Herein,we design block copolymers with well controlled chemical composition and molecular weight for cathode interlayer applications.The block copolymer coated cathodes display high optical transmittance and low work function.Conductivity studies reveal that the block copolymer thin film has abundant conductive channels and excellent longitudinal electron conductivity due to the interpenetrating networks formed by the polymer blocks.Applications of the cathode interlayers in organic solar cells provide higher power conversion efficiency and better stability compared to the most widelyapplied ZnO counterparts.Furthermore,no post-treatment is needed which enables excellent processability of the block copolymer based cathode interlayer.