RESUMEN
Four novel all-in-one structured cuprous iodide hybrid materials are presented. Isomerization of the alkyl chain on the ligand improved material thermal stability and regulated their luminescence to warm and near-white light emission, with the internal quantum yield increasing from 5% to 83%. This provides a reasonable route for designing white light emitting cuprous iodide materials for solid-state lighting in future.
RESUMEN
Recently, all-polymer solar cells (all-PSCs) have received increasing attention and made tremendous progress. However, the power conversion efficiency (PCE) of all-PSCs still lags behind the polymer-donor-small-molecule-acceptor based organic solar cells, owing to the excessive phase separation with poor miscibility between polymer donor and acceptor. In this research, an "end-capped" ternary strategy is proposed by introducing PM6TPO as a third component to fabricate highly efficient all-PSCs. The PM6:PM6TPO:PY-IT based ternary devices exhibit impressive PCE of 17.0% with enhanced light absorption and optimal morphology, and the introduction of PM6TPO significantly reduces the phase separation. The ternary devices also exhibit improved stability, outstanding tolerance of active layer thickness, and high performance of 1 cm2 unit cells. More importantly, the "end-capped" ternary strategy enables efficient and facile improvement of all-PSCs performance without additional selection and complicated synthesis for the third component.
RESUMEN
The high-performance organic solar cells (OSCs) tend to choose the polymers with high molecular weight as donors, which easily produce good crystallinity to facilitate intermolecular charge transfer. However, these polymers usually accompanied by the low solubility and synthetic difficulty, increasing batch-to-batch variations. The proposal of conjugated mesopolymers (molar mass (Mn ) in 1-10 kDa) can overcome these problems. Herein, a new mesopolymer, MePBDFClH as donor material is designed and synthesized, and firstly applied in OSCs. As a comparison, other lower molecular weight mesopolymer of MePBDFClL and higher molecular weight polymer of PBDFCl with same structure are also prepared and investigated. Because of its appropriate phase separation and miscibility in the blend film, the MePBDFClH exhibits the highest power conversion efficiency (PCE) of 15.06% among the three materials. Meanwhile, the champion PCE is a new record for benzo[1,2-b:4,5-b']difuran-based photovoltaic materials. Importantly, comparing to the pronounced PCE decrease of polymer PBDFCl by about 12%, a slightly PCE difference for mespolymer MePBDFClL is only less than 5%, reducing the batch-to-batch variation. This work not only suggests that the benzo[1,2-b:4,5-b']difuran unit is a promising electron-donating core but also shows that the mesopolymers have great potentials to produce the low-differentiated and high-performance organic photovoltaic materials.
RESUMEN
Copper(I) halide complexes are well sought-after materials due to their rich structural diversities and photophysical properties. Profoundly, there is a direct relationship between each structural variation and luminescence of these complexes, for a purported use. In this review, recent publications within the last 2 years about copper(I) halide complexes, centering on their structural dimensionalities with derivatives of nitrogen, phosphorus, and sulfur ligands, have been considered alongside their effects on luminescence.
RESUMEN
Three new luminescent metal-organic frameworks (LMOFs), [Zn(tppa)(ndc)] n (1), [Cd(tppa)(oba)] n (2), [Zn2(tppa)(bpdc)2] n (3) (tppa = tri(4-pyridylphenyl)amine, ndc = 1,4-naphthalenedicarboxylic acid, oba = 4,4'-oxydibenzoic acid, bpdc = 4,4'-biphenyldicarboxylic acid) have been synthesized by solvothermal method. Complexes 1 and 2 are 2-D two-fold interpenetrating structures, aligning into a 3-D structure through C-Hâ¯π stacking interactions, while 3 is a 5-fold interpenetrating three-dimensional structure. The internal quantum yields (IQYs) of complexes 1-3 are 32.7%, 45.7% and 24.0% (λ ex = 365 nm), separately. Furthermore, all the complexes show different luminescence signal changes towards aromatic volatile organic compounds (AVOCs). Complex 1 exhibits a high sensitivity in the detection of both Fe3+ and Cr3+ with large quenching coefficients of K sv 2.57 × 104 M-1 and 2.96 × 104 M-1, respectively. All these results demonstrated potential applications in chemical sensing.