Poor thermostability of Sb2S3 in vacuum hinders the possibility of achieving high-quality crystalline films. In order to enhance the photovoltaic properties of Sb2S3 planar heterojunction solar cells, a selenylation-based post-treatment approach has been employed. Selenylation performed over 15 min on the Sb2S3 film resulted in an enhancement in the conversion efficiency from ~ 0.01 to 2.20%. Effect of the selenylation on the evolution of morphology, crystal structure, composition distributions, and photovoltaic behavior has been investigated. The variation in the energy levels of Sb2S3/CdS junction has been also been discussed. Results show that selenylation not only enhanced the crystallinity of Sb2S3 film but also provided a suitable energy level which facilitated charge transport from absorber to the buffer layer.

As a synthetic renewable and biodegradable material, the application of polylactide (PLA) in the green flexible electronics has attracted intensive attention due to the increasingly serious issue of electronic waste. Unfortunately, the development of PLA-based optoelectronic devices is greatly hindered by the poor heat resistance and mechanical property of PLA. To overcome these limitations, herein, we report a facile and promising route to fabricate silver nanowires/PLA (AgNW/PLA) film with largely improved properties by utilizing the stereocomplex (SC) crystallization between poly(L-lactide) (PLLA) and poly(D-lactide) (PDLA). Through embedding the AgNW networks into the PLLA:PDLA blend matrix via a transfer method, the AgNW/PLLA:PDLA film with both high transparency and excellent conductivity was obtained. Compared with the AgNW/PLLA film, the formation of SC crystallites in the composites matrix could significantly enhance not only heat resistance but also mechanical strength of the AgNW/PLLA:PDLA film. Exceptionally, the AgNW/PLLA:PDLA film exhibited superior flexibility and could maintain excellent electrical conductivity stability even under the condition of 10,000 repeated bending cycles and 100 tape test cycles. In addition, the organic light-emitting diodes (OLEDs) with the AgNW/PLLA:PDLA films as electrodes were successfully fabricated in this work for the first time and they exhibited highly flexible, luminous, as well as hydrolytic degradation properties. This work could provide a low-cost and environment-friendly avenue towards fabricating high-performanced PLA-based biodegradable electronics.

A two-dimensional graphene-like carbon nitride (g-CN) monolayer decorated with the superatomic cluster NLi₄ was studied for reversible hydrogen storage by first-principles calculations. Molecular dynamics simulations show that the g-CN monolayer has good thermal stability at room temperature. The NLi₄ is firmly anchored on the g-CN monolayer with a binding energy of −6.35 eV. Electronic charges are transferred from the Li atoms of NLi₄ to the g-CN monolayer, mainly due to the hybridization of Li(2s), C(2p), and N(2p) orbitals. Consequently, a spatial local electrostatic field is formed around NLi₄, leading to polarization of the adsorbed hydrogen molecules and further enhancing the electrostatic interactions between the Li atoms and hydrogen. Each NLi₄ can adsorb nine hydrogen molecules with average adsorption energies between −0.152 eV/H₂ and −0.237 eV/H₂. This range is within the reversible hydrogen storage energy window. Moreover, the highest achieved gravimetric capacity is up to 9.2 wt%, which is superior to the 5.5 wt% target set by the U.S. Department of Energy. This study shows that g-CN monolayers decorated with NLi₄ are a good candidate for reversible hydrogen storage.