Boosting photovoltaic performance for Sb2S3solar cells by ionic liquid-assisted hydrothermal synthesis.

Bulk and surface trap-states in the Sb2S3films are considered one of the crucial energy loss mechanisms for achieving high photovoltaic performance in planar Sb2S3solar cells. Because ionic liquid additives offer interesting physicochemical properties to control the synthesis of inorganic material, in this work we propose the addition of 1-Butyl-3-methylimidazolium hydrogen sulfate (BMIMHS) into a Sb2S3hydrothermal precursor solution as a facile way to fabricate low-defect Sb2S3solar cells. Lower presence of small particles on the surface, as well as higher crystallinity are demonstrated in the BMIMHS-assisted Sb2S3films. Moreover, analyses of dark current density-voltageJ-Vcurves, surface photovoltage transient and intensity-modulated photocurrent spectroscopy have suggested that adding BMIMHS results in high-quality Sb2S3films and a successful defect passivation. Consequently, the best-performing BMIMHS-assisted device exhibits a 15.4% power conversion efficiency enhancement compared to that of control device. These findings show that ionic liquid BMIMHS can effectively be used to obtain high-quality Sb2S3films with low-defects and improved optoelectronic properties.

Sb2O3 nanoparticles anchored on N-doped graphene nanoribbons as improved anode for sodium-ion batteries.

Sodium-ion batteries (SIBs) are emerging as a promising alternative to conventional lithium-ion technology, due to the abundance of sodium resources. Still, major drawbacks for the commercial application of SIBs lie in the slow kinetic processes and poor cycling performance of the devices. In this work, a hybrid nanocomposite of Sb2O3 nanoparticles anchored on N-doped graphene nanoribbons (GNR) is implemented as anode material in SIBs. The obtained Sb2O3/N-GNR anode delivers a reversible specific capacity of 642 mA h g-1 after 100 cycles at 0.1 A g-1 and exhibits a good rate capability. Even after 500 cycles at 5 A g-1, the specific capacity is maintained at about 405 mA h g-1. Such good Na storage performance is mainly ascribed to the beneficial effect of N doping for charge transfer and to the improved microstructure that facilitates the Na+ diffusion through the overall electrode.