Ligand-free Cs2PdBr6 perovskite microcrystals with narrow bandgap and high photoelectrochemical performance in aqueous solution

The exploration of efficient lead-free perovskite photoelectric active materials to develop high-performance photoelectrochemical(PEC)systems in aqueous solution is crucial to expand their PEC applications.Herein,we successfully constructed a high-performance PEC platform using ligand-free perovskite Cs2PdBr6 microcrystals(MCs)as the photoactive substance.The Cs2PdBr6 MCs showed narrow bandgap,wide absorption range,high electronic mobility and good stability in aqueous solutions.Particularly,the Cs2PdBr6 MCs exhibited an excellent photoresponse,the photocurrent density could reach as high as 98μA/cm^(2)under 10.18 mW/cm^(2)light irradiation in the absence of other electron acceptors.In addition of the extremely wide range of response wavelength,wide pH range and accelerated interfacial carrier transfer,the Cs2PdBr6 MCs demonstrated the significant potential of photocathode active material for applications in PEC sensors and optoelectronic devices.Therefore,this work indicates that Cs2PdBr6 MCs design is a highly efficient way to solve the intrinsic issues of perovskite material,predicting a promising strategy for high performance PEC application in aqueous ambience.

Target-triggered inhibiting oxidase-mimicking activity of platinum nanoparticles for ultrasensitive colorimetric detection of silver ion

The development of efficient methods for the detection of hazardous and toxic elements is extremely important for environmental security and public health. In this work, we developed a facile colorimetric assaying system for Ag+ detection in aqueous solution. Chitosan-stabilized platinum nanoparticles(ChPtNPs) were synthesized and severed as an artificial oxidase to catalyze the oxidation of the substrate3,30,5,50-tetramethylbenzidine(TMB) and generate color signal. In the presence of Ag+, due to the strong metallophilic interactions between Ag+ and Pt2+ on the surface of Ch-PtNPs, Ag+ can weaken the affinity to the substrates and inactivate the catalytic activity of Ch-PtNPs, leading to decreased absorbance signal to varying degrees depending on Ag+ amount. Combing the specific binding between Ch-PtNPs and Ag+ with signal amplification procedure based on the Ch-PtNPs-catalyzed TMB oxidation, a sensitive,selective, simple, cost-effective, and rapid detection method for Ag+ can be realized. Ag+ ions in tap and lake waters have been successfully detected. We ensured that the proposed method can be a potential alternative for Ag+ determination in environmental samples.