Facile synthesis of ZnO/ZnS hollow nanorods via Kirkendall effect with enhanced photocatalytic degradation of methylene blue.

Because of the growing concerns about environmental issues, the search of proficient semiconductor catalysts for pollutants degradation from contaminated water is one of the interesting areas of research. Due to the larger surface area, hollow nanomaterials with hollow interior and outer thickness illustrate a class of significant nanostructured materials. The enhanced surface area provides remarkable applications of the hollow nanomaterials in catalysis. In Kirkendall effect, pores are formed owing to the diverse diffusion rates of two nanomaterials in a diffusion couple. Here, we have introduced the facile hydrothermal synthesis of hollow nanorods of ZnO/ZnS via Kirkendall effect using ZnO nanorods (NRs). The morphologies, optical properties, compositions, and crystal structures of the as synthesized materials are systematically studied using UV-vis, PXRD, FESEM, TEM, EDS, XPS, etc. The process of synthesis and growth mechanism of hollow NRs is suggested based on the Kirkendall effect. A hollow nanomaterial, envisaged being highly efficient for molecule adsorption on its surface, the as synthesized materials were used for the photocatalytic degradation of methylene blue (MB) dye. MB degradation efficiency of 96% within 60 min was performed over ZnO/ZnS hollow NRs, which was 2.6-fold greater than that of ZnO. The rate constant of ZnO/ZnS heterostructure was 0.045 min-1, which was 5.5 times larger than that of bare ZnO. We have concluded our work in the directions towards the synthesis of various semiconductor hollow nanostructures for the varied catalytic reactions.

Ag2S/Ag Heterostructure: A Promising Electrocatalyst for the Hydrogen Evolution Reaction.

Different metal chalcogenides, being a potential candidate for hydrogen evolution catalysts, have attracted enormous attention in the field of water splitting. In the present study, Ag2S/Ag is revealed as an efficient catalyst for hydrogen evolution. When a sacrificial template of the CuS nanostructure is used, Ag2S/Ag heterostructures are synthesized following a simple wet-chemical technique. Two different routes, wet chemical and hydrothermal, are followed to modulate the morphology of the CuS templates from flower ball to wirelike structures, which subsequently results in the formation of Ag2S nanostructure. Finally, the Ag layer is deposited on Ag2S with the help of a photoreduction technique. The unique heterostructure of Ag2S/Ag shows efficient catalytic activity in the H2 evolution reaction. A Ag2S/Ag wire can successfully generate a 10 mA/cm2 current density at a -0.199 V potential. Ag2S/Ag contains the micronanostructure where nanoplates of Ag2S/Ag assemble to give rise to microstructures such as flower balls and wire.

Construction of CuS/Au Heterostructure through a Simple Photoreduction Route for Enhanced Electrochemical Hydrogen Evolution and Photocatalysis.

An efficient Hydrogen evolution catalyst has been developed by decorating Au nanoparticle on the surface of CuS nanostructure following a green and environmental friendly approach. CuS nanostructure is synthesized through a simple wet-chemical route. CuS being a visible light photocatalyst is introduced to function as an efficient reducing agent. Photogenerated electron is used to reduce Au(III) on the surface of CuS to prepare CuS/Au heterostructure. The as-obtained heterostructure shows excellent performance in electrochemical H2 evolution reaction with promising durability in acidic condition, which could work as an efficient alternative for novel metals. The most efficient CuS-Au heterostructure can generate 10 mA/cm2 current density upon application of 0.179 V vs. RHE. CuS-Au heterostructure can also perform as an efficient photocatalyst for the degradation of organic pollutant. This dual nature of CuS and CuS/Au both in electrocatalysis and photocatalysis has been unveiled in this study.

Synthesis of Monometallic (Au and Pd) and Bimetallic (AuPd) Nanoparticles Using Carbon Nitride (C3N4) Quantum Dots via the Photochemical Route for Nitrophenol Reduction.

In this study, we report the synthesis of monometallic (Au and Pd) and bimetallic (AuPd) nanoparticles (NPs) using graphitic carbon nitride (g-C3N4) quantum dots (QDs) and photochemical routes. Eliminating the necessity of any extra stabilizer or reducing agent, the photochemical reactions have been carried out using a UV light source of 365 nm where C3N4 QD itself functions as a suitable stabilizer as well as a reducing agent. The g-C3N4 QDs are excited upon irradiation with UV light and produce photogenerated electrons, which further facilitate the reduction of metal ions. The successful formation of Au, Pd, and AuPd alloy nanoparticles is evidenced by UV-vis, powder X-ray diffraction, X-ray photon spectroscopy, and energy-dispersive spectroscopy techniques. The morphology and distribution of metal nanoparticles over the C3N4 QD surface has been systematically investigated by high-resolution transmission electron microscopy (HRTEM) and SAED analysis. To explore the catalytic activity of the as-prepared samples, the reduction reaction of 4-nitrophenol with excellent performance is also investigated. It is noteworthy that the synthesis of both monometallic and bimetallic NPs can be accomplished by using a very small amount of g-C3N4, which can be used as a promising photoreducing material as well as a stabilizer for the synthesis of various metal nanoparticles.