Faze Wang

Ammonia intercalated flower-like MoS2 nanosheet film as electrocatalyst for high efficient and stable hydrogen evolution

Ammonia intercalated flower-like MoS2 electrocatalyst film assembled by vertical orientated ultrathin nanosheet on graphite sheethas been successfully synthesized using one-step hydrothermal method. In this strategy, ammonia can effectively insert into the parallel plane of the MoS2 nanosheets, leading to the expansion of lattice and phase transfer from 2H to 1T, generating more active unsaturated sulfur atoms. The flower-like ammoniated MoS2 electrocatalysts with more active sites and large surface area exhibited excellent HER activity with a small Tafel slope and low onset overpotential, resulting a great enhancement in hydrogen evolution. The high efficient activity and recyclable utilization, as well as large-scale, indicate that it is a very promising electrocatalyst to replace Pt in industry application.

Visible light photocatalytic H2-production activity of wide band gap ZnS nanoparticles based on the photosensitization of graphene

Visible light photocatalytic H(2) production from water splitting is considered an attractive way to solve the increasing global energy crisis in modern life. In this study, a series of zinc sulfide nanoparticles and graphene (GR) sheet composites were synthesized by a two-step hydrothermal method, which used zinc chloride, sodium sulfide, and graphite oxide (GO) as the starting materials. The as-prepared ZnS-GR showed highly efficient visible light photocatalytic activity in hydrogen generation. The morphology and structure of the composites obtained by transmission electron microscope and x-ray diffraction exhibited a small crystallite size and a good interfacial contact between the ZnS nanoparticles and the two-dimensional (2D) GR sheet,which were beneficial for the photocatalysis. When the content of the GR in the catalyst was 0.1%, the ZG0.1 sample exhibited the highest H(2)-production rate of 7.42 μmol h(−1) g(−1), eight times more than the pure ZnS sample. This high visible-light photocatalytic H(2) production activity is attributed to the photosensitization of GR. Irradiated by visible light, the electrons photogenerated from GR transfer to the conduction band of ZnS to participate in the photocatalytic process. This study presents the visible-light photocatalytic activity of wide bandgap ZnS and its application in H(2) evolution.

A Simple and Sensitive Colorimetric Detection of Silver Ions Based on Cationic Polymer-Directed AuNPs Aggregation

This paper describes a simple and sensitive colorimetric sensor employing single-stranded DNA (ssDNA) ligand, cationic polymer, and gold nanoparticles (AuNPs) to detect silver ions. The positively charged polymer can electrostatically interact with ssDNA and destroy the charge balance leading to induction of AuNP aggregation. Silver ions (Ag+) can bind to cytosine (C)-rich nucleic acids to form the C-Ag+-C hair-pin structure, which can prevent its interaction with polymers. The resulting cationic polymer could aggregate AuNPs causing a remarkable change in colour. The concentration of Ag+ can be determined visually. This sensing platform exhibits high sensitivity and selectivity towards Ag+ versus other metal ions, with a detection limit of 48.6 nM. The assay did not require any labelling or modifying steps. This method is simple, effective, and convenient and can in principle be used to detect other metal ions or small molecules.

Regulation of hemin peroxidase catalytic activity by arsenic-binding aptamers for the colorimetric detection of arsenic(III)

The catalytic activity of higher concentration of hemin can be temporarily inhibited by arsenic-binding aptamers, and it will recover in the presence of As(III) due to the exhaustion of aptamers, so the subsequent TMB molecules can be oxidized thoroughly and cause a remarkable increase of absorbance value at 442 nm, which enables the colorimetric detection of As(III) with high selectivity and a detection limit of 6 ppb.

Electrochemically induced Ti3+ self-doping of TiO2 nanotube arrays for improved photoelectrochemical water splitting

AbstractWe report a facile electrochemical reduction method to synthesize Ti3+-self-doped TiO2 nanotube arrays (TNTs), where the effects of reduction duration and potential on the photoelectrochemical performance were systematically investigated. The X-ray photoelectron spectroscopy and electron paramagnetic resonance spectra confirmed the presence of Ti3+ in the TNTs. Under the optimum reduction condition, the Ti3+-self-doped TNTs exhibited remarkably enhanced photocurrent density and photoconversion efficiency, which were nearly 3.1 and 1.75 times that of pristine TNTs, respectively. The enhancement of PEC performance is due to the improved electrical conductivity, accelerated charge transfer rate at the TNTs/electrolyte interface, as well as the improved visible light response, which is elucidated by electrochemical impedance spectra, Mott–Schottky, and UV–Vis diffuse reflection spectra.

InP nanopore arrays for photoelectrochemical hydrogen generation

We report a facile and large-scale fabrication of highly ordered one-dimensional (1D) indium phosphide (InP) nanopore arrays (NPs) and their application as photoelectrodes for photoelectrochemical (PEC) hydrogen production. These InP NPs exhibit superior PEC performance due to their excellent light-trapping characteristics, high-quality 1D conducting channels and large surface areas. The photocurrent density of optimized InP NPs is 8.9 times higher than that of planar counterpart at an applied potential of +0.3 V versus RHE under AM 1.5G illumination (100 mW cm(-2)). In addition, the onset potential of InP NPs exhibits 105 mV of cathodic shift relative to planar control. The superior performance of the nanoporous samples is further explained by Mott-Schottky and electrochemical impedance spectroscopy ananlysis.

Galvanic displacement assembly of ultrathin Co3O4 nanosheet arrays on nickel foam for a high-performance supercapacitor

High-performance supercapacitors are very desirable for many portable electronic devices, electric vehicles and high-power electronic devices. Herein, a facile and binder-free synthesis method, galvanic displacement of the precursor followed by heat treatment, is used to fabricate ultrathin Co3O4 nanosheet arrays on nickel foam substrate. When used as a supercapacitor electrode the prepared Co3O4 on nickel foam exhibits a maximum specific capacitance of 1095 F g-1 at a current density of 1 A g-1 and good cycling stability of 71% retention after 2000 cycling tests. This excellent electrochemical performance can be ascribed to the high specific surface area of each Co3O4 nanosheet that comprises numerous nanoparticles.

Engineering MoSx/Ti/InP Hybrid Photocathode for Improved Solar Hydrogen Production

Due to its direct band gap of ~1.35 eV, appropriate energy band-edge positions, and low surface-recombination velocity, p-type InP has attracted considerable attention as a promising photocathode material for solar hydrogen generation. However, challenges remain with p-type InP for achieving high and stable photoelectrochemical (PEC) performances. Here, we demonstrate that surface modifications of InP photocathodes with Ti thin layers and amorphous MoSx nanoparticles can remarkably improve their PEC performances. A high photocurrent density with an improved PEC onset potential is obtained. Electrochemical impedance analyses reveal that the largely improved PEC performance of MoSx/Ti/InP is attributed to the reduced charge-transfer resistance and the increased band bending at the MoSx/Ti/InP/electrolyte interface. In addition, the MoSx/Ti/InP photocathodes function stably for PEC water reduction under continuous light illumination over 2 h. Our study demonstrates an effective approach to develop high-PEC-performance InP photocathodes towards stable solar hydrogen production.

Unique Three-Dimensional InP Nanopore Arrays for Improved Photoelectrochemical Hydrogen Production

Ordered three-dimensional (3D) nanostructure arrays hold promise for high-performance energy harvesting and storage devices. Here, we report the fabrication of InP nanopore arrays (NPs) in unique 3D architectures with excellent light trapping characteristic and large surface areas for use as highly active photoelectrodes in photoelectrochemical (PEC) hydrogen evolution devices. The ordered 3D NPs were scalably synthesized by a facile two-step etching process of (1) anodic etching of InP in neutral 3 M NaCl electrolytes to realize nanoporous structures and (2) wet chemical etching in HCl/H3PO4 (volume ratio of 1:3) solutions for removing the remaining top irregular layer. Importantly, we demonstrated that the use of neutral electrolyte of NaCl instead of other solutions, such as HCl, in anodic etching of InP can significantly passivate the surface states of 3D NPs. As a result, the maximum photoconversion efficiency obtained with ∼15.7 μm thick 3D NPs was 0.95%, which was 7.3 and 1.4 times higher than that of planar and 2D NPs. Electrochemical impedance spectroscopy and photoluminescence analyses further clarified that the improved PEC performance was attributed to the enhanced charge transfer across 3D NPs/electrolyte interfaces, the improved charge separation at 3D NPs/electrolyte junction, and the increased PEC active surface areas with our unique 3D NP arrays.

A highly sensitive resonance scattering based sensor using unmodified gold nanoparticles for daunomycin detection in aqueous solution

A sensitive sensor for detection of daunomycin (DNR) was developed by using free-labeled gold nanoparticles (AuNPs) and DNR aptamer. In the absence of DNR, free aptamer could absorb onto the surface of AuNPs to prevent them from aggregating in high salt solution. In the presence of DNR, the aptamer was firstly exhausted due to the formation of a DNR/aptamer complex, which lead to the remarkable change of resonance scattering (RS) intensity at 550 nm. Such sensor showed high selectivity and a detection limit of 17.1 nM. Based on the advantage of the sensor, the proposed sensing method is believed to be implemented to the on-site and real-time DNR detection in food safety and other applications.