Yan-Ru Liu

Two-step synthesis of binary Ni–Fe sulfides supported on nickel foam as highly efficient electrocatalysts for the oxygen evolution reaction

A facile two-step method has been used to synthesize binary Ni–Fe sulfides supported on nickel foam (NF) as electrocatalysts for the oxygen evolution reaction (OER). Firstly, NiFe hydroxide nanosheets have been electrodeposited on NF (NiFe/NF) as a precursor with a large surface area. Secondly, the as-prepared NiFe/NF has been subjected to a hydrothermal sulfuration process in order to prepare NiFeS/NF as an efficient electrocatalyst for the OER. The as-prepared samples have been characterized by XRD, XPS and SEM. The SEM images show that the NiFeS film was composed of needle-like nanostructures covering the surface of the NF. The corresponding OER performances in alkaline media have been systematically investigated. NiFeS/NF shows a superior overpotential of 65 mV at 10 mA cm−2, which is much lower than most Ni-based electrocatalysts. The overpotential of 189 mV at 100 mA cm−2 of NiFeS/NF suggests very promising OER activity for industrial applications. The electrochemically active surface area (251.25 cm2) of NiFeS/NF is obviously larger than that of NiFeS/NF (173.75 cm2) and NiFeS/NF (205.00 cm2). However, the stability of NiFeS/NF is not very good due to the intrinsic nature of metal sulfides in alkaline solution. An approach of electrodeposition of Fe hydroxide film on NiFeS/NF (NiFeS–Fe/NF) has been used to protect NiFeS/NF for better stability for the OER. The OER performances of NiFeS–Fe/NF demonstrate enhanced stability but lower activity with 101.6 mV at 10 mA cm−2. Therefore, there may be an optimal balance between activity and stability of transition metal sulfides for the OER.

NiSe@NiOOH Core-Shell Hyacinth-like Nanostructures on Nickel Foam Synthesized by in Situ Electrochemical Oxidation as an Efficient Electrocatalyst for the Oxygen Evolution Reaction.

NiSe@NiOOH core-shell hyacinth-like nanostructures supported on nickel foam (NF) have been successfully synthesized by a facile solvothermal selenization and subsequent in situ electrochemical oxidation (ISEO). First, the unique NiSe/NF nanopillar arrays were prepared in N,N-dimethylformamide (DMF) as a precursor template that can provide a large surface area, excellent conductivity, and robust support. Next, amorphous NiOOH covering the surface of NiSe nanopillars was fabricated by ISEO, as confirmed by XPS andEDX spectroscopy. SEM images revealed the hyacinth-like morphology of NiSe@NiOOH/NF with NiOOH as the shell and NiSe as the core. The electrochemical performance of NiSe@NiOOH/NF for the oxygen evolution reaction (OER) was investigated. NiSe@NiOOH/NF demonstrates an obviously enhanced OER activity with much lower overpotential of 332 mV at 50 mA cm(-2) compared to other Ni-based electrocatalysts. The low charge-transfer resistance (Rct), large electrochemical double-layer capacitance (Cdl) of electrochemically active surface areas (ECSAs), and excellent long-term stability of NiSe@NiOOH/NF confirm the enhancement of its electrochemical performance for the OER, which can be ascribed to the large amount of active sites derived from the amorphous NiOOH shell and the good conductivity and stability derived from the NiSe core. In addition, the synergistic effect between the NiSe core and NiOOH shell could serve for a highly efficient OER electrocatalyst.

In situ sulfurized CoMoS/CoMoO4 shell–core nanorods supported on N-doped reduced graphene oxide (NRGO) as efficient electrocatalyst for hydrogen evolution reaction

Many strategies, such as doping metal, designing low-dimensional nanostructures, and enhancing the utilization of active sites based on a conductive support, have been intensively pursued to improve the intrinsic activity of transition metal chalcogenides for the hydrogen evolution reaction (HER). However, integrating all the above-mentioned merits into one electrocatalyst is still a significant challenge. Herein, we have successfully prepared uniform CoMoS/CoMoO4 (CMS) shell–core nanorods, with a diameter of 60 nm and a length of 800 nm, supported on N-doped reduced graphene oxide (NRGO). The obtained CMS/NRGO can combine many advantages, including transition metal doping, one-dimensional nanorods, and the superior conductivity of NRGO, resulting in very promising HER properties and excellent stability. The optimum sulfurization temperature for unsupported CMS nanorods has been explored using uniform CoMoO4 nanorods as a precursor. Although CMS-3 prepared with a sulfurization temperature of 300 °C has been found to possess the optimum activity for the HER, when adopting NRGO as a support, CMS-3/NRGO exhibits an impressive enhancement in HER performances with a low overpotential of 80 mV, a small Tafel slope of 58 mV dec−1, and a large exchange current density of 428 μA cm−2. In addition, the electrocatalytic activity of CMS-3/NRGO shows a negligible delay after 1000 cycles, indicating its robust electrochemical stability in acid electrolyte solution. Therefore, adopting low-temperature sulfurization of one-dimensional metal oxide precursors supported on NRGO may be a promising strategy for obtaining excellent electrocatalysts for the HER.

Controllable synthesis of three dimensional electrodeposited Co–P nanosphere arrays as efficient electrocatalysts for overall water splitting

Novel three dimensional (3D) electrodeposited Co–P nanosphere arrays on FTO (Co–P/FTO) have been successfully prepared as efficient bifunctional electrocatalysts for overall water splitting in alkaline media. The morphologies and properties of the 3D Co–P nanosphere arrays can be controlled by the electrolyte concentration. At the middle concentration, Co–P nanospheres have a more homogeneous size and array distribution and a rough surface, implying a larger surface area and an increased number of active sites for water splitting. The electrochemical measurements confirm the best electrocatalytic performances of Co–P/FTO at the middle concentration. They show excellent activity, with an overpotential of 125 mV for HER, 420 mV for OER and Tafel slopes of 54 mV dec−1 and 83 mV dec−1, respectively. The fabricated bifunctional systems of Co–P/Co–P can efficiently catalyse HER and OER at the same time, solving the incompatible problem of different media between HER and OER. Therefore, controlling the synthesis of 3D Co–P/FTO nanosphere arrays through electrodeposition can provide a facile way for the bifunctional electrocatalysis of both HER and OER.

Novel Ni3S2@NiOOH hybrid nanostructure supported on Ni foam as high-efficient electrocatalyst for hydrogen evolution reaction

Novel Ni3S2@NiOOH hybrid nanostructures have been synthesized using Ni foam (NF) as support and Ni source through a facile low-temperature sulfurization and following in situ electrochemical oxidation process. The structure and composition of the as-prepared samples were characterized by XRD, XPS and SEM. The uniform film composed of volcanic-like Ni3S2 nanostrucutres covered on the surface of Ni foam after 300 °C sulfurization in H2S/N2 for 1h. The similar film of Ni3S2@NiOOH hybrid nanostructure has been obtained after electrochemical treatment of Ni3S2/NF in 1.0 M KOH (called ET-Ni3S2/NF). The electrocatalytic performances of all the samples for hydrogen evolution reaction (HER) have been investigated. The obtained ET-Ni3S2/NF shows smaller onset potential and Tafel slope than Ni3S2/NF due to the formation of NiOOH nanoplates on the surface of NF. The synergistic effect between Ni3S2 and NiOOH may be responsible for the enhancement of the HER activity.

Facile synthesis of TiO2 nanoplates decorated with Ag nanoparticles for electro-oxidation of hydrazine

Abstract TiO2 nanoplates decorated with Ag nanoparticles have been synthesized by a facile method. The as-prepared Ag/TiO2 nanoplates have been characterized using transmission electron microscopy and X-ray diffraction. Transmission electron microscopy results show that TiO2 nanoplates have a uniform side length of about 40 nm and mono-dispersed morphology, which implies that TiO2 nanoplates may be pomising supports. Ag nanoparticles with diameter ranging from 10 to 20 nm can be observed to disperse homogeneously on the surface of TiO2 nanoplates. The electro-oxidation of Ag/TiO2 nanoplates for hydrazine oxidation has been investigated in detail. The results show that Ag/TiO2 nanoplates have excellent electrocatalytic activity. The electro-oxidation of hydrazine may be an irreversible process being controlled by diffusion of hydrazine.