Publications by authors named "Renzheng Jiang"

Understanding the reconstruction mechanism to rationally design cost-effective electrocatalysts for oxygen evolution reaction (OER) is still challenging. Herein, a defect-rich NiMoO precatalyst is used to explore its OER activity and reconstruction mechanism. In situ generated oxygen vacancies, distorted lattices, and edge dislocations expedite the deep reconstruction of NiMoO to form polycrystalline Ni (oxy)hydroxides for alkaline oxygen evolution.

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Hybrid cocatalysts have great application potential for improving the photocatalytic hydrogen evolution performance of semiconductors. The interfaces between components of hybrid cocatalysts make a great contribution to the improvement, but the associated mechanisms remain unclear. Herein, we prepared and tested three comparative CdS-based photocatalysts with NiS, NiS/NiS, and NiS as the cocatalysts separately.

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Earth-abundant transition metal-based bifunctional electrocatalysts are promising alternatives to noble metals for overall water electrolysis, but restricted by low activity and durability. Herein, a three-dimensional phosphorus-doped nickel molybdate/nickel molybdate hydrate @phosphates core-shell nanorod clusters on nickel foam self-supported electrode was fabricated by a combined hydrothermal and phosphating process. The phosphorus doping and phosphate coating induced by phosphating process bring in a synergistic effect to improve the electrical conductivity, provide abundant active surface sites and accelerate the surface reaction for nickel molybdate/nickel molybdate hydrate (NiMoO/NiMoO·nHO) heterostructures.

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The intriguing features of two-dimensional (2D) materials such as better charge carrier separation and abundant surface reaction sites endow them with potential applications as cocatalysts in photocatalysis. In this paper, a ternary 2D nickel hydroxide/sulfides nanosheet composed of Ni(OH), NiS and NiS was loaded on CdS nanospheres by a simple chemical deposition route. The composition of nickel hydroxide/sulfides was determined clearly through an overall analysis using X-ray diffraction, transmission electron microscopy and X-ray photoelectron spectroscopy.

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In order to improve the sonocatalytic activity of TiO(2), Al(2)O(3)/TiO(2), Y(2)O(3)/TiO(2) and Fe(2)O(3)/TiO(2) composites were prepared using mechanical mixing, liquid boiling, ultrasonic dispersion and heat-treated methods. And then, a series of degradation experiments were carried out under ultrasonic irradiation. Also, the influences of heat-treated temperature and heat-treated time on the sonocatalytic activity of Al(2)O(3)/TiO(2), Y(2)O(3)/TiO(2) and Fe(2)O(3)/TiO(2), and ultrasonic irradiation time and solution acidity on the sonocatalytic degradation of Acid red B were investigated by UV-vis spectra.

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In this work, the emphasis was mainly placed on investigating the sonocatalytic activity of TiO(2)-ZnO mixed with Er(3+):YAlO(3), namely, Er(3+):YAlO(3)/TiO(2)-ZnO composite. It is able to utilize the sonoluminescence light to improve the sonocatalytic degradation of organic dyes. The Er(3+):YAlO(3) as up-conversion luminescence agent was synthesized by sol-gel and auto-combustion method, and then Er(3+):YAlO(3)/TiO(2)-ZnO composite as sonocatalyst were prepared by ultrasonic dispersion and liquids boil method.

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The previous work proved that the bovine serum albumin (BSA) could be damaged under the combined action of ultrasonic irradiation and ZnO. In this work, the assisted sonocatalytic damage of BSA using metronidazole (MTZ) as a sensitizer was further investigated by means of UV-vis and fluorescence spectra. The results indicated that the adding of MTZ could obviously promote the sonocatalytic damage of BSA under ultrasonic irradiation in the presence of nano-sized ZnO powder.

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The CeO(2)/TiO(2), SnO(2)/TiO(2) and ZrO(2)/TiO(2) composites were prepared by dispersing various nano-sized oxides (CeO(2), SnO(2), ZrO(2) and TiO(2)) with ultrasound and mixing TiO(2) with CeO(2), SnO(2) and ZrO(2), respectively, in boiling water in a molar ratio of 4:1, followed by calcining temperature 500 degrees C for 60 min. Then a series of sonocatalytic degradation experiments were carried out under ultrasonic irradiation in the presence of CeO(2)/TiO(2), SnO(2)/TiO(2) and ZrO(2)/TiO(2) composites and nano-sized TiO(2) powder. Also, the influences of heat-treatment temperature and heat-treatment time on the sonocatalytic activities of CeO(2)/TiO(2), SnO(2)/TiO(2) and ZrO(2)/TiO(2) composites, and of irradiation time and solution acidity on the sonocatalytic degradation of Acid Red B were investigated by UV-vis spectra.

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