首页> 外文期刊>催化剂现代研究(英文) >High Efficient Photocatalytic Degradation of 3,7-Bis(Dimethylamino)-Phenothiazin-5-Ium Chloride Dye and Kinetics of H2 Evolution of N2H4H2O by Synthesized CdS/NiS Nanocomposite by Electrochemical Method
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High Efficient Photocatalytic Degradation of 3,7-Bis(Dimethylamino)-Phenothiazin-5-Ium Chloride Dye and Kinetics of H2 Evolution of N2H4H2O by Synthesized CdS/NiS Nanocomposite by Electrochemical Method

机译:通过电化学方法,通过电化学方法合成Cds / NIS纳米复合材料高效光催化降解3,7-双(二甲基氨基)-phenothia- 5-Ⅱ型-5-氯化物染料和N2H4H2O的H2进化动力学

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CdS/NiS nanocomposites were synthesized by electrochemical method. Ni and Cd is one of the important II-VI semiconducting materials with a direct band gap of 3.26 eV which finds applications in electrical conductivity and photo-catalysis. The synthesized nanocomposites were characterized by BET, UV-VIS, XRD, FE-SEM (EDAX) techniques. X-Ray diffraction (XRD) reveals crystallite size to be 23.22 nm which was calculated using Williamson-Hall (W-H) plot method. The energy of the band gap for CdS/NiS could be thus estimated to be 3.26 eV. The photocatalytic activity of the sample was evaluated by the degradation of textile dye methylene Blue (MB) in aqueous solutions under UV radiation. Hydrogen energy is regarded as a promising alternative in terms of energy conversion and storage. Hydrogen Evolution Reaction (HER) was carried out in both visible light and UV light by using Hydrazine (N2H4H2O) in the presence of CdS/NiS nanocomposite. The synthesized photocatalyst shows applicable performance for kinetics of Hydrogen Evolution Reaction (HER) in Visible light and UV light. The decomposition of hydrazine (N2H4H2O) proceeded rapidly to generate free hydrogen rich gas through OH radical contact with CdS/NiS nanocomposite at room temperature. The rate of HER is limited by either proton adsorption onto an active site or evolution of formed hydrogen from the surface. A high Tafel slope is indicative of proton adsorption as the rate limiting step, while a lower Tafel slope (20 - 45 mV) indicates that the evolution of molecules hydrogen from the catalyst is rate limiting. In the present case the Tafel slopes for visible light 23.5 mV and 42.5 mV for UV light. Blank experiments show poor activity for HER i.e. 10.1 - 13.5 mV.
机译:通过电化学方法合成CDS / NIS纳米复合材料。 Ni和CD是具有3.26eV的直接带隙的重要II-VI半导体材料之一,可在电导率和光催化中找到应用。通过BET,UV-Vis,XRD,Fe-SEM(EDAX)技术表征合成的纳米复合材料。 X射线衍射(XRD)揭示了用威廉姆森 - 霍尔(W-H)图法计算的结晶尺寸为23.22nm。因此,CDS / NIS的带隙的能量可以估计为3.26eV。通过在UV辐射下水溶液中的纺织染料亚甲基蓝(MB)的降解来评估样品的光催化活性。在能量转换和储存方面被认为是氢能量的有希望的替代品。在CDS / NIS纳米复合材料存在下,通过使用肼(N2H4H2O)在可见光和UV光中进行氢进化反应(其)。合成的光催化剂显示出可见光和紫外光的氢进化反应(她)的动力学的适用性。肼(N2H4H2O)的分解迅速进行,通过在室温下与CDS / NIS纳米复合材料的OH自由基接触产生游离氢气。她的速率受到质子吸附到活性位点或从表面形成的形成氢的演变的限制。高Tafel斜率表示质子吸附作为速率限制步骤,而下塔拉斐尔斜率(20-45mV)表明来自催化剂的分子氢的演变是速率限制。在当前情况下,Tafel倾斜23.5mV和42.5mV的UV光。空白实验表明,她的活动差,即10.1-13.5 mV。

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