tio2掺杂钆电催化剂的酸性析氢增强

M. Alsawat
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引用次数: 1

摘要

采用两种不同原子浓度的六水硝酸钆,叔丁醇钛为钛前驱体,二甲亚砜为溶剂,合成了掺杂钆的TiO2 NPs,即TiO2- gd1.0和TiO2- gd6.0。利用傅里叶红外光谱(FTIR)、热重差热分析(TGA-DTA)、x射线衍射(XRD)、扫描电子显微镜(SEM)和透射电子显微镜(TEM)对NPs的结构和形貌进行了表征。采用线性扫描伏安法(LSV)测试了两种合成的TiO2-Gd1.0和TiO2-Gd6.0在酸性电解质(0.5 M H2SO4)中作为析氢反应(HER)的电催化剂。将LSV数据拟合到Tafel方程,并对描述HER动力学的各种电化学参数进行了评价和讨论。结果表明,掺杂Gd3+后,TiO2 NPs表面HER的动力学显著增强,且与TiO2 NPs中Gd3+离子的原子浓度成正比。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Enhanced Acidic Hydrogen Evolution on TiO2-Doped Gadolinium Electrocatalysts
Gadolinium-doped TiO2 NPs, namely TiO2-Gd1.0 and TiO2-Gd6.0 have been synthesized using two different atomic concentrations of gadolinium(III) nitrate hexahydrate in presence of titanium(IV) tert-butoxide as a titanium precursor and dimethyl sulfoxide as a solvent. The structure and morphology of these NPs have been characterized by Fourier transform infrared spectroscopy (FTIR), thermogravimetric-differential thermal analysis (TGA-DTA), X-ray diffraction (XRD), scanning electron microscopy (SEM), and transmission electron microscopy (TEM). The two synthesized TiO2-Gd1.0 and TiO2-Gd6.0 were tested as electrocatalysts for hydrogen evolution reaction (HER) in an acidic electrolyte (0.5 M H2SO4) based on linear sweep voltammetry (LSV) measurements. LSV data were fitted to Tafel equation and the various electrochemical parameters describing the HER kinetics were evaluated and discussed. Results demonstrate that the kinetics of the HER on the surface of TiO2 NPs significantly enhanced upon doping it with Gd3+, proportionally to the atomic concentration of the Gd3+ cations in the TiO2 NPs.
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