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首页> 外文期刊>Dalton transactions: An international journal of inorganic chemistry >Photocatalyzed preferential oxidation of CO under simulated sunlight using Au-transition metal oxide-sepiolite catalysts
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Photocatalyzed preferential oxidation of CO under simulated sunlight using Au-transition metal oxide-sepiolite catalysts

机译:使用Au-过渡金属氧化物 - 海泡石催化剂在模拟阳光下CO的光催化优先氧化

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In the present study a series of Au-transition metal oxides supported on a clay mineral such as sepiolite were tested in the preferential oxidation of CO in an excess of H-2 under simulated solar light irradiation and in the absence of light, at 30 degrees C and atmospheric pressure. Transition metal oxides (ZnO, Fe2O3, NiO, MnO2, and Co3O4) were dispersed over the sepiolite surface where, subsequently, Au nanoparticles with an average particle size between 2 and 3 nm were successfully deposited-precipitated. The obtained photocatalysts were characterized by XRD, XRF, DRUV-Vis, N-2 adsorption-desorption and HRTEM in order to evaluate the optical, structural and chemical properties of the prepared samples. Despite the low amount of gold (nominal 1.0 wt%), the catalysts exhibited an outstanding behavior under light irradiation, with reaction rates between 4.5 and 5.2 mmol COox g(cat)(-1) h(-1) for the Au-NiSep, Au-CoSep and Au-ZnSep samples. These photocatalysts exhibited a high dispersion of the respective transition metal oxides over the sepiolite support and the presence of low-coordinated hemispherical gold nanoparticles. The superior photocatalytic efficiency of these samples was ascribed to the reduction of the electron-hole pair recombination of photogenerated charge carriers by the excitation of the localized surface plasmon resonance of the Au nanoparticles. The BET surface area and the gold particle size seemed to be relevant factors affecting the catalytic performance.
机译:在本研究中,在模拟的太阳能光照射下,在过量的H-2中优先氧化在含量的H-2中,在含有Sepiolite上的粘土矿物如海硫酸盐的一系列Au-过渡金属氧化物。 C和大气压。将过渡金属氧化物(ZnO,Fe 2 O 3,NiO,MnO 2和CO 3O4)分散在海硫醇石表面上,随后,成功地沉积沉淀平均粒径2至3nm的Au纳米颗粒。所获得的光催化剂的特征在于XRD,XRF,DRUV-Vis,N-2吸附 - 解吸和HRTEM,以评估制备样品的光学,结构和化学性质。尽管金量较少(标称1.0wt%),但催化剂在光照照射下表现出突出的行为,对于Au-Nisep的4.5和5.2mmol CoOx G(CAT)(-1)H(-1)之间的反应速率,Au-cosep和au-znsep样品。这些光催化剂在海泡石载体上表现出相应的过渡金属氧化物的高分散体和低配位的半球形金纳米颗粒。通过激发Au纳米颗粒的局部表面等离子体共振的激发,将这些样品的卓越的光催化效率归因于通过激发局部表面等离子体共振的激发光发性电荷载体的电子 - 空穴对重组。 BET表面积和金粒径似乎是影响催化性能的相关因素。

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