首页> 外文会议>Asia-Pacific Congress on Catalysis:Abstracts vol.1; 20031012-15; Dalian(CN) >Electronic Structures and Photocatalytic Properties of New Vanadates Semiconductor Photocatalysts
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Electronic Structures and Photocatalytic Properties of New Vanadates Semiconductor Photocatalysts

机译:新型钒酸盐半导体光催化剂的电子结构和光催化性能

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Semiconductor photocatalysts have attracted increasing interests because of their functions in generating "clean-energy" hydrogen from water and air/water purification. However, most of the photocatalysts developed up to now have wide band gaps that they only respond to the ultra violet (UV) light, which occupies only about 4% of the solar spectrum. Research and development of visible light driven photocatalysts is indispensable from the viewpoint of efficient utilization of solar energy. Recently, we have succeeded in developing the world-first visible light responding photocatalysts, (In_(1-x)Ni_x)TaO_4 (x = 0~0.2). The photocatalysts can split water into H_2 and O_2 in a 2:1 stoichiometric manner, under visible light irradiation (λ > 420nm). Moreover, with 5d metal Ta being substituted by 4d metal Mb or 3d metal V, a systematic variation on the photophysical and photocatalytic properties reflecting strong effects of electronic structures was observed. In this study, we focused our concerns on the transition metal V and further substituted In by the trivalent rare earth elements to investigate the effects of f electron on the electronic and photophysical properties of the catalysts. Understandings on the relations among the materials syntheses, crystal, electronic structures, and photocatalytie activities of these new photocatalysts, obtained from theoretical calculations based on the first-principle method and experiments included crystal structure analyses, UV-vis diffuse reflectance spectroscopy, photocatalytie activity measurement, etc., will be discussed.
机译:半导体光催化剂因其从水和空气/水净化中产生“清洁能源”氢的功能而吸引了越来越多的兴趣。但是,迄今为止开发的大多数光催化剂都具有宽带隙,它们仅对紫外线(UV)产生反应,而紫外线仅占太阳光谱的4%。从有效利用太阳能的观点来看,可见光驱动的光催化剂的研究和开发是必不可少的。最近,我们成功开发了世界上第一个可见光响应型光催化剂(In_(1-x)Ni_x)TaO_4(x = 0〜0.2)。在可见光(λ> 420nm)下,光催化剂可以以2:1的化学计量比将水分解为H_2和O_2。此外,用5d金属Ta替代4d金属Mb或3d金属V,观察到反映电子结构的强效应的光物理和光催化性能的系统变化。在这项研究中,我们将注意力集中在过渡金属V上,并进一步用三价稀土元素取代In来研究f电子对催化剂电子和光物理性质的影响。通过基于第一原理方法的理论计算和实验获得对这些新型光催化剂的材料合成,晶体,电子结构和光催化活性之间关系的理解,包括晶体结构分析,紫外-可见漫反射光谱,光催化活性测量等等。

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