Alammar Tarek, Mudring Anja-Verena
Department of Chemistry, College of Science, King Faisal University, P.O Box 400, Al-Ahsa 31982, Saudi Arabia.
Department of Biological & Chemical Engineering, Intelligent Advanced Materials, Aarhus University, Aarhus 8200, Denmark.
Inorg Chem. 2024 Apr 8;63(14):6132-6140. doi: 10.1021/acs.inorgchem.3c02874. Epub 2024 Mar 27.
Employing ionic liquid-assisted microwave synthesis and moderate heat treatment allows for the preparation of otherwise difficult-to-obtain perovskite-type BaSnZrO solid solutions (0 ≤ ≤ 1). The impact of substituting Sn for the crystal structure, crystallinity, morphology, and photocatalytic performance was investigated. The obtained materials are characterized by X-ray diffraction, scanning electron microscopy, Brunauer-Emmett-Teller (BET) surface area analysis, X-ray photoelectron spectroscopy, UV-Vis diffuse reflectance spectroscopy, photoluminescence spectroscopy, and Raman and IR spectroscopy. SEM images show that the morphology of the samples varies from rods for = 0, 0.2 to spherical for = 0.5, 0.8, 1. Upon Zr for Sn substitution, the band gap changes from 3.1 to 5.0 eV as the valence and conduction bands move to lower and higher energies. The photocatalytic activities of the BaSnZrO samples in the hydroxylation of terephthalic acid (TA) follow the order BaSnZrO> BaSnZrO> BaSnO> BaSnZrO> BaZrO. The superior photocatalytic activity of BaSnZrO can be attributed to the synergistically favorable combination of a suitable band structure, band gap size, and increased surface area-to-volume ratio, resulting in a diminished crystalline particle size unattainable from samples prepared via traditional synthetic routes or without ionic liquid.
采用离子液体辅助微波合成和适度热处理,可以制备出其他方法难以获得的钙钛矿型BaSnZrO固溶体(0≤≤1)。研究了用Sn替代对晶体结构、结晶度、形貌和光催化性能的影响。通过X射线衍射、扫描电子显微镜、布鲁诺尔-埃米特-泰勒(BET)表面积分析、X射线光电子能谱、紫外-可见漫反射光谱、光致发光光谱以及拉曼光谱和红外光谱对所得材料进行了表征。扫描电子显微镜图像显示,样品的形貌从=0、0.2时的棒状变化为=0.5、0.8、1时的球状。随着Zr替代Sn,当价带和导带向更低和更高能量移动时,带隙从3.1 eV变为5.0 eV。BaSnZrO样品在对苯二甲酸(TA)羟基化反应中的光催化活性顺序为BaSnZrO>BaSnZrO>BaSnO>BaSnZrO>BaZrO。BaSnZrO优异的光催化活性可归因于合适的能带结构、带隙尺寸以及增加的表面积与体积比之间协同有利的组合,从而导致通过传统合成路线或不使用离子液体制备的样品无法获得的减小的晶体粒径。