首页> 外文期刊>Inorganic Chemistry: A Research Journal that Includes Bioinorganic, Catalytic, Organometallic, Solid-State, and Synthetic Chemistry and Reaction Dynamics >Tetragonal to Monoclinic Crystalline Phases Change of BiVO4 via Microwave-Hydrothermal Reaction: In Correlation with Visible-Light-Driven Photocatalytic Performance
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Tetragonal to Monoclinic Crystalline Phases Change of BiVO4 via Microwave-Hydrothermal Reaction: In Correlation with Visible-Light-Driven Photocatalytic Performance

机译:通过微波 - 水热反应转移到单斜晶相变为BIVO4的变化:与可见光催化的光催化性能相关

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Explicit control of the crystalline phases and morphology of semiconducting BiVO4 crystals has been successfully synthesized via microwave-hydrothermal condition (MW-HT) without requiring any template/surfactant, doping of metal ions, and altering pH of reaction solution. Unambiguously, the crystalline phase of BiVO4 crystal has transformed from tetragonal zircon type (tz) to monoclinic scheelite (m) via mixed-phase (m-tz) by altering microwave-irradiation time at fixed microwave-irradiation power (800 W) without changing any precursor concentrations throughout the reaction. X-ray diffraction and Rietveld refinement studies confirmed the phase transformation of BiVO4 crystals that occurs by controlling the irradiation time (10-22 min) and temperature (116-195 degrees C). The changes in VO43- tetrahedron bond strength and bond length attributed to phase transitions in BiVO4 crystals were corroborated by Raman spectra. Field emission scanning electron microscope revealed the sequential growth and rational morphological evolution of spherical-shaped zircon type tz-BiVO4 particles to preferentially oriented (010) and (110)-faceted decahedron-shaped scheelite m-BiVO4 crystals. The UV-reflectance and photoluminescence analyses revealed reduction in the optical bandgap and efficient charge separation with tunneling of excitons through interfaces, owing to phase transitions from tetragonal to monoclinic in BiVO4 crystals. High-resolution transmission electron microscopy images revealed the formation of heterojunctions between both the phases of BiVO4 crystals. The photocatalytic degradation of Rhodamine-B dye under natural sunlight showed maximum efficiency of 95% with highest rate kinetics (kappa(avg) = 0.0718/min) using mixed-phase BiVO4 (m:tz-60:40) crystals, whereas under simulated sunlight, monoclinic phase BiVO4 crystals showed high degradation efficiency of 87% with low rate kinetics (kappa(avg) = 0.0436/min) for 200 min. The free-radical trapping tests revealed that
机译:通过微波 - 水热条件(MW-HT)成功地合成了半导体BIVO4晶体的结晶相和形态的明确控制,而不需要任何模板/表面活性剂,金属离子的掺杂,并改变反应溶液的pH。明确地,通过在固定微波照射功率(800 W)以固定微波照射功率(800W)以固定的微波照射时间(800 W)在不变化的情况下通过混合相(M-TZ),Bivo4晶体的结晶相通过混合相(M-TZ)转化为单斜晶体(M)转化为单斜晶体(M)。不变化在整个反应中的任何前体浓度。 X射线衍射和RIETVELD细化研究证实了通过控制照射时间(10-22分钟)和温度(116-195℃)而发生的BIVO4晶体的相变。归因于BIVO4晶体中相转变的VO43-四向量键合强度和键合长度的变化通过拉曼光谱来证实。场发射扫描电子显微镜揭示了球形锆石型TZ-Bivo4颗粒的顺序增长和合理形态学,优先取向(010)和(110) - 甲状二管状的白皮岩M-Bivo4晶体。 UV反射率和光致发光分析显示光学带隙的降低和通过界面与激子隧道的有效电荷分离,由于在BiVo4晶体中的四边形到单斜移到单斜移。高分辨率透射电子显微镜图像显示BIVO4晶体的两相之间的杂交功能。自然阳光下的罗丹明-B染料的光催化降解显示最大效率为95%,最高速率动力学(Kappa(AVG)= 0.0718 / min),使用混合相BIVO4(M:TZ-60:40)晶体,而在模拟下阳光,单斜晶相体Bivo4晶体显示出高速率动力学(Kappa(AVG)= 0.0436 / min)的高降解效率为200分钟。自由基诱捕测试显示

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