Sharmin Fahmida, Basith M A
Nanotechnology Research Laboratory, Department of Physics, Bangladesh University of Engineering and Technology, Dhaka 1000, Bangladesh.
ACS Omega. 2022 Sep 23;7(39):34901-34911. doi: 10.1021/acsomega.2c03457. eCollection 2022 Oct 4.
Sillenite-type members of the bismuth ferrite family have demonstrated outstanding potential as novel photocatalysts in environmental remediation such as organic pollutant degradation. This investigation has developed a low temperature one-step hydrothermal technique to fabricate sillenite bismuth ferrite BiFeO (S-BFO) via co-substitution of 10% Gd and 10% Cr in Bi and Fe sites of BiFeO, respectively, by tuning hydrothermal reaction temperatures. Rietveld refined X-ray diffraction patterns of the as-synthesized powder materials revealed the formation of S-BFO at a reaction temperature of 120-160 °C. A further increase in the reaction temperature destroyed the desired sillenite structure. With the increase in the reaction temperature from 120 to 160 °C, the morphology of S-BFO gradually changed from irregular shape to spherical powder nanomaterials. The high-resolution TEM imaging demonstrated the polycrystalline nature of the S-BFO(160) nanopowders synthesized at 160 °C. The as-synthesized samples exhibited considerably high absorbance in the visible region of the solar spectrum, with the lowest band gap of 1.76 eV for the sample S-BFO(160). Interestingly, S-BFO(160) exhibited the highest photocatalytic performance under solar irradiation, toward the degradation of rhodamine B and methylene blue dyes owing to homogeneous phase distribution, regular powder-like morphology, lowest band gap, and quenching of electron-hole pair recombination. The photodegradation of a colorless organic pollutant (ciprofloxacin) was also examined to ensure that the degradation is photocatalytic and not dye-sensitized. In summary, Gd and Cr co-doping have proven to be a compelling energy-saving and low-cost approach for the formulation of sillenite-phase bismuth ferrite with promising photocatalytic activity.
铋铁氧体家族中的硅铈矿型成员已展现出作为新型光催化剂在环境修复(如有机污染物降解)方面的巨大潜力。本研究开发了一种低温一步水热法,通过分别在BiFeO的Bi位和Fe位共取代10%的Gd和10%的Cr,并调节水热反应温度来制备硅铈矿型铋铁氧体BiFeO(S-BFO)。对合成后的粉末材料进行的Rietveld精修X射线衍射图谱显示,在120 - 160 °C的反应温度下形成了S-BFO。反应温度的进一步升高破坏了所需的硅铈矿结构。随着反应温度从120 °C升高到160 °C,S-BFO的形态逐渐从不规则形状变为球形粉末纳米材料。高分辨率透射电镜成像证明了在160 °C合成的S-BFO(160)纳米粉末的多晶性质。合成后的样品在太阳光谱的可见光区域表现出相当高的吸光度,样品S-BFO(160)的带隙最低,为1.76 eV。有趣的是,由于均匀的相分布、规则的粉末状形态、最低的带隙以及电子 - 空穴对复合的猝灭,S-BFO(160)在太阳辐射下对罗丹明B和亚甲基蓝染料的降解表现出最高的光催化性能。还对无色有机污染物(环丙沙星)的光降解进行了研究,以确保降解是光催化的而非染料敏化的。总之,Gd和Cr共掺杂已被证明是一种引人注目的节能且低成本的方法,用于制备具有有前景的光催化活性的硅铈矿相铋铁氧体。