Singla Shelly, Devi Pooja, Basu Soumen
Materials Science and Sensor Application, Central Scientific Instruments Organisation, Chandigarh 160030, India.
School of Chemistry and Biochemistry, Thapar Institute of Engineering and Technology, Patiala 147004, India.
Materials (Basel). 2023 Aug 17;16(16):5661. doi: 10.3390/ma16165661.
In this study, a series of BiVO/BiOBr composites with varying mole ratios were successfully synthesized using a hydrothermal method. The in-situ synthesis strategy facilitated the formation of a close interfacial contact between BiVO and BiOBr at the depletion zone, resulting in improved charge segregation, migration, reduced charge recombination, enhanced solar light absorption capacity, promoting narrow band gap, and large surface area. This study investigates the influence of different mole ratios of BiVO and BiOBr in a BiVO/BiOBr nanocomposite on the photocatalytic degradation of tetracycline (TC), a pharmaceutical pollutant, and photoelectrocatalytic water splitting (PEC) under solar light irradiation. Maximum decomposition efficiency of ~90.4% (with a rate constant of 0.0159 min) for TC was achieved with 0.5 g/L of 3:1 BiVO: BiOBr (31BVBI) photocatalyst within 140 min. The degraded compounds resulting from the TC abatement were analyzed using GC-MS. Furthermore, TC standards exhibited 78.2% and 87.7% removal of chemical oxygen demand (COD) and total organic carbon (TOC), respectively, while TC tablets showed 64.6% COD removal and 73.8% TOC removal. The PEC water splitting experiments demonstrated that the 31BVBI photoanode achieved the highest photocurrent density of approximately 0.2198 mA/cm at 1.23 V vs. RHE, resulting in the generation of approximately 1.864 mmolcm s of hydrogen, while remaining stable for 21,600 s. The stability of the photocatalyst was confirmed by post-degradation characterizations, which revealed intact crystalline planes, shape, and surface area. Comparisons with existing physicochemical methods used in industries indicate that the reported photocatalyst possesses strong surface catalytic properties and has the potential for application in industrial wastewater treatment and hydrogen generation, offering an advantageous alternative to costly and time-consuming processes.
在本研究中,采用水热法成功合成了一系列不同摩尔比的BiVO/BiOBr复合材料。原位合成策略促进了BiVO和BiOBr在耗尽区形成紧密的界面接触,从而改善了电荷分离、迁移,减少了电荷复合,增强了太阳光吸收能力,促进了窄带隙的形成以及增大了表面积。本研究考察了BiVO/BiOBr纳米复合材料中不同摩尔比的BiVO和BiOBr对药物污染物四环素(TC)的光催化降解以及太阳光照射下光电催化水分解(PEC)的影响。在140分钟内,0.5 g/L的3:1 BiVO:BiOBr(31BVBI)光催化剂对TC的最大分解效率达到约90.4%(速率常数为0.0159 min)。使用气相色谱 - 质谱联用仪(GC - MS)分析了TC降解产生的化合物。此外,TC标准品分别实现了78.2%的化学需氧量(COD)去除率和87.7%的总有机碳(TOC)去除率,而TC片剂的COD去除率为64.6%,TOC去除率为73.8%。PEC水分解实验表明,31BVBI光阳极在相对于可逆氢电极(RHE)为1.23 V时实现了约0.2198 mA/cm的最高光电流密度,产生了约1.864 mmolcm s的氢气,同时在21600 s内保持稳定。降解后表征证实了光催化剂的稳定性,其晶体平面、形状和表面积保持完整。与工业中使用的现有物理化学方法的比较表明,所报道的光催化剂具有很强的表面催化性能,在工业废水处理和制氢方面具有应用潜力,为昂贵且耗时的工艺提供了一种有利的替代方案。