Waghchoure Nehal Ashok, Patel Atul, Raikar Laxman G, Gandhi Jemi, Jayadevan Kampurath Poduvattil, Prakash Halan
Energy and Environmental Chemistry Laboratory, Department of Chemistry, Birla Institute of Technology and Science, Pilani, K K Birla Goa Campus Zuarinagar Goa 403726 India
RSC Adv. 2025 Jul 1;15(28):22250-22266. doi: 10.1039/d5ra02938d. eCollection 2025 Jun 30.
Photocatalysis is promising for the degradation of antibiotic pollutants in water, which are known to cause the emergence of harmful antibiotic-resistant bacteria (ARB). Importantly, photocatalytic degradation of antibiotic pollutants in water with loss of antibacterial activity in an energy-efficient manner needs to be explored. Here, for the first time, we report degradation of tetracycline (TC), a known antibiotic pollutant in water, with removal of its antibiotic activity by cubic-barium stannate (BaSnO, BSO) perovskite photocatalytic nanoparticles under a blue LED light (367 nm) irradiation, (BSO/LED) system. XRD results revealed a single cubic phase of BSO with a crystallite size of 35 nm. FESEM and TEM images showed that BSO had cubic block-like morphology. BET analysis revealed the mesopores nature of BSO with a surface area of 1.1 m g. XPS confirmed the existence of Ba and Sn ions. The bandgap energy of BSO was determined to be ∼3.2 eV. Importantly, photolysis of BSO under blue LED light caused complete degradation of TC in water, with a pseudo-first-order rate constant ( ) value determined as 0.0824 min. Radical scavenging and ESR results revealed O and holes were profoundly generated in the BSO/LED system, causing degradation of TC along with antibiotic activity removal. Electrical energy per order ( ) was determined as 13.63 kWh per m per order, revealing that the BSO/LED system is energy-efficient. Further, BSO was reused four times, highlighting its stability. Degradation byproducts were predicted to be non-toxic by ecological structure activity relationship analysis. Thus, the study discloses an effective photocatalytic degradation of TC along with removal of its antibacterial activity that is needed to prevent hazardous ARB, by a stable non-lead-perovskite nano-photocatalyst under an energy-efficient LED source.
光催化对于水中抗生素污染物的降解具有广阔前景,已知这些污染物会导致有害的抗生素抗性细菌(ARB)的出现。重要的是,需要探索以节能方式对水中抗生素污染物进行光催化降解并使其失去抗菌活性的方法。在此,我们首次报道了在蓝色发光二极管(LED)灯(367 nm)照射下,立方锡酸钡(BaSnO,BSO)钙钛矿光催化纳米颗粒对水中已知抗生素污染物四环素(TC)的降解及其抗生素活性的去除(BSO/LED体系)。X射线衍射(XRD)结果显示BSO为单一立方相,微晶尺寸为35 nm。场发射扫描电子显微镜(FESEM)和透射电子显微镜(TEM)图像表明BSO具有立方块状形态。比表面积(BET)分析揭示了BSO的介孔性质,其表面积为1.1 m²/g。X射线光电子能谱(XPS)证实了Ba和Sn离子的存在。确定BSO的带隙能量约为3.2 eV。重要的是,在蓝色LED光下BSO的光解导致水中TC完全降解,确定其伪一级反应速率常数()值为0.0824 min⁻¹。自由基清除和电子顺磁共振(ESR)结果表明,在BSO/LED体系中大量产生了超氧阴离子(O₂⁻)和空穴,导致TC降解并去除其抗生素活性。每降解一个数量级所需电能(Eo)确定为每立方米每数量级13.63 kWh,表明BSO/LED体系具有节能性。此外,BSO可重复使用四次,突出了其稳定性。通过生态结构活性关系分析预测降解副产物无毒。因此,该研究揭示了一种在节能LED光源下,由稳定的无铅钙钛矿纳米光催化剂对TC进行有效光催化降解并去除其抗菌活性的方法,这对于预防有害的ARB是必要的。