Mohammad Akbar, Baig Mirza Talha, Tauqeer Mohd, Kim Hyo-Jin, Park Chae-Hee, Choi Chang-Hyung
School of Chemical Engineering, Yeungnam University, Gyeongsan, 38541, Gyeongbuk, Republic of Korea.
Department of Chemistry, Kocaeli University, Kocaeli, 41380, Turkey.
J Environ Manage. 2025 Aug 29;393:127010. doi: 10.1016/j.jenvman.2025.127010.
The present review focuses on the bismuth-based heterojunction photocatalysts for the degradation of tetracycline (TC) antibiotic. The frequent usage of antibiotics causes several environmental and health concerns due to their widespread occurrence and persistence in aquatic ecosystems. In this context, bismuth-based photocatalysts have extended noteworthy interest for their tunable structures, visible-light activity, suitable band gap energies, and unique physicochemical properties. However, their distinct use is limited by inadequate charge separation and reduced conduction band potentials. To address these limitations, the development of Type-II, Z-scheme, p-n heterojunctions, and more recently, S-scheme heterojunctions has been studied and reviewed to improve the charge carrier dynamics and light absorption. In this review, various bismuth-based heterojunctions, detailing their synthesis methods, structural properties, and mechanism involve therein. Notably, few of bismuth-based heterojunction photocatalysts stand out as the most efficient, owing to their strong visible-light absorption, multistep charge transfer channels, and active surface chemistry. The heterojunction photocatalysts exhibit significant enhancements in photocatalytic efficiency by expediting the separation of photogenerated charges and reducing recombination rates but have certain limitations. The degradation of TC reached over 90 % in short time period, highlighting the efficacy of the photocatalysts reported over time. The synergistic roles of reactive species, including hydroxyl radicals (•OH), superoxide radicals (•O), and photogenerated holes (h), in the degradation of TC are discussed. Further, this review highlights the limitations and prospects of the conventional mechanisms and S-scheme heterojunction based-mechanism, respectively. Theoretical aspects were reviewed to enhance bismuth-based photocatalysis and what important major steps need to be taken for a strong heterojunction formation. The review highlights the design of bismuth-based photocatalysts with anticipated extended light response, strong heterojunction formation, stability, scalability, development of thin-film designs, and degradation of other pollutants.
本综述聚焦于用于降解四环素(TC)抗生素的铋基异质结光催化剂。抗生素的频繁使用因其在水生生态系统中的广泛存在和持久性而引发了若干环境和健康问题。在此背景下,铋基光催化剂因其可调控的结构、可见光活性、合适的带隙能量以及独特的物理化学性质而受到了显著关注。然而,它们的独特用途受到电荷分离不足和导带电位降低的限制。为了解决这些限制,人们研究并综述了II型、Z型、p-n异质结以及最近的S型异质结的发展,以改善电荷载流子动力学和光吸收。在本综述中,详细介绍了各种铋基异质结,包括它们的合成方法、结构性质以及其中涉及的机理。值得注意的是,少数铋基异质结光催化剂因其强烈的可见光吸收、多步电荷转移通道和活性表面化学而脱颖而出,成为最有效的光催化剂。异质结光催化剂通过加速光生电荷的分离和降低复合率,在光催化效率方面有显著提高,但也存在一定局限性。TC的降解在短时间内达到了90%以上,突出了所报道的光催化剂随时间的有效性。讨论了包括羟基自由基(•OH)、超氧自由基(•O)和光生空穴(h)在内的活性物种在TC降解中的协同作用。此外,本综述分别强调了传统机理和基于S型异质结机理的局限性和前景。对理论方面进行了综述,以增强铋基光催化作用以及形成强异质结需要采取的重要主要步骤。该综述强调了具有预期扩展光响应、强异质结形成、稳定性、可扩展性、薄膜设计开发以及其他污染物降解能力的铋基光催化剂的设计。