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SEPARATION AND PURIFICATION TECHNOLOGY · 2024 · IF 8.1

Boosted antibiotic elimination over 2D/2D mesoporous CeO2/BiOCl S-scheme photocatalyst

Huiling Tang,Hengchao E,Chunxia Yao,Xuesheng Wang,Jiaxin Zhou,Wei Song,Zhijie Zhang

Exploring efficient photocatalysts holds significant importance for the prevention and treatment of antibiotic pollution. This research reports a 2D/2D CeO 2 /BiOCl S-scheme photocatalyst constructed by mesoporous CeO 2 and BiOCl nanosheets (NSs). Efficient charge separation and transfer was achieved by the synergistic effect of large-area contact and S-scheme charge transfer mechanism, which significantly enhanced the photocatalytic performance of CeO 2 /BiOCl. Experimental results demonstrated that the CeO 2 /BiOCl photocatalyst displayed superior photocatalytic activity to the individual components, which could efficiently eliminate four types of antibiotics, namely tetracycline (TC), chlortetracycline (CTC), doxycycline (DOC), and oxytetracycline (OTC) under UV light irradiation. Particularly, the sample of 0.4CeO 2 /BiOCl exhibited the highest catalytic efficiency, with a TC degradation rate constant of 0.01524 min −1 , which was 1.85 and 22.74 times higher than that of single CeO 2 and BiOCl, respectively. Moreover, liquid chromatograph-mass spectrometer (LC-MS) analysis is employed to reveal the degradation pathways of TC. This work offers an insightful idea for the fabrication of novel S-scheme photocatalysts applied in environmental purification.

CAS / MDL: 64-17-5
研究领域: 环境科学 · 材料科学
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JOURNAL OF COLLOID AND INTERFACE SCIENCE · 2022 · IF 9.965

BiOI@CeO2@Ti3C2 MXene composite S-scheme photocatalyst with excellent bacteriostatic properties

Zhipeng Mao,Wei Hao,Wei Wang,Fubin Ma,Chengcheng Ma,Shougang Chen

As an influential antifouling material, photocatalytic materials have drawn attention increasingly over recent years owing to their potential bacteriostatic property in the domain of marine antifouling. Herein, a flower-like BiOI@CeO 2 @Ti 3 C 2 S-scheme photocatalyst was contrived and prepared by hydrothermal method . The innovative combination of Ti 3 C 2 and narrow band gap semiconductor BiOI was implemented to modify CeO 2 and the photocatalytic bacteriostatic mechanism of BiOI@CeO 2 @Ti 3 C 2 was elucidated. Schottky junction was formed between CeO 2 and Ti 3 C 2 , and a p-n junction was formed between CeO 2 and BiOI. By photoelectrochemical characterization, BCT-10 exhibits the best photoelectrochemical performance of which photogenerated carrier transport can be performed more readily at 10 % CeO 2 @Ti 3 C 2 addition. 99.76 % and 99.89 % of photocatalytic bacteriostatic efficiency of BCT-10 against Escherichia coli and Staphylococcus aureus were implemented respectively, which were 2.98 and 3.07 times higher than that of pure CeO 2 . The ternary heterojunction can suppress photogenerated electron-hole complexes more effectively and enhance the photocatalytic bacteriostatic effect of CeO 2 , which also provided a new concept to the further broadened application of CeO 2 in the marine bacteriostatic and antifouling field.

CAS / MDL: 7681-11-0 2408-70-0
研究领域: 材料科学 · 环境科学 · 微生物学
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SEPARATION AND PURIFICATION TECHNOLOGY · 2024 · IF 8.1

Synergistic adsorption-photocatalytic degradation of tetracycline by S-scheme InVO4/ZnIn2S4 heterojunction: mechanism, toxicity assessment, and potential applications

Liying Sun,Xuesong He,Bin Liu,Shuming Zhang,Zheng Xiang,Xin Wang,Yang Wang

The development of materials with dual adsorption/photocatalytic functions for the removal of difficult-to-degrade organics is a very promising and challenging strategy. In this paper, a novel S-scheme heterojunction photocatalyst, InVO 4 /ZnIn 2 S 4 , was successfully synthesized with a unique hierarchical structure, which provides plenty of accessible adsorption/photocatalytic sites with a high light-harvesting rate (by multiple reflections). The experimental results show that optimized InVO 4 /ZnIn 2 S 4 (5-IV/ZIS) has superior removal performance, whose adsorption-photocatalytic synergistic removal of tetracycline (TET) can reach 69.31 % after 15 min and 90.69 % after 45 min. Based on the analysis of the mechanism, the excellent removal performance can be attributed to the adsorption of the target onto the material by hydrogen bonding, followed by the degradation of the adsorbed target by active substances ( h + > O 2 •− > e - > 1 O 2 > • OH) generated by the S-scheme heterojunction. In addition, the possible pathways for the photocatalytic removal of TET on 5-IV/ZIS were investigated by HPLC-MS analysis. T.E.S.T. and E. coli inhibition experiments demonstrated a significant reduction in the toxicity of TET after the photocatalytic reaction. In conclusion, the novel multifunctional photocatalyst 5-IV/ZIS prepared in this study can be used for the efficient treatment of organic compounds in wastewater with a bright application prospect.

研究领域: 环境科学 · 材料科学 · 生物学
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INTERNATIONAL JOURNAL OF HYDROGEN ENERGY · 2025 · IF 8.3

Interfacial charge transfer via Mo–S bonds in MoSe2/Mn0.5Cd0.5S S-scheme heterojunction for efficient photocatalytic H2 evolution

Jingting Sun,Shangshang Wang,Xingyu Liu,Huan Yu,Jiaming Li,Chao Liu,Qinfang Zhang,Zhigang Zou

Photocatalytic hydrogen production (PHE) technology has emerged as a sustainable approach to convert solar energy into hydrogen energy, exhibiting significant potential for clean energy applications. In this study, an ultrasonic-assisted method was adopted to fabricate S-scheme MoSe 2 /Mn 0.5 Cd 0.5 S (MoSe 2 /MCS) composites, where intimate heterostructures are formed through interfacial Mo–S bonds between MCS and MoSe 2 . The atomic-level Mo–S bonds establish charge transport pathways and enable directional control of charge transfer. The as-constructed S-scheme MoSe 2 /MCS photocatalysts exhibit two critical advantages: enhanced charge carrier separation rate and improved overall redox capacity. Under visible-light irradiation, the MoSe 2 /MCS composites significantly outperform pure MCS in PHE performance. The optimal 5-MoSe 2 /MCS composite demonstrates the superior PHE activity, achieving an apparent quantum yield value of 71.16 % at 400 nm and remarkable photocatalytic stability. Key characterization techniques, including (solution-based) time-resolved photoluminescence technique, theoretical calculation, photoelectrochemical measurements, were employed to elucidate the positive correlation between ion-carrier interaction and charge separation efficiency, thereby enhancing the PHE performance. Based on experimental analysis and theoretical calculation, a plausible PHE mechanism for the S-scheme MCS composites is revealed and discussed in detail. These findings provide valuable insights for designing high-efficiency S-scheme heterostructured composites with interfacial chemical bonds.

研究领域: 材料科学 · 物理化学 · 纳米催化 · 能源材料 · 光催化
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JOURNAL OF ALLOYS AND COMPOUNDS · 2025 · IF 6.3

Interface-engineered CdZnS/PDI S-scheme photocatalyst with synergistic effects for enhanced hydrogen production

Wei Cai,Jincheng Liu,Zewei Liao,Yijun Luo,Xiaoyan Xiang,Bingjie Li,Wenxin Yang,Yanxiong Fang

Overcoming limited charge separation and inefficient solar utilization remains critical for photocatalytic hydrogen evolution. This study addresses these challenges by constructing an organic-inorganic composite photocatalyst by integrating CdZnS nanoparticles with perylene-3,4,9,10-tetracarboxylic diimide (PDI) nanosheets via controlled assembly. Optimizing the PDI content yielded a remarkable hydrogen evolution rate of 7.09 mmol·g −1 ·h −1 under visible light irradiation, representing a 2.3-fold enhancement over pristine CdZnS. This superior photocatalytic performance originates from synergistic effects: exceptional light harvesting by PDI supramolecular structures, enhanced charge mobility via π-π conjugation pathways, and efficient charge separation with high redox potential preservation enabled by the S-scheme heterojunction mechanism. This work establishes a strategic paradigm for developing high-efficiency heterojunction photocatalysts through rational interface engineering.

研究领域: 光催化 · 材料科学 · 纳米技术 · 能量转换 · 环境科学
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