g-C3N4/g-C3N5纳米片异质结光催化剂增强抗生素的光降解和抗菌活性

IF 4.3 3区 化学 Q2 CHEMISTRY, MULTIDISCIPLINARY
ACS Omega Pub Date : 2025-09-16 DOI:10.1021/acsomega.5c04579
Aslisha Champati, , , Pratyush Kumar Sahu, , , Alaka Rath, , , Brundabana Naik*, , and , Abanti Pradhan*, 
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引用次数: 0

摘要

通过热聚合和kbr辅助剥离,设计了一种有机C-N聚合物纳米复合材料g-C3N4/g-C3N5 (ECN45),研究了其作为光催化剂光降解有机抗生素污染物和抗菌活性的潜力。石墨化氮化碳(g-C3N4)是一种二维材料,被认为是一种很有前途的光催化剂;然而,它具有较高的光生电子-空穴对复合频率,并且对可见光的吸收范围窄至450 nm。因此,在g-C3N4上形成1D g-C3N5异质结可以使g-C3N4的电荷复合最小化。此外,由于缺乏足够的表面活化,体复合材料(BCN45)暴露于KBr剥离,导致g-C3N4/g-C3N5薄片(ECN45)。由于偶氮键和π共轭键的存在,与原始元素相比,该1D/2D杂化催化剂的带隙减小了1.81 eV。与原始形式相比,纳米复合材料显示出向可见光光谱的红移。通过TEM, SEM-EDX, BET, XRD, UVDRS, FTIR, XPS, PL和电化学分析技术对纳米复合材料的形态,光谱和物理化学研究进行了证实。在pH为3的酸性环境下,最低浓度为10 mg L-1,降解时间为120 min,降解率约为93.1%。进一步,通过抑菌区试验、MIC(最低抑菌浓度)和微生物体光催化细胞渗漏,考察催化剂对革兰氏阴性菌大肠杆菌(E. coli)和革兰氏阳性菌金黄色葡萄球菌(S. aureus)的抑菌作用。此外,还解释了形成的2D/1D异质结构对CIP降解和抗菌活性所表现出的合理的Z-scheme机制。增强的光活性归因于一维/二维杂化纳米结构的协同效应,扩展共轭导致丰富的光收获,以及z -图式异质结使光生电荷分离更好。该方法为建立具有高效光催化活性的有效无金属复合材料奠定了基础。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Enhanced Photodegradation of Antibiotics and Antimicrobial Activity by a g-C3N4/g-C3N5 Nanosheet Heterojunction Photocatalyst

An organic C–N polymeric nanocomposite, g-C3N4/g-C3N5 sheet (ECN45), was designed through thermal polymerization, followed by KBr-assisted exfoliation, to investigate its potential as a photocatalyst for the photodegradation of organic antibiotic pollutants and antimicrobial activities. Graphitic carbon nitride (g-C3N4) is a 2D material recognized as a highly promising photocatalyst; however, it possesses an elevated frequency of photogenerated electron–hole pair recombination and a constricted absorption range for visible light of up to 450 nm. Therefore, the formation of a heterojunction of 1D g-C3N5 upon g-C3N4 can minimize the charge recombination of g-C3N4. Furthermore, due to a lack of sufficient surface activation, the bulk composite (BCN45) was exposed to KBr exfoliation, resulting in a g-C3N4/g-C3N5 sheet (ECN45). The 1D/2D hybrid catalyst exhibits a reduction in band gap of up to 1.81 eV due to the presence of azo linkages and π-conjugated bonds compared to its pristine elements. The nanocomposite shows a red shift toward the visible light spectrum compared to its pristine forms. The morphological, spectroscopic, and physicochemical investigations of the nanocomposite are confirmed by TEM, SEM-EDX, BET, XRD, UVDRS, FTIR, XPS, PL, and electrochemical analysis techniques. The photocatalytic application is shown by the composite for degrading the antibiotic CIP (ciprofloxacin) for about 93.1% at an acidic environment of pH 3 at its lowest concentration of 10 mg L–1 in 120 min. Further, the catalyst is examined to show antimicrobial action against Gram-negative bacteria Escherichia coli (E. coli) and Gram-positive bacteria Staphylococcus aureus (S. aureus) with the help of the inhibition zone test, MIC (minimum inhibition concentration), and photocatalytic cellular leakage of the microbial body. Also, the plausible Z-scheme mechanisms exhibited by the formed 2D/1D heterostructure for CIP degradation and antimicrobial activity are explained. The enhanced photoactivity is attributed to the synergistic effects of 1D/2D hybrid nanostructure, extended conjugation leading to enriched light harvesting, and Z-scheme heterojunction for better photogenerated charge separation. This approach makes grounds to establish an effective metal-free composite showing efficient photocatalytic activity.

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来源期刊
ACS Omega
ACS Omega Chemical Engineering-General Chemical Engineering
CiteScore
6.60
自引率
4.90%
发文量
3945
审稿时长
2.4 months
期刊介绍: ACS Omega is an open-access global publication for scientific articles that describe new findings in chemistry and interfacing areas of science, without any perceived evaluation of immediate impact.
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