Heterointerface engineering is an effective strategy to design and construct high-performance photocatalysts. Herein, polyaniline (PANI) nanoparticles and ZnTi layered double hydroxide (ZnTi-LDH) nanosheets were integrated to form organic-inorganic heterostructure (PANI/LDH) via d-π electronic coupling using in-situ polymerization for photocatalytic oxidation/reduction towards tetracycline (TC) and Cr(VI). The photocatalytic activity was closely related to feed amount of aniline (Ani) in the polymerization process, which the abundant PANI nanoparticles were evenly distributed on the surface of ZnTi-LDH nanosheets at the proper Ani feed amount, and thus reinforced d-π electronic coupling at the organic-inorganic interfaces more efficiently. Density functional theory calculations further verified the existence of d-π overlap at the PANI/LDH heterointerface. The strong d-π coupling boosted charge separation and transfer to improve photocatalytic efficiency. As a result, the optimal PANI/LDH exhibited outstanding photocatalytic activities with 97.8 % Cr(VI) reducing rate and 87.8 % TC removal rate in the single Cr(VI) and TC system, as well as high simultaneous removal rate of Cr(VI) and TC in TC/Cr(VI) coexistence system, respectively. Subsequently, the photocatalytic enhanced mechanisms were put forward to remove Cr(VI) and TC under visible-light. Finally, the aquatic toxicity of the photolytic products was evaluated using Chlorella sp. as an ecological indicator, showing that the PANI/LDH had a notable detoxification efficiency of TC and Cr(VI).
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http://dx.doi.org/10.1016/j.jcis.2025.01.050 | DOI Listing |
Int J Mol Sci
November 2024
Research Group Experimental Pharmacology (EFAR), Center for Neurosciences (C4N), Vrije Universiteit Brussel (VUB), Laarbeeklaan 103, 1090 Brussels, Belgium.
J Environ Sci (China)
March 2024
The Key Lab of Pollution Control and Ecosystem Restoration in Industry Clusters, Ministry of Education, School of Environment and Energy, South China University of Technology, Guangzhou 510006, China. Electronic address:
Amino acids (AAs) including D- and L- enantiomers are a group of organic nitrogen species in ambient aerosol. Due to the low abundances of AAs (level of ng/m) and the matrix effects by coexistent components, it is challenging to quantify AA enantiomers in ambient aerosols especially under pollution conditions. In this study, we present an optimized method for analyzing AA enantiomers in atmospheric aerosol samples including a pretreatment process and the detection by high performance liquid chromatography coupled to a fluorescence detector (HPLC-FLD).
View Article and Find Full Text PDFNucleic Acids Res
April 2023
CSIR-Centre for Cellular and Molecular Biology (CSIR-CCMB), Hyderabad, Telangana 500007, India.
Biosens Bioelectron
February 2022
College of Life Science and Technology, Huazhong University of Science and Technology, Wuhan, 430074, China. Electronic address:
Chiral analysis of amino acids (AAs) is of great importance in medical science due to the distinctive effect of AA isomers on human health. Although various chiral recognition techniques have been developed, the quantitative chiral recognition of low-level AA isomers remains challenging. Here, we combined the fiber optic SPR with an enzyme-substrate recognition mechanism to construct a direct-assay-type chiral AA biosensor.
View Article and Find Full Text PDFInorg Chem
January 2021
MOE Key Laboratory of Bioinorganic and Synthetic Chemistry, School of Chemistry, Sun Yat-sen University, Guangzhou 510275, Guangdong, China.
The postcoordinated interligand-coupling strategy provides a useful and complementary protocol for synthesizing polydentate ligands. Herein, diastereoselective photoreactions of Λ-[Ir(pq)(d-AA)] () and Λ-[Ir(pq)(l-AA)] (, where pq is 2-phenylquinoline and AA is an amino acid) are reported in the presence of O under mild conditions. Diastereomer is dehydrogenatively oxidized into an imino acid complex, while diastereomer mainly occurs via interligand C-N cross-dehydrogenative coupling between quinoline at the C8 position and AA ligands at room temperature, affording Λ-[Ir(pq)(l-pq-AA)].
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