Ligand-variable metal clusters charge transfer in Ce-Por-MOF/AgNWs and their application in photoelectrochemical sensing of ronidazole

A photoelectrochemical sensing platform based on ligand-variable metal clusters charge transfer was established for the quantitative assay of ronidazole (RNZ) using Ce-porphyrin-metal–organic frameworks/silver nanowires (Ce-Por-MOFs/AgNWs). Rod-like Ce-Por-MOFs and well-dispersed sub-50 nm AgNWs wer...

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Veröffentlicht in:Mikrochimica acta (1966) 2022-10, Vol.189 (10), p.383-383, Article 383
Hauptverfasser: Kang, Jinsheng, Ma, Xionghui, Wu, Yuwei, Pang, Chaohai, Li, Shuhuai, Li, Jianping, Xiong, Yuhao, Luo, Jinhui, Wang, Mingyue, Xu, Zhi
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container_issue 10
container_start_page 383
container_title Mikrochimica acta (1966)
container_volume 189
creator Kang, Jinsheng
Ma, Xionghui
Wu, Yuwei
Pang, Chaohai
Li, Shuhuai
Li, Jianping
Xiong, Yuhao
Luo, Jinhui
Wang, Mingyue
Xu, Zhi
description A photoelectrochemical sensing platform based on ligand-variable metal clusters charge transfer was established for the quantitative assay of ronidazole (RNZ) using Ce-porphyrin-metal–organic frameworks/silver nanowires (Ce-Por-MOFs/AgNWs). Rod-like Ce-Por-MOFs and well-dispersed sub-50 nm AgNWs were prepared using a hydrothermal method and polyol strategy, and then through simple drop coating to yield Ce-Por-MOFs/AgNWs nanocomposites. We investigated the intrinsic semiconducting properties of the composites. More importantly, it was found that the variable-valence metal node can provide electronic defect states similar to those caused by multi-metal doping, synergizing with the surface plasmon effect of AgNWs, which significantly improved the photoelectric conversion efficiency, thereby resulting in excellent optoelectronic properties. In combination with molecular imprinting, a competitive type trace photoelectrochemical sensor for RNZ was constructed using Fe 2+ as the electron donor and probe. Under optimal conditions, the sensor response is proportional to the logarithm of RNZ concentration in the range 0.1–104 nM with a detected limit of 0.038 nM. The recoveries ranged from 87.2 to 116% with relative standard deviations (RSDs) 
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Rod-like Ce-Por-MOFs and well-dispersed sub-50 nm AgNWs were prepared using a hydrothermal method and polyol strategy, and then through simple drop coating to yield Ce-Por-MOFs/AgNWs nanocomposites. We investigated the intrinsic semiconducting properties of the composites. More importantly, it was found that the variable-valence metal node can provide electronic defect states similar to those caused by multi-metal doping, synergizing with the surface plasmon effect of AgNWs, which significantly improved the photoelectric conversion efficiency, thereby resulting in excellent optoelectronic properties. In combination with molecular imprinting, a competitive type trace photoelectrochemical sensor for RNZ was constructed using Fe 2+ as the electron donor and probe. Under optimal conditions, the sensor response is proportional to the logarithm of RNZ concentration in the range 0.1–104 nM with a detected limit of 0.038 nM. The recoveries ranged from 87.2 to 116% with relative standard deviations (RSDs) &lt; 6.5% ( n  = 3) in milk sample. This work reveals the charge-transfer process of variable-valence metal nodes in MOFs during photoelectrochemical processes, which will provide new insights for the sensing application of variable-valence metal MOFs. 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Rod-like Ce-Por-MOFs and well-dispersed sub-50 nm AgNWs were prepared using a hydrothermal method and polyol strategy, and then through simple drop coating to yield Ce-Por-MOFs/AgNWs nanocomposites. We investigated the intrinsic semiconducting properties of the composites. More importantly, it was found that the variable-valence metal node can provide electronic defect states similar to those caused by multi-metal doping, synergizing with the surface plasmon effect of AgNWs, which significantly improved the photoelectric conversion efficiency, thereby resulting in excellent optoelectronic properties. In combination with molecular imprinting, a competitive type trace photoelectrochemical sensor for RNZ was constructed using Fe 2+ as the electron donor and probe. Under optimal conditions, the sensor response is proportional to the logarithm of RNZ concentration in the range 0.1–104 nM with a detected limit of 0.038 nM. The recoveries ranged from 87.2 to 116% with relative standard deviations (RSDs) &lt; 6.5% ( n  = 3) in milk sample. This work reveals the charge-transfer process of variable-valence metal nodes in MOFs during photoelectrochemical processes, which will provide new insights for the sensing application of variable-valence metal MOFs. 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The recoveries ranged from 87.2 to 116% with relative standard deviations (RSDs) &lt; 6.5% ( n  = 3) in milk sample. This work reveals the charge-transfer process of variable-valence metal nodes in MOFs during photoelectrochemical processes, which will provide new insights for the sensing application of variable-valence metal MOFs. Graphical abstract</abstract><cop>Vienna</cop><pub>Springer Vienna</pub><doi>10.1007/s00604-022-05477-1</doi><tpages>1</tpages><orcidid>https://orcid.org/0000-0001-8554-4928</orcidid></addata></record>
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subjects Analytical Chemistry
Characterization and Evaluation of Materials
Charge transfer
Chemistry
Chemistry and Materials Science
Ligands
Metal clusters
Metal-organic frameworks
Microengineering
Molecular imprinting
Nanochemistry
Nanocomposites
Nanotechnology
Nanowires
Optoelectronics
Original Paper
Photoelectricity
Polyols
Porphyrins
Sensors
Silver
title Ligand-variable metal clusters charge transfer in Ce-Por-MOF/AgNWs and their application in photoelectrochemical sensing of ronidazole
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