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基于原始赤铁矿纳米阵列的过氧化氢光电化学传感及机理研究

Photoelectrochemical sensing and mechanism investigation of hydrogen peroxide using a pristine hematite nanoarrays.

作者信息

Lv Jiaqi, Fan Ming, Zhang Ling, Zhou Qian, Wang Li, Chang Zhixian, Chong Ruifeng

机构信息

Henan Joint International Research Laboratory of Environmental Pollution Control Materials, Henan Provincial Engineering Research Center of Green Anticorrosion Technology for Magnesium Alloys, College of Chemistry and Chemical Engineering, Henan University, Kaifeng, 475004, China.

Henan Joint International Research Laboratory of Environmental Pollution Control Materials, Henan Provincial Engineering Research Center of Green Anticorrosion Technology for Magnesium Alloys, College of Chemistry and Chemical Engineering, Henan University, Kaifeng, 475004, China.

出版信息

Talanta. 2022 Jan 15;237:122894. doi: 10.1016/j.talanta.2021.122894. Epub 2021 Oct 2.

Abstract

In this paper, a facile hydrothermal combined with subsequent two-step post-calcination method was used to fabricate hematite (α-FeO) nanoarrays on fluorine-doped SnO glass (FTO). The morphology, crystalline phase, optical property and surface chemical states of the fabricated α-FeO photoelectrode were characterized by scanning electron microscopy, X-ray diffraction, ultraviolet visible spectroscopy and X-ray photoelectron spectroscopy correspondingly. The α-FeO photoelectrode exhibits excellent photoelectrochemical (PEC) response toward hydrogen peroxide (HO) in aqueous solutions, with a low detection limit of 20 μM (S/N = 3) and wide linear range (0.01-0.09, 0.3-4, and 6-16 mM). Additionally, the α-FeO photoelectrode shows satisfying reproducibility, stability, selectivity and good feasibility for real samples. Mechanism analysis indicates, comparing with HO, HO possesses much more fast reaction kinetics over α-FeO surface, thus the recombination of photogenerated charges are reduced, followed by much more photogenerated electrons are migrated to the counter electrode via external circuit. The insight on the enhanced photocurrent, which is corelative to the concentration of HO in aqueous solution, will stimulate us to further optimize the surface structure of α-FeO to gain highly efficient α-FeO based sensors.

摘要

本文采用简便的水热法结合后续两步煅烧方法,在氟掺杂的SnO玻璃(FTO)上制备赤铁矿(α-Fe₂O₃)纳米阵列。通过扫描电子显微镜、X射线衍射、紫外可见光谱和X射线光电子能谱分别对制备的α-Fe₂O₃光电极的形貌、晶相、光学性质和表面化学状态进行了表征。α-Fe₂O₃光电极在水溶液中对过氧化氢(H₂O₂)表现出优异的光电化学(PEC)响应,检测限低至20 μM(信噪比=3),线性范围宽(0.01 - 0.09、0.3 - 4和6 - 16 mM)。此外,α-Fe₂O₃光电极对实际样品具有良好的重现性、稳定性、选择性和可行性。机理分析表明,与H₂O相比,H₂O₂在α-Fe₂O₃表面具有更快的反应动力学,从而减少了光生电荷的复合,更多的光生电子通过外电路迁移到对电极。对与水溶液中H₂O₂浓度相关的增强光电流的深入了解,将促使我们进一步优化α-Fe₂O₃的表面结构,以获得高效的基于α-Fe₂O₃的传感器。

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