Phuong Thao Dao Vu, Dien Nguyen Dac, Tam Phuong Dinh
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引用次数: 0
Abstract
This work studies gold nanoparticle (AuNP) nucleation and growth mechanism from deep eutectic solvent (DES)-based choline chloride and glycerol (glyceline) onto glassy carbon electrode (GCE) and its application for DNA biosensor. Investigation of the current density transients indicated that the AuNPs were formed by the simultaneous presence of Au diffusion-controlled 3D nucleation and growth and residual water reaction over the Au nuclei growing surfaces. The AuNP structure was characterized by the field emission scanning electron microscopy, energy dispersive X-ray spectroscopy, and X-ray diffraction. AuNPs were used to fabricate electrochemical DNA sensor. The hybridization was monitored by cyclic voltammetry and electrochemical impedance spectroscopy measurement using potassium ferri/ferrocyanide redox probes \({\left[Fe{(CN)}_{6}\right]}^{3-/4-}\) as the indicator probe. Results show that the biosensor exhibited a linear correlation to the logarithm of the target DNA concentration ranged from 1.10−14 M to 1.10−9 M, and the limit of detection was 1.10−14 M. Furthermore, the findings indicate that the prepared electrode exhibited excellent reproducibility and long-term stability when applied for determining M. tuberculosis samples.
这项工作研究了基于深共晶溶剂(DES)的氯化胆碱和甘油(甘氨酸)在玻璃碳电极(GCE)上的金纳米粒子(AuNP)成核和生长机制及其在 DNA 生物传感器中的应用。对电流密度瞬态的研究表明,AuNPs 是由金扩散控制的三维成核和生长以及金核生长表面的残余水反应同时存在而形成的。场发射扫描电子显微镜、能量色散 X 射线光谱和 X 射线衍射对 AuNP 结构进行了表征。利用 AuNPs 制作了电化学 DNA 传感器。使用铁/铁氰化钾氧化还原探针({left[Fe{(CN)}_{6}\right]}^{3-/4-})作为指示探针,通过循环伏安法和电化学阻抗谱测量来监测杂交。结果表明,该生物传感器与目标 DNA 浓度的对数在 1.10-14 M 到 1.10-9 M 之间呈现线性相关,检测限为 1.10-14 M。
期刊介绍:
The Journal of Solid State Electrochemistry is devoted to all aspects of solid-state chemistry and solid-state physics in electrochemistry.
The Journal of Solid State Electrochemistry publishes papers on all aspects of electrochemistry of solid compounds, including experimental and theoretical, basic and applied work. It equally publishes papers on the thermodynamics and kinetics of electrochemical reactions if at least one actively participating phase is solid. Also of interest are articles on the transport of ions and electrons in solids whenever these processes are relevant to electrochemical reactions and on the use of solid-state electrochemical reactions in the analysis of solids and their surfaces.
The journal covers solid-state electrochemistry and focusses on the following fields: mechanisms of solid-state electrochemical reactions, semiconductor electrochemistry, electrochemical batteries, accumulators and fuel cells, electrochemical mineral leaching, galvanic metal plating, electrochemical potential memory devices, solid-state electrochemical sensors, ion and electron transport in solid materials and polymers, electrocatalysis, photoelectrochemistry, corrosion of solid materials, solid-state electroanalysis, electrochemical machining of materials, electrochromism and electrochromic devices, new electrochemical solid-state synthesis.
The Journal of Solid State Electrochemistry makes the professional in research and industry aware of this swift progress and its importance for future developments and success in the above-mentioned fields.