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用于毛细管参比电极的钛支架上的微孔Ag/AgCl

Microporous Ag/AgCl on a Titanium Scaffold for Use in Capillary Reference Electrodes.

作者信息

Robinson Emily E A, Troudt Blair K, Bühlmann Philippe

机构信息

Department of Chemistry, University of Minnesota, 207 Pleasant St. SE, Minneapolis, Minnesota 55455, United States.

出版信息

Anal Chem. 2024 Feb 6;96(5):2236-2243. doi: 10.1021/acs.analchem.3c05382. Epub 2024 Jan 26.

DOI:10.1021/acs.analchem.3c05382
PMID:38277487
Abstract

AgCl-coated silver fabricated with the thermal-electrolytic method can be used to prepare more reproducible reference electrodes than Ag/AgCl prepared with alternative methods such as electrolytic and chemical AgCl deposition or thermal fabrication. However, thermal-electrolytic fabrication requires a scaffold material upon which to build the layers upon. Platinum and rhodium have been used for this purpose as they are mechanically strong and chemically inert, but their cost is prohibitive for wider application. Herein, we report the stability of Ag/AgCl reference electrodes built atop a titanium scaffold using the thermal-electrolytic method and the use of these Ti/Ag/AgCl constructs in capillary-based reference electrodes. Electrochemical characterization shows that the probable presence of small amounts of oxygen at the Ti/Ag interface does not affect the reference electrode performance; in particular, over a wide pH range, the half-cell potential is pH independent. The electrical resistance of the Ti/Ag/AgCl/KCl system is dominated by the charge transfer resistance at the interface of the AgCl to KCl solution but is kept very small by the large AgCl surface area and a high solution concentration of chloride. The resulting high exchange current minimizes the effect of system impurities on the reference half-cell potential. Capillary-based reference electrodes comprising Ti/Ag/AgCl show exceptionally low potential drifts (as low as 0.03 ± 2.01 μV/h) and standard deviations of the potential at or below ±0.5 mV over a 60 h period. These capillary-based reference electrodes are suitable for very small sample volumes while still providing a free-flowing liquid junction that prevents reference electrode contamination.

摘要

采用热电解法制备的涂覆有氯化银的银电极,相较于通过电解和化学氯化银沉积或热制备等其他方法制备的银/氯化银电极,可用于制备重现性更高的参比电极。然而,热电解制备需要一种支架材料来构建各层。铂和铑已被用于此目的,因为它们机械强度高且化学惰性强,但成本过高,无法广泛应用。在此,我们报告了使用热电解法在钛支架上构建的银/氯化银参比电极的稳定性,以及这些钛/银/氯化银结构在毛细管基参比电极中的应用。电化学表征表明,钛/银界面可能存在的少量氧气不会影响参比电极性能;特别是在较宽的pH范围内,半电池电位与pH无关。钛/银/氯化银/氯化钾系统的电阻主要由氯化银与氯化钾溶液界面处的电荷转移电阻决定,但由于氯化银的大表面积和高浓度的氯化物溶液,电阻保持非常小。由此产生的高交换电流使系统杂质对参比半电池电位的影响最小化。包含钛/银/氯化银的毛细管基参比电极在60小时内显示出极低的电位漂移(低至0.03±2.01μV/h),电位的标准偏差在±0.5mV或更低。这些毛细管基参比电极适用于非常小的样品体积,同时仍提供防止参比电极污染的自由流动液接界。

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