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结合电子电容器的固体接触离子选择电极进行快速恒电位电容测量。

Rapid Constant Potential Capacitive Measurements with Solid-Contact Ion-Selective Electrodes Coupled to Electronic Capacitor.

作者信息

Kraikaew Pitchnaree, Sailapu Sunil Kumar, Bakker Eric

机构信息

Department of Inorganic and Analytical Chemistry, University of Geneva, Quai Ernest-Ansermet 30, CH-1211 Geneva, Switzerland.

Instituto de Microelectrónica de Barcelona, IMB-CNM (CSIC), C/del Til·lers, Campus UAB, 08193 Bellaterra, Barcelona, Spain.

出版信息

Anal Chem. 2020 Oct 20;92(20):14174-14180. doi: 10.1021/acs.analchem.0c03254. Epub 2020 Sep 30.

DOI:10.1021/acs.analchem.0c03254
PMID:32940460
Abstract

A constant potential capacitive readout of solid-contact ion-selective electrodes (SC-ISE) allows one to obtain easily identifiable current transients that can be integrated to obtain a charge vs logarithmic activity relationship. The resulting readout can therefore be much more sensitive than traditional open-circuit potentiometry. Unfortunately, however, comparatively long measurement times and significant baseline current drifts make it currently difficult to fully realize the promise of this technique. We show here that this challenge is overcome by placing the SC-ISE in series with an electronic capacitor, with pH probes as examples. Kirchhoff's law is shown to be useful to choose an adequate range of added capacitances so that it dominates the overall cell value. Two different ion-to-electron transducing materials, functionalized single-wall carbon nanotubes (f-SWCNTs) and poly(3-octylthiophene) (POT), were explored as solid-contact transducing layers. The established SC-ISE-based f-SWCNT transducer is found to be compatible with a wide range of external capacitances up to 100 μF, while POT layers require a narrower range of 1-4.7 μF. Importantly, the time for a charging transient to reach equilibrium was found to be less than 10 s, which is dramatically faster than without added electronic component. Owing to the ideal behavior of capacitor, the response current decays rapidly to zero, making the determination of the integrated charge practically applicable.

摘要

固体接触离子选择电极(SC-ISE)的恒电位电容读出方式能够让人获得易于识别的电流瞬变信号,这些信号经积分后可得到电荷与对数活度的关系。因此,所得的读出结果可能比传统的开路电位分析法更为灵敏。然而,不幸的是,相对较长的测量时间和显著的基线电流漂移使得目前难以充分实现该技术的前景。我们在此表明,以pH探头为例,将SC-ISE与一个电子电容器串联可克服这一挑战。结果表明,基尔霍夫定律有助于选择合适的附加电容范围,以便其在整个电池值中占主导地位。研究了两种不同的离子-电子转换材料,即功能化单壁碳纳米管(f-SWCNT)和聚(3-辛基噻吩)(POT)作为固体接触转换层。已建立的基于SC-ISE的f-SWCNT传感器被发现与高达100 μF的广泛外部电容兼容,而POT层所需的电容范围较窄,为1-4.7 μF。重要的是,发现充电瞬变达到平衡的时间小于10秒,这比不添加电子元件时要快得多。由于电容器的理想特性,响应电流迅速衰减至零,使得积分电荷的测定切实可行。

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