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原位电化学电子顺磁共振波谱法作为探测双电层电容的工具。

In situ electrochemical electron paramagnetic resonance spectroscopy as a tool to probe electrical double layer capacitance.

机构信息

School of Chemistry, University of Manchester, Oxford Road, Manchester, M13 9PL, UK.

School of Pharmacy and Biomolecular Science, Liverpool John Moores University, James Parsons Building, Byrom Street, Liverpool, L3 3AF, UK.

出版信息

Chem Commun (Camb). 2018 Apr 12;54(31):3827-3830. doi: 10.1039/C8CC00450A.

Abstract

Electron paramagnetic resonance (EPR) spectroscopy is applied in situ to monitor the electrochemical capacitance of activated carbon in aqueous solutions, thereby revealing aspects of the charge storage mechanism. The EPR signal of activated carbon increases during the charging process and returns reversibly when discharged. Simulation of the spectral lineshape and its temperature dependence indicate that two kinds of spins exist: spin at defects giving rise to a narrow signal, and spins associated with surface-bound aromatic moieties causing a broad signal. A potential-dependent response of the narrow feature is seen in each of the electrolyte solutions used, while changes of the broad feature occur only at higher electrolyte concentrations. The results suggest that the observed increase of unpaired electron density on activated carbon is due to the formation of radical species due to reduction of functional groups. The potential dependence of the broad feature at higher electrolyte concentrations may be related to the further adsorption of ions into the deep porous structure of activated carbon.

摘要

电子顺磁共振(EPR)光谱学被应用于原位监测活性炭在水溶液中的电化学电容,从而揭示了电荷存储机制的一些方面。在充电过程中,活性炭的 EPR 信号增加,在放电时可恢复性地返回。对谱线形状及其温度依赖性的模拟表明存在两种自旋:缺陷引起的窄信号自旋,以及与表面结合的芳族基团引起的宽信号自旋。在所使用的每种电解质溶液中都观察到窄特征的与电位有关的响应,而宽特征的变化仅在更高的电解质浓度下发生。结果表明,在活性炭上观察到的不成对电子密度的增加是由于官能团还原形成自由基物种所致。在较高电解质浓度下宽特征的电位依赖性可能与离子进一步吸附到活性炭的深多孔结构中有关。

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