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首页> 外文期刊>Journal of Electroanalytical Chemistry: An International Journal Devoted to All Aspects of Electrode Kinetics, Interfacial Structure, Properties of Electrolytes, Colloid and Biological Electrochemistry >Influence of viscosity on chronoamperometry of reversible redox system on rough and nanoparticles deposited Pt electrode: Aqueous/glycerol and RTIL medium
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Influence of viscosity on chronoamperometry of reversible redox system on rough and nanoparticles deposited Pt electrode: Aqueous/glycerol and RTIL medium

机译:粘度对粗糙和纳米颗粒沉积的Pt电极上可逆氧化还原系统计时电流的影响:水性/甘油和RTIL介质

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Recently developed theories allow us to predict expected electrochemical response from quantitative surface texture information obtained from various microscopies. We generalized power spectrum based chronoamperometry theory involving species with unequal diffusion coefficient of electroactive species in presence of uncompensated solution resistance. Chronoamperometric response in two viscous media, like ionic liquid and glycerol, is studied and it shows strong influence of electrode roughness up to longer time scales. Measurements were carried out for two reversible charge transfer systems: (i) solution of Fe(CN)(6)(3-) and Fe(CN)(6)(4-) in 3 M NaNO3 at various compositions of glycerol and (ii) ferrocene in [bmim][BF4] RTIL. Viscous medium induces suppression in growth of diffusion length which allows us to see enhanced and prolonged roughness effect in chronoamperometry. It is found that the enhanced viscosity: (i) induces delay, through enhanced ohmic contribution, in the onset of anomalous regime and (ii) causes dilation in roughness influenced time regime (the enlargement of roughness influenced region). These two effects allow determination of microscopic area from short time chronoamperometric data which is not possible in non viscous aqueous medium. The corrections in the chronoamperometric current for the electric double layer and the random convective flow are also accomplished. (C) 2016 Elsevier B.V. All rights reserved.
机译:最近发展的理论使我们能够根据从各种显微镜获得的定量表面纹理信息来预测预期的电化学响应。我们推广了基于功率谱的计时电流法理论,该理论涉及在不补偿溶液电阻的情况下电活性物质扩散系数不相等的物质。研究了两种粘性介质(如离子液体和甘油)中的计时安培响应,该响应在较长的时间范围内显示出电极粗糙度的强烈影响。对两种可逆电荷转移系统进行了测量:(i)在各种甘油组成下,Fe(CN)(6)(3-)和Fe(CN)(6)(4-)在3 M NaNO3中的溶液和( ii)[bmim] [BF4] RTIL中的二茂铁。粘性介质会抑制扩散长度的增长,这使我们能够看到计时电流法中增强和延长的粗糙度效果。发现增加的粘度:(i)通过增加的欧姆贡献在异常状态的发生中引起延迟,并且(ii)在粗糙度影响的时间范围中引起膨胀(粗糙度影响的区域的扩大)。这两种作用使得可以从短时间计时电流数据确定微观区域,这在非粘性水性介质中是不可能的。还完成了双电层和随机对流的计时电流校正。 (C)2016 Elsevier B.V.保留所有权利。

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