On the importance of correcting for the uncompensated Ohmic resistance in model experiments of the Oxygen Reduction Reaction

被引:185
作者
van der Vliet, Dennis [1 ,2 ]
Strmcnik, Dusan S. [2 ]
Wang, Chao [2 ]
Stamenkovic, Vojislav R. [2 ]
Markovic, Nenad M. [2 ]
Koper, Marc T. M. [1 ]
机构
[1] Leiden Univ, Leiden Inst Chem, NL-2300 RA Leiden, Netherlands
[2] Argonne Natl Lab, Div Mat Sci, Argonne, IL 60439 USA
关键词
Ohmic drop; Oxygen Reduction Reaction; Voltammetry; Rotating disk electrode; SINGLE-CRYSTAL; FUEL-CELLS; ELECTRODE; SURFACES; CATALYSTS; ALLOY; DROP; DISK; ELECTROCATALYSTS; NANOPARTICLES;
D O I
10.1016/j.jelechem.2010.05.016
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
When measuring the current due to the Oxygen Reduction Reaction (ORR) and hydrogen oxidation reaction (HOR) on Pt and Pt alloys in aqueous electrolyte, it is important to take care of two major sources of error that are relatively easy to correct for. First, when measuring ORR voltammetry, adsorption processes are superimposed on the current. Second, the system resistance causes an Ohmic drop that may have a profound effect on the measured curves, especially at the higher currents close to the diffusion limiting current. More importantly, we show that it also influences the kinetic part of the potential curve in such a way that the Tafel slope may be determined incorrectly when failing to correct for Ohmic drop. Finally, because electrolyte resistance lowers with increasing temperature, failure to compensate for Ohmic drop may lead to erroneous conclusions about the temperature-dependent activity of a catalyst as well as the corresponding activation energies. (C) 2010 Elsevier B.V. All rights reserved.
引用
收藏
页码:29 / 34
页数:6
相关论文
共 44 条
[1]   Specificity of the kinetics of H2, evolution to the structure of single-crystal Pt surfaces, and the relation between opd and upd H [J].
Barber, J ;
Morin, S ;
Conway, BE .
JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 1998, 446 (1-2) :125-138
[4]   THE KINETICS OF THE HYDROGEN EVOLUTION REACTION AT HIGH CURRENT DENSITIES [J].
BOCKRIS, JO ;
AZZAM, AM .
TRANSACTIONS OF THE FARADAY SOCIETY, 1952, 48 (02) :145-160
[5]   RECENT DEVELOPMENTS IN THE STUDY OF HYDROGEN OVERPOTENTIAL [J].
BOCKRIS, JO .
CHEMICAL REVIEWS, 1948, 43 (03) :525-577
[6]   Oxygen reduction activity of Pt and Pt-Mn-Co electrocatalysts sputtered on nano-structured thin film support [J].
Bonakdarpour, Arman ;
Stevens, Krystal ;
Vernstrom, George D. ;
Atanasoski, Radoslav ;
Schmoeckel, Alison K. ;
Debe, Mark K. ;
Dahn, Jeff R. .
ELECTROCHIMICA ACTA, 2007, 53 (02) :688-694
[7]   ELECTROANALYTICAL CONTROLLED-POTENTIAL INSTRUMENTATION [J].
BOOMAN, GL ;
HOLBROOK, WB .
ANALYTICAL CHEMISTRY, 1963, 35 (12) :1793-&
[8]   Enhanced activity for oxygen reduction reaction on "Pt3CO" nanoparticles:: Direct evidence of percolated and sandwich-segregation structures [J].
Chen, Shuo ;
Ferreira, Paulo J. ;
Sheng, Wenchao ;
Yabuuchi, Naoaki ;
Allard, Lawrence F. ;
Shao-Horn, Yang .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2008, 130 (42) :13818-13819
[9]   Electrocatalytic reduction of oxygen by FePt alloy nanoparticles [J].
Chen, Wei ;
Kim, Jaemin ;
Sun, Shonheng ;
Chen, Shaowei .
JOURNAL OF PHYSICAL CHEMISTRY C, 2008, 112 (10) :3891-3898
[10]   OHMIC DROP DISTORTION OF ANODIC STRIPPING CURVES FROM A THIN MERCURY-FILM ELECTRODE [J].
DEVRIES, WT ;
VANDALEN, E .
JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 1966, 12 (01) :9-&