Evaluation of Alkylamine Modified Pt Nanoparticles as Oxygen Reduction Reaction Electrocatalyst for Fuel Cells via Electrochemical Impedance Spectroscopy

被引:22
|
作者
Joshi, Prerna [1 ]
Okada, Toshihiko [1 ]
Miyabayashi, Keiko [1 ]
Miyake, Mikio [2 ]
机构
[1] Shizuoka Univ, Grad Sch Integrated Sci & Technol, Dept Engn, Shizuoka 4328561, Japan
[2] Univ Technol Malaysia, Malaysia Japan Int Inst Technol, Dept Environm Engn & Green Technol, Kuala Lumpur 54100, Malaysia
关键词
DOUBLE-LAYER CAPACITANCE; PLATINUM NANOPARTICLES; CATHODE CATALYST; CHARGE-TRANSFER; PT(111); ELECTRODES; OXIDATION; MECHANISM; KINETICS; MODEL;
D O I
10.1021/acs.analchem.8b00247
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Organically (octyl amine, OA) surface modified electrocatalyst (OA-Pt/CB) was studied for its oxygen reduction reaction (ORR) activity via dc methods and its charge and mass transfer properties were studied via electrochemical impedance spectroscopy (EIS). Comparison with a commercial catalyst (TEC10V30E) with similar Pt content was also carried out. In EIS, both the catalysts showed a single time-constant with an emerging high-frequency semicircle of very small diameter which was fitted using suitable equivalent circuits. The organically modified catalyst showed lower charge-transfer resistance and hence, low polarization resistance in high potential region as compared to the commercial catalyst. The dominance of kinetic processes was observed at 0.925-1.000 V, whereas domination of diffusion based processes was observed at lower potential region for the organic catalyst. No effect due to the presence of carbon was observed in the EIS spectra. Using the hydrodynamic method, higher current penetration depth was obtained for the organically modified catalyst at 1600 rpm. Exchange current density and Tafel slopes for both the electrocatalysts were calculated from the polarization resistance obtained from EIS which was in correlation with the results obtained from dc methods.
引用
收藏
页码:6116 / 6123
页数:8
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