RRDE experiments on noble-metal and noble-metal-free catalysts: Impact of loading on the activity and selectivity of oxygen reduction reaction in alkaline solution

被引:87
作者
Zhang, Gaixia [1 ]
Wei, Qiliang [1 ]
Yang, Xiaohua [1 ]
Tavares, Ana C. [1 ]
Sun, Shuhui [1 ]
机构
[1] Inst Natl Rech Sdentif INRS Enengie, Mat & Thecommunicat, 1650 Blvd Lionel Boulet, Varennes J3X IS2, PQ, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
Oxygen reduction reaction; Rotating ring-disk electrode; Catalyst loading; Hydrogen peroxide selectivity; Electron transfer number; HYDROGEN-PEROXIDE; AIR BATTERIES; DISK ELECTRODE; H2O2; RELEASE; ELECTROCATALYSTS; PERFORMANCE; CARBON; DENSITY; IRON; ELECTROREDUCTION;
D O I
10.1016/j.apcatb.2017.01.001
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Oxygen reduction reaction (ORR) is at the core of various applications, such as fuel cells, metal-air batteries and H2O2 electro-generation. Depending on the targeted application, catalysts that follow a "direct four-electron (4e(-))" pathway or "two-electron (2e(-))" pathway are envisaged. We have systematically investigated the impact of the electrocatalyst loading on the rotating ring-disk electrode (RRDE), on their activity and selectivity towards ORR in alkaline medium (0.1 M and 1M KOH). Four representative catalysts, including a noble metal catalyst (commercial 20 wt% Pt/C, ETEK), metal-free catalysts (Printex carbon black and graphene), and non-noble metal catalyst (Fe/N/C), were selected because they exhibit different behaviours for ORR following a "direct four-electron (4e-)" pathway, "two-electron (2e-)" pathway, or a "series 2e(-) + 2e(-)" pathway. The results confirmed that the catalyst loading influences the activity and the selectivity of the catalysts, with lower loadings favoring the H2O2 electrogeneration, and researchers should pay attention to it. Moreover, in order to make possible comparison between results coming from different research groups, we recommend reasonable loading ranges for each type of catalyst. (C) 2017 Elsevier B.V. All rights reserved.
引用
收藏
页码:115 / 126
页数:12
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