Effect of carbon precursor and initial pH on cobalt-doped carbon xerogel for oxygen reduction

被引:18
|
作者
Abidin, Azim Fitri Zainul [1 ]
Loh, Kee Shyuan [1 ]
Wong, Wai Yin [1 ]
Mohamad, Abu Bakar [1 ,2 ]
Puspasari, Ifa [3 ]
机构
[1] Univ Kebangsaan Malaysia, Fuel Cell Inst, Ukm Bangi 43600, Selangor, Malaysia
[2] Univ Kebangsaan Malaysia, Dept Chem & Proc Engn, Fac Engn & Built Environm, Ukm Bangi 43600, Selangor, Malaysia
[3] Univ Islam Indonesia, Dept Chem Engn, Jl Kaliurang KM 14,5 Sleman, Yogyakarta 55584, Indonesia
关键词
Carbon xerogel; Cobalt doping; Oxygen reduction reaction; Catalyst; FUEL-CELL; COSE2; NANOPARTICLES; AEROGELS; ELECTROCATALYST; CATALYSTS; PERFORMANCE; POWER; IRON; GELS;
D O I
10.1016/j.ijhydene.2018.05.015
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
In this study, cobalt-doped carbon xerogel (Co-CX) was synthesised via sol-gel polymerisation of phenolic compounds (i.e., resorcinol, phenol and m-cresol) and formaldehyde, and this polymerisation was catalysed by cobalt nitrate and followed by a carbonisation process. The effect of the initial pH value (5.5, 6.5 and 7.5) as well as the type of carbon precursors on the structural properties of Co-CX was investigated via field emission scanning electron microscope (FESEM), Brunauer-Emmett-Teller (BET) and X-ray diffractometry (XRD). The catalytic activity of Co-CX for the oxygen reduction reaction (ORR) in 0.1 M KOH was studied using a rotating ring-disk electrode (RRDE) technique. The structural properties and ORR activities were affected by different initial pH values as well as the type of carbon precursor. A carbon precursor consisting of resorcinol-formaldehyde with an initial pH value of 7.5 exhibited the best catalytic activity. The initial pH plays an important role in promoting micro/mesopores. The FESEM and BET results revealed that Co doping promotes the formation of additional pores. The RRDE result indicated that Co-CX exhibited good catalytic activity that tends to favour a four-electron pathway. (C) 2018 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:11047 / 11055
页数:9
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