摘要
用改良Hummers法和碳热还原法分别制备了石墨烯和碳化钴钼。用透射电镜(TEM)、扫描电子显微镜(SEM)和X射线衍射仪(XRD)表征了材料的形貌和结构。用循环伏安(CV)表征了其氧还原(ORR)催化性能,结果表明,复合材料的氧还原峰电流和起峰电位均大大优于单一材料。旋转圆盘电极(RDE)实验表明复合材料的氧还原反应为高效的四电子转移过程。含有6 mg·cm^(-2)石墨烯/碳化钴钼复合材料作为阴极催化剂的微生物燃料电池(MFCs)最大功率密度为418 mW·m^(-2),达到商业铂碳的68.3%。因此,廉价的石墨烯/碳化钴钼复合材料作为MFCs阴极氧还原催化剂具有巨大的应用潜力。
Graphene and Co-Mo carbide were prepared by a modified Hummers' method and carbothermal reduction,respectively. The morphologies of the materials were studied using transmission electron microscopy( TEM) and scanning electron microscopy( SEM),and the structures were characterized using X-ray diffraction( XRD). The electrocatalytic activities of the materials for oxygen reduction were measured by cyclic voltammetry( CV). The results revealed that a graphene /Co-Mo carbide composite exhibited better electrocatalytic activity towards oxygen reduction than pure graphene or Co-Mo carbide,with a higher oxygen reduction peak current and greater positive onset potential. The rotating disk electrode( RDE) test revealed that the oxygen reduction reaction in the graphene / Co-Mo carbide composite proceeded via an efficient four-electron transfer process. A microbial fuel cell( MFC) assembled using 6 mg·cm^(-2)of the graphene / Co-Mo carbide composite as a catalytic cathode delivered a power density of 418 m W·m-2,which was 68. 3% of the value of an MFC using a Pt/C-catalyst cathode,meaning inexpensive graphene / Co-Mo carbide composites have great potential for application as oxygen reduction catalysts in MFC cathodes.
作者
郭文显
陈妹琼
张敏
柳鹏
张燕
蔡志泉
程发良
GUO Wenxian CHEN Meiqiong ZHANG Min LIU Peng ZHANG Yan CAI Zhiquan CHENG Faliang(Dongguan Key Laboratory of Green Energy,Department of City and Environment Science, City College of Dongguan University of Technology,Dongguan 523419, China Guangdong Engineering and Technology Research Center for Advanced Nanomaterials, Dongguan University of Technology, Dongguan 523808, China)
出处
《环境工程学报》
CAS
CSCD
北大核心
2016年第11期6529-6535,共7页
Chinese Journal of Environmental Engineering
基金
国家自然科学基金资助项目(21505019
21475022
21375016)
东莞市科技计划项目(2014106101020
2014106101022
2012108101016)