催化作用
质子交换膜燃料电池
碱性燃料电池
甲醇
金属有机骨架
无机化学
热重分析
钴
电解质
电化学
沸石咪唑盐骨架
化学
咪唑酯
化学工程
材料科学
电极
有机化学
物理化学
工程类
吸附
作者
Williane da Silva Freitas,Barbara Mecheri,Carmelo Lo Vecchio,Irene Gatto,Vincenzo Baglio,Valerio C.A. Ficca,Atanu Patra,E. Placidi,Alessandra D’Epifanio
标识
DOI:10.1016/j.jpowsour.2022.232135
摘要
Metal-organic frameworks were used as metal-nitrogen-carbon templates to synthesize Co–N–C catalysts through a facile synthesis approach that combined a cobalt-based zeolitic imidazolate framework (ZIF) structure and conductive carbon support. The spectroscopic, structural, and thermogravimetric analysis confirmed the synthesis of the Co-based ZIF, used to prepare catalysts with different ZIF/carbon support ratios by pyrolysis under inert atmosphere. Electrochemical characterization at alkaline pH demonstrated high activity towards oxygen reduction reaction (ORR). In addition to ORR activity, the Co–N–C electrocatalysts showed high methanol tolerance in the preliminary tests in a half-cell configuration. When assembled at the cathode side of both a hydrogen-fed anion exchange membrane fuel cell and an alkaline direct methanol fuel cell (ADMFC), the Co–N–C electrocatalysts showed competitive performance with the state-of-the-art Pt/C and other platinum-group-metal-free materials, using a FUMASEP® FAA-3-50 membrane. Exceptionally high performance (higher than 45 mW cm−2) was achieved in ADMFC fed with high methanol concentration (up to 10 M), due to the high methanol tolerance of Co–N–C electrocatalysts. Normalizing the performance to Pt loading, a value of 31.0 mW mgPt−1 was obtained, which is the highest power up to now recorded with this kind of membrane and one of the highest values in the literature for ADMFCs.
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