直接乙醇燃料电池
塔菲尔方程
化学
甘油
乙醇
质子交换膜燃料电池
甲醇
催化作用
开路电压
碱性燃料电池
离子交换
功率密度
电催化剂
乙醇燃料
核化学
无机化学
电化学
化学工程
离子
生物化学
电极
有机化学
电压
物理化学
功率(物理)
工程类
物理
量子力学
作者
Khalid Zakaria,Matthew R. McKay,Ravikumar Thimmappa,Maksudul Hasan,Mohamed Mamlouk,Keith Scott
标识
DOI:10.1002/celc.201900502
摘要
Abstract The direct oxidation reaction of glycerol (GOR) was studied and compared to that of methanol (MOR) and ethanol (EOR) in both acid and alkaline media using commercial Pt/C, PtRu/C, Pd/C and PdNi/C electrocatalysts. The results show that GOR and MOR in alkaline media is better than that in acid media, in contrast to ethanol. Among the studied catalysts, PtRu/C showed the lowest onset potential and the highest catalytic activity for GOR and MOR in alkaline media, providing the lowest onset potential and a Tafel slope (TS) of 63 mV dec −1 , which could be attributed to the high surface poisoning tolerance. In fuel cells, the open circuit voltage of alkaline anion exchange membrane fuel cells (AEMFCs) was higher than that of the proton exchange membrane fuel cells (PEMFCs). In the kinetic region (up to 20 mA cm −2 ), the power density and cell performance were higher for AEMFCs than those of PEMFCs. However, the power density peaks were higher for PEMFCs than those for AEMFCs. Both the cell performance and the power density increased with increasing temperature. Regardless of the temperature and the media, glycerol crossover is comparable to that of ethanol but much less than that of methanol.
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