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作 者:吴燕妮[1] 李顺华[1] 肖晓鹏 郑梦琪[1] 陈志胜[1] 闫鹏[1] 王赵志[1]
机构地区:[1]肇庆学院,化学化工学院,广东肇庆526061
出 处:《化学研究与应用》2015年第5期684-688,共5页Chemical Research and Application
基 金:广东省自然科学基金博士启动项目(S2012040007383)资助;广东省教育厅科技创新项目(2013KJCX0193)资助;肇庆学院2014年大学生创新创业训练项目(DC201440)资助
摘 要:分别采用高压有机溶剂法和回流法不同的制备方法,制备了含铂20%(w)的催化剂Pt/C-HP(高压有机溶剂法)和Pt/C-Reflux(回流法)。实验发现:对于甲醇的阳极氧化过程,高压有机溶胶法制得的催化剂活性较高,催化剂Pt/C-HP甲醇氧化峰电流密度是Pt/C-Reflux的1.5倍,且远远高于商业催化剂JM3000含铂20%(w)Pt/C催化剂,催化剂Pt/C-Reflux甲醇氧化峰电流密度与商业催化剂JM3000催化剂相当。采用X射线衍射(XRD)、透射电镜(TEM)、循环伏安法(CV)等方法对催化剂进行表征的结果表明:高压有机溶胶法制得的催化剂分散性比回流法制得的催化剂好,使得前者催化剂的电化学活性比表面积得到了显著的提高。High-pressure colloidal method( denoted as Pt/C-HP) and the reflux method( denoted as Pt/C-Reflux) were used to syn-thesis catalyst 20%( w) Pt/C. We found that Pt/C-HP showed much higher activity than Pt/C-Reflux during the anodic oxidation of methanol. The peak current density for Pt/C-HP was 1. 5 times as high as that of Pt/C-Reflux and it was also much higher than that of the commercial JM3000(20%w)Pt/C catalyst. The peak current density for Pt/C-Reflux is similar with the commercial JM3000 (20%,w)Pt/C catalyst. X-ray diffraction analysis(XRD),transmission electron microscopy(TEM)and the cyclic voltammograms CV method) etc. revealed that the dispersion for Pt/C-HP is better than that of Pt/C-Reflux whereas the electrochemical special sur-face area of Pt/C-HP increased significantly.
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