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作 者:韩梦飞 顾军[1] 薛盛鼎 祝苏君 黄润生[1] HAN Meng-Fei;GU Jun;XUE Sheng-Ding;ZHU Su-Jun;HUANG Run-Sheng(School of Physics,Nanjing University,Nanjing 210093,China)
机构地区:[1]南京大学物理学院,南京210093
出 处:《无机化学学报》2023年第7期1253-1260,共8页Chinese Journal of Inorganic Chemistry
基 金:南通市基础科学基金项目(No.JC2021109);国家重点研发计划(No.2022YFE0207600)资助。
摘 要:为提高PtCo/C合金催化剂的电化学性能,采用微波法合成铂钴锰催化剂前驱体,经高温热处理形成合金,最后通过酸处理得到铂钴锰合金催化剂(PtCoMn/C)。电化学测试结果表明:适量锰的添加可提升PtCo/C催化剂的活性和耐久性。PtCo Mn/C催化剂在0.9 V(vs RHE)电压下的质量比活性(MA)达到0.666 A·mgPt^(-1),是传统Pt/C的2.66倍,是PtCo/C催化剂的1.30倍。在30000圈催化剂加速耐久性测试中,PtCoMn/C合金催化剂的电化学活性面积(ECSA)和质量比活性(MA)仅下降6.9%和27.1%,均远低于Pt/C催化剂。The precursor of PtCoMn alloy catalyst was synthesized with ethylene glycol as reducing agent under microwave heating.After high temperature heat treatment,the alloy was formed.Finally,the PtCoMn alloy catalyst was obtained by acid treatment.The composition,structure,and morphology of the catalyst were characterized by elemental analysis,X-ray diffraction,and transmission electron microscopy.The surface electronic structure and properties of the catalyst were studied by X-ray photoelectron spectroscopy and electrochemical workstation.The results showed that the activity and durability of the catalyst can be improved by the addition of proper amount of Mn.The mass specific activity(MA)of PtCoMn/C catalyst was 0.666 A·mgPt^(-1) at 0.9 V(vs RHE),which was 2.66 times that of conventional Pt/C and 1.30 times that of PtCo/C catalyst.In the 30000-cycle catalyst accelerated durability test,electrochemical active area(ECSA)and MA of PtCoMn/C alloy catalyst only decreased by 6.9%and 27.1%,both of which were much lower than Pt/C catalyst.
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