功能材料
功能材料
공능재료
JOURNAL OF FUNCTIONAL MATERIALS
2010年
3期
500-504
,共5页
吴红军%阮琴%王宝辉%腾佳%付波
吳紅軍%阮琴%王寶輝%騰佳%付波
오홍군%원금%왕보휘%등가%부파
RuO_2%Co_3O_4%CeO_2%阳极%析氧
RuO_2%Co_3O_4%CeO_2%暘極%析氧
RuO_2%Co_3O_4%CeO_2%양겁%석양
RuO_2%Ce%electrocatalytic activity%oxygen evolution%mixed oxide
采用溶胶-凝胶法制备RuO_2-Co_3O_4-CeO_2(Ru-Co-Ce)复合氧化物电极,利用SEM、XRD对电极表面形貌及物相结构进行了表征,并通过循环伏安及阳极极化曲线等手段对1.0mol/L KOH溶液中电极的析氧反应(OER)活性及其动力学进行了系统研究.结果表明,稀土CeO_2可细化RuO_2晶相,提高电极活性表面积,其中40%(摩尔分数)CeO_2复合氧化物电极具有最大的伏安电荷86.23mC/cm~2,在过电位η=0.60V(Ag/AgCl)时,其反应表观活化能可低至22.76kJ/mol,具有最佳的析氧活性.电极在低过电位及高过电位区域Tafel斜率分别约为40、120mV,电极对OH-的反应级数均为1.0.
採用溶膠-凝膠法製備RuO_2-Co_3O_4-CeO_2(Ru-Co-Ce)複閤氧化物電極,利用SEM、XRD對電極錶麵形貌及物相結構進行瞭錶徵,併通過循環伏安及暘極極化麯線等手段對1.0mol/L KOH溶液中電極的析氧反應(OER)活性及其動力學進行瞭繫統研究.結果錶明,稀土CeO_2可細化RuO_2晶相,提高電極活性錶麵積,其中40%(摩爾分數)CeO_2複閤氧化物電極具有最大的伏安電荷86.23mC/cm~2,在過電位η=0.60V(Ag/AgCl)時,其反應錶觀活化能可低至22.76kJ/mol,具有最佳的析氧活性.電極在低過電位及高過電位區域Tafel斜率分彆約為40、120mV,電極對OH-的反應級數均為1.0.
채용용효-응효법제비RuO_2-Co_3O_4-CeO_2(Ru-Co-Ce)복합양화물전겁,이용SEM、XRD대전겁표면형모급물상결구진행료표정,병통과순배복안급양겁겁화곡선등수단대1.0mol/L KOH용액중전겁적석양반응(OER)활성급기동역학진행료계통연구.결과표명,희토CeO_2가세화RuO_2정상,제고전겁활성표면적,기중40%(마이분수)CeO_2복합양화물전겁구유최대적복안전하86.23mC/cm~2,재과전위η=0.60V(Ag/AgCl)시,기반응표관활화능가저지22.76kJ/mol,구유최가적석양활성.전겁재저과전위급고과전위구역Tafel사솔분별약위40、120mV,전겁대OH-적반응급수균위1.0.
Ti-supported RuO_2-Co_3O_4-CeO_2(Ru-Co-Ce)electrodes were prepared by sol-gel process.The surface morphology and phase structure of the coating anode were characterized by SEM and XRD.Electrocatalytic activity and oxygen evolution reaction (OER) kinetics on these electrodes in 1.0mol/L KOH solution were studied recording cyclic voltammetry and polarisation curve.The results showed that the appropriate content of CeO_2 could reduced the grain size and increased active surface area.Mixed oxide electrodes with 40mol% CeO_2 had the greatest voltammetric charge,86.23mC/cm~2,and the standard electrochemical energy of activation for OER at 0.60V was 22.76kJ/mol.Catalytic performance was the best.Tafel slopes at low and high overpotential were 40 and 120mV,respectively.The order of reaction order with respect to [OH-] are both 1.0.The oxygen evolution reaction kinetics equation on these electrodes were presented,which could account for the values of the experimental results.