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纳米碳管-钙钛石复合催化剂氧电极交换电流密度的测试与分析

The test and analysis of the exchange current density of the carbon nanotube and perovskite compound oxygen electrodes
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摘要 以纳米碳管与钙钛石制备了复合催化剂氧电极,分析了电极中氧还原的催化机理,利用稳态阴极极化测试法,测试并分析了所制氧电极的交换电流密度.结果表明:复合催化剂催化能力优于单一催化剂;不同种类钙钛石催化能力大小顺序为:La0.8Sr0.2CoO3>La0.6Ca0.4CoO3>La0.6Ni0.4CoO3>La0.8Sr0.2MnO3,正交试验确定的最佳氧电极催化剂配比为:纳米碳管0.1 g,La0.6Sr0.4CoO30.02 g,Na2SO40.1 g,PTFE 0.5 mL,此时,交换电流密度最大,达0.1441 mA/cm2;单因素试验结果显示,复合催化剂中w(La0.8Sr0.2CoO3)=9.09%,w(Na2SO4)=45.45%时电极的阴极极化程度最小. The compound oxygen electrodes with carbon nanotube and perovskite were prepared, the catalysis mechanism of oxygen reduce was analyzed. With the method of cathode polazation curves, the exchange current densities of the oxygen electrodes were tested. The results show that:The compound catalyst ability is superior to singie catalyst. The catalyze ability of different kinds perovskite is La0.8 Sr0.2 CoO3 〉 La0.6 Ca0.4 CoO3 〉 La0.6Ni0.4CoO3 〉 La0.8Sr0.2MnO3. The best proportion of compound catalyzer is 0.1 g carbon nanotube and 0.1 g Na2SO4 and 0.02 g La0.6Sr0.4CoO3 and 0.5 mL PTFE by exchange current density is biggest 0. 1441 mA/cm^2. The experi orthogonal experiment. Under this condition, mental result of single factor shows that:The electric pole cathode polarization is minimum when La0.8Sr0.2CoO3 content is 9.09% and Na2SO4 content is 45.45 %.
出处 《郑州轻工业学院学报(自然科学版)》 CAS 2006年第4期8-11,共4页 Journal of Zhengzhou University of Light Industry:Natural Science
基金 河南省科技攻关项目(0324210004) 郑州轻工业学院大学生科技课题资助项目
关键词 交换电流密度 纳米碳管 钙钛石 氧电极 exchange current density carbon nanotube perovskite oxygen electrode
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  • 1马紫峰,林维明.固体氧化物燃料电池电极材料研究ILa1—xSrxMnO3的合成及其电导特性[J].电源技术,1993,17(6):1-5. 被引量:7
  • 2刘社田,于作龙,吴越.钙钛矿型复合氧化物LaM_yM_(1-y)~'O_3的氧化还原性能的研究[J].无机材料学报,1994,9(4):443-449. 被引量:7
  • 3[1]Chartouni D, Kuriyama N, Kiyobayashi T, et al. J Chen. Air-metal hy dride secondary battery with long cycle life[J]. Journal of Alloys and Compounds, 2002, 330 - 332:766 - 770. 被引量:1
  • 4[3]Bursell M, Pirjamali M, Kiros Y.La0.6Ca0.4O3, La0.16Ca0.9MnO3 and LaNiO3 as bifunctional oxygen electrodes [ J ]. Electrochimica Acta, 2002, 47:1 651 - 1 660. 被引量:1
  • 5[4]Churl K L, Kathryn A S, Frank R M. Thermal treatment of La0.6 Ca0.4 CoO3 perovskites for bifunctional air electrodes[J ]. J Electrochem Soc, 1997, 144(11) :3 801 - 3 806. 被引量:1
  • 6[5]Manoharan R, Shukla A K. Oxides supported carbon air-electrodes for alkaline solution power devices[J]. Electrochimica Acta, 1985, 30(2): 205 - 209. 被引量:1
  • 7Muller S, Striebel K, Haas O. La0.6Ca0.4CoO3 :A stable and powerful catalyst for bifunctional air electrodes [ J ]. Electrochimica Acta, 1994,39 (11 - 12) :1661--1668. 被引量:1
  • 8Lee Churl K,Striebel Kathryn A, Mclamon Frank R. Thermal treatment of La0.6Ca0.4CoO3 perovskites for bifunctional air electrodes[J]. J Electrochem Soc, 1997,144 ( 11 ) :3801--3806. 被引量:1
  • 9Tiwari S K, Koenig J F, Poillerat Get al. Electrocatalysis of oxygen evolution/reduction on LaNiO3 prepared by a novel malic acid-aided method [ J ]. Journal of Applied Electroche mistry, 1998,28 : 114--119. 被引量:1
  • 10Bursell M,Pirjamali M, Kiros Y. La0.6Ca0.4O3, La0.6Ca0.9MnO3 and LaNiO3 as bifunctional oxygen electrodes [ J ].Electrochimica Acta ,2002 , 4 7 : 1651--1660. 被引量:1

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