期刊文献+

银/二氧化锰复合催化剂的制备及其对氧还原的电化学活性

Synthesis and Electrochemical Activity of Silver and Manganese Dioxide Composites for Oxygen Reduction Reaction
原文传递
导出
摘要 通过化学还原法,在多壁碳纳米管(MWCNT)负载的二氧化锰纳米颗粒表面上进一步沉积银纳米颗粒,制备银/二氧化锰电极材料(Ag/MnO2/MWCNT).利用循环伏安(CV)和线性扫描技术(LSV),测试了这些催化剂对碱性溶液中氧还原反应(ORR)的电化学活性.结果表明,MnO2为5%(wt%)与10%的催化剂对ORR均表现出强的电活性,它们的ORR起始电位约为0.02 V(vs. Hg/Hg O).在Ag/5%MnO2/MWCNT电极上,ORR的极限扩散电流密度是2.86×10-(-3)A/cm-2(1 200 r/min),高于Ag/MWCNT.Levich方程分析表明,在Ag/5%MnO2/MWCNT催化剂上,ORR电子转移数明显大于Ag/MWCNT,说明在Ag/5%MnO2/MWCNT上氧气能更彻底地还原.结果表明,适量MnO2的加入能明显改善Ag/MWCNT对ORR的电活性. Silver/manganese dioxide/multi-walled carbon nanotubes(Ag/MnO2/MWCNT) composites with different MnO2 loadings were prepared by chemical reduction method. Cyclic voltammetry and linear sweep voltammetry were used to investigate the electroactivity of the samples for oxygen reduction reaction(ORR) in the alkaline solution. The results show that both Ag/5% MnO2/MWCNT and Ag/10% MnO2/MWCNT exhibit a high electrocatalytic activity,with the onset potential of ca. 0. 02 V(vs. Hg/Hg O) and the ORR limiting current density of 5% Ag/MnO2/MWCNT is 2. 86 x 10-(-3)A/cm-2(1 200 r/min),higher than that of Ag/MWCNT. Levich analysis is shown that Ag/5% MnO2/MWCNT possesses a much greater electron-transfer number for ORR than Ag/MWCNT,which indicates the more complete reduction of oxygen on the Ag/5%MnO2/MWCNT.
作者 阳铮 易清风 向柏霖 Yang Zheng;Yi Qingfeng;Xiang Bolin(School of Chemistry and Chemical Engineering, Hunan University of Science and Technology, Xiangtan 411201, China;School of Chemistry and Chemical Engineering, Huaihua University, Huaihua 418000, China)
出处 《湖南科技大学学报(自然科学版)》 CAS 北大核心 2018年第1期71-77,共7页 Journal of Hunan University of Science And Technology:Natural Science Edition
基金 国家自然科学基金资助项目(21376070) 湖南省自然科学基金资助项目(14JJ2096)
关键词 纳米银 二氧化锰 氧还原 燃料电池 silver nanoparticles manganese dioxide Oxygen reduction fuel cell
  • 相关文献

参考文献6

二级参考文献73

  • 1邹勇进,孙立贤,徐芬,杨黎妮.以新亚甲基蓝为电子媒介体的大肠杆菌微生物燃料电池的研究[J].高等学校化学学报,2007,28(3):510-513. 被引量:17
  • 2肖占文 杨邦朝 等.计算机控制的电化学暂态测量系统[J].功能材料,1998,29:802-802.
  • 3KIM B H, KIM H J, HYUN M S, et al. Direct electrode reaction of Fe (III)-reducing bacterium, Shewanella putrefaciens[J]. J Microbiol Biotechol, 1999, 9 : 127-131.
  • 4OH S E, LOGAN B E. Proton exchange membrane and electrode surface areas as factors that affect power[J]. Biotech Prod Process Eng, 2006, 70 : 162-169.
  • 5HEIJNE A T, HAMELERS H V M, WILDE V D,et al.Power generation using different cation, anion and ultrafiltration membranes in microbial fuel cells[J]. Environ Sci Technol, 2006, 40 : 5200-5205.
  • 6ZHANG T, ZENG Y L, CHEN S L, et al. Improved performances of E.coli-catalyzed microbial fuel cells with composite graphite/PTFE anodes[J]. Electrochemistry Communications, 2007, 9(3) : 349-353.
  • 7GIL G C, CHANG I S, KIM B H, et al.Operational parameters affecting the performance of a mediator-less microbial fuel cell [J]. Biosens Bioelectron, 2003, 18:327-334.
  • 8LOGAN B E, HAMELERS B. ROZENDAL R, et al. Microbial fuel cells: Methodology and technology[J]. Environ Sci Technol, 2006, 40 : 5181.
  • 9ZHAO F, HARNISCH F, SCHRODER U,et al. Application of pyrolysed iron (II) phthalocyanine and CoTMPP based oxygen reduction catalysts as cathode materials in microbial fuel cells [J]. Electrochem Cornm, 2005, 7 : 1405-1410.
  • 10WEI Z D, HUANG W Z, ZHANG S T, et al. Carbon-based air electrodes carrying MnOz in zinc-air batteries [J]. Journal of Power Sources, 2000, 91:83-85.

共引文献69

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部