期刊文献+

电弧放电法制备石墨烯的硝酸改性及其电化学性能增强 被引量:5

Nitric Acid Modification of Graphene Nanosheets Prepared by ArcDischarge Method and Their Enhanced Electrochemical Properties
在线阅读 下载PDF
导出
摘要 采用电弧放电法大规模制备了层数少,导电率高,结晶性好的石墨烯纳米片(GNSs).通过扫描电镜(SEM)和透射电镜(TEM)表征发现制得的石墨烯形貌良好.然而电化学测试表明GNSs作为电极材料的电容性能不好.为了增加材料表面电化学反应活性点,促进GNSs在水系电解液中的润湿性,我们对所制备的GNSs表面进行了硝酸改性处理.结果显示硝酸处理后的石墨烯纳米片(H-GNSs)表面新增了较多的含氧氮官能团,其亲水性得到了显著提高.对H-GNSs的电化学研究表明:硝酸改性处理后的GNSs在2mol·L-1KOH溶液中电流密度为0.5A·g-1时,比电容可达65.5F·g-1,约为改性前的30倍;此外,H-GNSs作为电极材料连续进行2000次充放电测试后还展示出了良好的循环稳定性,是一种潜在的超级电容器电极材料. Large-scale synthesis of few-layer graphene nanosheets (GNSs) with high crystallinity and electrical conductivity (1680 S. m^(-1)) is achieved by an arc-discharge method. The GNSs exhibited good morphologies as observed using scanning electron microscopy (SEM) and transmission electron microscopy (TEM). However, electrochemical testing showed that the performance of the graphene (GNS) electrodes in supercapacitors was poor. To increase the surface active sites for electrochemical reactions and promote the wettability by aqueous electrolyte of the GNSs, a nitdc acid treatment was used to chemically modify their surface. The acid treatment introduced more oxygen/nitrogen-containing functional groups onto the GNS surface, and clearly enhanced the hydrophilicity. The nitric-acid-modified GNSs (H-GNSs) showed vastly better electrode performance, with a maximum specific capacitance of 65.5 F. g^(-1) (about 30 times that of original GNSs) at a current density of 0.5 A. g^(-1) in 2 mol· L^(-1) KOH electrolyte. In addition, the H-GNS electrode showed good cycling stability and lifetime after running 2000 cycles. Therefore, H-GNSs may be an attractive candidate as electrode materials for supercapacitors.
出处 《物理化学学报》 SCIE CAS CSCD 北大核心 2012年第7期1726-1732,共7页 Acta Physico-Chimica Sinica
基金 中国科学院"百人计划"项目 中国博士后科学基金(20100480728) 甘肃省青年科技基金计划项目(1107RJYA274)资助~~
关键词 石墨烯 电弧放电 化学改性 比电容 超级电容器 Graphene Arc-discharge Chemical modification Specific capacitance Supercapacitor
  • 相关文献

参考文献42

  • 1Winter, M.; Brodd, R. J. Chem. Rev. 2004, 104, 4245. doi: 10.1021/cr020730k.
  • 2Conway, B. E. J. Electrochem. Soc. 1991, 138, 1539. doi: 10.1149/1.2085829.
  • 3Xiortg, S. L.; Yuan, C. Z.; Zhang, X. G.; Xi, B. J.; Qian, Y. T. Chem. Eur. J. 2009, 15, 5320. doi: 10.1002/chem.200802671.
  • 4Wu, Z. S.; Wang, D. W.; Ren, W. C.; Zhao, J. P.; Zhou, G. M.; Li, F.; Cheng, H. M. Adv. Funct. Mater. 2010, 20, 3595. doi: 10.1002/adfm.201001054.
  • 5Lang, J. W.; Kong, L. B.; Wu, W. J.; Luo, Y. C.; Kang, L. Chem. Commun. 2008, 4213.
  • 6Li, . M.; Van Zijll, M.; Chiang, S.; Pan, N. d. Power Sources 2011, 196, 6003. doi: 10.1016/j.jpowsour.2011.02.092.
  • 7Chang, J. K.; Tsai, W. T. J. Electrochem. Soc. 2005, 152, A2063.
  • 8Zhang, H.; Cao, G. E; Wang, Z. Y.; Yang, Y. S.; Shi, Z. J.; Gu, Z. N. Electrochem. Commun. 2008, 10, 1056. doi: 10.1016/ j.elecom.2008.05.007.
  • 9Nam, K. W.; Kim, K. B. 3". Electrochem. Soc. 2002, 149, A346.
  • 10Lei, Z. B.; Christov, N.; Zhao, X. S. Energy Environ. Sci. 2011, 4, 1866. doi: 10.1039/clee01094h.

二级参考文献2

共引文献10

同被引文献75

引证文献5

二级引证文献23

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