首页> 外文期刊>Journal of Environmental Management >Photocatalytic hydrogen production from dye contaminated water and electrochemical supercapacitors using carbon nanohorns and TiO_2 nanoflower heterogeneous catalysts
【24h】

Photocatalytic hydrogen production from dye contaminated water and electrochemical supercapacitors using carbon nanohorns and TiO_2 nanoflower heterogeneous catalysts

机译:光催化氢气生产从染料污染的水和电化学超级电容器使用碳纳米植物和TiO_2纳米辊异质催化剂

获取原文
获取原文并翻译 | 示例
       

摘要

In this research, efficient and novel catalysts based on hierarchical carbon nanohorns-titanium nanoflowers have been prepared by one-pot solvothermal process. Hydrogen generation from dye-contaminated water and dye degradation along with electrochemical supercapacitance performance have been investigated using the synthesized hierarchical catalyst to produce 4500 μmol g~(-1) h~(-1) of hydrogen from the photocatalytically generated aqueous methylene blue and methyl orange dyes, which were degraded up to 90% under natural solar light irradiation. These results offer a new path to generate hydrogen from the aqueous dyes. The catalysts electrode showed 164.6 F g~(-1) supercapacitance at 5 mV s~(-1) scan rate, which is nearly 1.3 and 1.65-times higher than that of pristine titanium nanoflower and carbon nanohorns electrodes, respectively. Such superior results were achieved due to good crystallinity, improved optical absorption strength, strong chemical composition between the two components, and hierarchical morphology as demonstrated from XRD, UV-DRS, TEM, XPS, and Raman spectral characterizations.
机译:在该研究中,通过单罐溶剂热法制备基于等级碳纳米醇钛纳米辊的高效和新的催化剂。使用合成的等级催化剂研究了从染料污染的水和染料降解的氢气和染料降解的氢气从光催化生成的亚甲基蓝和甲基产生4500μmolg〜(-1)H〜(-1)氢橙色染料,在天然太阳光照照射下降低至90%。这些结果提供了一种从水性染料中产生氢的新途径。催化剂电极以5mV S〜(-1)扫描速率,催化剂电极显示出164.6fg〜(-1)超水分,其分别比原始钛纳米λ和碳纳米荷尔电极高的1.3%。由于良好的结晶度,改善的光学吸收强度,两种组分之间的强化学组成,以及从XRD,UV-DRS,TEM,XPS和拉曼光谱特性所证明的分层形态之间实现了这种优异的结果。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号