首页> 外文期刊>International journal of hydrogen energy >Rh nanospheres anchored TaON@Ta_2O_5 nanophotocatalyst for efficient hydrogen evolution from photocatalytic water splitting under visible light irradiation
【24h】

Rh nanospheres anchored TaON@Ta_2O_5 nanophotocatalyst for efficient hydrogen evolution from photocatalytic water splitting under visible light irradiation

机译:Rh纳米球锚定的TaON @ Ta_2O_5纳米光催化剂可在可见光照射下从光催化水分解中高效释放氢

获取原文
获取原文并翻译 | 示例
       

摘要

Rh nanospheres anchored TaON Ta2O5 with shell-core structure was synthesized from in situ Rh3+-doped Ta2O5 by one-step high-temperature ammonolysis, which exhibited efficient visible light photoactivity for H-2-evolution (39.41 mu mol.g(-1).h(-1)), much higher than unmodified Ta3N5 Ta2O5 (21.75 mu.mol.g(-1).h(-1)). Rh-modifying inhibited the phase transformation from TaON to Ta3N5 during the nitridation process, and increased the specific surface area and active sites, and extended the optical absorption throughout visible light region due to localized surface plasmon resonance (LSPR) effect. Relative intensities of peaks at 827 cm(-1) for Ta-O bonds increased with increasing Rh-modifying amounts, which was beneficial to improving the stability. Notably, constructing novel Rh/TaON/Ta2O5 hetero-junctions including a Rh/TaON Schottky junction and an n-n TaON/Ta2O5 mutant hetero-junction facilitated photogenerated carriers directed transfer from inner to surface active sites, and decreased travel distance of charge carriers, and formed built-in electric fields to accelerating charge separation. Synergetic effects of the enhanced photocatalytic H-2-evolution activity were discussed in detail. This work provided a promising strategy to further design and develop efficient and stable Ta-based photocatalysts for solar water splitting. (C) 2019 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
机译:通过一步高温氨解由原位掺杂Rh3 +的Ta2O5合成了具有壳核结构的锚定TaON Ta2O5的Rh纳米球,其对H-2-演化显示出有效的可见光光活性(39.41μmol.g(-1) .h(-1)),比未改性的Ta3N5 Ta2O5(21.75μmol.g(-1).h(-1))高得多。 Rh修饰在氮化过程中抑制了从TaON到Ta3N5的相变,并增加了比表面积和活性位,并且由于局部表面等离子体激元共振(LSPR)效应而将光吸收扩展到整个可见光区域。 Ta-O键在827 cm(-1)处的峰的相对强度随Rh修饰量的增加而增加,这有利于提高稳定性。值得注意的是,构建新型的Rh / TaON / Ta2O5异质结,包括Rh / TaON肖特基结和nn TaON / Ta2O5突变异质结,有助于光生载流子直接从内部转移到表面活性位,并缩短了电荷载流子的迁移距离,并且形成内置电场以加速电荷分离。详细讨论了增强的光催化H-2-演化活性的协同效应。这项工作为进一步设计和开发用于太阳能水分解的高效,稳定的Ta基光催化剂提供了有希望的策略。 (C)2019氢能出版物有限公司。由Elsevier Ltd.出版。保留所有权利。

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