...
首页> 外文期刊>ACS Sustainable Chemistry & Engineering >Fabrication of Octahedral Cu@Graphitic Carbon Cage Complex Porous Structures and Their Microwave-Driven Catalytic Activity
【24h】

Fabrication of Octahedral Cu@Graphitic Carbon Cage Complex Porous Structures and Their Microwave-Driven Catalytic Activity

机译:八面体Cu @石墨碳笼复合多孔结构的制备及其微波驱动催化活性

获取原文
获取原文并翻译 | 示例

摘要

A novel porous octahedral Cu@graphitic carbon cage (Cu@GCC) was successfully fabricated by rapid room-temperature synthesis of a Cu-based metal organic framework (MOF) with further pyrolysis in N-2. The as-obtained Cu@GCCs show a unique structure where well-dispersed Cu nanoparticles (NPs) were encapsulated in porous carbon cages. Compared to Cu/Cu2O@GCCs, CuO/Cu2OP GCCs, a graphitic carbon matrix, and pure Cu, the Cu@GCCs exhibited the best catalytic activity toward the degradation of lomefloxacin (LOM) and methylene blue (MB) under microwave irradiation (MI). Microwave -driven enhanced catalytic activity of Cu@GCCs was mainly ascribed to synergistic contributions of plasmonic Cu NPs and carbon cages as well as their unique open porous structure facilitating the mass transfer and highly efficient microwave energy harvesting. The Cu NPs play a pivotal role of oxidation active center in this catalytic process. The longevity and reusability of Cu@GCCs were enhanced by the protective role of the carbon layer. The main active species were identified to be holes (h(+).) and superoxide radicals (center dot O-2(-)) by various scavengers, and new insights into the catalytic mechanism from the localized surface plasmon resonance (LSPR) effect of metallic nanostructures were also provided. This work offers a new strategy for the design of metal@GCC catalysts and explores their potential applications in environmental remediation.
机译:通过快速室温合成Cu基金属有机骨架(MOF)的快速室温合成,通过N-2进一步热解成功制造了一种新的多孔八面体Cu @石墨碳笼(Cu @ gcc)。所获得的Cu @ gccs显示出独特的结构,其中将分散的Cu纳米颗粒(NPS)包封在多孔碳笼中。与Cu / Cu2O @ GCCs,CuO / Cu2op GCC,石墨碳基质和纯Cu,Cu @ Gccs在微波辐射下表现出朝向洛美昔粒(LOM)和亚甲基蓝(MB)的降解的最佳催化活性(MI )。 Cu @ gccs的微波驱动增强催化活性主要归因于等离子体Cu NPS和碳笼的协同贡献以及它们独特的开放式多孔结构,便于传质和高效微波能量收获。 Cu NPS在该催化过程中发挥氧化活性中心的枢转作用。通过碳层的保护作用,Cu @ gccs的寿命和可重用性得到了增强。通过各种清除剂鉴定主要活性物质是孔(H(+)。)和超氧化物自由基(中央点O-2()),并从局部表面等离子体共振(LSPR)效应中进入催化机制的新见解还提供了金属纳米结构。这项工作为金属@ GCC催化剂设计提供了一种新的策略,并探讨了它们在环境修复中的潜在应用。

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