...
首页> 外文期刊>Journal of Materials Chemistry, A. Materials for energy and sustainability >Ionic liquid-derived Fe-N/C catalysts for highly efficient oxygen reduction reaction without any supports, templates, or multi-step pyrolysis
【24h】

Ionic liquid-derived Fe-N/C catalysts for highly efficient oxygen reduction reaction without any supports, templates, or multi-step pyrolysis

机译:离子液体衍生的Fe-N / C催化剂,无需任何载体,模板或多步热解即可进行高效的氧还原反应

获取原文
获取原文并翻译 | 示例
   

获取外文期刊封面封底 >>

       

摘要

The development of efficient and low-cost non-precious-metal electrocatalysts such as Fe-N/C for the oxygen reduction reaction (ORR) is crucial for fuel cells and metal-air batteries. Here, we report a class of highly efficient Fe-N/C electrocatalysts derived from versatile imidazolium-based ionic liquids (ILs) with a halogen-coordinated iron anion. Without any supports, templates, or multi-step pyrolysis, the as-prepared Fe-N/C catalysts exhibited superior activity in the ORR to the state-of-the-art Pt/C in alkaline electrolytes by 44 mV in half-wave potential. More interestingly, owing to the versatile configuration of the imidazolium-based IL precursors, a diverse range of catalyst structures was successfully modulated. Based on this, it was clearly revealed that the electrical conductivity, type/amount of N dopants, and "effective porosity" (not the conventional total surface area) jointly determined the electrocatalytic activity. A pivotal radar chart is further proposed to successfully predict activity in the ORR merely from the structures of Fe-N/C catalysts. The proposed ILs platform would provide a valuable toolbox for the molecular design of precursors to tune the structures of Fe-N/C electrocatalysts towards excellent activity in the ORR in a highly flexible manner, and facilitate the long-term challenging study of relationships between processing, structure and activity.
机译:高效,低成本的非贵金属电催化剂(例如用于氧还原反应(ORR)的Fe-N / C)的开发对于燃料电池和金属空气电池至关重要。在这里,我们报告了一类高效的Fe-N / C电催化剂,其由具有卤素配位铁阴离子的多功能咪唑基离子液体(IL)衍生而来。在没有任何载体,模板或多步热解的情况下,所制备的Fe-N / C催化剂在ORR中的活性比碱性电解质中最新技术的Pt / C高一半,半波为44 mV。潜在。更有趣的是,由于基于咪唑鎓的IL前体的通用配置,成功地调节了多种催化剂结构。基于此,清楚地表明,电导率,N掺杂剂的类型/量和“有效孔隙率”(不是常规的总表面积)共同决定了电催化活性。还提出了一个枢轴雷达图,仅从Fe-N / C催化剂的结构成功预测ORR中的活性。提议的离子液体平台将为前体的分子设计提供有价值的工具箱,以高度灵活的方式将铁-碳/碳电催化剂的结构调整为在ORR中具有出色的活性,并促进对加工之间关系的长期挑战性研究,结构和活动。

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