首页> 外文期刊>Applied Surface Science >An ingenious approach for ZIFs derived N-doped hierarchical porous carbon hybrids with FeCo alloy nanoparticles as efficient bifunctional oxygen electrocatalysts
【24h】

An ingenious approach for ZIFs derived N-doped hierarchical porous carbon hybrids with FeCo alloy nanoparticles as efficient bifunctional oxygen electrocatalysts

机译:ZIFs衍生的N掺杂的分级多孔碳杂化体的巧妙方法,其中FeCo合金纳米颗粒为有效的双功能氧电催化剂

获取原文
获取原文并翻译 | 示例

摘要

An ingenious approach is proposed to achieve exceedingly efficient bifunctional oxygen electrocatalysts of oxygen reduction reaction (ORR) and oxygen evolution reaction (OER). Hierarchical porous structure constituted by nanotubes and nanobulks with high specific surface area and encapsulated FeCo alloy nanoparticles is successfully prepared via the hybrid of Fe(II)-doped ZIF-8 (FeZIF) and cobalt (III) acetylacetonate (Co(acac)(3)), which is greatly redound to mass transfer and electron transport. Interestingly, Co(acac)(3) plays dual-roles during preparation process, which not only generates new metal species but improves porous structure. Moreover, FeZIF acts as a self-sacrificing template and iron source. Owing to the coaction of the unique porous structure, bimetal-N active sites and FeCo alloy, the resultant catalyst carbonized at 850 degrees C exhibits a prominent ORR activity with a positive half-wave potential of 0.864 V (vs the reversible hydrogen electrode, RHE), and a low operating potential of 1.675 V at a current density of 10 mA cm(-2) for OER in alkaline media. The potential gap (Delta E) of overall oxygen electrode is 0.81 V, which surpass that of numerous non-noble metal-based catalysts reported to date, indicating a promising bifunctional oxygen electrocatalyst.
机译:提出了一种巧妙的方法来实现氧还原反应(ORR)和氧释放反应(OER)的极其高效的双功能氧电催化剂。通过掺杂Fe(II)的ZIF-8(FeZIF)和乙酰丙酮钴(III)(Co(acac)(3)的混合物)成功制备了由具有高比表面积的纳米管和纳米块以及包封的FeCo合金纳米颗粒组成的分层多孔结构)),这对于传质和电子传输是非常重要的。有趣的是,Co(acac)(3)在制备过程中起双重作用,不仅产生新的金属物种,而且改善了多孔结构。此外,FeZIF充当自牺牲模板和铁源。由于独特的多孔结构,双金属N活性位和FeCo合金的共同作用,在850℃碳化的所得催化剂显示出显着的ORR活性,正半波电势为0.864 V(与可逆氢电极RHE相比) ),以及在碱性介质中OER的电流密度为10 mA cm(-2)时的1.675 V低工作电势。整个氧电极的电势差(Delta E)为0.81 V,超过迄今为止报道的许多基于非贵金属的催化剂的电势差,表明有希望的双功能氧电催化剂。

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