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On an Easy Way to Prepare Fe, S, N Tri-Doped Mesoporous Carbon Materials as Efficient Electrocatalysts for Oxygen Reduction Reaction

机译:以一种简单的方法来制备Fe,S,N三掺杂的介孔碳材料,作为有效的氧还原反应的有效电催化剂

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摘要

Recently, precious metal-free and heteroatom functionalized carbon materials are widely considered as the promising candidates for oxygen reduction reaction (ORR). However, it is still a challenge to controllably prepare the carbon-based electrocatalysts with desirable activities. Herein, we demonstrate a simple strategy to synthesize the Fe/S/N tri-doped mesoporous carbon (Fe-S,N-C) materials as electrocatalysts for ORR. The resultant Fe-S,N-C catalyst possesses high content of pyridinic N (also including Fe-N-x), graphitic N atoms, thiophene S atoms, and abundant defects, as well as the high surface area and desirable mesoporous microstructure. Thus, in alkaline medium, the Fe-S,N-C shows an expected high ORR activity with a onset potential of 0.95V and half-wave potential of 0.83V. Meanwhile, the ORR proceeded on Fe-S,N-C via the four-electron transfer pathway. What is more, the as-prepared catalyst shows excellent electrocatalytic stability and good methanol tolerance, suggesting its potential applications in fuel cells and metal-air battery.
机译:最近,珍贵的无金属和杂原子官能化碳材料被广泛认为是氧还原反应的有希望的候选者(ORR)。然而,可控制地制备具有所需活动的碳基电催化剂仍然是一项挑战。在此,我们证明了一种简单的策略,以将Fe / S / N三掺杂的介孔碳(Fe-S,N-C)材料合成为ORR的电催化剂。得到的Fe-S,N-C催化剂具有高含量的吡啶N(也包括Fe-N-X),石墨N原子,噻吩S原子和丰富的缺陷,以及高表面积和所需的介孔微观结构。因此,在碱性培养基中,Fe-S,N-C显示出一种预期的高润发活性,起始电位为0.95V,半波电位为0.83V。同时,ORR通过四电子转移途径进行FE-S,N-C.更重要的是,制备的催化剂显示出优异的电催化稳定性和良好的甲醇耐受性,旨在提出其在燃料电池和金属 - 空气电池中的潜在应用。

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