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双金属沸石咪唑骨架衍生的铁、钴和氮共掺杂碳纳米多面体电催化剂用于高效氧还原。

Bimetal Zeolitic Imidazolite Framework-Derived Iron-, Cobalt- and Nitrogen-Codoped Carbon Nanopolyhedra Electrocatalyst for Efficient Oxygen Reduction.

出版信息

ACS Appl Mater Interfaces. 2018 Apr 18;10(15):12651-12658. doi: 10.1021/acsami.8b00512. Epub 2018 Apr 3.

DOI:10.1021/acsami.8b00512
PMID:29611701
Abstract

Replacing precious metal electrocatalysts with high-performance and low-cost nonprecious metal electrocatalysts (NPMCs) is crucial for the commercialization of fuel cell technologies. Herein, we present a novel and facile route for synthesis of iron-, cobalt-, and nitrogen-codoped carbon nanopolyhedra electrocatalysts (Fe,Co,N-CNP) by one-step pyrolysis of a new type of Fe/Co bimetal zeolitic imidazolate framework (Fe,Co-ZIF) crystals that were self-assembled by oxygen-free solvothermal reaction of Fe and Co with 2-methylimidazole. During the pyrolysis process, the Fe ions in Fe,Co-ZIF not only effectively inhibit the aggregation of Co nanoparticles but also increase the specific surface area (SSA) and N content of the resultant electrocatalysts. The optimized Fe,Co,N-CNP(0.3) (Fe/Co molar ratio of 0.3 in Fe,Co-ZIF) electrocatalyst exhibited a highly promising activity for oxygen reduction reaction (ORR) with a positive half-wave potential ( E) of 0.875 V (29 mV higher than that of the commercial Pt/C), excellent methanol tolerance, and electrochemical stability in the alkaline electrolyte. Also, Fe,Co,N-CNP(0.3) presents comparable ORR catalytic activity as Pt/C in the acidic electrolyte with E of 0.764 V and superior methanol tolerance and electrochemical stability. The outstanding ORR performance of Fe,Co,N-CNP(0.3) is ascribed to the synergistic contribution of homogeneous Fe, Co, and N codoping structure, high SSA, and hierarchically porous structure for rapid mass transport. This novel and rational methodology for controlled synthesis of ZIFs-derived nitrogen-doped porous carbon nanopolyhedras offers new prospects in developing highly efficient NPMCs for ORR.

摘要

用高性能、低成本的非贵金属电催化剂(NPMCs)替代贵金属电催化剂对于燃料电池技术的商业化至关重要。在此,我们提出了一种通过一步热解新型 Fe/Co 双金属沸石咪唑酯骨架(Fe/Co-ZIF)晶体来合成铁、钴和氮共掺杂碳纳米多面体电催化剂(Fe,Co,N-CNP)的新方法,该晶体由无氧气溶剂热反应自组装而成 Fe 和 Co 与 2-甲基咪唑。在热解过程中,Fe,Co-ZIF 中的 Fe 离子不仅有效地抑制了 Co 纳米粒子的聚集,而且提高了所得电催化剂的比表面积(SSA)和 N 含量。优化后的 Fe,Co,N-CNP(0.3)(Fe/Co-ZIF 中 Fe/Co 的摩尔比为 0.3)电催化剂在碱性电解质中对氧还原反应(ORR)表现出极高的活性,半波电位(E)为 0.875 V(比商业 Pt/C 高 29 mV),具有出色的甲醇耐受性和电化学稳定性。此外,在酸性电解质中,Fe,Co,N-CNP(0.3) 具有与 Pt/C 相当的 ORR 催化活性,E 为 0.764 V,甲醇耐受性和电化学稳定性更高。Fe,Co,N-CNP(0.3) 出色的 ORR 性能归因于均匀的 Fe、Co 和 N 共掺杂结构、高 SSA 和分级多孔结构对快速质量传输的协同贡献。这种用于可控合成 ZIFs 衍生氮掺杂多孔碳纳米多面体的新颖且合理的方法为开发高效 ORR 的 NPMCs 提供了新的前景。

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