Jungwon Lee, Eun Young Shin, Seokhyeon Jeon, Sanghee Yang, Sungjin Park
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引用次数: 0
Abstract
The oxygen reduction reaction (ORR), occurred at cathodes in fuel cells, eco-friendly energy-conversion system, requires efficient electrocatalysts to overcome sluggish reaction kinetics. In this work, to enhance the ORR performance by decreasing potentials, we developed carbonized zeolite-imidazolate frameworks (ZIF) containing Co atoms (Co–C). The final product is produced by two-step process including (i) the formation of ZIF with Co species, and (ii) carbonization of the ZIF using high temperature treatment. Morphological characterizations revealed that the Co–C has polygon-shaped ZIF-based materials with metallic Co particles wrapped by layered carbon structures. The amount of Co atoms is found to be ~ 4 wt%, possessing a large surface area of 718 m2/g. X-ray photoelectron spectroscopy measurements further supported the formation of sp2 carbon structures with N-doping. The Co–C products exhibit an efficient electrocatalytic ORR performance in alkaline media, with their onset and half-wave potentials as of 0.97 and 0.86 V, comparable to those of Pt/C. Furthermore, Co–C shows the excellent cyclic durability and stability against for methanol poisoning. Collectively, this system including Co-based active species on ZIF networks provides a promise route for the development of efficient ORR electrocatalysts.
氧还原反应(ORR)发生在环保能源转换系统燃料电池的阴极上,需要高效的电催化剂来克服反应动力学的迟缓。在这项工作中,为了通过降低电位来提高氧还原反应的性能,我们开发了含有钴原子(Co-C)的碳化沸石-咪唑酸盐框架(ZIF)。最终产品由两步工艺制成,包括 (i) 形成含 Co 物种的 ZIF,以及 (ii) 通过高温处理对 ZIF 进行碳化。形态特征显示,Co-C 具有多角形的 ZIF 基材料,金属 Co 粒子被层状碳结构包裹。Co 原子的含量约为 4 wt%,具有 718 m2/g 的大表面积。X 射线光电子能谱测量进一步证实了 N 掺杂形成的 sp2 碳结构。Co-C 产品在碱性介质中表现出高效的电催化 ORR 性能,其起始电位和半波电位分别为 0.97 V 和 0.86 V,与 Pt/C 相当。此外,Co-C 对甲醇中毒表现出卓越的循环耐久性和稳定性。总之,这种在 ZIF 网络上含有 Co 基活性物种的体系为开发高效 ORR 电催化剂提供了一条可行的途径。
期刊介绍:
Topics in Catalysis publishes topical collections in all fields of catalysis which are composed only of invited articles from leading authors. The journal documents today’s emerging and critical trends in all branches of catalysis. Each themed issue is organized by renowned Guest Editors in collaboration with the Editors-in-Chief. Proposals for new topics are welcome and should be submitted directly to the Editors-in-Chief.
The publication of individual uninvited original research articles can be sent to our sister journal Catalysis Letters. This journal aims for rapid publication of high-impact original research articles in all fields of both applied and theoretical catalysis, including heterogeneous, homogeneous and biocatalysis.