Yurika Taniguchi , Shinya Kokuryo , Ryuji Takada , Xinran Yang , Koji Miyake , Yoshiaki Uchida , Norikazu Nishiyama
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引用次数: 0
摘要
近年来,掺杂杂原子的碳因其电性能而成为廉价的高性能电催化材料,受到越来越多的关注。精确控制掺杂杂原子碳的合成方法对于提高其性能和扩大其应用范围非常重要。在本研究中,我们开发了一种氟吡啶药用沸石模板法,用于氮/氟(N/F)共掺杂碳。与使用吡啶制备的氮掺杂碳相比,氮/氟共掺杂碳在氧还原反应(ORR)中表现出更好的催化性能。特别是,与文献报道的商用铂载碳黑和 N/F 共掺碳相比,优化的 N/F 共掺碳显示出更高的半波电位(0.87 V vs. RHE)。使用各种 N/F 共掺杂碳进行的比较研究表明,半离子键 C-F 可能会提高 ORR 活性。相反,共价或离子 C-F 对提高 ORR 活性的贡献微乎其微。
Fluoropyridine-medicated zeolite templating method for N/F co-doped carbon with high electrocatalytic performance on oxygen reduction reaction
Heteroatom-doped carbons have attracted increasing attention in recent years as inexpensive high-performance electrocatalytic materials owing to their electrical properties. A precisely controlled synthesis method for heteroatom-doped carbons is important to improve their performance and expand their applications. In this study, we developed a fluoropyridine-medicated zeolite templating method for Nitrogen/Fluorine (N/F) co-doped carbons. The N/F co-doped carbons showed better catalytic performances for oxygen reduction reaction (ORR) than N-doped carbon prepared using pyridine. In particular, the optimized N/F co-doped carbon exhibited a higher half-wave potential (0.87 V vs. RHE) than commercial Pt-loaded carbon black and N/F co-doped carbons reported in the literature. The comparative studies using various N/F co-doped carbons revealed that semi-ionic bonded C-F might improve ORR activity. In contrast, the contribution from covalent or ionic C-F to improving ORR activity would be negligible.
期刊介绍:
Electrochemistry Communications is an open access journal providing fast dissemination of short communications, full communications and mini reviews covering the whole field of electrochemistry which merit urgent publication. Short communications are limited to a maximum of 20,000 characters (including spaces) while full communications and mini reviews are limited to 25,000 characters (including spaces). Supplementary information is permitted for full communications and mini reviews but not for short communications. We aim to be the fastest journal in electrochemistry for these types of papers.