She Yiyi, Lu Zhouguang, Ni Meng, Li Li, Leung Michael K H
‡Department of Materials Science and Engineering, South University of Science and Technology of China, Shenzhen, Guangdong, China.
§Department of Building and Real Estate, The Hong Kong Polytechnic University, ZN713, South Tower, 7/F , Block Z, Hong Kong, China.
ACS Appl Mater Interfaces. 2015 Apr 8;7(13):7214-21. doi: 10.1021/acsami.5b00222. Epub 2015 Mar 25.
Developing metal-free catalysts for oxygen reduction reaction (ORR) is a great challenge in the development of fuel cells. Nitrogen and sulfur codoped carbon with remarkably high nitrogen content up to 13.00 at % was successfully fabricated by pyrolysis of homogeneous mixture of exfoliated graphitic flakes and ionic liquid 1-butyl-3-methylimidazolium bis(trifluoromethanesulfonyl)imide ([Bimi][Tf2N]). The exfoliated graphite flakes served as a structure-directing substance as well as additional carbon source in the fabrication. It was demonstrated that the use of graphite flakes increased the nitrogen doping level, optimized the composition of active nitrogen configurations, and enlarged the specific surface area of the catalysts. Electrochemical characterizations revealed that the N and S codoped carbon fabricated by this method exhibited superior catalytic activities toward ORR under both acidic and alkaline conditions. Particularly in alkaline solution, the current catalyst compared favorably to the conventional 20 wt % Pt/C catalyst via four-electron transfer pathway with better ORR selectivity. The excellent catalytic activity was mainly ascribed to high nitrogen doping content, appropriate constitution of active nitrogen configurations, large specific surface area, and synergistic effect of N and S codoping.
开发用于氧还原反应(ORR)的无金属催化剂是燃料电池发展中的一项重大挑战。通过对剥离的石墨薄片与离子液体1-丁基-3-甲基咪唑双(三氟甲磺酰)亚胺([Bimi][Tf2N])的均匀混合物进行热解,成功制备了氮含量高达13.00 at%的氮硫共掺杂碳。在制备过程中,剥离的石墨薄片既作为结构导向物质,又作为额外的碳源。结果表明,使用石墨薄片提高了氮掺杂水平,优化了活性氮构型的组成,并增大了催化剂的比表面积。电化学表征表明,通过该方法制备的氮硫共掺杂碳在酸性和碱性条件下均对ORR表现出优异的催化活性。特别是在碱性溶液中,当前催化剂通过四电子转移途径与传统的20 wt% Pt/C催化剂相比具有更好的ORR选择性。优异的催化活性主要归因于高氮掺杂含量、活性氮构型的适当组成、大比表面积以及氮硫共掺杂的协同效应。