Zhao Haoyue, Song Beibei, Li Han, Li Xinyu, Ge Can, Wu Qilong, Chen Jun, Wang Zhe, Yan Guilong, Fang Jian
College of Textile and Clothing Engineering, Soochow University, Suzhou, Jiangsu, 215123, China.
JC STEM lab of Sustainable Fibers and Textiles, School of Fashion and Textiles, The Hong Kong Polytechnic University, Hung Hom, Kowloon, Hong Kong, 999077, China.
Small. 2025 Jan;21(4):e2407700. doi: 10.1002/smll.202407700. Epub 2024 Nov 27.
Carbon-supported single-atom catalysts (SACs) have shown great potential in electrocatalysis, whereas traditional synthesis methods typically involve energy-intensive carbonization processes and unfavorable atomic migration and aggregation. Herein, an energy-efficient and universal strategy is developed to rapidly fabricate various SACs on nitrogen-doped hierarchically porous carbon nanofibers (M-TM/NPCNFs, TM = Fe, Co, Ni, FeCo, and FeNi) by electrospinning and controllable microwave heating technique. Such microwave heating technique enables an ultrafast heating rate (ramping to 900 °C in 5 min) to greatly suppress the random migration and aggregation of metal species. Meanwhile, the energy consumption and time can be reduced to 2.5% and less than half an hour, respectively, compared to traditional pyrolysis methods. As a proof of concept, the synthesized M-Fe/NPCNFs with abundant Fe-N sites exhibit remarkable oxygen reduction reaction (ORR) activity with a high half-wave potential (E = 0.88 V) in alkaline media, excellent performance in Zn-air battery with a large discharge specific capacity (801 mAh g) and long-term cycle durability (over 1000 h), demonstrating the great potential of the microwave heating technique in efficient fabrication of SACs for energy related applications.
碳负载单原子催化剂(SACs)在电催化领域已展现出巨大潜力,然而传统合成方法通常涉及能源密集型的碳化过程以及不利的原子迁移和聚集。在此,我们开发了一种节能且通用的策略,通过静电纺丝和可控微波加热技术,在氮掺杂的分级多孔碳纳米纤维(M-TM/NPCNFs,TM = Fe、Co、Ni、FeCo和FeNi)上快速制备各种SACs。这种微波加热技术能够实现超快的加热速率(5分钟内升温至900°C),从而极大地抑制金属物种的随机迁移和聚集。同时,与传统热解方法相比,能耗和时间可分别降低至2.5%和不到半小时。作为概念验证,合成的具有丰富Fe-N位点的M-Fe/NPCNFs在碱性介质中表现出显著的氧还原反应(ORR)活性,半波电位高(E = 0.88 V),在锌空气电池中具有优异性能,放电比容量大(801 mAh g)且长期循环耐久性好(超过1000小时),证明了微波加热技术在高效制备用于能源相关应用的SACs方面具有巨大潜力。