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Scalable synthesis of bi-functional high-performance carbon nanotube sponge catalysts and electrodes with optimum C-N-Fe coordination for oxygen reduction reaction

机译:具有最佳C-N-Fe配位的双功能高性能碳纳米管海绵催化剂和电极的可扩展合成,用于氧还原反应

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摘要

Oxygen reduction reaction (ORR) is essential in various electrochemical energy conversion processes, but its sluggish kinetics calls for catalysts made of platinum or its alloys. Although their high catalytic activity has been hardly challenged, the high price of the precious metal has limited their wide applications. Nitrogen-doped carbonaceous materials have been reported as alternatives due to the low cost of carbon and nitrogen precursors, but the low-cost has accompanied by low catalytic activity and poor stability, particularly in acidic media. Here we developed 3-dimentional (3D) N/Fe-containing carbon nanotube (CNT) sponges showing striking improvements in catalytic activity and stability in both acidic and basic solutions. The onset potential and limiting current density in 0.5 M H2SO4 or 0.1 M KOH were comparable to those of Pt/C (20 wt% Pt). More importantly, cyclic voltammetry (CV) tests up to 30000 cycles suggest their excellent long-term stability even better than those of Pt/C. We believe that the key for the high performance is pyridinic nitrogen coordinated with iron in 3D CNTs, according to the comparative studies with their variants whose characteristics include iron-deficiency as well as nitrogen doping with weak iron coordination. This study demonstrates that a proper doping, coordination, and morphology design of CNT bulks could lead to an outstanding performance, and the findings will be of great value for further improving non-precious metal catalysts. The self-standing and porous sponge-like 3D structure could substantially facilitate the mass transfer for ORR and, therefore, potentially act as a gas diffusion layer in electrochemical cells. The unique bi-functionality with a low cost but a high performance could make fuel cells as commercially viable options in the future.
机译:氧还原反应(ORR)在各种电化学能量转换过程中必不可少,但其反应迟缓的动力学要求使用铂或其合金制成的催化剂。尽管几乎没有挑战其高催化活性,但是贵金属的高价限制了它们的广泛应用。由于碳和氮前体的低成本,已经报道了氮掺杂的碳质材料的替代品,但是低成本伴随着低的催化活性和差的稳定性,特别是在酸性介质中。在这里,我们开发了3维(3D)含N / Fe的碳纳米管(CNT)海绵,在酸性和碱性溶液中均显示出惊人的催化活性和稳定性。在0.5 M H2SO4或0.1 M KOH中的起始电势和极限电流密度与Pt / C(20 wt%Pt)相当。更重要的是,循环伏安法(CV)测试高达30000个循环,表明其出色的长期稳定性甚至优于Pt / C。根据对3D CNT中铁的配位作用的比较研究,我们认为高性能的关键是吡啶铁氮与铁配位,其变体的特征包括铁缺乏以及铁配位弱的氮掺杂。这项研究表明,对CNT块进行适当的掺杂,配位和形态设计可能会导致出色的性能,这一发现对于进一步改进非贵金属催化剂具有重要的价值。自立且多孔的海绵状3D结构可以大大促进ORR的质量传递,因此有可能在电化学电池中充当气体扩散层。具有低成本但高性能的独特双功能性将使燃料电池成为将来在商业上可行的选择。

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  • 来源
    《Energy & environmental science》 |2015年第6期|1799-1807|共9页
  • 作者单位

    Texas A&M Univ, Dept Mech Engn, College Stn, TX 77843 USA;

    Texas A&M Univ, Dept Mat Sci & Engn, College Stn, TX 77843 USA;

    Texas A&M Univ, Dept Mat Sci & Engn, College Stn, TX 77843 USA;

    Texas A&M Univ, Dept Mech Engn, College Stn, TX 77843 USA|Texas A&M Univ, Dept Mat Sci & Engn, College Stn, TX 77843 USA;

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  • 入库时间 2022-08-17 23:11:36

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