物理化学学报 >> 2019, Vol. 35 >> Issue (5): 472-485.doi: 10.3866/PKU.WHXB201806131

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碳基非贵金属氧还原电催化剂的活性位结构研究进展

杨晓冬1,陈驰2,周志有3,*(),孙世刚3   

  1. 1 华侨大学材料科学与工程学院,福建 厦门 361021
    2 中国科学院上海高等研究院,上海 201210
    3 厦门大学化学化工学院,能源材料化学创新中心,固体表面物理化学国家重点实验室,福建 厦门 361005
  • 收稿日期:2018-04-11 发布日期:2018-10-19
  • 通讯作者: 周志有 E-mail:zhouzy@xmu.edu.cn
  • 作者简介:周志有,现任厦门大学化学与化工学院教授。主要研究领域:电催化,燃料电池,非铂电催化剂和电化学原位红外光谱
  • 基金资助:
    国家自然科学基金(21703184);国家自然科学基金(91645121);国家重点研发计划(2017YFA0206500)

Advances in Active Site Structure of Carbon-Based Non-Precious Metal Catalysts for Oxygen Reduction Reaction

Xiaodong YANG1,Chi CHEN2,Zhiyou ZHOU3,*(),Shigang SUN3   

  1. 1 College of Materials Science and Engineering, Huaqiao University, Xiamen 361021, Fujian Province, P. R. China
    2 Shanghai Advanced Research Institute, Chinese Academy of Sciences, Shanghai 201210, P. R. China
    3 Collaborative Innovation Center of Chemistry for Energy Materials, State Key Laboratory of Physical Chemistry of Solid Surfaces, College of Chemistry and Chemical Engineering, Xiamen University, Xiamen 361005, Fujian Province, P. R. China
  • Received:2018-04-11 Published:2018-10-19
  • Contact: Zhiyou ZHOU E-mail:zhouzy@xmu.edu.cn
  • Supported by:
    the National Natural Science Foundation of China(21703184);the National Natural Science Foundation of China(91645121);the National Key Research and Development Program of China(2017YFA0206500)

摘要:

以热解型Fe/N/C为代表的碳基非贵金属材料被认为是当前最具潜力替代铂的非贵金属氧还原催化剂,其综合性能的进一步突破,对于推动质子交换膜燃料电池商业化应用具有重要意义。对热解型Fe/N/C催化剂活性位结构的深入认识是实现催化剂高活性位密度和高稳定性理性设计的关键。本文总结了热解型Fe/N/C活性位的研究进展,重点介绍了非晶态铁氮配位活性中心、氮掺杂和碳缺陷三类活性位构型。由于热解型Fe/N/C是非均相的,结构非常复杂,导致在活性位认识上还存在诸多争议,本文总结阐述了活性位结构的不同观点。最后,我们展望了Fe/N/C催化剂活性位研究的未来方向。

关键词: 氧还原反应, 碳基非贵金属催化剂, 活性位, 电催化, 燃料电池

Abstract:

Carbon-based non-precious metal catalysts, represented by pyrolyzed Fe/N/C, are the most promising catalysts to replace platinum for the oxygen reduction reaction (ORR). Therefore, further improvement of their performance will be significant for commercialization of proton exchange membrane fuel cells. Unveiling the nature of active sites at the atomic scale paves the way for rational designs of Fe/N/C catalysts with high activity and durability. Herein, we review the advances in the active site structure of carbon-based non-precious metal catalysts. Three types of active sites are discussed in the order of their ORR activity, namely, iron/nitrogen-containing sites, nitrogen-containing sites, and carbon defects. In the iron/nitrogen-containing sites, some of iron atoms are amorphous and positioned in a porphyrin-like plane structure with single-iron-atom coordinated to nitrogen. Iron in porphyrin-like sites is believed to directly bind to dioxygen with electron transfer from eg-orbitals (dz2) of iron to antibonding orbitals of dioxygen. Factors governing the energy level of eg-orbitals (dz2) are certainly effected the ORR activity, including coordination number, atom type, axial ligand effect and electron-donating/withdrawing capability of the carbon matrix. The structures of porphyrin-like iron centers are described as four-coordinate FeN4, five-coordinate N-FeN2+2, O2-FeN4C12 and Fe-N2+2 bridging two graphene edges. Moreover, some highly active sites are proposed with basic N-group or defective carbon neighboring the Fe-N center. It is worth noting that surface probing is a powerful tool to identify porphyrin-like iron sites, as well as to estimate its density and turnover frequency. The prospect of surface probe is combined with spectroscopy techniques that will be tremendously helpful in providing further insights of pyrolyzed Fe/N/C. Besides the iron in porphyrin-like sites, other iron atoms are incorporated into crystalline iron nanoparticles and clusters, which are speculated to facilitate electron transfer from nitrogen-doped carbon to dioxygen. However, the role of crystalline iron remains uncertain, because conflicting experimental results are often observed when crystalline iron is removed. Nonetheless, it is undoubted that the iron doping highly boosts the ORR activity of carbon-based catalysts. The next category consists of the nitrogen-containing sites. Various models have been developed to describe the nitrogen-doping carbon catalysts. These include synthesis of planar nitrogen by the layer-by-layer space-confined method, controlled-synthesis of nitrogen on highly-oriented pyrolytic graphite, and selective graft of acetyl group on pyridinic-nitrogen. Strong evidences from models of nitrogen-doping carbon catalysts identify the ortho-carbon atom of the pyridinic ring is the reactive site. The last sites, dopant-free defective carbon, are also found to contribute to ORR. Exploring and summarizing the active sites of pyrolyzed Fe/N/C deepen our understanding of the structure-performance relationship and paves the way for new synthetic strategies. It is expected that the activity as well as stability of pyrolyzed Fe/N/C can be further improved, by exploring the active sites and the ORR mechanism.

Key words: Oxygen reduction reaction, Carbon-based non-precious metal catalyst, Active site, Electrocatalysis, Fuel cell

MSC2000: 

  • O646