Li Wensheng, Sun Lingtao, Hu Rong, Liao Wenli, Li Zhongbin, Li Yanrong, Guo Chaozhong
College of Chemistry and Chemical Engineering, Chongqing University, Chongqing 400044, China.
Research Institute for New Materials Technology, Engineering Research Center of New Energy Storage Devices and Applications, Chongqing University of Arts and Sciences, Chongqing 402160, China.
Materials (Basel). 2017 May 20;10(5):564. doi: 10.3390/ma10050564.
The great challenge of boosting the oxygen reduction reaction (ORR) activity of non-noble-metal electrocatalysts is how to achieve effective exposure and full utilization of nitrogen-rich active sites. To realize the goals of high utilization of active sites and fast electron transport, here we report a new strategy for synthesis of an iron and nitrogen co-doped carbon nanolayers-wrapped multi-walled carbon nanotubes as ORR electrocatalyst (N-C@CNT-Fe) via using partially carbonized hemoglobin as a single-source precursor. The onset and half-wave potentials for ORR of N-C@CNT-Fe are only 45 and 54 mV lower than those on a commercial Pt/C (20 wt.% Pt) catalyst, respectively. Besides, this catalyst prepared in this work has been confirmed to follow a four-electron reaction mechanism in ORR process, and also displays ultra-high electrochemical cycling stability in both acidic and alkaline electrolytes. The enhancement of ORR activity can be not only attributed to full exposure and utilization of active site structures, but also can be resulted from the improvement of electrical conductivity owing to the introduction of CNT support. The analysis of X-ray photoelectric spectroscopy shows that both Fe-N and graphitic-N species may be the ORR active site structures of the prepared catalyst. Our study can provide a valuable idea for effective improvement of the electrocatalytic activity of non-noble-metal ORR catalysts.
提高非贵金属电催化剂的氧还原反应(ORR)活性面临的巨大挑战是如何实现富氮活性位点的有效暴露和充分利用。为了实现活性位点高利用率和快速电子传输的目标,在此我们报道一种新的合成策略,即通过使用部分碳化的血红蛋白作为单源前驱体,制备一种铁和氮共掺杂的碳纳米层包裹多壁碳纳米管作为ORR电催化剂(N-C@CNT-Fe)。N-C@CNT-Fe的ORR起始电位和半波电位分别仅比商业Pt/C(20 wt.% Pt)催化剂低45 mV和54 mV。此外,本工作制备的这种催化剂已被证实在ORR过程中遵循四电子反应机理,并且在酸性和碱性电解质中均表现出超高的电化学循环稳定性。ORR活性的提高不仅归因于活性位点结构的充分暴露和利用,还可归因于由于引入CNT载体而导致的电导率提高。X射线光电子能谱分析表明,Fe-N和石墨氮物种可能是所制备催化剂的ORR活性位点结构。我们的研究可为有效提高非贵金属ORR催化剂的电催化活性提供有价值的思路。