Tanasa Eugenia, Maxim Florentina Iuliana, Erniyazov Tugce, Iacob Matei-Tom, Skála Tomáš, Tanase Liviu Cristian, Ianăși Cătălin, Moisescu Cristina, Miron Cristina, Ardelean Ioan, Antohe Vlad-Andrei, Fagadar-Cosma Eugenia, Stamatin Serban N
Faculty of Applied Chemistry and Materials Science, Politehnica University of Bucharest, Splaiul Independentei Str. No. 313, 060042 Bucharest, Romania.
Nano-SAE Research Centre, University of Bucharest, Atomistilor 405, 077125 Magurele, Ilfov, Romania.
Nanomaterials (Basel). 2021 May 1;11(5):1198. doi: 10.3390/nano11051198.
Polymer electrolyte membrane fuel cells require cheap and active electrocatalysts to drive the oxygen reduction reaction. Nitrogen-doped carbons have been extensively studied regarding their oxygen reduction reaction. The work at hand looks beyond the nitrogen chemistry and brings to light the role of oxygen. Nitrogen-doped nanocarbons were obtained by a radio-frequency plasma route at 0, 100, 250, and 350 W. The lateral size of the graphitic domain, determined from Raman spectroscopy, showed that the nitrogen plasma treatment decreased the crystallite size. Synchrotron radiation photoelectron spectroscopy showed a similar nitrogen chemistry, albeit the nitrogen concentration increased with the plasma power. Lateral crystallite size and several nitrogen moieties were plotted against the onset potential determined from oxygen reduction reaction curves. There was no correlation between the electrochemical activity and the sample structure, as determine from Raman and synchrotron radiation photoelectron spectroscopy. Near-edge X-ray absorption fine structure (NEXAFS) was performed to unravel the carbon and nitrogen local structure. A difference analysis of the NEXAFS spectra showed that the oxygen surrounding the pyridinic nitrogen was critical in achieving high onset potentials. The work shows that there were more factors at play, other than carbon organization and nitrogen chemistry.
聚合物电解质膜燃料电池需要廉价且活性高的电催化剂来驱动氧还原反应。氮掺杂碳在氧还原反应方面已得到广泛研究。手头的这项工作超越了氮化学范畴,揭示了氧的作用。通过射频等离子体路线在0、100、250和350瓦功率下制备了氮掺杂纳米碳。由拉曼光谱确定的石墨域横向尺寸表明,氮等离子体处理减小了微晶尺寸。同步辐射光电子能谱显示出类似的氮化学性质,尽管氮浓度随等离子体功率增加。将横向微晶尺寸和几种氮基团与由氧还原反应曲线确定的起始电位作图。由拉曼光谱和同步辐射光电子能谱确定,电化学活性与样品结构之间没有相关性。进行近边X射线吸收精细结构(NEXAFS)分析以揭示碳和氮的局部结构。NEXAFS光谱的差异分析表明,吡啶氮周围的氧对于实现高起始电位至关重要。这项工作表明,除了碳结构和氮化学之外,还有更多因素在起作用。