Chakraborty Arup, Devivaraprasad Ruttala, Bera Bapi, Neergat Manoj
Department of Energy Science and Engineering, Indian Institute of Technology Bombay (IITB), Powai, Mumbai-400076, India.
Phys Chem Chem Phys. 2017 Sep 27;19(37):25414-25422. doi: 10.1039/c7cp04285j.
Carbon is heat-treated with a nitrogen-containing precursor (ammonia) to obtain nitrogen-doped carbon and the composition is estimated using CHN and XPS analysis. The active site density of the carbon and nitrogen-doped carbon is quantified using 1,2-dihydroxybenzene (catechol) molecules as an adsorbate in phosphate buffer (pH 7) solution. The features of the voltammograms of the catechol-adsorbed high surface area carbon and nitrogen-doped carbon are similar to that of the polished nitrogen-grafted glassy carbon electrode (GCE) reported in the literature. At the same time, the polished GCE does not show any well-defined catechol adsorption features. It is found that the adsorption charge (obtained by integrating the peak area, after subtracting the background) is in the order of N/C 900 > N/C 1000 > N/C 800 > N/C 700 > C. A similar trend is observed in their oxygen reduction reaction (ORR) activity in 0.1 M KOH. Moreover, the turnover frequency (ToF) of the catalysts is calculated and it is comparable to that reported in the literature using other methods for non-precious catalysts. Therefore, the adsorption charge can be correlated with the active site density of the carbon and nitrogen-doped carbon samples.
用含氮前驱体(氨)对碳进行热处理以获得氮掺杂碳,并使用CHN和XPS分析来估算其组成。在磷酸盐缓冲液(pH 7)溶液中,以1,2 - 二羟基苯(儿茶酚)分子作为吸附质,对碳和氮掺杂碳的活性位点密度进行定量。儿茶酚吸附的高表面积碳和氮掺杂碳的伏安图特征与文献报道的抛光氮接枝玻碳电极(GCE)相似。同时,抛光的GCE未显示出任何明确的儿茶酚吸附特征。发现吸附电荷(通过减去背景后对峰面积进行积分获得)的顺序为N/C 900 > N/C 1000 > N/C 800 > N/C 700 > C。在它们于0.1 M KOH中的氧还原反应(ORR)活性中也观察到类似趋势。此外,计算了催化剂的周转频率(ToF),其与文献中使用其他方法对非贵金属催化剂报道的结果相当。因此,吸附电荷可以与碳和氮掺杂碳样品的活性位点密度相关联。