Wu Tianxing, Zhang Haimin, Zhang Xian, Zhang Yunxia, Zhao Huijun, Wang Guozhong
Key Laboratory of Materials Physics, Centre for Environmental and Energy Nanomaterials, Anhui Key Laboratory of Nanomaterials and Nanostructures, Institute of Solid State Physics, Chinese Academy of Sciences, Hefei 230031, P. R. China.
Phys Chem Chem Phys. 2015 Nov 7;17(41):27527-33. doi: 10.1039/c5cp04252f.
In this work, chitosan whiskers (CWs) were first extracted using low-cost and earth-abundant crab shells as materials by a series of chemical processes, and then assembled into chitosan whisker microspheres (CWMs) via a simple photochemical polymerization approach. Subsequently, a cementite (Fe3C) nanocrystal@N-doped graphitic carbon (Fe3C@NGC) nanocomposite was successfully fabricated by high temperature pyrolysis of CWMs adsorbed with ferric acetylacetonate (Fe(acac)3) at 900 °C. It was found that a suitable growth atmosphere generated inside CWMs during high temperature pyrolysis is critically important to form Fe3C nanocrystal cores, concurrently accompanying a structural transformation from chitosan whiskers to mesoporous graphitic carbon shells with natural nitrogen (N) doping properties, resulting in the formation of a core-shell structure Fe3C@NGC nanocomposite. The resulting samples were evaluated as electrocatalysts for oxygen reduction reaction (ORR). In comparison with sole N-doped graphitic carbon without Fe3C nanocrystals obtained by direct pyrolysis of chitosan whisker microspheres at 900 °C (CWMs-900), Fe3C@NGC showed significantly improved ORR catalytic activity. The tolerance to fuel cell molecules (e.g., methanol) and the durability of Fe3C@NGC are obviously superior to commercial Pt/C catalysts in alkaline media. The high ORR performance of Fe3C@NGC could be due to its large surface area (313.7 m(2) g(-1)), a synergistic role of Fe3C nanocrystals, N doping in graphitic carbon creating more catalytic active sites, and a porous structure of the nanocomposite facilitating mass transfer to efficiently improve the utilization of these catalytic active sites.
在本工作中,首先以低成本且储量丰富的蟹壳为原料,通过一系列化学工艺提取壳聚糖晶须(CWs),然后通过简单的光化学聚合方法将其组装成壳聚糖晶须微球(CWMs)。随后,通过在900℃下对吸附有乙酰丙酮铁(Fe(acac)3)的CWMs进行高温热解,成功制备了渗碳体(Fe3C)纳米晶体@N掺杂石墨碳(Fe3C@NGC)纳米复合材料。研究发现,高温热解过程中在CWMs内部产生的合适生长气氛对于形成Fe3C纳米晶体核至关重要,同时伴随着从壳聚糖晶须到具有天然氮(N)掺杂特性的介孔石墨碳壳的结构转变,从而形成核壳结构的Fe3C@NGC纳米复合材料。将所得样品评估为氧还原反应(ORR)的电催化剂。与通过在900℃下直接热解壳聚糖晶须微球获得的不含Fe3C纳米晶体的单一N掺杂石墨碳(CWMs-900)相比,Fe3C@NGC表现出显著提高的ORR催化活性。在碱性介质中,Fe3C@NGC对燃料电池分子(如甲醇)的耐受性和耐久性明显优于商业Pt/C催化剂。Fe3C@NGC的高ORR性能可能归因于其大表面积(313.7 m(2) g(-1))、Fe3C纳米晶体的协同作用、石墨碳中的N掺杂产生更多催化活性位点以及纳米复合材料的多孔结构促进传质以有效提高这些催化活性位点的利用率。