Hubei Key Laboratory of Electrochemical Power Sources, Key Laboratory of Analytical Chemistry for Biology and Medicine (Ministry of Education), Department of Chemistry, Wuhan University, Wuhan 430072, China.
Phys Chem Chem Phys. 2013 Nov 14;15(42):18482-90. doi: 10.1039/c3cp53760a.
A Fe/N co-doped ternary nanocarbon hybrid, with uniform bamboo-like carbon nanotubes (CNTs) in situ grown on/between the single/few-layer graphene sheets interspaced by carbon nanosphere aggregates, was prepared through a one-pot heat treatment of a precursor mixture containing graphene oxide, Vulcan XC-72 carbon nanospheres, nitrogen rich melamine and small amounts of Fe ions. Physical characterization including electron microscopic images, N2 adsorption-desorption isotherms, pore size distribution, XPS, XRD, Mössbauer spectra, and EDX revealed that the 0-D/1-D/2-D ternary hybrid architecture not only offered an optimized morphology for high dispersion of each nanocarbon moiety, while the carbon nanosphere interspaced graphene sheets have provided a platform for efficient reaction between Fe ions and melamine molecules, resulting in uniform nucleation and growth of CNTs and formation of high density Fe-N coordination assemblies that have been believed to be the active centers for the oxygen reduction reaction (ORR) in carbon-based nonprecious metal electrocatalysts. In the absence of graphene oxides or carbon nanospheres, a similar heat treatment was found to result in large amounts of elemental Fe and Fe carbides and entangled CNTs with wide diameter distributions. As a result, the ternary Fe/N-doped nanocarbon hybrid exhibits ORR activity much higher than the Fe-N doped single or binary nanocarbon materials prepared under similar heat treatment conditions, and approaching that of the state-of-the-art carbon-supported platinum catalyst (Pt/C) in acidic media, as well as superior stability and methanol tolerance to Pt/C.
一种 Fe/N 共掺杂三元纳米碳杂化材料,具有均匀的竹状碳纳米管(CNTs)原位生长在/之间的单/少层石墨烯片之间,由包含氧化石墨烯、Vulcan XC-72 碳纳米球、富氮三聚氰胺和少量 Fe 离子的前体混合物通过一步热处理制备而成。物理特性包括电子显微镜图像、N2 吸附-解吸等温线、孔径分布、XPS、XRD、Mössbauer 光谱和 EDX 表明,0-D/1-D/2-D 三元杂化结构不仅提供了优化的形态,使每个纳米碳部分高度分散,而且碳纳米球间隔的石墨烯片为 Fe 离子和三聚氰胺分子之间的有效反应提供了平台,导致 CNTs 的均匀成核和生长以及高密度 Fe-N 配位组装的形成,据信这是碳基非贵金属电催化剂中氧还原反应(ORR)的活性中心。在没有氧化石墨烯或碳纳米球的情况下,类似的热处理被发现会导致大量的元素 Fe 和 Fe 碳化物以及具有宽直径分布的缠结 CNTs。因此,三元 Fe/N 掺杂纳米碳杂化材料表现出比在类似热处理条件下制备的 Fe-N 掺杂单或二元纳米碳材料更高的 ORR 活性,并且在酸性介质中接近最先进的碳载铂催化剂(Pt/C)的活性,以及优于 Pt/C 的稳定性和甲醇耐受性。