Han Xiao, Zheng Zhiping, Chen Jiayu, Xue Yakun, Li Huiqi, Zheng Jun, Xie Zhaoxiong, Kuang Qin, Zheng Lansun
State Key Laboratory of Physical Chemistry of Solid Surfaces & Department of Chemistry, College of Chemistry and Chemical Engineering, Xiamen University, Xiamen 361005, P. R. China.
Institute of Physical Science and Information Technology, Anhui University, Hefei 230601, P. R. China.
Nanoscale. 2019 Jul 14;11(26):12610-12618. doi: 10.1039/c9nr02914a. Epub 2019 Jun 24.
In the past decade, tremendous efforts have been devoted to the search for the alternatives to Pt-based catalysts for the oxygen reduction reaction (ORR) in fuel cells and metal-air batteries. Recently, metal-nitrogen-carbon (M-N-C) systems, especially 3d transition metals (TM) and their alloys encapsulated in nitrogen-doped carbon based materials (TM@N-C), have attracted increasing attention due to their low cost and high ORR activity. Here, a simple and novel strategy is developed to synthesize sandwich-structured TM@N-C composites, in which ultrafine Fe nanoparticles are encapsulated in nitrogen-doped carbon nanotubes (N-CNTs) grafted on both sides of reduced graphene oxide (rGO) sheets by pyrolysis of ammonium ferric citrate-functionalized zeolitic imidazolate framework-8@graphene oxide (Fe@ZIF-8@GO). The resulting Fe@N-CNTs@rGO composites naturally integrate zero-dimensional (0D) Fe nanoparticles, one-dimensional (1D) N-CNTs, and two-dimensional (2D) graphene into a three-dimensional (3D) hierarchical architecture with highly dispersed active sites, a large surface area, and abundant porosity. Because of these structural advantages, the sandwich-structured Fe@N-CNTs@rGO composites display a half-wave potential of 0.83 V in a 0.1 M KOH solution for the ORR, comparable to that of commercial Pt/C catalysts, and more excellent durability and resistance to fuel molecules. The proposed strategy paves a new way for the synthesis of non-precious high-performance electrocatalysts for energy conversion applications.
在过去十年中,人们付出了巨大努力来寻找用于燃料电池和金属空气电池中氧还原反应(ORR)的铂基催化剂替代品。最近,金属氮碳(M-N-C)体系,特别是封装在氮掺杂碳基材料(TM@N-C)中的3d过渡金属(TM)及其合金,因其低成本和高ORR活性而受到越来越多的关注。在此,我们开发了一种简单新颖的策略来合成三明治结构的TM@N-C复合材料,其中通过柠檬酸铁铵功能化的沸石咪唑酯骨架-8@氧化石墨烯(Fe@ZIF-8@GO)的热解,将超细铁纳米颗粒封装在接枝于还原氧化石墨烯(rGO)片两侧的氮掺杂碳纳米管(N-CNTs)中。所得的Fe@N-CNTs@rGO复合材料自然地将零维(0D)铁纳米颗粒、一维(1D)N-CNTs和二维(2D)石墨烯整合到具有高度分散的活性位点、大表面积和丰富孔隙率的三维(3D)分级结构中。由于这些结构优势,三明治结构的Fe@N-CNTs@rGO复合材料在0.1 M KOH溶液中对ORR的半波电位为0.83 V,与商业Pt/C催化剂相当,并且具有更优异的耐久性和对燃料分子的耐受性。所提出的策略为合成用于能量转换应用的非贵金属高性能电催化剂开辟了一条新途径。