National Institute of Advanced Industrial Science and Technology (AIST), Ikeda, Osaka 563-8577, Japan.
J Am Chem Soc. 2009 Mar 4;131(8):2778-9. doi: 10.1021/ja808830a.
Carbon-supported Fe@Pt core-shell nanoparticle (NP) catalysts with Fe cores in different crystal states have been successfully synthesized by a sequential reduction process. Unexpectedly, in contrast to its crystallized counterpart, iron in the amorphous state exerts a distinct and powerful ability as the core for the Fe@Pt NPs. The resultant NPs are far more active for ammonia borane oxidation (by up to 354%) than the commercial Pt/C catalysts. Furthermore, these NPs combine low cost, long-term stability, and easy recovery functions.
通过顺序还原法成功制备了具有不同晶体状态 Fe 核的负载于碳的 Fe@Pt 核壳纳米粒子(NP)催化剂。出乎意料的是,与晶态的 Fe 相比,非晶态的 Fe 作为 Fe@Pt NPs 的核表现出明显而强大的能力。与商业 Pt/C 催化剂相比,所得的 NPs 对硼烷氨氧化的活性提高了 354%。此外,这些 NPs 还具有成本低、长期稳定性和易于回收等功能。