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一锅法合成具有高催化性能的三金属 Au@PdPt 核壳纳米粒子。

One-pot synthesis of trimetallic Au@PdPt core-shell nanoparticles with high catalytic performance.

机构信息

Department of Chemistry and KI for the NanoCentury, KAIST , Daejeon 305-701, Korea, and Center for Nanomaterials and Chemical Reactions, Institute for Basic Science (IBS), Daejeon 305-701, Korea.

出版信息

ACS Nano. 2013 Sep 24;7(9):7945-55. doi: 10.1021/nn403027j. Epub 2013 Aug 8.

Abstract

The development of an efficient synthesis method to produce multimetallic nanoparticles (NPs) with a desirable structure is strongly required to clarify the structure-composition-property relationship of NPs and to investigate their possible applications. However, the controlled synthesis of NPs consisting of multiple (n ≥ 3) noble metal components has been relatively unexplored in comparison to bimetallic NPs. In the present work, we have demonstrated a facile one-pot aqueous approach for the controlled synthesis of trimetallic Au@PdPt core-shell NPs with a well-defined octahedral Au core and a highly crystalline dendritic Pd-Pt alloy shell (Auoct@PdPt NPs). The simultaneous reduction of multiple metal precursors with dual reducing agents, namely, ascorbic acid and hydrazine, gave a fine control over the nucleation and growth kinetics of NPs, resulting in the formation of novel Auoct@PdPt NPs. The prepared NPs showed excellent catalytic performance for methanol electrooxidation, which can be attributed to their optimized binding strength toward adsorbate molecules due to the improved charge transfer between core and shell of the NPs. The present strategy can offer a convenient and valuable way to fabricate multicomponent nanostructures with desired structures and functions.

摘要

开发一种有效的合成方法来制备具有理想结构的多金属纳米粒子(NPs),对于阐明 NPs 的结构-组成-性能关系以及研究它们的潜在应用具有重要意义。然而,与双金属 NPs 相比,由多种(n≥3)贵金属组分组成的 NPs 的可控合成相对较少被探索。在本工作中,我们展示了一种简便的一锅水相法,用于可控合成具有明确八面体 Au 核和高度结晶树枝状 Pd-Pt 合金壳(Auoct@PdPt NPs)的三金属 Au@PdPt 核壳 NPs。使用两种还原剂,即抗坏血酸和水合肼,同时还原多种金属前体,可以很好地控制 NPs 的成核和生长动力学,从而形成新颖的 Auoct@PdPt NPs。所制备的 NPs 在甲醇电氧化中表现出优异的催化性能,这归因于它们由于 NPs 核壳之间的电荷转移得到改善,从而对吸附分子具有优化的结合强度。本策略为制备具有所需结构和功能的多组分纳米结构提供了一种简便而有价值的方法。

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