Nguyen Quynh N, Kim Eun Mi, Ding Yong, Janssen Annemieke, Wang Chenxiao, Li Kei Kwan, Kim Junseok, Fichthorn Kristen A, Xia Younan
School of Chemistry and Biochemistry, Georgia Institute of Technology, Atlanta, Georgia 30332, United States.
Department of Chemical Engineering, The Pennsylvania State University, University Park, Pennsylvania 16803, United States.
J Am Chem Soc. 2024 May 1;146(17):12040-12052. doi: 10.1021/jacs.4c01725. Epub 2024 Mar 30.
This study demonstrates the crucial role of reduction kinetics in phase-controlled synthesis of noble-metal nanocrystals using Ru nanocrystals as a case study. We found that the reduction kinetics played a more important role than the templating effect from the preformed seed in dictating the crystal structure of the deposited overlayers despite their intertwined effects on successful epitaxial growth. By employing two different polyols, a series of Ru nanocrystals with tunable sizes of 3-7 nm and distinct patterns of crystal phase were synthesized by incorporating different types of Ru seeds. Notably, the use of ethylene glycol and triethylene glycol consistently resulted in the formation of Ru shell in natural hexagonal close-packed () and metastable face-centered cubic () phases, respectively, regardless of the size and phase of the seed. Quantitative measurements and theoretical calculations suggested that this trend was a manifestation of the different reduction kinetics associated with the precursor and the chosen polyol, which, in turn, affected the reduction pathway (solution versus surface) and packing sequence of the deposited Ru atoms. This work not only underscores the essential role of reduction kinetics in controlling the packing of atoms and thus the phase taken by Ru nanocrystals but also suggests a potential extension to other noble-metal systems.
本研究以钌纳米晶体为例,证明了还原动力学在贵金属纳米晶体相控合成中的关键作用。我们发现,尽管还原动力学和预先形成的晶种的模板效应在成功的外延生长中相互交织,但在决定沉积覆盖层的晶体结构方面,还原动力学比晶种的模板效应发挥着更重要的作用。通过使用两种不同的多元醇,通过引入不同类型的钌晶种,合成了一系列尺寸可调(3 - 7纳米)且具有不同晶相模式的钌纳米晶体。值得注意的是,无论晶种的尺寸和相如何,使用乙二醇和三甘醇分别始终导致形成天然六方密堆积()相和亚稳态面心立方()相的钌壳。定量测量和理论计算表明,这种趋势是与前驱体和所选多元醇相关的不同还原动力学的体现,进而影响了还原途径(溶液相还是表面相)以及沉积的钌原子的堆积顺序。这项工作不仅强调了还原动力学在控制原子堆积从而控制钌纳米晶体所采取的相方面的重要作用,还暗示了对其他贵金属体系的潜在扩展。