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用于可调谐合成单原子、团簇和纳米颗粒催化剂的非晶态到晶态转变:金属元素(铜、钴、镍、钇、铯)在多孔二维超薄氧化铝纳米片上的分散

Amorphous-to-Crystalline Transformation for Tunable Synthesis of Single Atom, Cluster, and Nanoparticle Catalysts: Dispersion of Metal Elements (Cu, Co, Ni, Y, Cs) on Holey 2D Ultra-Thin AlO Nanosheets.

作者信息

Wang Yaping, Zhang Tingshi, Huang Xinlian, Zeng Yurong, Wei Siyuan, Zhuang Zanyong, Zhu Chongbing, Yu Yan

机构信息

College of Materials Science and Engineering, Fuzhou University, New Campus, Minhou, Fujian, 350108, China.

Key Laboratory of Advanced Materials Technologies, Fuzhou University, Fuzhou, 350108, China.

出版信息

Small Methods. 2025 Jul;9(7):e2402072. doi: 10.1002/smtd.202402072. Epub 2025 Apr 10.

DOI:10.1002/smtd.202402072
PMID:40211597
Abstract

Herein, a versatile amorphous-to-crystalline transformation (ACT) strategy is described, to furnish various metals (Cu, Co, Ni, Cs, and Y) based atomically dispersed catalysts (ADCs) on thin holey 2D AlO. This approach, which involves adjusting reactant stoichiometry, enables the continuous modulation of particle size of ADCs at an atomical level, giving the ultrafine products as single atom, cluster, or nanoparticle catalysts. This synthesis method allows a straightforward analysis and comparison of the reactivity of the ADCs catalysts based on the dispersion of the active metal. In the case of Cu, the cluster catalyst 0.2-Cu/AlO outperforms the single atom catalyst 0.1-Cu/AlO and the nanoparticle catalyst 0.3-Cu/AlO in the oxidation of refractory organic molecules, thanks to its superior electron transport and surface adsorption properties. These findings are well supported by the Density functional theory (DFT) calculations. Additionally, this method facilitates the preparation of atomic clusters with a very small size of 0.5-1 nm, composed of just a few atoms, as exemplified by Ni-based ADCs. The developed synthesis enriches the library of ADCs and demonstrates the potential of amorphous-to-crystalline transformation in creating advanced ultrasmall functional materials.

摘要

本文描述了一种通用的非晶态到晶态转变(ACT)策略,用于在有孔的二维薄AlO上制备各种基于金属(铜、钴、镍、铯和钇)的原子分散催化剂(ADC)。这种方法通过调整反应物化学计量比,能够在原子水平上连续调节ADC的粒径,从而得到作为单原子、团簇或纳米颗粒催化剂的超精细产物。这种合成方法基于活性金属的分散情况,能够直接分析和比较ADC催化剂的反应活性。以铜为例,在难熔有机分子的氧化反应中,团簇催化剂0.2-Cu/AlO优于单原子催化剂0.1-Cu/AlO和纳米颗粒催化剂0.3-Cu/AlO,这得益于其优异的电子传输和表面吸附性能。密度泛函理论(DFT)计算很好地支持了这些发现。此外,这种方法有助于制备尺寸非常小(0.5-1纳米)、仅由几个原子组成的原子团簇,如镍基ADC所示。所开发的合成方法丰富了ADC的种类,并展示了非晶态到晶态转变在制备先进的超小型功能材料方面的潜力。

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