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通过在流动反应器中一次性注入无卤前驱体连续制备Ag@Pd纳米立方体和Pd基纳米框架。

Synthesis of Ag@Pd Nanocubes and Pd-based Nanoframes via One-Shot Injection of a Halide-Free Precursor for Continuous Production in a Flow Reactor.

作者信息

Yu Hansong, He Jianlong, Li Kei Kwan, Huang Qijia, Ding Yong, Xia Younan

机构信息

School of Materials Science and Engineering, Georgia Institute of Technology, Atlanta, Georgia, 30332, United States.

School of Chemistry and Biochemistry, Georgia Institute of Technology, Atlanta, Georgia, 30332, United States.

出版信息

Chemistry. 2025 Apr 22;31(23):e202500201. doi: 10.1002/chem.202500201. Epub 2025 Mar 21.

Abstract

Noble-metal open nanostructures have remarkable catalytic capabilities toward a wide range of reactions. In particular, Pd-based open nanostructures have been synthesized and validated for superior catalytic performance toward formic acid oxidation. However, most of the syntheses are based on dropwise addition, making it challenging to increase the production volume. In this work, we present a facile approach to the synthesis of Ag@Pd core-frame nanocubes and then Pd-based nanoframes through one-shot injection. In a typical synthesis, Ag nanocubes are dispersed in an aqueous solution of ascorbic acid and polyvinylpyrrolidone at room temperature, followed by the injection of Pd(NH)(NO) precursor in one shot. The Pd(NH)(NO) precursor has a much slower reduction kinetics relative to NaPdCl, preventing self-nucleation and enabling controlled deposition of Pd atoms on the Ag nanocubes. The lower reduction potential of Pd(NH)(NO) also helps minimize the galvanic replacement reaction, facilitating uniform deposition of Pd atoms. After selectively etching away the Ag template, Pd-based nanoframes with a rigid cubic structure are obtained. Finally, the synthesis is successfully adapted to a continuous flow system, generating Ag@Pd nanocubes with comparable quality to those obtained via one-shot synthesis, demonstrating a practical route to large-scale production of Pd-based nanoframes with HO etching.

摘要

贵金属开放纳米结构对多种反应具有卓越的催化能力。特别是,基于钯的开放纳米结构已被合成并验证对甲酸氧化具有优异的催化性能。然而,大多数合成方法基于滴加,这使得扩大产量具有挑战性。在这项工作中,我们提出了一种简便的方法来合成Ag@Pd核框架纳米立方体,然后通过一次注射合成基于钯的纳米框架。在典型的合成中,将银纳米立方体在室温下分散在抗坏血酸和聚乙烯吡咯烷酮的水溶液中,然后一次性注射Pd(NH)(NO)前驱体。与NaPdCl相比,Pd(NH)(NO)前驱体的还原动力学要慢得多,可防止自核化并使钯原子在银纳米立方体上可控沉积。Pd(NH)(NO)较低的还原电位也有助于最小化电化置换反应,促进钯原子的均匀沉积。选择性蚀刻掉银模板后,获得具有刚性立方结构的基于钯的纳米框架。最后,该合成方法成功应用于连续流动系统,生成了与通过一次注射合成获得的质量相当的Ag@Pd纳米立方体,证明了一种通过HO蚀刻大规模生产基于钯的纳米框架的实用途径。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/78e2/12015395/430b22219106/CHEM-31-e202500201-g005.jpg

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