Issue 44, 2024

Asymmetric magnetic nanosnowman loaded with AgPd nanocage toward NIR-enhanced catalytic activity

Abstract

Although bimetallic noble nanostructures often possess high activity in nanocatalysis, their controllable fabrication, tunable catalytic activity, and easy separation remain significant challenges. In this study, an Fe3O4@AgPd/Polydopamine (Fe3O4@AgPd/PDA) nanosnowman loaded with an AgPd nanocage was designed by a one-step template-disposition-redox polymerization method. The AgPd nanocage endowed the product with high catalytic activity for the reduction of organic pollutants (4-NP, MO, MB). Interestingly, under near-infrared (NIR) light, the catalytic kinetics of the Fe3O4@AgPd/PDA nanosnowman on catalytic reduction of organic pollutants increased by 2.6, 1.57, and 5.45 times, respectively. The asymmetric nanostructure facilitated the separation of electron–hole pairs, promoted electron transfer, and accelerated the catalytic activity. Density functional theory (DFT) analysis indicated that the electron transfer between the AgPd alloy and the Fe3O4 nanosphere played a critical role on the high catalytic activity. Moreover, Fe3O4@AgPd/PDA also demonstrated excellent catalytic activity in the Heck carbon–carbon coupling reaction with a >95% conversion rate and >99% selectivity. Owing to the well-encapsulated PDA shell and outstanding magnetic properties, the Fe3O4@AgPd/PDA nanosnowman exhibited good cyclic catalytic activity. With its multi-mode catalysis, NIR-enhanced catalytic activity, and easy separation, the Fe3O4@AgPd/PDA nanosnowman exhibits great application potential in nanocatalysis.

Graphical abstract: Asymmetric magnetic nanosnowman loaded with AgPd nanocage toward NIR-enhanced catalytic activity

Supplementary files

Article information

Article type
Paper
Submitted
26 Aug 2024
Accepted
10 Oct 2024
First published
14 Oct 2024

Dalton Trans., 2024,53, 17864-17879

Asymmetric magnetic nanosnowman loaded with AgPd nanocage toward NIR-enhanced catalytic activity

J. Jin, H. Li, H. Wang, Q. Fang, Y. Xu, W. Kong, X. Chen, K. C. Leung, H. Wang and S. Xuan, Dalton Trans., 2024, 53, 17864 DOI: 10.1039/D4DT02425G

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