Natural halloysite nanotubes enclosing PdAg alloy nanoparticles as nanoreactors with enhanced catalytic performance
- Authors
- Zhou, Tao; Liu, Zhe; Kim, Kyeounghak; Yu, Taekyung
- Issue Date
- Dec-2025
- Publisher
- Academic Press
- Keywords
- Halloysite nanotubes; PdAg nanoparticles; Nanoreactor; Recyclability; Spatially confinement catalysis
- Citation
- Journal of Colloid and Interface Science, v.700, pp 1 - 14
- Pages
- 14
- Indexed
- SCIE
SCOPUS
- Journal Title
- Journal of Colloid and Interface Science
- Volume
- 700
- Start Page
- 1
- End Page
- 14
- URI
- https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/208692
- DOI
- 10.1016/j.jcis.2025.138531
- ISSN
- 0021-9797
1095-7103
- Abstract
- Hollow nanoreactors, with their void-confinement effects and stable carrier properties, hold great promise for catalytic applications. In this study, we present a green and versatile method to confine PdAg alloy nanoparticles (NPs) within halloysite nanotubes (HNTs), creating highly efficient catalysts (PdxAgy@HNTs-OH) for the reduction of toxic pollutants like 4-nitrophenol (4-NP), Methyl Orange (MO), and Congo Red (CR). PdAg NPs are selectively anchored to the inner surface of HNTs, with the exclusively lumen-confined PdAg3@HNTs-OH exhibiting superior activity compared to dual-surface-loaded counterparts (d-PdAg3@HNTs), directly evidencing the critical role of void confinement. Experimental and density functional theory (DFT) studies reveal that HNTs modulate the electronic structure of PdAg NPs, reducing energy barriers for 4-NP adsorption and intermediate conversion. This electronic optimization, combined with spatial confinement, ensures exceptional catalytic performance. The work establishes a dual engineering strategy that integrates electronic regulation with nanoscale spatial control to design high-performance catalytic nanoreactors.
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