Journal
ADVANCED MATERIALS
Volume 34, Issue 43, Pages -Publisher
WILEY-V C H VERLAG GMBH
DOI: 10.1002/adma.202205153
Keywords
cell-mimicking; hollow structures; hydrogenation reactions; nanoreactors; polymers
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Funding
- National Natural Science Foundation of China [21902157]
- Liaoning Provincial Natural Science Foundation of China [2019-BS-239]
- National Postdoctoral Program for Innovative Talents [BX20180296]
- China Postdoctoral Science Foundation [2018M641720]
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Hollow nanostructures with fascinating properties have attracted extensive research interest. In this study, a top-down chemical surgery strategy was introduced to precisely control the synthesis of cell-mimicking complex hollow architectures. The transformation process was tracked and demonstrated the ability to accurately confine gold nanoparticles. By selectively depositing palladium nanoparticles, bimetallic catalysts with excellent hydrogenation performance were obtained.
Hollow nanostructures with fascinating properties have inspired numerous interests in broad research fields. Cell-mimicking complex hollow architectures with precise active components distributions are particularly important, while their synthesis remains highly challenging. Herein, a top-down chemical surgery strategy is introduced to engrave the 3-aminophenol formaldehyde resin (APF) spheres at nanoscale. Undergoing the cleavage of (Ar)C-N bonds with ethanol as chemical scissors and subsequent repolymerization process, the Solid APF transform to multilevel hollow architecture with precise nanospatial distribution of organic functional groups (e.g., hydroxymethyl and amine). The transformation is tracked by electron microscopy and solid-state nuclear magnetic resonance techniques, the category and dosage of alcohol are pivotal for constructing multilevel hollow structures. Moreover, it is demonstrated the evolution of nanostructures accompanied with unique organic microenvironments is able to accurately confine multiple gold (Au) nanoparticles, leading to the formation of pomegranate-like particles. Through selectively depositing palladium (Pd) nanoparticles onto the outer shell, bimetallic Au@APF@Pd catalysts are formed, which exhibit excellent hydrogenation performance with turnover frequency (TOF) value up to 11257 h(-1). This work provides an effective method for precisely manipulating the nanostructure and composition of polymers at nanoscale and sheds light on the design of catalysts with precise spatial active components.
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