Author
Listed:
- Kang Xia
(The University of Tokyo)
- Takafumi Yatabe
(The University of Tokyo)
- Kentaro Yonesato
(The University of Tokyo)
- Soichi Kikkawa
(Tokyo Metropolitan University)
- Seiji Yamazoe
(Tokyo Metropolitan University)
- Ayako Nakata
(National Institute for Materials Science (NIMS))
- Ryo Ishikawa
(The University of Tokyo)
- Naoya Shibata
(The University of Tokyo)
- Yuichi Ikuhara
(The University of Tokyo)
- Kazuya Yamaguchi
(The University of Tokyo)
- Kosuke Suzuki
(The University of Tokyo)
Abstract
Owing to their remarkable properties, gold nanoparticles are applied in diverse fields, including catalysis, electronics, energy conversion and sensors. However, for catalytic applications of colloidal gold nanoparticles, the trade-off between their reactivity and stability is a significant concern. Here we report a universal approach for preparing stable and reactive colloidal small (~3 nm) gold nanoparticles by using multi-dentate polyoxometalates as protecting agents in non-polar solvents. These nanoparticles exhibit exceptional stability even under conditions of high concentration, long-term storage, heating and addition of bases. Moreover, they display excellent catalytic performance in various oxidation reactions of organic substrates using molecular oxygen as the sole oxidant. Our findings highlight the ability of inorganic multi-dentate ligands with structural stability and robust steric and electronic effects to confer stability and reactivity upon gold nanoparticles. This approach can be extended to prepare metal nanoparticles other than gold, enabling the design of novel nanomaterials with promising applications.
Suggested Citation
Kang Xia & Takafumi Yatabe & Kentaro Yonesato & Soichi Kikkawa & Seiji Yamazoe & Ayako Nakata & Ryo Ishikawa & Naoya Shibata & Yuichi Ikuhara & Kazuya Yamaguchi & Kosuke Suzuki, 2024.
"Ultra-stable and highly reactive colloidal gold nanoparticle catalysts protected using multi-dentate metal oxide nanoclusters,"
Nature Communications, Nature, vol. 15(1), pages 1-11, December.
Handle:
RePEc:nat:natcom:v:15:y:2024:i:1:d:10.1038_s41467-024-45066-9
DOI: 10.1038/s41467-024-45066-9
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