Please use this identifier to cite or link to this item: https://doi.org/10.1038/s41467-020-17068-w
Title: Heterophase fcc-2H-fcc gold nanorods
Authors: Fan, Z.
Bosman, M. 
Huang, Z.
Chen, Y.
Ling, C.
Wu, L.
Akimov, Y.A.
Laskowski, R.
Chen, B.
Ercius, P.
Zhang, J.
Qi, X.
Goh, M.H.
Ge, Y.
Zhang, Z.
Niu, W.
Wang, J.
Zheng, H.
Zhang, H.
Issue Date: 2020
Publisher: Nature Research
Citation: Fan, Z., Bosman, M., Huang, Z., Chen, Y., Ling, C., Wu, L., Akimov, Y.A., Laskowski, R., Chen, B., Ercius, P., Zhang, J., Qi, X., Goh, M.H., Ge, Y., Zhang, Z., Niu, W., Wang, J., Zheng, H., Zhang, H. (2020). Heterophase fcc-2H-fcc gold nanorods. Nature Communications 11 (1) : 3293. ScholarBank@NUS Repository. https://doi.org/10.1038/s41467-020-17068-w
Rights: Attribution 4.0 International
Abstract: The crystal phase-based heterostructures of noble metal nanomaterials are of great research interest for various applications, such as plasmonics and catalysis. However, the synthesis of unusual crystal phases of noble metals still remains a great challenge, making the construction of heterophase noble metal nanostructures difficult. Here, we report a one-pot wet-chemical synthesis of well-defined heterophase fcc-2H-fcc gold nanorods (fcc: face-centred cubic; 2H: hexagonal close-packed with stacking sequence of “AB”) at mild conditions. Single particle-level experiments and theoretical investigations reveal that the heterophase gold nanorods demonstrate a distinct optical property compared to that of the conventional fcc gold nanorods. Moreover, the heterophase gold nanorods possess superior electrocatalytic activity for the carbon dioxide reduction reaction over their fcc counterparts under ambient conditions. First-principles calculations suggest that the boosted catalytic performance stems from the energetically favourable adsorption of reaction intermediates, endowed by the unique heterophase characteristic of gold nanorods. © 2020, The Author(s).
Source Title: Nature Communications
URI: https://scholarbank.nus.edu.sg/handle/10635/198177
ISSN: 2041-1723
DOI: 10.1038/s41467-020-17068-w
Rights: Attribution 4.0 International
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