Please use this identifier to cite or link to this item: https://doi.org/10.1038/s41467-020-18080-w
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dc.titleAtomically-precise dopant-controlled single cluster catalysis for electrochemical nitrogen reduction
dc.contributor.authorYao, C.
dc.contributor.authorGuo, N.
dc.contributor.authorXi, S.
dc.contributor.authorXu, C.-Q.
dc.contributor.authorLiu, W.
dc.contributor.authorZhao, X.
dc.contributor.authorLi, J.
dc.contributor.authorFang, H.
dc.contributor.authorSu, J.
dc.contributor.authorChen, Z.
dc.contributor.authorYan, H.
dc.contributor.authorQiu, Z.
dc.contributor.authorLyu, P.
dc.contributor.authorChen, C.
dc.contributor.authorXu, H.
dc.contributor.authorPeng, X.
dc.contributor.authorLi, X.
dc.contributor.authorLiu, B.
dc.contributor.authorSu, C.
dc.contributor.authorPennycook, S.J.
dc.contributor.authorSun, C.-J.
dc.contributor.authorLi, J.
dc.contributor.authorZhang, C.
dc.contributor.authorDu, Y.
dc.contributor.authorLu, J.
dc.date.accessioned2021-08-19T05:01:14Z
dc.date.available2021-08-19T05:01:14Z
dc.date.issued2020
dc.identifier.citationYao, C., Guo, N., Xi, S., Xu, C.-Q., Liu, W., Zhao, X., Li, J., Fang, H., Su, J., Chen, Z., Yan, H., Qiu, Z., Lyu, P., Chen, C., Xu, H., Peng, X., Li, X., Liu, B., Su, C., Pennycook, S.J., Sun, C.-J., Li, J., Zhang, C., Du, Y., Lu, J. (2020). Atomically-precise dopant-controlled single cluster catalysis for electrochemical nitrogen reduction. Nature Communications 11 (1) : 4389. ScholarBank@NUS Repository. https://doi.org/10.1038/s41467-020-18080-w
dc.identifier.issn2041-1723
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/198310
dc.description.abstractThe ability to precisely engineer the doping of sub-nanometer bimetallic clusters offers exciting opportunities for tailoring their catalytic performance with atomic accuracy. However, the fabrication of singly dispersed bimetallic cluster catalysts with atomic-level control of dopants has been a long-standing challenge. Herein, we report a strategy for the controllable synthesis of a precisely doped single cluster catalyst consisting of partially ligand-enveloped Au4Pt2 clusters supported on defective graphene. This creates a bimetal single cluster catalyst (Au4Pt2/G) with exceptional activity for electrochemical nitrogen (N2) reduction. Our mechanistic study reveals that each N2 molecule is activated in the confined region between cluster and graphene. The heteroatom dopant plays an indispensable role in the activation of N2 via an enhanced back donation of electrons to the N2 LUMO. Moreover, besides the heteroatom Pt, the catalytic performance of single cluster catalyst can be further tuned by using Pd in place of Pt as the dopant. © 2020, The Author(s).
dc.publisherNature Research
dc.rightsAttribution 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.sourceScopus OA2020
dc.typeArticle
dc.contributor.departmentCHEMISTRY
dc.contributor.departmentMATERIALS SCIENCE AND ENGINEERING
dc.contributor.departmentPHYSICS
dc.description.doi10.1038/s41467-020-18080-w
dc.description.sourcetitleNature Communications
dc.description.volume11
dc.description.issue1
dc.description.page4389
dc.published.statePublished
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