Zhang, J., Wu, X., Cheong, W. C., Chen, W., Lin, R., Li, J., Zheng, L., Yan, W., Gu, L., Chen, C., Peng, Q., Wang, D., & Li, Y. (2018). Cation vacancy stabilization of single-atomic-site Pt 1 /Ni(OH) x catalyst for diboration of alkynes and alkenes Nature Communications, 9(1), Article 1002. https://doi.org/10.1038/s41467-018-03380-z
Zhang, Jian ; Wu, Xi ; Cheong, Weng Chon et al. / Cation vacancy stabilization of single-atomic-site Pt 1 /Ni(OH) x catalyst for diboration of alkynes and alkenes In: Nature Communications. 2018 ; Vol. 9, No. 1.
@article{50ab6a3590ce482bbd5adb811e83c735,
title = " Cation vacancy stabilization of single-atomic-site Pt 1 /Ni(OH) x catalyst for diboration of alkynes and alkenes ",
abstract = " Development of single-atomic-site catalysts with high metal loading is highly desirable but proved to be very challenging. Although utilizing defects on supports to stabilize independent metal atoms has become a powerful method to fabricate single-atomic-site catalysts, little attention has been devoted to cation vacancy defects. Here we report a nickel hydroxide nanoboard with abundant Ni 2+ vacancy defects serving as the practical support to achieve a single-atomic-site Pt catalyst (Pt 1 /Ni(OH) x ) containing Pt up to 2.3 wt% just by a simple wet impregnation method. The Ni 2+ vacancies are found to have strong stabilizing effect of single-atomic Pt species, which is determined by X-ray absorption spectrometry analyses and density functional theory calculations. This Pt 1 /Ni(OH) x catalyst shows a high catalytic efficiency in diboration of a variety of alkynes and alkenes, yielding an overall turnover frequency value upon reaction completion for phenylacetylene of ~3000 h -1 , which is much higher than other reported heterogeneous catalysts.",
author = "Jian Zhang and Xi Wu and Cheong, {Weng Chon} and Wenxing Chen and Rui Lin and Jia Li and Lirong Zheng and Wensheng Yan and Lin Gu and Chen Chen and Qing Peng and Dingsheng Wang and Yadong Li",
note = "Publisher Copyright: {\textcopyright} 2018 The Author(s).",
year = "2018",
month = dec,
day = "1",
doi = "10.1038/s41467-018-03380-z",
language = "English",
volume = "9",
journal = "Nature Communications",
issn = "2041-1723",
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Zhang, J, Wu, X, Cheong, WC, Chen, W, Lin, R, Li, J, Zheng, L, Yan, W, Gu, L, Chen, C, Peng, Q, Wang, D & Li, Y 2018, ' Cation vacancy stabilization of single-atomic-site Pt 1 /Ni(OH) x catalyst for diboration of alkynes and alkenes ', Nature Communications, vol. 9, no. 1, 1002. https://doi.org/10.1038/s41467-018-03380-z
Cation vacancy stabilization of single-atomic-site Pt 1 /Ni(OH) x catalyst for diboration of alkynes and alkenes . / Zhang, Jian; Wu, Xi; Cheong, Weng Chon et al.
In:
Nature Communications, Vol. 9, No. 1, 1002, 01.12.2018.
Research output: Contribution to journal › Article › peer-review
TY - JOUR
T1 - Cation vacancy stabilization of single-atomic-site Pt 1 /Ni(OH) x catalyst for diboration of alkynes and alkenes
AU - Zhang, Jian
AU - Wu, Xi
AU - Cheong, Weng Chon
AU - Chen, Wenxing
AU - Lin, Rui
AU - Li, Jia
AU - Zheng, Lirong
AU - Yan, Wensheng
AU - Gu, Lin
AU - Chen, Chen
AU - Peng, Qing
AU - Wang, Dingsheng
AU - Li, Yadong
N1 - Publisher Copyright:
© 2018 The Author(s).
PY - 2018/12/1
Y1 - 2018/12/1
N2 - Development of single-atomic-site catalysts with high metal loading is highly desirable but proved to be very challenging. Although utilizing defects on supports to stabilize independent metal atoms has become a powerful method to fabricate single-atomic-site catalysts, little attention has been devoted to cation vacancy defects. Here we report a nickel hydroxide nanoboard with abundant Ni 2+ vacancy defects serving as the practical support to achieve a single-atomic-site Pt catalyst (Pt 1 /Ni(OH) x ) containing Pt up to 2.3 wt% just by a simple wet impregnation method. The Ni 2+ vacancies are found to have strong stabilizing effect of single-atomic Pt species, which is determined by X-ray absorption spectrometry analyses and density functional theory calculations. This Pt 1 /Ni(OH) x catalyst shows a high catalytic efficiency in diboration of a variety of alkynes and alkenes, yielding an overall turnover frequency value upon reaction completion for phenylacetylene of ~3000 h -1 , which is much higher than other reported heterogeneous catalysts.
AB - Development of single-atomic-site catalysts with high metal loading is highly desirable but proved to be very challenging. Although utilizing defects on supports to stabilize independent metal atoms has become a powerful method to fabricate single-atomic-site catalysts, little attention has been devoted to cation vacancy defects. Here we report a nickel hydroxide nanoboard with abundant Ni 2+ vacancy defects serving as the practical support to achieve a single-atomic-site Pt catalyst (Pt 1 /Ni(OH) x ) containing Pt up to 2.3 wt% just by a simple wet impregnation method. The Ni 2+ vacancies are found to have strong stabilizing effect of single-atomic Pt species, which is determined by X-ray absorption spectrometry analyses and density functional theory calculations. This Pt 1 /Ni(OH) x catalyst shows a high catalytic efficiency in diboration of a variety of alkynes and alkenes, yielding an overall turnover frequency value upon reaction completion for phenylacetylene of ~3000 h -1 , which is much higher than other reported heterogeneous catalysts.
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U2 - 10.1038/s41467-018-03380-z
DO - 10.1038/s41467-018-03380-z
M3 - Article
C2 - 29520021
AN - SCOPUS:85048279423
SN - 2041-1723
VL - 9
JO - Nature Communications
JF - Nature Communications
IS - 1
M1 - 1002
ER -
Zhang J, Wu X, Cheong WC, Chen W, Lin R, Li J et al. Cation vacancy stabilization of single-atomic-site Pt 1 /Ni(OH) x catalyst for diboration of alkynes and alkenes Nature Communications. 2018 Dec 1;9(1):1002. doi: 10.1038/s41467-018-03380-z