Single atom catalysts in Van der Waals gaps
Single-atom catalysts provide efficiently utilized active sites to improve catalytic activities while improving the stability and enhancing the activities to the level of their bulk metallic counterparts are grand challenges. Herein, we demonstrate a family of single-atom catalysts with different in...
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Published in | Nature communications Vol. 13; no. 1; pp. 6863 - 9 |
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Main Authors | , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
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London
Nature Publishing Group UK
11.11.2022
Nature Publishing Group Nature Portfolio |
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Abstract | Single-atom catalysts provide efficiently utilized active sites to improve catalytic activities while improving the stability and enhancing the activities to the level of their bulk metallic counterparts are grand challenges. Herein, we demonstrate a family of single-atom catalysts with different interaction types by confining metal single atoms into the van der Waals gap of two-dimensional SnS
2
. The relatively weak bonding between the noble metal single atoms and the host endows the single atoms with more intrinsic catalytic activity compared to the ones with strong chemical bonding, while the protection offered by the layered material leads to ultrahigh stability compared to the physically adsorbed single-atom catalysts on the surface. Specifically, the trace Pt-intercalated SnS
2
catalyst has superior long-term durability and comparable performance to that of commercial 10 wt% Pt/C catalyst in hydrogen evolution reaction. This work opens an avenue to explore high-performance intercalated single-atom electrocatalysts within various two-dimensional materials.
A family of single-atom catalysts synthesized by intercalating metal single atoms into the van der Waals gap of two-dimensional SnS
2
is reported. The materials are applied as hydrogen evolving catalysts with good durability and overpotential. |
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AbstractList | A family of single-atom catalysts synthesized by intercalating metal single atoms into the van der Waals gap of two-dimensional SnS2 is reported. The materials are applied as hydrogen evolving catalysts with good durability and overpotential. Single-atom catalysts provide efficiently utilized active sites to improve catalytic activities while improving the stability and enhancing the activities to the level of their bulk metallic counterparts are grand challenges. Herein, we demonstrate a family of single-atom catalysts with different interaction types by confining metal single atoms into the van der Waals gap of two-dimensional SnS2. The relatively weak bonding between the noble metal single atoms and the host endows the single atoms with more intrinsic catalytic activity compared to the ones with strong chemical bonding, while the protection offered by the layered material leads to ultrahigh stability compared to the physically adsorbed single-atom catalysts on the surface. Specifically, the trace Pt-intercalated SnS2 catalyst has superior long-term durability and comparable performance to that of commercial 10 wt% Pt/C catalyst in hydrogen evolution reaction. This work opens an avenue to explore high-performance intercalated single-atom electrocatalysts within various two-dimensional materials.A family of single-atom catalysts synthesized by intercalating metal single atoms into the van der Waals gap of two-dimensional SnS2 is reported. The materials are applied as hydrogen evolving catalysts with good durability and overpotential. Single-atom catalysts provide efficiently utilized active sites to improve catalytic activities while improving the stability and enhancing the activities to the level of their bulk metallic counterparts are grand challenges. Herein, we demonstrate a family of single-atom catalysts with different interaction types by confining metal single atoms into the van der Waals gap of two-dimensional SnS 2 . The relatively weak bonding between the noble metal single atoms and the host endows the single atoms with more intrinsic catalytic activity compared to the ones with strong chemical bonding, while the protection offered by the layered material leads to ultrahigh stability compared to the physically adsorbed single-atom catalysts on the surface. Specifically, the trace Pt-intercalated SnS 2 catalyst has superior long-term durability and comparable performance to that of commercial 10 wt% Pt/C catalyst in hydrogen evolution reaction. This work opens an avenue to explore high-performance intercalated single-atom electrocatalysts within various two-dimensional materials. A family of single-atom catalysts synthesized by intercalating metal single atoms into the van der Waals gap of two-dimensional SnS 2 is reported. The materials are applied as hydrogen evolving catalysts with good durability and overpotential. Single-atom catalysts provide efficiently utilized active sites to improve catalytic activities while improving the stability and enhancing the activities to the level of their bulk metallic counterparts are grand challenges. Herein, we demonstrate a family of single-atom catalysts with different interaction types by confining metal single atoms into the van der Waals gap of two-dimensional SnS2. The relatively weak bonding between the noble metal single atoms and the host endows the single atoms with more intrinsic catalytic activity compared to the ones with strong chemical bonding, while the protection offered by the layered material leads to ultrahigh stability compared to the physically adsorbed single-atom catalysts on the surface. Specifically, the trace Pt-intercalated SnS2 catalyst has superior long-term durability and comparable performance to that of commercial 10 wt% Pt/C catalyst in hydrogen evolution reaction. This work opens an avenue to explore high-performance intercalated single-atom electrocatalysts within various two-dimensional materials.Single-atom catalysts provide efficiently utilized active sites to improve catalytic activities while improving the stability and enhancing the activities to the level of their bulk metallic counterparts are grand challenges. Herein, we demonstrate a family of single-atom catalysts with different interaction types by confining metal single atoms into the van der Waals gap of two-dimensional SnS2. The relatively weak bonding between the noble metal single atoms and the host endows the single atoms with more intrinsic catalytic activity compared to the ones with strong chemical bonding, while the protection offered by the layered material leads to ultrahigh stability compared to the physically adsorbed single-atom catalysts on the surface. Specifically, the trace Pt-intercalated SnS2 catalyst has superior long-term durability and comparable performance to that of commercial 10 wt% Pt/C catalyst in hydrogen evolution reaction. This work opens an avenue to explore high-performance intercalated single-atom electrocatalysts within various two-dimensional materials. Single-atom catalysts provide efficiently utilized active sites to improve catalytic activities while improving the stability and enhancing the activities to the level of their bulk metallic counterparts are grand challenges. Herein, we demonstrate a family of single-atom catalysts with different interaction types by confining metal single atoms into the van der Waals gap of two-dimensional SnS 2 . The relatively weak bonding between the noble metal single atoms and the host endows the single atoms with more intrinsic catalytic activity compared to the ones with strong chemical bonding, while the protection offered by the layered material leads to ultrahigh stability compared to the physically adsorbed single-atom catalysts on the surface. Specifically, the trace Pt-intercalated SnS 2 catalyst has superior long-term durability and comparable performance to that of commercial 10 wt% Pt/C catalyst in hydrogen evolution reaction. This work opens an avenue to explore high-performance intercalated single-atom electrocatalysts within various two-dimensional materials. |
ArticleNumber | 6863 |
Author | Liu, Wei Liu, Lixuan Yang, Weiwei Wang, Erqing Zhai, Pengbo Zhou, Wu Ajayan, Pulickel M. Jiang, Huaning Wei, Yi Gong, Yongji Chen, Qian Gu, Xiaokang Xu, Mingquan Zou, Xiaolong |
Author_xml | – sequence: 1 givenname: Huaning surname: Jiang fullname: Jiang, Huaning organization: School of Materials Science and Engineering, Beihang University – sequence: 2 givenname: Weiwei surname: Yang fullname: Yang, Weiwei organization: School of Materials Science and Engineering, Beihang University, School of Materials and Chemistry, University of Shanghai for Science and Technology – sequence: 3 givenname: Mingquan surname: Xu fullname: Xu, Mingquan organization: School of Physical Sciences and CAS Key Laboratory of Vacuum Physics, University of Chinese Academy of Sciences – sequence: 4 givenname: Erqing surname: Wang fullname: Wang, Erqing organization: Shenzhen Geim Graphene Center and Low-Dimensional Materials and Devices Laboratory, Tsinghua-Berkeley Shenzhen Institute, Tsinghua University – sequence: 5 givenname: Yi surname: Wei fullname: Wei, Yi organization: State Key Laboratory of Organic-Inorganic Composites, Beijing Key Laboratory of Electrochemical Process and Technology for Materials, Beijing University of Chemical Technology – sequence: 6 givenname: Wei surname: Liu fullname: Liu, Wei organization: School of Materials Science and Engineering, Beihang University – sequence: 7 givenname: Xiaokang surname: Gu fullname: Gu, Xiaokang organization: School of Materials Science and Engineering, Beihang University – sequence: 8 givenname: Lixuan surname: Liu fullname: Liu, Lixuan organization: School of Materials Science and Engineering, Beihang University – sequence: 9 givenname: Qian surname: Chen fullname: Chen, Qian organization: School of Materials Science and Engineering, Beihang University – sequence: 10 givenname: Pengbo surname: Zhai fullname: Zhai, Pengbo organization: School of Materials Science and Engineering, Beihang University, College of Physics, Qingdao University – sequence: 11 givenname: Xiaolong orcidid: 0000-0002-3987-6865 surname: Zou fullname: Zou, Xiaolong organization: Shenzhen Geim Graphene Center and Low-Dimensional Materials and Devices Laboratory, Tsinghua-Berkeley Shenzhen Institute, Tsinghua University – sequence: 12 givenname: Pulickel M. orcidid: 0000-0001-8323-7860 surname: Ajayan fullname: Ajayan, Pulickel M. organization: School of Material Science & NanoEngineering, Rice University – sequence: 13 givenname: Wu orcidid: 0000-0002-6803-1095 surname: Zhou fullname: Zhou, Wu email: wuzhou@ucas.ac.cn organization: School of Physical Sciences and CAS Key Laboratory of Vacuum Physics, University of Chinese Academy of Sciences – sequence: 14 givenname: Yongji orcidid: 0000-0003-1432-6813 surname: Gong fullname: Gong, Yongji email: yongjigong@buaa.edu.cn organization: School of Materials Science and Engineering, Beihang University, Center for Micro-Nano Innovation of Beihang University |
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Snippet | Single-atom catalysts provide efficiently utilized active sites to improve catalytic activities while improving the stability and enhancing the activities to... A family of single-atom catalysts synthesized by intercalating metal single atoms into the van der Waals gap of two-dimensional SnS2 is reported. The materials... |
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SubjectTerms | 147/135 147/137 147/143 639/301/299/886 639/638/263/915 639/925/357/1018 Bonding strength Catalysts Catalytic activity Chemical bonds Chemical synthesis Chemical vapor deposition Durability Electrocatalysts Humanities and Social Sciences Hydrogen Hydrogen evolution reactions Laboratories multidisciplinary Noble metals Science Science (multidisciplinary) Single atom catalysts Tin disulfide Transmission electron microscopy Two dimensional materials |
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Title | Single atom catalysts in Van der Waals gaps |
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