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New Spiral Form of Carbon Nitride with Ultrasoftness and Tunable Electronic Structures

[Image: see text] The structural diversity and multifunctionality of carbon nitride materials distinct from pure carbon materials are drawing increasing interest. Using first-principles calculations, we proposed a stable spiral structure of carbon nitride, namely spiral-C(3)N, which is composed of s...

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Autores principales: Bu, Hongxia, Yang, Bo, Yuan, Huimin, Yuan, Xiaojuan, Wang, Hui, Qi, Siyun, Ma, Xikui, Zhao, Mingwen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2020
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7807741/
https://www.ncbi.nlm.nih.gov/pubmed/33458503
http://dx.doi.org/10.1021/acsomega.0c04997
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author Bu, Hongxia
Yang, Bo
Yuan, Huimin
Yuan, Xiaojuan
Wang, Hui
Qi, Siyun
Ma, Xikui
Zhao, Mingwen
author_facet Bu, Hongxia
Yang, Bo
Yuan, Huimin
Yuan, Xiaojuan
Wang, Hui
Qi, Siyun
Ma, Xikui
Zhao, Mingwen
author_sort Bu, Hongxia
collection PubMed
description [Image: see text] The structural diversity and multifunctionality of carbon nitride materials distinct from pure carbon materials are drawing increasing interest. Using first-principles calculations, we proposed a stable spiral structure of carbon nitride, namely spiral-C(3)N, which is composed of sp(2)-hybridized carbon and pyridine nitrogen with a 60° helical symmetry along the z-direction. The stability was verified from the cohesive energy, phonon spectrum, and elastic constants. Despite the strong covalent bonds of the spiral framework, the spiral-C(3)N exhibits a hardness lower than 12.00 GPa, in sharp contrast to the superhardness of cubic carbon nitrides reported in previous literature, which can be attributed to the unique porous configuration. The softness of the spiral-C(3)N was also confirmed by the small ideal strengths, which are, respectively, 33.00 GPa at a tensile strain of 0.22 along the [1̅21̅0] direction and 18.00 GPa at a shear strain of 0.52 in the (0001)[1̅21̅0] direction. Electronic band structure of spiral-C(3)N exhibits metallic features. A metal–semiconductor transition can be triggered by hydrogenation of the pyridine nitrogen atoms of spiral-C(3)N. Such a new three-dimensional spiral framework of sp(2)-hyperdized carbon and nitrogen atoms not only enriches the family of carbon nitride materials but also finds application in energy conversion and storage.
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spelling pubmed-78077412021-01-15 New Spiral Form of Carbon Nitride with Ultrasoftness and Tunable Electronic Structures Bu, Hongxia Yang, Bo Yuan, Huimin Yuan, Xiaojuan Wang, Hui Qi, Siyun Ma, Xikui Zhao, Mingwen ACS Omega [Image: see text] The structural diversity and multifunctionality of carbon nitride materials distinct from pure carbon materials are drawing increasing interest. Using first-principles calculations, we proposed a stable spiral structure of carbon nitride, namely spiral-C(3)N, which is composed of sp(2)-hybridized carbon and pyridine nitrogen with a 60° helical symmetry along the z-direction. The stability was verified from the cohesive energy, phonon spectrum, and elastic constants. Despite the strong covalent bonds of the spiral framework, the spiral-C(3)N exhibits a hardness lower than 12.00 GPa, in sharp contrast to the superhardness of cubic carbon nitrides reported in previous literature, which can be attributed to the unique porous configuration. The softness of the spiral-C(3)N was also confirmed by the small ideal strengths, which are, respectively, 33.00 GPa at a tensile strain of 0.22 along the [1̅21̅0] direction and 18.00 GPa at a shear strain of 0.52 in the (0001)[1̅21̅0] direction. Electronic band structure of spiral-C(3)N exhibits metallic features. A metal–semiconductor transition can be triggered by hydrogenation of the pyridine nitrogen atoms of spiral-C(3)N. Such a new three-dimensional spiral framework of sp(2)-hyperdized carbon and nitrogen atoms not only enriches the family of carbon nitride materials but also finds application in energy conversion and storage. American Chemical Society 2020-12-24 /pmc/articles/PMC7807741/ /pubmed/33458503 http://dx.doi.org/10.1021/acsomega.0c04997 Text en © 2020 The Authors. Published by American Chemical Society This is an open access article published under a Creative Commons Non-Commercial No Derivative Works (CC-BY-NC-ND) Attribution License (http://pubs.acs.org/page/policy/authorchoice_ccbyncnd_termsofuse.html) , which permits copying and redistribution of the article, and creation of adaptations, all for non-commercial purposes.
spellingShingle Bu, Hongxia
Yang, Bo
Yuan, Huimin
Yuan, Xiaojuan
Wang, Hui
Qi, Siyun
Ma, Xikui
Zhao, Mingwen
New Spiral Form of Carbon Nitride with Ultrasoftness and Tunable Electronic Structures
title New Spiral Form of Carbon Nitride with Ultrasoftness and Tunable Electronic Structures
title_full New Spiral Form of Carbon Nitride with Ultrasoftness and Tunable Electronic Structures
title_fullStr New Spiral Form of Carbon Nitride with Ultrasoftness and Tunable Electronic Structures
title_full_unstemmed New Spiral Form of Carbon Nitride with Ultrasoftness and Tunable Electronic Structures
title_short New Spiral Form of Carbon Nitride with Ultrasoftness and Tunable Electronic Structures
title_sort new spiral form of carbon nitride with ultrasoftness and tunable electronic structures
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7807741/
https://www.ncbi.nlm.nih.gov/pubmed/33458503
http://dx.doi.org/10.1021/acsomega.0c04997
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