Towards the selective growth of two-dimensional ordered CxNy compounds via epitaxial substrate mediation
We have theoretically explored the mechanism of selective growth of ordered 2D CxNy compounds on various epitaxial substrates, which can be achieved under distinct chemical potential windows by establishing the substrate mediated thermodynamic phase diagrams as well as the kinetics pathways. Accordi...
Gespeichert in:
Veröffentlicht in: | Science bulletin 2024-07, Vol.69 (14), p.2212-2220 |
---|---|
Hauptverfasser: | , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 2220 |
---|---|
container_issue | 14 |
container_start_page | 2212 |
container_title | Science bulletin |
container_volume | 69 |
creator | Gong, Xiaoshu Dong, Ruikang Wang, Jinlan Ma, Liang |
description | We have theoretically explored the mechanism of selective growth of ordered 2D CxNy compounds on various epitaxial substrates, which can be achieved under distinct chemical potential windows by establishing the substrate mediated thermodynamic phase diagrams as well as the kinetics pathways. Accordingly, the optimal experimental conditions, e.g., the temperature and partial pressure of feedstock, are also suggested.
[Display omitted]
Two-dimensional (2D) ordered carbon–nitrogen binary compounds (CxNy) show great potential in many fields owing to their diverse structures and outstanding properties. However, the scalable and selective synthesis of 2D CxNy compounds remain a challenge due to the variable C/N stoichiometry induced coexistence of graphitic, pyridinic, and pyrrolic N species and the competitive growth of graphene. Here, this work systematically explored the mechanism of selective growth of a series of 2D ordered CxNy compounds, namely, the g-C3N4, C2N, C3N, and C5N, on various epitaxial substrates via first-principles calculations. By establishing the thermodynamic phase diagram, it is revealed that the individualized surface interaction and symmetry match between 2D CxNy compounds and substrates together enable the selective epitaxial growth of single crystal 2D CxNy compounds within distinct chemical potential windows of feedstock. The kinetics behaviors of the diffusion and attachment of the decomposed feedstock C/N atoms to the growing CxNy clusters further confirmed the feasibility of the substrate mediated selective growth of 2D CxNy compounds. Moreover, the optimal experimental conditions, including the temperature and partial pressure of feedstock, are suggested for the selective growth of targeted 2D CxNy compound on individual epitaxial substrates by carefully considering the chemical potential of carbon/nitrogen as the functional of experimental parameters based on the standard thermochemical tables. This work provides an insightful understanding on the mechanism of selective epitaxial growth of 2D ordered CxNy compounds for guiding the future experimental design. |
doi_str_mv | 10.1016/j.scib.2024.04.057 |
format | Article |
fullrecord | <record><control><sourceid>proquest_elsev</sourceid><recordid>TN_cdi_proquest_miscellaneous_3053974955</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S2095927324003062</els_id><sourcerecordid>3053974955</sourcerecordid><originalsourceid>FETCH-LOGICAL-e241t-db9038006a81096e55c4e140db9c22f990fd9d6590bdfd52b13d683c14655bc33</originalsourceid><addsrcrecordid>eNo9kMtqwzAQRU1poSHND3SlZTd2R5JlR9BNCX1BaDfpWsjSuFGwrdRSHv37KqQUBmaYuXe4nCy7pVBQoNX9pgjGNQUDVhaQStQX2YSBFLlkc3r5P9f8OpuFsAEAWkpWQj3J1it_0KMNJK6RBOzQRLdH8jX6Q1wT35J48Ll1PQ7B-UF3xI8WR7RkcXz_Icb3W78bkn3vNMGti_rokijsmhBHHZH0aJ2OyXqTXbW6Czj769Ps8_lptXjNlx8vb4vHZY6spDG3jQQ-B6j0nIKsUAhTIi0h7Q1jrZTQWmkrIaGxrRWsodxWc25oWQnRGM6n2d3573b03zsMUfUuGOw6PaDfBcVBcFmXUogkfThLMeXZOxxV4oiDSZHHxEFZ7xQFdWKsNqdbo06MFaQSNf8FjM1y5g</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>3053974955</pqid></control><display><type>article</type><title>Towards the selective growth of two-dimensional ordered CxNy compounds via epitaxial substrate mediation</title><source>Alma/SFX Local Collection</source><creator>Gong, Xiaoshu ; Dong, Ruikang ; Wang, Jinlan ; Ma, Liang</creator><creatorcontrib>Gong, Xiaoshu ; Dong, Ruikang ; Wang, Jinlan ; Ma, Liang</creatorcontrib><description>We have theoretically explored the mechanism of selective growth of ordered 2D CxNy compounds on various epitaxial substrates, which can be achieved under distinct chemical potential windows by establishing the substrate mediated thermodynamic phase diagrams as well as the kinetics pathways. Accordingly, the optimal experimental conditions, e.g., the temperature and partial pressure of feedstock, are also suggested.
[Display omitted]
Two-dimensional (2D) ordered carbon–nitrogen binary compounds (CxNy) show great potential in many fields owing to their diverse structures and outstanding properties. However, the scalable and selective synthesis of 2D CxNy compounds remain a challenge due to the variable C/N stoichiometry induced coexistence of graphitic, pyridinic, and pyrrolic N species and the competitive growth of graphene. Here, this work systematically explored the mechanism of selective growth of a series of 2D ordered CxNy compounds, namely, the g-C3N4, C2N, C3N, and C5N, on various epitaxial substrates via first-principles calculations. By establishing the thermodynamic phase diagram, it is revealed that the individualized surface interaction and symmetry match between 2D CxNy compounds and substrates together enable the selective epitaxial growth of single crystal 2D CxNy compounds within distinct chemical potential windows of feedstock. The kinetics behaviors of the diffusion and attachment of the decomposed feedstock C/N atoms to the growing CxNy clusters further confirmed the feasibility of the substrate mediated selective growth of 2D CxNy compounds. Moreover, the optimal experimental conditions, including the temperature and partial pressure of feedstock, are suggested for the selective growth of targeted 2D CxNy compound on individual epitaxial substrates by carefully considering the chemical potential of carbon/nitrogen as the functional of experimental parameters based on the standard thermochemical tables. This work provides an insightful understanding on the mechanism of selective epitaxial growth of 2D ordered CxNy compounds for guiding the future experimental design.</description><identifier>ISSN: 2095-9273</identifier><identifier>ISSN: 2095-9281</identifier><identifier>EISSN: 2095-9281</identifier><identifier>DOI: 10.1016/j.scib.2024.04.057</identifier><language>eng</language><publisher>Elsevier B.V</publisher><subject>2D ordered carbon–nitrogen compounds ; Epitaxial substrate ; First-principles calculation ; Growth mechanism ; Thermodynamic phase diagram</subject><ispartof>Science bulletin, 2024-07, Vol.69 (14), p.2212-2220</ispartof><rights>2024 Science China Press</rights><rights>Copyright © 2024 Science China Press. Published by Elsevier B.V. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>315,781,785,27929,27930</link.rule.ids></links><search><creatorcontrib>Gong, Xiaoshu</creatorcontrib><creatorcontrib>Dong, Ruikang</creatorcontrib><creatorcontrib>Wang, Jinlan</creatorcontrib><creatorcontrib>Ma, Liang</creatorcontrib><title>Towards the selective growth of two-dimensional ordered CxNy compounds via epitaxial substrate mediation</title><title>Science bulletin</title><description>We have theoretically explored the mechanism of selective growth of ordered 2D CxNy compounds on various epitaxial substrates, which can be achieved under distinct chemical potential windows by establishing the substrate mediated thermodynamic phase diagrams as well as the kinetics pathways. Accordingly, the optimal experimental conditions, e.g., the temperature and partial pressure of feedstock, are also suggested.
[Display omitted]
Two-dimensional (2D) ordered carbon–nitrogen binary compounds (CxNy) show great potential in many fields owing to their diverse structures and outstanding properties. However, the scalable and selective synthesis of 2D CxNy compounds remain a challenge due to the variable C/N stoichiometry induced coexistence of graphitic, pyridinic, and pyrrolic N species and the competitive growth of graphene. Here, this work systematically explored the mechanism of selective growth of a series of 2D ordered CxNy compounds, namely, the g-C3N4, C2N, C3N, and C5N, on various epitaxial substrates via first-principles calculations. By establishing the thermodynamic phase diagram, it is revealed that the individualized surface interaction and symmetry match between 2D CxNy compounds and substrates together enable the selective epitaxial growth of single crystal 2D CxNy compounds within distinct chemical potential windows of feedstock. The kinetics behaviors of the diffusion and attachment of the decomposed feedstock C/N atoms to the growing CxNy clusters further confirmed the feasibility of the substrate mediated selective growth of 2D CxNy compounds. Moreover, the optimal experimental conditions, including the temperature and partial pressure of feedstock, are suggested for the selective growth of targeted 2D CxNy compound on individual epitaxial substrates by carefully considering the chemical potential of carbon/nitrogen as the functional of experimental parameters based on the standard thermochemical tables. This work provides an insightful understanding on the mechanism of selective epitaxial growth of 2D ordered CxNy compounds for guiding the future experimental design.</description><subject>2D ordered carbon–nitrogen compounds</subject><subject>Epitaxial substrate</subject><subject>First-principles calculation</subject><subject>Growth mechanism</subject><subject>Thermodynamic phase diagram</subject><issn>2095-9273</issn><issn>2095-9281</issn><issn>2095-9281</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><recordid>eNo9kMtqwzAQRU1poSHND3SlZTd2R5JlR9BNCX1BaDfpWsjSuFGwrdRSHv37KqQUBmaYuXe4nCy7pVBQoNX9pgjGNQUDVhaQStQX2YSBFLlkc3r5P9f8OpuFsAEAWkpWQj3J1it_0KMNJK6RBOzQRLdH8jX6Q1wT35J48Ll1PQ7B-UF3xI8WR7RkcXz_Icb3W78bkn3vNMGti_rokijsmhBHHZH0aJ2OyXqTXbW6Czj769Ps8_lptXjNlx8vb4vHZY6spDG3jQQ-B6j0nIKsUAhTIi0h7Q1jrZTQWmkrIaGxrRWsodxWc25oWQnRGM6n2d3573b03zsMUfUuGOw6PaDfBcVBcFmXUogkfThLMeXZOxxV4oiDSZHHxEFZ7xQFdWKsNqdbo06MFaQSNf8FjM1y5g</recordid><startdate>20240730</startdate><enddate>20240730</enddate><creator>Gong, Xiaoshu</creator><creator>Dong, Ruikang</creator><creator>Wang, Jinlan</creator><creator>Ma, Liang</creator><general>Elsevier B.V</general><scope>7X8</scope></search><sort><creationdate>20240730</creationdate><title>Towards the selective growth of two-dimensional ordered CxNy compounds via epitaxial substrate mediation</title><author>Gong, Xiaoshu ; Dong, Ruikang ; Wang, Jinlan ; Ma, Liang</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-e241t-db9038006a81096e55c4e140db9c22f990fd9d6590bdfd52b13d683c14655bc33</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>2D ordered carbon–nitrogen compounds</topic><topic>Epitaxial substrate</topic><topic>First-principles calculation</topic><topic>Growth mechanism</topic><topic>Thermodynamic phase diagram</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Gong, Xiaoshu</creatorcontrib><creatorcontrib>Dong, Ruikang</creatorcontrib><creatorcontrib>Wang, Jinlan</creatorcontrib><creatorcontrib>Ma, Liang</creatorcontrib><collection>MEDLINE - Academic</collection><jtitle>Science bulletin</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Gong, Xiaoshu</au><au>Dong, Ruikang</au><au>Wang, Jinlan</au><au>Ma, Liang</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Towards the selective growth of two-dimensional ordered CxNy compounds via epitaxial substrate mediation</atitle><jtitle>Science bulletin</jtitle><date>2024-07-30</date><risdate>2024</risdate><volume>69</volume><issue>14</issue><spage>2212</spage><epage>2220</epage><pages>2212-2220</pages><issn>2095-9273</issn><issn>2095-9281</issn><eissn>2095-9281</eissn><abstract>We have theoretically explored the mechanism of selective growth of ordered 2D CxNy compounds on various epitaxial substrates, which can be achieved under distinct chemical potential windows by establishing the substrate mediated thermodynamic phase diagrams as well as the kinetics pathways. Accordingly, the optimal experimental conditions, e.g., the temperature and partial pressure of feedstock, are also suggested.
[Display omitted]
Two-dimensional (2D) ordered carbon–nitrogen binary compounds (CxNy) show great potential in many fields owing to their diverse structures and outstanding properties. However, the scalable and selective synthesis of 2D CxNy compounds remain a challenge due to the variable C/N stoichiometry induced coexistence of graphitic, pyridinic, and pyrrolic N species and the competitive growth of graphene. Here, this work systematically explored the mechanism of selective growth of a series of 2D ordered CxNy compounds, namely, the g-C3N4, C2N, C3N, and C5N, on various epitaxial substrates via first-principles calculations. By establishing the thermodynamic phase diagram, it is revealed that the individualized surface interaction and symmetry match between 2D CxNy compounds and substrates together enable the selective epitaxial growth of single crystal 2D CxNy compounds within distinct chemical potential windows of feedstock. The kinetics behaviors of the diffusion and attachment of the decomposed feedstock C/N atoms to the growing CxNy clusters further confirmed the feasibility of the substrate mediated selective growth of 2D CxNy compounds. Moreover, the optimal experimental conditions, including the temperature and partial pressure of feedstock, are suggested for the selective growth of targeted 2D CxNy compound on individual epitaxial substrates by carefully considering the chemical potential of carbon/nitrogen as the functional of experimental parameters based on the standard thermochemical tables. This work provides an insightful understanding on the mechanism of selective epitaxial growth of 2D ordered CxNy compounds for guiding the future experimental design.</abstract><pub>Elsevier B.V</pub><doi>10.1016/j.scib.2024.04.057</doi><tpages>9</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 2095-9273 |
ispartof | Science bulletin, 2024-07, Vol.69 (14), p.2212-2220 |
issn | 2095-9273 2095-9281 2095-9281 |
language | eng |
recordid | cdi_proquest_miscellaneous_3053974955 |
source | Alma/SFX Local Collection |
subjects | 2D ordered carbon–nitrogen compounds Epitaxial substrate First-principles calculation Growth mechanism Thermodynamic phase diagram |
title | Towards the selective growth of two-dimensional ordered CxNy compounds via epitaxial substrate mediation |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-15T11%3A06%3A38IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_elsev&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Towards%20the%20selective%20growth%20of%20two-dimensional%20ordered%20CxNy%20compounds%20via%20epitaxial%20substrate%20mediation&rft.jtitle=Science%20bulletin&rft.au=Gong,%20Xiaoshu&rft.date=2024-07-30&rft.volume=69&rft.issue=14&rft.spage=2212&rft.epage=2220&rft.pages=2212-2220&rft.issn=2095-9273&rft.eissn=2095-9281&rft_id=info:doi/10.1016/j.scib.2024.04.057&rft_dat=%3Cproquest_elsev%3E3053974955%3C/proquest_elsev%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=3053974955&rft_id=info:pmid/&rft_els_id=S2095927324003062&rfr_iscdi=true |