Mateus Silva Rêgo , Mário Rocha dos Santos , Marcelo Lopes Pereira Junior , Eduardo Costa Girão , Vincent Meunier , Paloma Vieira Silva
{"title":"基于二维联苯网络的单石墨炔层的结构、力学和电子特性","authors":"Mateus Silva Rêgo , Mário Rocha dos Santos , Marcelo Lopes Pereira Junior , Eduardo Costa Girão , Vincent Meunier , Paloma Vieira Silva","doi":"10.1016/j.cartre.2025.100506","DOIUrl":null,"url":null,"abstract":"<div><div>Graphene is a promising material for the development of applications in nanoelectronic devices, but the lack of a band gap necessitates the search for ways to tune its electronic properties. In addition to doping, defects, and nanoribbons, a more radical alternative is the development of 2D forms with structures that are in clear departure from the honeycomb lattice, such as graphynes, with the distinctive property of involving carbon atoms with both hybridizations <span><math><mrow><mi>s</mi><mi>p</mi></mrow></math></span> and <span><math><mrow><mi>s</mi><msup><mrow><mi>p</mi></mrow><mrow><mn>2</mn></mrow></msup></mrow></math></span>. The density and details of how the acetylenic links are distributed allow for a variety of electronic signatures. Here we propose a graphyne system based on the recently synthesized biphenylene monolayer. We demonstrate that this system features highly localized states with a spin-polarized semiconducting configuration. We study its stability and show that the system’s structural details directly influence its highly anisotropic electronic properties. Finally, we show that the symmetry of the frontier states can be further tuned by modulating the size of the acetylenic chains forming the system.</div></div>","PeriodicalId":52629,"journal":{"name":"Carbon Trends","volume":"20 ","pages":"Article 100506"},"PeriodicalIF":3.1000,"publicationDate":"2025-04-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Structural, mechanical, and electronic properties of single graphyne layers based on a 2D biphenylene network\",\"authors\":\"Mateus Silva Rêgo , Mário Rocha dos Santos , Marcelo Lopes Pereira Junior , Eduardo Costa Girão , Vincent Meunier , Paloma Vieira Silva\",\"doi\":\"10.1016/j.cartre.2025.100506\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Graphene is a promising material for the development of applications in nanoelectronic devices, but the lack of a band gap necessitates the search for ways to tune its electronic properties. In addition to doping, defects, and nanoribbons, a more radical alternative is the development of 2D forms with structures that are in clear departure from the honeycomb lattice, such as graphynes, with the distinctive property of involving carbon atoms with both hybridizations <span><math><mrow><mi>s</mi><mi>p</mi></mrow></math></span> and <span><math><mrow><mi>s</mi><msup><mrow><mi>p</mi></mrow><mrow><mn>2</mn></mrow></msup></mrow></math></span>. The density and details of how the acetylenic links are distributed allow for a variety of electronic signatures. Here we propose a graphyne system based on the recently synthesized biphenylene monolayer. We demonstrate that this system features highly localized states with a spin-polarized semiconducting configuration. We study its stability and show that the system’s structural details directly influence its highly anisotropic electronic properties. Finally, we show that the symmetry of the frontier states can be further tuned by modulating the size of the acetylenic chains forming the system.</div></div>\",\"PeriodicalId\":52629,\"journal\":{\"name\":\"Carbon Trends\",\"volume\":\"20 \",\"pages\":\"Article 100506\"},\"PeriodicalIF\":3.1000,\"publicationDate\":\"2025-04-17\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Carbon Trends\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S2667056925000562\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"MATERIALS SCIENCE, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Carbon Trends","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2667056925000562","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"MATERIALS SCIENCE, MULTIDISCIPLINARY","Score":null,"Total":0}
Structural, mechanical, and electronic properties of single graphyne layers based on a 2D biphenylene network
Graphene is a promising material for the development of applications in nanoelectronic devices, but the lack of a band gap necessitates the search for ways to tune its electronic properties. In addition to doping, defects, and nanoribbons, a more radical alternative is the development of 2D forms with structures that are in clear departure from the honeycomb lattice, such as graphynes, with the distinctive property of involving carbon atoms with both hybridizations and . The density and details of how the acetylenic links are distributed allow for a variety of electronic signatures. Here we propose a graphyne system based on the recently synthesized biphenylene monolayer. We demonstrate that this system features highly localized states with a spin-polarized semiconducting configuration. We study its stability and show that the system’s structural details directly influence its highly anisotropic electronic properties. Finally, we show that the symmetry of the frontier states can be further tuned by modulating the size of the acetylenic chains forming the system.