{"title":"Two-dimensional multifunctional metal-organic frameworks with large in-plane negative Poisson ratios and photocatalytic water splitting properties.","authors":"Wei Lin, Huimiao Wang, Yaling Luo, Xiaofeng Liu, ZhongJun Li, Weiduo Zhu, Xingxing Li, Zhao Chen, Haidi Wang","doi":"10.1039/d4mh01275e","DOIUrl":null,"url":null,"abstract":"<p><p>Auxetic materials with multifunctional properties are highly sought after for application in modern nano-devices. However, the majority of reported inorganic auxetic materials exhibit low negative Poisson's ratios (NPR), poor flexibility, and limited functionality. In this study, we employ density-functional-theory (DFT) first-principles simulations to design a series of two-dimensional (2D) metal-organic frameworks (MOFs) M<sub>2</sub>C<sub>4</sub>X<sub>4</sub> (M = Cu, Ag, Au; X = O, S, NCN) that display intriguing auxetic behavior, superior flexibility and appropriate photocatalytic water-splitting properties. These M<sub>2</sub>C<sub>4</sub>X<sub>4</sub> MOFs are assembled from carbon tetragon motifs and exist in both <i>cis</i>- and <i>trans</i>-isomer forms, with the NPR ranging from -0.17 to -0.90. Notably, <i>trans</i>-Cu<sub>2</sub>C<sub>4</sub>(NCN)<sub>4</sub> exhibits a high NPR of -0.90, while <i>cis</i>-Cu<sub>2</sub>C<sub>4</sub>(NCN)<sub>4</sub> achieves an NPR of -0.67. Both isomers demonstrate excellent flexibility, characterized by ultra-low Young's modulus and high fracture strengths. Furthermore, their direct band gaps, strong light-harvesting capabilities, and long excited-state lifetimes make them promising candidates for the photocatalytic oxygen evolution reaction in water. These results provide a viable strategy for the design and synthesis of novel optoelectronic multifunctional materials.</p>","PeriodicalId":87,"journal":{"name":"Materials Horizons","volume":" ","pages":""},"PeriodicalIF":12.2000,"publicationDate":"2024-10-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Materials Horizons","FirstCategoryId":"88","ListUrlMain":"https://doi.org/10.1039/d4mh01275e","RegionNum":2,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0
Abstract
Auxetic materials with multifunctional properties are highly sought after for application in modern nano-devices. However, the majority of reported inorganic auxetic materials exhibit low negative Poisson's ratios (NPR), poor flexibility, and limited functionality. In this study, we employ density-functional-theory (DFT) first-principles simulations to design a series of two-dimensional (2D) metal-organic frameworks (MOFs) M2C4X4 (M = Cu, Ag, Au; X = O, S, NCN) that display intriguing auxetic behavior, superior flexibility and appropriate photocatalytic water-splitting properties. These M2C4X4 MOFs are assembled from carbon tetragon motifs and exist in both cis- and trans-isomer forms, with the NPR ranging from -0.17 to -0.90. Notably, trans-Cu2C4(NCN)4 exhibits a high NPR of -0.90, while cis-Cu2C4(NCN)4 achieves an NPR of -0.67. Both isomers demonstrate excellent flexibility, characterized by ultra-low Young's modulus and high fracture strengths. Furthermore, their direct band gaps, strong light-harvesting capabilities, and long excited-state lifetimes make them promising candidates for the photocatalytic oxygen evolution reaction in water. These results provide a viable strategy for the design and synthesis of novel optoelectronic multifunctional materials.