{"title":"氧化锌纳米粉体表面对 β-二酮的吸附:吸附物对二酮结构的依赖性","authors":"","doi":"10.1016/j.susc.2024.122554","DOIUrl":null,"url":null,"abstract":"<div><p>Surface modification has been established to control chemical, mechanical, and electronic properties of oxide surfaces. Surface chemistry of β-diketones on ZnO nanomaterials presents an opportunity to investigate the dependence of the adsorbate structure on the type of diketone and, specifically, on the presence of electron-donating and electron-withdrawing functional groups. This work compares the adsorption of 1,1,1-trifluoro-2,4-pentane-dione (trifluoroacetylacetone, tfacH) and 1,1,1,5,5,5-hexafluoro-2,4-pentane-dione (hexafluoroacetylacetone, hfacH) on ZnO nanopowder by interrogating the molecular structure of adsorbates with spectroscopic and computational methods. Despite the fact that in the gas phase the enol structure dominates for hfacH and the diketone has substantial presence for tfacH, once these compounds are adsorbed on ZnO, the diketonate is the majority of surface species for hfacH and dissociated enolate is dominant for tfacH. Moreover, given the amphoteric nature of ZnO, it is proposed that on a surface of basic oxide, the O-H dissociation of the enol form could be driven to completion for hfacH, and this proposal is confirmed by comparing chemistry of hfacH on ZnO and MgO surfaces.</p></div>","PeriodicalId":22100,"journal":{"name":"Surface Science","volume":null,"pages":null},"PeriodicalIF":2.1000,"publicationDate":"2024-07-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Adsorption of β-diketones on a surface of ZnO nanopowder: Dependence of the adsorbate on the diketone structure\",\"authors\":\"\",\"doi\":\"10.1016/j.susc.2024.122554\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>Surface modification has been established to control chemical, mechanical, and electronic properties of oxide surfaces. Surface chemistry of β-diketones on ZnO nanomaterials presents an opportunity to investigate the dependence of the adsorbate structure on the type of diketone and, specifically, on the presence of electron-donating and electron-withdrawing functional groups. This work compares the adsorption of 1,1,1-trifluoro-2,4-pentane-dione (trifluoroacetylacetone, tfacH) and 1,1,1,5,5,5-hexafluoro-2,4-pentane-dione (hexafluoroacetylacetone, hfacH) on ZnO nanopowder by interrogating the molecular structure of adsorbates with spectroscopic and computational methods. Despite the fact that in the gas phase the enol structure dominates for hfacH and the diketone has substantial presence for tfacH, once these compounds are adsorbed on ZnO, the diketonate is the majority of surface species for hfacH and dissociated enolate is dominant for tfacH. Moreover, given the amphoteric nature of ZnO, it is proposed that on a surface of basic oxide, the O-H dissociation of the enol form could be driven to completion for hfacH, and this proposal is confirmed by comparing chemistry of hfacH on ZnO and MgO surfaces.</p></div>\",\"PeriodicalId\":22100,\"journal\":{\"name\":\"Surface Science\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":2.1000,\"publicationDate\":\"2024-07-14\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Surface Science\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0039602824001055\",\"RegionNum\":4,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"CHEMISTRY, PHYSICAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Surface Science","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0039602824001055","RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
Adsorption of β-diketones on a surface of ZnO nanopowder: Dependence of the adsorbate on the diketone structure
Surface modification has been established to control chemical, mechanical, and electronic properties of oxide surfaces. Surface chemistry of β-diketones on ZnO nanomaterials presents an opportunity to investigate the dependence of the adsorbate structure on the type of diketone and, specifically, on the presence of electron-donating and electron-withdrawing functional groups. This work compares the adsorption of 1,1,1-trifluoro-2,4-pentane-dione (trifluoroacetylacetone, tfacH) and 1,1,1,5,5,5-hexafluoro-2,4-pentane-dione (hexafluoroacetylacetone, hfacH) on ZnO nanopowder by interrogating the molecular structure of adsorbates with spectroscopic and computational methods. Despite the fact that in the gas phase the enol structure dominates for hfacH and the diketone has substantial presence for tfacH, once these compounds are adsorbed on ZnO, the diketonate is the majority of surface species for hfacH and dissociated enolate is dominant for tfacH. Moreover, given the amphoteric nature of ZnO, it is proposed that on a surface of basic oxide, the O-H dissociation of the enol form could be driven to completion for hfacH, and this proposal is confirmed by comparing chemistry of hfacH on ZnO and MgO surfaces.
期刊介绍:
Surface Science is devoted to elucidating the fundamental aspects of chemistry and physics occurring at a wide range of surfaces and interfaces and to disseminating this knowledge fast. The journal welcomes a broad spectrum of topics, including but not limited to:
• model systems (e.g. in Ultra High Vacuum) under well-controlled reactive conditions
• nanoscale science and engineering, including manipulation of matter at the atomic/molecular scale and assembly phenomena
• reactivity of surfaces as related to various applied areas including heterogeneous catalysis, chemistry at electrified interfaces, and semiconductors functionalization
• phenomena at interfaces relevant to energy storage and conversion, and fuels production and utilization
• surface reactivity for environmental protection and pollution remediation
• interactions at surfaces of soft matter, including polymers and biomaterials.
Both experimental and theoretical work, including modeling, is within the scope of the journal. Work published in Surface Science reaches a wide readership, from chemistry and physics to biology and materials science and engineering, providing an excellent forum for cross-fertilization of ideas and broad dissemination of scientific discoveries.