Bei Wu, Xiaocheng Liu, Peigen Liu, Geng Wu, Lin Tian, Xiao Han, Junmin Li, Xun Hong
{"title":"通过结晶到非晶相变策略合成非晶金属氧化物","authors":"Bei Wu, Xiaocheng Liu, Peigen Liu, Geng Wu, Lin Tian, Xiao Han, Junmin Li, Xun Hong","doi":"10.1038/s44160-024-00704-4","DOIUrl":null,"url":null,"abstract":"Amorphous metal oxide (AMO) nanomaterials are attractive because of their unique short-range order structure, but controllable synthesis is still challenging. Here we report a Li+-assisted liquid-phase reduction method, which converts a series of crystalline metal oxides into amorphous structures (RuOx, PtOx, CuOx, NiOx, PdOx, MnOx and NiCoOx). Taking RuO2 as an example, in situ Raman and X-ray absorption spectroscopy indicate that the reduction of Ru–O coordination number and distortion of the medium-range structure of Ru–Ru during the amorphization process are caused by naphthalene radical anions and lithium ions. Theoretical calculations indicate that Li⁺ insertion in RuOx strengthens its electrostatic interaction with the naphthalene radical anion, accelerating the stripping of oxygen from Li⁺-inserted RuOx. The introduction of positive charge by Li⁺ insertion can disrupt the internal charge balance of crystal ruthenium oxide, and therefore reduce the formation energy of intermediates for producing amorphous RuOx. This strategy paves a way for achieving the controllable synthesis of AMOs. A Li⁺-assisted liquid-phase reduction method is reported, which converts crystalline metal oxides into amorphous metal oxides. The electrostatic interaction between the naphthalene radical anions and Li⁺-inserted metal oxides is found to promote the amorphization process.","PeriodicalId":74251,"journal":{"name":"Nature synthesis","volume":"4 3","pages":"370-379"},"PeriodicalIF":0.0000,"publicationDate":"2025-01-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Synthesis of amorphous metal oxides via a crystalline to amorphous phase transition strategy\",\"authors\":\"Bei Wu, Xiaocheng Liu, Peigen Liu, Geng Wu, Lin Tian, Xiao Han, Junmin Li, Xun Hong\",\"doi\":\"10.1038/s44160-024-00704-4\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Amorphous metal oxide (AMO) nanomaterials are attractive because of their unique short-range order structure, but controllable synthesis is still challenging. Here we report a Li+-assisted liquid-phase reduction method, which converts a series of crystalline metal oxides into amorphous structures (RuOx, PtOx, CuOx, NiOx, PdOx, MnOx and NiCoOx). Taking RuO2 as an example, in situ Raman and X-ray absorption spectroscopy indicate that the reduction of Ru–O coordination number and distortion of the medium-range structure of Ru–Ru during the amorphization process are caused by naphthalene radical anions and lithium ions. Theoretical calculations indicate that Li⁺ insertion in RuOx strengthens its electrostatic interaction with the naphthalene radical anion, accelerating the stripping of oxygen from Li⁺-inserted RuOx. The introduction of positive charge by Li⁺ insertion can disrupt the internal charge balance of crystal ruthenium oxide, and therefore reduce the formation energy of intermediates for producing amorphous RuOx. This strategy paves a way for achieving the controllable synthesis of AMOs. A Li⁺-assisted liquid-phase reduction method is reported, which converts crystalline metal oxides into amorphous metal oxides. The electrostatic interaction between the naphthalene radical anions and Li⁺-inserted metal oxides is found to promote the amorphization process.\",\"PeriodicalId\":74251,\"journal\":{\"name\":\"Nature synthesis\",\"volume\":\"4 3\",\"pages\":\"370-379\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2025-01-03\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Nature synthesis\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.nature.com/articles/s44160-024-00704-4\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"0\",\"JCRName\":\"CHEMISTRY, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Nature synthesis","FirstCategoryId":"1085","ListUrlMain":"https://www.nature.com/articles/s44160-024-00704-4","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"0","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
Synthesis of amorphous metal oxides via a crystalline to amorphous phase transition strategy
Amorphous metal oxide (AMO) nanomaterials are attractive because of their unique short-range order structure, but controllable synthesis is still challenging. Here we report a Li+-assisted liquid-phase reduction method, which converts a series of crystalline metal oxides into amorphous structures (RuOx, PtOx, CuOx, NiOx, PdOx, MnOx and NiCoOx). Taking RuO2 as an example, in situ Raman and X-ray absorption spectroscopy indicate that the reduction of Ru–O coordination number and distortion of the medium-range structure of Ru–Ru during the amorphization process are caused by naphthalene radical anions and lithium ions. Theoretical calculations indicate that Li⁺ insertion in RuOx strengthens its electrostatic interaction with the naphthalene radical anion, accelerating the stripping of oxygen from Li⁺-inserted RuOx. The introduction of positive charge by Li⁺ insertion can disrupt the internal charge balance of crystal ruthenium oxide, and therefore reduce the formation energy of intermediates for producing amorphous RuOx. This strategy paves a way for achieving the controllable synthesis of AMOs. A Li⁺-assisted liquid-phase reduction method is reported, which converts crystalline metal oxides into amorphous metal oxides. The electrostatic interaction between the naphthalene radical anions and Li⁺-inserted metal oxides is found to promote the amorphization process.