Jielin Huang , Jie Wang , Haonan Duan , Songsong Chen , Junping Zhang , Li Dong , Xiangping Zhang
{"title":"在离子液体中构建介孔 CeO2 单晶颗粒,促进二氧化碳和醇类向碳酸盐的转化","authors":"Jielin Huang , Jie Wang , Haonan Duan , Songsong Chen , Junping Zhang , Li Dong , Xiangping Zhang","doi":"10.1016/S1872-2067(24)60117-8","DOIUrl":null,"url":null,"abstract":"<div><div>Catalysts for CO<sub>2</sub> value-added conversion have been extensively explored, but there is still a lack of systematic design for catalysts that achieve efficient CO<sub>2</sub> conversion under mild conditions. Herein, we explored a mesoporous CeO<sub>2</sub> single-crystal formed with the regulation of ionic liquids, which catalyzed the effective carbonylation reaction with CO<sub>2</sub> under mild reaction conditions. By altering the synthetic environment, a series of uniform mesoporous CeO<sub>2</sub> particles with atomically aligned single-crystal frameworks were constructed, which have different surface physicochemical properties and primary aggregation degree. The prepared mesoporous CeO<sub>2</sub> single-crystal achieved efficient activation of CO<sub>2</sub> and alcohols at 0.5 MPa CO<sub>2</sub> and 100 °C, and the CeO<sub>2</sub>-IL-M catalyst shows optimal catalytic performance in the synthesis of ethylene carbonate with 46.22 mmol g<sup>–1</sup> h<sup>–1</sup>, which was 50.6 times as high as that of the CeO<sub>2</sub> obtained without ionic liquids. Subsequently, the catalytic pathway and mechanism of carbonylation reaction with CO<sub>2</sub> on mesoporous CeO<sub>2</sub> single-crystal were studied <em>via</em> React-IR spectra and C<sup>18</sup>O<sub>2</sub> labeling experiments. The research provides a new strategy for controllable nanoscale assembly of mesoporous single-crystal materials and expands the application range of single-crystal materials, aiming to develop novel catalytic materials to meet industrial needs.</div></div>","PeriodicalId":9832,"journal":{"name":"Chinese Journal of Catalysis","volume":"66 ","pages":"Pages 152-167"},"PeriodicalIF":15.7000,"publicationDate":"2024-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Constructing mesoporous CeO2 single-crystal particles in ionic liquids for enhancing the conversion of CO2 and alcohols to carbonates\",\"authors\":\"Jielin Huang , Jie Wang , Haonan Duan , Songsong Chen , Junping Zhang , Li Dong , Xiangping Zhang\",\"doi\":\"10.1016/S1872-2067(24)60117-8\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Catalysts for CO<sub>2</sub> value-added conversion have been extensively explored, but there is still a lack of systematic design for catalysts that achieve efficient CO<sub>2</sub> conversion under mild conditions. Herein, we explored a mesoporous CeO<sub>2</sub> single-crystal formed with the regulation of ionic liquids, which catalyzed the effective carbonylation reaction with CO<sub>2</sub> under mild reaction conditions. By altering the synthetic environment, a series of uniform mesoporous CeO<sub>2</sub> particles with atomically aligned single-crystal frameworks were constructed, which have different surface physicochemical properties and primary aggregation degree. The prepared mesoporous CeO<sub>2</sub> single-crystal achieved efficient activation of CO<sub>2</sub> and alcohols at 0.5 MPa CO<sub>2</sub> and 100 °C, and the CeO<sub>2</sub>-IL-M catalyst shows optimal catalytic performance in the synthesis of ethylene carbonate with 46.22 mmol g<sup>–1</sup> h<sup>–1</sup>, which was 50.6 times as high as that of the CeO<sub>2</sub> obtained without ionic liquids. 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引用次数: 0
摘要
二氧化碳增值转化催化剂已被广泛探索,但在温和条件下实现二氧化碳高效转化的催化剂仍缺乏系统设计。在此,我们探索了一种在离子液体调节下形成的介孔 CeO2 单晶,它能在温和的反应条件下催化 CO2 的有效羰基化反应。通过改变合成环境,构建了一系列具有原子排列单晶框架的均匀介孔CeO2颗粒,它们具有不同的表面理化性质和初级聚集度。所制备的介孔 CeO2 单晶在 0.5 MPa CO2 和 100 ℃条件下实现了对 CO2 和醇类的高效活化,CeO2-IL-M 催化剂在合成碳酸乙烯酯中表现出最佳催化性能,其催化活性为 46.22 mmol g-1 h-1,是不含离子液体的 CeO2 催化剂的 50.6 倍。随后,通过 React-IR 光谱和 C18O2 标记实验研究了介孔 CeO2 单晶与 CO2 发生羰基化反应的催化途径和机理。该研究为介孔单晶材料的纳米尺度可控组装提供了新策略,拓展了单晶材料的应用范围,旨在开发新型催化材料以满足工业需求。
Constructing mesoporous CeO2 single-crystal particles in ionic liquids for enhancing the conversion of CO2 and alcohols to carbonates
Catalysts for CO2 value-added conversion have been extensively explored, but there is still a lack of systematic design for catalysts that achieve efficient CO2 conversion under mild conditions. Herein, we explored a mesoporous CeO2 single-crystal formed with the regulation of ionic liquids, which catalyzed the effective carbonylation reaction with CO2 under mild reaction conditions. By altering the synthetic environment, a series of uniform mesoporous CeO2 particles with atomically aligned single-crystal frameworks were constructed, which have different surface physicochemical properties and primary aggregation degree. The prepared mesoporous CeO2 single-crystal achieved efficient activation of CO2 and alcohols at 0.5 MPa CO2 and 100 °C, and the CeO2-IL-M catalyst shows optimal catalytic performance in the synthesis of ethylene carbonate with 46.22 mmol g–1 h–1, which was 50.6 times as high as that of the CeO2 obtained without ionic liquids. Subsequently, the catalytic pathway and mechanism of carbonylation reaction with CO2 on mesoporous CeO2 single-crystal were studied via React-IR spectra and C18O2 labeling experiments. The research provides a new strategy for controllable nanoscale assembly of mesoporous single-crystal materials and expands the application range of single-crystal materials, aiming to develop novel catalytic materials to meet industrial needs.
期刊介绍:
The journal covers a broad scope, encompassing new trends in catalysis for applications in energy production, environmental protection, and the preparation of materials, petroleum chemicals, and fine chemicals. It explores the scientific foundation for preparing and activating catalysts of commercial interest, emphasizing representative models.The focus includes spectroscopic methods for structural characterization, especially in situ techniques, as well as new theoretical methods with practical impact in catalysis and catalytic reactions.The journal delves into the relationship between homogeneous and heterogeneous catalysis and includes theoretical studies on the structure and reactivity of catalysts.Additionally, contributions on photocatalysis, biocatalysis, surface science, and catalysis-related chemical kinetics are welcomed.