首页> 外文期刊>能源化学:英文版 >Surface functionalized N-C-TiO_(2)/C nanocomposites derived from metal-organic framework in water vapour for enhanced photocatalytic H generation
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Surface functionalized N-C-TiO_(2)/C nanocomposites derived from metal-organic framework in water vapour for enhanced photocatalytic H generation

机译:表面官能化N-C-TiO_(2)/ C纳米复合材料衍生自水蒸汽中的金属有机骨架,用于增强的光催化H发电

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摘要

Surface-functionalized nitrogen/carbon co-doped polymorphic TiO_(2) phase junction nanoparticles uniformly distributed in porous carbon matrix were synthesized by a simple one-step pyrolysis of titanium based metal-organic framework(MOF),NH_(2)-MIL^(-1)25(Ti) at 700°C under water vapour atmosphere.Introducing water vapour during the pyrolysis of NH_(2)-MIL^(-1)25(Ti) not only functionalizes the derived porous carbon matrix with carboxyl groups but also forms additional oxygen-rich N like interstitial/intraband states lying above the valence band of TiO2 along with the self-doped carbo n,which further narrows the energy band gaps of polymorphic TiO2 nanoparticles that enhance photocatalytic charge transfer efficiency.Without co-catalyst,sample N-C-TiO2/CArW demonstrates H_(2) evolution activity of 426 μmol gcat-1h^(-1),which remarkably outperforms commercial TiO_(2)(P-25) and N-C-TiO_(2)/CAr with a 5-fold and 3-fold H_(2) generation,respectively.This study clearly shows that water vapour atmosphere during the pyrolysis increases the hydrophilicity of the Ti-MOF derived composites by functionalizing porous carbon matrix with carboxylic groups,as well as enhancing the electrical conductivity and charge transfer efficiency due to the formation of additional localized oxygen-rich N like interstitial/intraband states.This work also demonstrates that by optimizing the anatase-rutile phase composition of the TiO2 polymorphs,tuning the energy band gaps by N/C co-doping and functionalizing the porous carbon matrix in the N-C-TiO2/C nanocomposites,the photocatalytic H_(2) generation activity can be further enhanced.
机译:通过简单的一步热解(MOF),NH_(2)-MIL ^,通过简单的单步热解合成表面官能化氮气/碳共掺杂多态性TiO_(2)相结纳米颗粒均匀分布在多孔碳基质中。 (-1)25(Ti)在700°C下在水蒸气气氛下。在NH_(2)-MIL ^( - 1)25(Ti)的热解期间,在热解期间的水蒸气不仅用羧基官能化衍生的多孔碳基质而且还形成额外的富含富含间质/内在状态的富含氧气/内在态,其伴随着TiO2的价带以及自掺杂的Carbo N,这进一步缩小了具有增强光催化电荷转移效率的多态性TiO2纳米颗粒的能带间隙。催化剂,样品NC-TiO2 /载体显示出426μmolGCAT-1H ^( - 1)的evolution活性,其显着优于商用TiO_(2)(P-25)和NC-TiO_(2)/汽车分别为5倍和3倍的H_(2)代。本研究清楚地表明水VAPOU在热解期间的R气氛通过用羧基官能化多孔碳基质来增加Ti-Mof衍生复合材料的亲水性,以及由于额外的局部氧气的富含性富含性富含型富含间质/内纳的富含型氧气的电导率和电荷转移效率该方面还证明,通过优化TiO 2多晶型物的锐钛矿 - 金红石相组合物,通过N / C共掺杂调节能带间隙并在NC-TiO 2 / C纳米复合材料中官能化,光催化H_ (2)可以进一步增强生成活动。

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  • 来源
    《能源化学:英文版》 |2021年第006期|P.485-495I0012|共12页
  • 作者单位

    College of Engineering Mathematics and Physical Sciences University of Exeter Exeter EX44QF United KingdomDepartment of Chemistry and Catalysis Research Center Technical University of Munich Garching 85748 Germany;

    College of Engineering Mathematics and Physical Sciences University of Exeter Exeter EX44QF United Kingdom;

    Catalysis Engineering Chemical Engineering Department Delft University of Technology van der Maasweg 9 2629 HZ Delft Netherlands;

    College of Engineering Mathematics and Physical Sciences University of Exeter Exeter EX44QF United Kingdom;

    Henan Key Laboratory of High Temperature Functional Ceramics Zhengzhou University Zhengzhou 450052 Henan China;

    Department of Chemistry University of Turin Via P.Giuria 7 10125 Turin Italy;

    Department of Chemistry and Catalysis Research Center Technical University of Munich Garching 85748 Germany;

    Catalysis Engineering Chemical Engineering Department Delft University of Technology van der Maasweg 9 2629 HZ Delft Netherlands;

    College of Engineering Mathematics and Physical Sciences University of Exeter Exeter EX44QF United Kingdom;

    College of Engineering Mathematics and Physical Sciences University of Exeter Exeter EX44QF United Kingdom;

  • 收录信息
  • 原文格式 PDF
  • 正文语种 chi
  • 中图分类 物理化学(理论化学)、化学物理学;
  • 关键词

    Metal-organic framework; TiO_(2); Porous carbon; Nanocomposite; Photocatalysis; Hydrogen generation;

    机译:金属有机框架;TiO_(2);多孔碳;纳米复合材料;光催化;氢气;
  • 入库时间 2022-08-19 04:57:47
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