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Stereodefined Codoping of sp-N and S Atoms in Few-Layer Graphdiyne for Oxygen Evolution Reaction

机译:几层石墨二炔中sp-N和S原子的立体定义共氧反应

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摘要

Developing metal-free catalysts with high catalytic activity for oxygen evolution reaction (OER) is essentially important for energy and environment-related techniques. Compared with individual element doping, doping carbon materials with multiple heteroelements has more advantages for enhancing the OER performance. However, doped sites for the different atoms are highly uncontrollable under the reported methods, which hinder the deeper understanding on the relationship between structure and property, and also limit the enhancement of catalytic activity. Our latest research has reported a method to site-controlled introducing a new form of nitrogen atoms, i.e. sp-hybridized nitrogen (sp-N), into graphdiyne, showing its potential advantages in OER catalysis. Since the sites of sp-N atoms are defined in graphdiyne, and the doping sites for S atoms are well understood, the relative position between N and S can be further defined. It gives us a chance to understand deeply the mechanism in the N, S heteroelements doped metal-free catalyst. Experimental results present that the codoping of sp-N and S atoms brought an excellent OER performance with low overpotential and high current density owning to the effectively synergistic effect of the stereodefined heteroatoms.
机译:开发对氧释放反应(OER)具有高催化活性的无金属催化剂对于能源和环境相关技术至关重要。与单元素掺杂相比,掺杂多种杂元素的碳材料在增强OER性能方面具有更多优势。然而,在所报道的方法下,对于不同原子的掺杂位点是高度不可控的,这阻碍了对结构和性质之间关系的更深入的理解,并且还限制了催化活性的提高。我们的最新研究报告了一种定点控制方法,可将一种新形式的氮原子(即sp-杂化氮(sp-N))引入石墨烯中,显示出其在OER催化中的潜在优势。因为sp-N原子的位点是在石墨二炔中定义的,并且S原子的掺杂位点是众所周知的,所以可以进一步定义N和S之间的相对位置。它使我们有机会深入了解N,S杂元素掺杂的无金属催化剂中的机理。实验结果表明,sp-N和S原子的共掺杂带来了优异的OER性能,具有较低的超电势和高电流密度,这归因于立体定义的杂原子的有效协同作用。

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  • 来源
    《Journal of the American Chemical Society》 |2019年第18期|7240-7244|共5页
  • 作者单位

    Harbin Inst Technol, Sch Chem & Chem Engn, MIIT Key Lab Crit Mat Technol New Energy Convers, Harbin 150001, Heilongjiang, Peoples R China|Chinese Acad Sci, Inst Proc Engn, State Key Lab Biochem Engn, 1 Beiertiao, Beijing 100190, Peoples R China;

    Chinese Acad Sci, Inst Proc Engn, State Key Lab Biochem Engn, 1 Beiertiao, Beijing 100190, Peoples R China|Univ Chinese Acad Sci, Beijing 100049, Peoples R China;

    Beijing Normal Univ, Dept Chem, Key Lab Theoret & Computat Photochem, Minist Educ, Beijing 100875, Peoples R China;

    Univ Sci & Technol China, CAS Ctr Excellence Nanosci, Natl Synchrotron Radiat Lab, Hefei 230029, Anhui, Peoples R China;

    Univ Sci & Technol China, CAS Ctr Excellence Nanosci, Natl Synchrotron Radiat Lab, Hefei 230029, Anhui, Peoples R China;

    Beijing Normal Univ, Dept Chem, Key Lab Theoret & Computat Photochem, Minist Educ, Beijing 100875, Peoples R China;

    Nanyang Technol Univ, Sch Mat Sci & Engn, Singapore 639798, Singapore;

    Chinese Acad Sci, Inst Phys, Beijing 100190, Peoples R China;

    Harbin Inst Technol, Sch Chem & Chem Engn, MIIT Key Lab Crit Mat Technol New Energy Convers, Harbin 150001, Heilongjiang, Peoples R China;

    Harbin Inst Technol, Sch Chem & Chem Engn, MIIT Key Lab Crit Mat Technol New Energy Convers, Harbin 150001, Heilongjiang, Peoples R China|Chinese Acad Sci, Inst Proc Engn, State Key Lab Biochem Engn, 1 Beiertiao, Beijing 100190, Peoples R China|Univ Chinese Acad Sci, Beijing 100049, Peoples R China;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
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