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首页> 外文期刊>ACS applied materials & interfaces >Non-Noble Metal Nanoparticles Supported by Postmodified Porous Organic Semiconductors: Highly Efficient Catalysts for Visible-Light-Driven On-Demand H-2 Evolution from Ammonia Borane
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Non-Noble Metal Nanoparticles Supported by Postmodified Porous Organic Semiconductors: Highly Efficient Catalysts for Visible-Light-Driven On-Demand H-2 Evolution from Ammonia Borane

机译:由后置多孔有机半导体支撑的非贵金属纳米颗粒:高效催化剂,用于从氨硼烷的可见光驱动的按需H-2进化

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摘要

From the viewpoint of controlling the visible light-driven activities of catalysts containing metal nano particles (NPs) by tuning, the microstructures-of semiconducting supports, we employed a postsynthetic thermal modification approach to prepare carbon nitride (C3N4) species featuring different microstructures and then we synthesized co and Ni NPs supported by these C3N4 species, Which were used to catalyze the room-temperature H-2 evolution from ammonia borane (NH3BH3). The systematic investigation showed that the catalysts had different activities under light irradiation. Compared with the pristine,C3N4-based catalyst, all the modified C3N4-based catalysts had enhanced activities. The highest active Co catalyst with,a total turnover frequency Of 93.8 min', was successfully obtained, which exceeded the values of all the reported heterogeneous noble metal-free catalysts. The structure characterizations indicated that the postmodified porous C3N4 species had the different band structures, photoluminescence lifetime, and photocurrent density under visible light irradiation) leading to the different separation efficiency of photogenerated charge carriers. These characteristics helped us regulate the electronic characteristics of Co and Ni NPs in the supported catalysts and then led to the significantly different and enhanced activity in the visible-light-driven H-2 evolution.
机译:从通过调节控制含有金属纳米颗粒(NPS)的催化剂的可见光驱动活性的观点来看,半导体支撑件的微观结构,我们采用了一种邮政的热改性方法来制备具有不同微观结构的碳氮化物(C3N4)物种。我们合成这些C3N4物种支持的CO和Ni NP,其用于催化来自氨硼烷(NH 3BH3)的室温H-2进化。系统的研究表明,催化剂在轻辐射下具有不同的活性。与原始C3N4的催化剂相比,所有改性的C3N4的催化剂具有增强的活性。成功获得了最高活性CO催化剂,总周转频率为93.8分钟',超过所有报告的异质贵金属催化剂的值。结构表征表明,后修补的多孔C3N4物种具有不同的带状结构,光致发光寿命和光电流密度,导致光生电电荷载体的不同分离效率。这些特性有助于我们调节支持的催化剂中CO和Ni NP的电子特性,然后导致可见光驱动的H-2进化中的显着不同和增强的活性。

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  • 来源
    《ACS applied materials & interfaces》 |2017年第38期|共8页
  • 作者单位

    Inner Mongolia Univ Sch Chem &

    Chem Engn Inner Mongolia Key Lab Coal Chem Hohhot 010021 Inner Mongolia Peoples R China;

    Inner Mongolia Univ Sch Chem &

    Chem Engn Inner Mongolia Key Lab Coal Chem Hohhot 010021 Inner Mongolia Peoples R China;

    Inner Mongolia Univ Sch Chem &

    Chem Engn Inner Mongolia Key Lab Coal Chem Hohhot 010021 Inner Mongolia Peoples R China;

    Inner Mongolia Univ Sch Chem &

    Chem Engn Inner Mongolia Key Lab Coal Chem Hohhot 010021 Inner Mongolia Peoples R China;

    Inner Mongolia Univ Sch Chem &

    Chem Engn Inner Mongolia Key Lab Coal Chem Hohhot 010021 Inner Mongolia Peoples R China;

  • 收录信息
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 化学工业;
  • 关键词

    hydrogen evolution; metal nanoparticle; semiconductor; catalyst; visible light irradiation;

    机译:氢气进化;金属纳米粒子;半导体;催化剂;可见光照射;

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