首页> 外文期刊>Energy & fuels >Construction of a Stable Two-Dimensional MAX Supported Protonated Graphitic Carbon Nitride (pg-C_3N_4)/Ti_3AIC_2/TiO_2 Z-Scheme Multiheterojunction System for Efficient Photocatalytic CO_2 Reduction through Dry Reforming of Methanol
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Construction of a Stable Two-Dimensional MAX Supported Protonated Graphitic Carbon Nitride (pg-C_3N_4)/Ti_3AIC_2/TiO_2 Z-Scheme Multiheterojunction System for Efficient Photocatalytic CO_2 Reduction through Dry Reforming of Methanol

机译:构造稳定的二维MAX负载质子化石墨氮化物(PG-C_3N_4)/ TI_3AIC_2 / TiO_2 Z方案多函数结,其通过干重重整甲醇的有效光催化CO_2降低

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摘要

In situ construction of two-dimensional (2D)/2D pg-C3N4/Ti3AlC2 MAX heterojunction was achieved using a protonated assisted sonication approach, while TiO2 nanoparticles were embedded over the layered heterostructure using a sol-gel method. This multiheterojunction system exhibits proficient charge transfer and superior activity toward photocatalytic reduction of CO2 through dry reforming of methanol (DRM). Using pg-C3N4/Ti3AlC2/TiO2 composite, H-2 and CO production rates at 91.9 and 4.97 mmol (g of cat.)(-1) h(-1) were achieved, which are 18- and 6-fold higher than using pristine pg-C3N4, respectively. The enhancement in photocatalytic activity is mainly attributed to intimate interfacial contact due to the formation of a multiheterojunction for better light absorption, boosted electron separation, and stronger photoreductive potential. More importantly, CO2 reduction with H2O produces CO-rich syngas; however, the methanol/water mixture promoted hydrogen-rich syngas production. Higher quantum yield and prolonged stability are further achieved over the composite catalyst, attributed to the exfoliated 2D Ti3AlC2 MAX structure with strong metal/support interaction. This work demonstrates DRM as a potential approach to get hydrogen-rich syngas and provides a new pathway for the construction of highly stable 2D MAX based structured composite for water splitting and CO2 reforming applications.
机译:使用质子化辅助超声处理方法实现二维(2D)/ 2D PG-C3N4 / Ti3AlC2最大函数的原位构造,而使用溶胶 - 凝胶法将TiO2纳米颗粒嵌入层状异质结构上。这种多千分之二官能系统通过干燥重整甲醇(DRM)表现出熟练的电荷转移和优异的光催化减少CO2。使用PG-C3N4 / TI3ALC2 / TiO2复合材料,H-2和CO生产率在91.9和4.97mmol(g猫)(g型)( - 1)H(-1),比高于18倍和6倍使用原始PG-C3N4。光催化活性的增强主要归因于互连的界面接触,由于形成多重结,以更好的光吸收,提升电子分离和更强的光导电位。更重要的是,二氧化碳减少与H2O产生共同的合成气;然而,甲醇/水混合物促进了富含氢的合成气生产。在复合催化剂上进一步实现了较高的量子产率和延长的稳定性,归因于具有强金属/载体相互作用的剥落的2D Ti3AlC2 Max结构。这项工作证明了DRM作为获得富含氢合成气的潜在方法,为施工高度稳定的2D最大结构化复合材料进行了新的途径,用于水分裂和CO2重整应用。

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  • 来源
    《Energy & fuels》 |2020年第3期|3540-3556|共17页
  • 作者

    Tahir Muhammad;

  • 作者单位

    Univ Teknol Malaysia Sch Chem & Energy Engn Dept Chem Engn Johor Baharu 81310 Johor Malaysia;

  • 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);
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
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