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首页> 外文期刊>Journal of Physics, D. Applied Physics: A Europhysics Journal >Hydroxy-carbonate-assisted synthesis of high porous graphitic carbon nitride with broken of hydrogen bonds as a highly efficient visible-light-driven photocatalyst
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Hydroxy-carbonate-assisted synthesis of high porous graphitic carbon nitride with broken of hydrogen bonds as a highly efficient visible-light-driven photocatalyst

机译:羟基碳酸酯辅助合成高多孔石墨碳氮化物,氢键破碎为高效的可见光光催化剂

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摘要

Graphite carbon nitride (g-C3N4) is a promising candidate as an efficient, affordable, and sustainable alternative photocatalyst owing to its unique physical and chemical properties. However, the photocatalytic activity of pristine g-C3N4 is still far below what is expected, because of its insufficient active site and high electron-hole recombination rates. Herein, we develop a novel strategy-a one-step hydroxy-carbonate-assisted route-to try to overcome these disadvantages in g-C3N4 nanosheets by creating substantial pores ranging from mesoporous to macropore, which are mainly caused by the partial breaking of hydrogen bonds and removing of magnesium oxide. Luxuriant pores in g-C3N4 not only serve as a reaction center by providing a large number of active sites at pore edges, but also effectively improve the photogenerated carrier separation by shortening their transfer lengths. The highly efficient visible-light photocatalytic activity of porous g-C3N4 nanosheets are demonstrated by degrading methyl blue (MB) and gentian violet (GV) as models, which its degradation rate constant is respectively more than 109 times and 12 times higher than those of pristine g-C3N4. Meanwhile, the high porous g-C3N4 has robust stability. The simple and effective strategy proposed here provides a direct route to highly functionalized g-C3N4 nanosheets and other layered semiconductors for various applications.
机译:石墨碳氮化物(G-C3N4)是由于其独特的物理和化学性质而作为有效,实惠和可持续的替代光催化剂的候选者。然而,由于其活性位点不足和高电子 - 空穴重组率,原始G-C3N4的光催化活性仍远低于预期的。在此,我们开发一种新的策略 - 一种通过产生从培养孔到大孔的大量孔来克服G-C3N4纳米片中的一步羟基 - 碳酸酯辅助途径 - 以克服巨孔,这主要是由氢气部分破碎引起的键合和去除氧化镁。 G-C3N4中的茂盛孔不仅可以通过在孔边缘提供大量活性位点,而且通过缩短其转移长度来有效地改善光生载体分离。通过降解甲基蓝(MB)和龙胆紫(GV)作为模型来证明多孔G-C3N4纳米片的高效可见光光催化活性,其降解率常数分别超过109倍,比原始G-C3N4。同时,高多孔G-C3N4具有稳定的稳定性。此处提出的简单有效的策略提供了用于各种应用的高官能化G-C3N4纳米片和其他层状半导体的直接路线。

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