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Enhanced pyrocatalysis of the pyroelectric BiFeO3/g-C3N4?heterostructure for dye decomposition driven by cold-hot temperature alternation

机译:热电bifeO3 / G-C3N4的增强过亚丙酸分析α异质结构,用于冷热温度交替驱动的染料分解

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The BiFeO3/g-C3N4?heterostructure, which is fabricated via a simple mixing-calcining method, benefits the significant enhancement of the pyrocatalytic performance. With the growth of g-C3N4?content in the heterostructure pyrocatalysts from 0 to 25%, the decomposition ratio of Rhodamine B (RhB) dye after 18 cold-hot temperature fluctuation (25–65 °C) cycles increases at first and then decreases, reaching a maximum value of ~94.2% at 10% while that of the pure BiFeO3?is ~67.7%. The enhanced dye decomposition may be due to the generation of the internal electric field which strengthens the separation of the positive and negative carriers and further accelerates their migrations. The intermediate products in the pyrocatalytic reaction also have been detected and confirmed, which proves the key role of the pyroelectric effect in realizing the dye decomposition using BiFeO3/g-C3N4?heterostructure catalyst. The pyroelectric BiFeO3/g-C3N4?heterostructure shows the potential application in pyrocatalytically degrading dye wastewater.
机译:BifeO3 / G-C3N4?异质结构,通过简单的混合煅烧方法制造,有利于热催化性能的显着提高。随着G-C3N4的生长,异质结构含量从0〜25%的含量,罗丹明B(RHB)染料的分解比在18次冷热温度波动(25-65℃)循环后开始增加,然后降低,最大值达到10%的最大值〜94.2%,而纯BifeO3的最大值为10%?是〜67.7%。增强型染料分解可能是由于产生的内部电场的产生,该内部电场增强了正极和负载体的分离并进一步加速了它们的迁移。过催化反应中的中间产物也已检测到并确认,这证明了热电效应在实现使用BifeO3 / G-C3N4α异质结构催化剂来实现染料分解的关键作用。热释电体3 / G-C3N4?异质结构显示出吡铜alytaly降解染料废水中的潜在应用。

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