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首页> 外文期刊>RSC Advances >Solvothermal method coupled with thermal decomposition for synthesis of non-stoichiometric BiO1.18I0.64 with excellent photocatalytic activity
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Solvothermal method coupled with thermal decomposition for synthesis of non-stoichiometric BiO1.18I0.64 with excellent photocatalytic activity

机译:溶剂热结合热分解法合成具有光催化活性的非化学计量比BiO1.18I0.64

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A series of non-stoichiometric BiOxI3-2x photocatalysts were successfully prepared by a solvothermal method combined with thermal decomposition. Among them, BiO1.18I0.64 exhibited the highest photocatalytic activity. The degradation rate of aniline (50 mg L-1) over the photocatalyst (1 g L-1) was about 92.5% after 3 h of white LED lamp irradiation. Density functional theory calculations demonstrated that a much faster velocity of relative movement between electron and hole, as well as an apparently enhanced internal electric field in BiO1.18I0.64 greatly facilitated separation of photogenerated electron-hole pairs, which significantly improved its photocatalytic activity. In addition, I-vacancies in BiO1.18I0.64 could play an important role in capturing holes and thereby inhibiting the recombination of photoinduced electron-hole pairs. It further accounted for the obviously enhanced photocatalytic activity of BiO1.18I0.64.
机译:通过溶剂热法与热分解相结合,成功制备了一系列非化学计量比的BiOxI3-2x光催化剂。其中,BiO1.18I0.64表现出最高的光催化活性。白色LED灯照射3小时后,苯胺(50 mg L-1)在光催化剂(1 g L-1)上的降解率约为92.5%。密度泛函理论计算表明,BiO1.18I0.64中电子与空穴之间的相对运动更快,并且内部电场明显增强,大大促进了光生电子-空穴对的分离,从而显着提高了其光催化活性。此外,BiO1.18I0.64中的I空位在捕获空穴中起着重要作用,从而抑制了光诱导电子-空穴对的重组。它进一步说明了BiO1.18I0.64的光催化活性明显增强。

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