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A direct Z-scheme g-C3N4/SnS2 photocatalyst with superior visible-light CO2 reduction performance

机译:一种直接Z形式G-C3N4 / SNS2光催化剂,具有优异的可见光CO2还原性能

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摘要

udud - SnS quantum dots anchored in situ on g-CN by a simple one-step hydrothermal method.udud - The internal electric field between g-CN and SnS was confirmed.udud - Internal-electric-field-induced direct Z-scheme g-CN/SnS charge transfer for enhanced photocatalytic CO reduction.udud - In situ FTIR analysis further proved the suggested photocatalytic mechanism.ududududPhotocatalytic reduction of CO to solar fuels is an ideal approach to simultaneously solve the global warming and energy crisis issues. Constructing a direct Z-scheme heterojunction is an effective way to overcome the drawbacks of single-component or conventional heterogeneous photocatalysts for photocatalytic CO reduction. Here, a novel type of direct Z-scheme g-CN/SnS heterojunction was constructed by depositing SnS quantum dots onto the g-CN surface in situ via a simple one-step hydrothermal method. -Cysteine not only acted as the sulfur source, but also grafted ammine groups onto g-CN in the hydrothermal process, which greatly enhanced the CO uptake of the composite. XPS analysis and density functional theory (DFT) calculation show that electron transfer occurred from g-CN to SnS, resulting in the formation of interfacial internal electric fields (IEF) between the two semiconductors at equilibrium. As a result, Z-scheme charge transfer took place under photoexcitation, with the electrons in SnS combining with the holes in g-CN, which improved the extraction and utilization of photoinduced electron in g-CN. The g-CN/SnS hybrid shows superior photocatalytic CO reduction as compared with individual g-CN and SnS, which should be attributed to the IEF-induced direct Z-scheme as well as improved CO adsorption capacity. In situ FTIR spectra illustrate that HCOOH appeared as an intermediate during the CO conversion, which can only be generated by g-CN according to the energy level of the photoinduced electrons, further confirming the Z-scheme configuration for the g-CN/SnS system.
机译:ud ud - 通过简单的一步水热法在G-cn上锚定的量子点。 ud ud - 确认了g-cn和sns之间的内部电场。 ud ud - 内电 - 菲尔德诱导的直接Z-Scheme G-CN / SNS电荷转移,用于增强的光催化CO降低。 UD UD - 原位FTIR分析进一步证明了建议的光催化机制。 ud ud ud ud Ud udPhotocatalytic减少Co到Solar燃料是同时解决全球变暖和能源危机问题的理想方法。构建直接Z形方案异质结是克服用于光催化CO的单组分或常规异质光催化剂的缺点的有效途径。这里,通过通过简单的单步水热法在原位沉积在G-CN表面上,构建一种新颖的直接Z形式G-CN / Sn的异质结。 - 胞嘧啶不仅用作硫源,还具有含硫源,还在水热过程中接枝到G-CN上,这大大提高了复合材料的共同吸收。 XPS分析和密度泛函理论(DFT)计算表明,从G-CN到SNS发生电子转移,导致两种半导体之间的界面内部电场(IEF)的形成。结果,Z方案电荷转移在光呼吸中发生,用SNS中的电子与G-CN中的孔组合,这改善了G-CN中光诱导电子的提取和利用。与单独的G-CN和SNS相比,G-CN / SNS杂种显示出优异的光催化CO降低,其应归因于IEF诱导的直接Z方案以及改善的CO吸附能力。原位FTIR光谱说明了在CO转换期间的HCOOH出现在CO转换期间,这只能通过G-CN根据光导电的能级产生,进一步证实了G-CN / SNS系统的Z方案配置。

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