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首页> 外文期刊>Journal of Materials Chemistry, A. Materials for energy and sustainability >Methylamine lead bromide perovskite/protonated graphitic carbon nitride nanocomposites: interfacial charge carrier dynamics and photocatalysis
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Methylamine lead bromide perovskite/protonated graphitic carbon nitride nanocomposites: interfacial charge carrier dynamics and photocatalysis

机译:甲胺铅溴化物钙钛矿/质子化石墨碳氮化物纳米复合材料:界面电荷载体动力学和光催化

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We demonstrate the decoration of methylamine lead bromide (MAPbBr(3), MA: CH3NH3+) perovskite nanoparticles on protonated graphitic carbon nitride (p-g-C3N4) sheets to form nanocomposites (NCs) for the first time. The intrinsic type II band structure of MAPbBr(3)/p-g-C3N4 NCs resulted in significant charge separation properties, which were greatly beneficial for related applications in photoelectric conversion. The interfacial charge transfer behavior of MAPbBr(3)/p-g-C3N4 NCs was analyzed via time-resolved photoluminescence (TRPL) spectroscopy and singular-value decomposition global fitting (SVD-GF), which revealed that photoexcited electrons in the conduction band (CB) and shallow-trap (ST) states of MAPbBr(3) could be transferred into the CB of g-C3N4. The fitting results for TRPL traces indicated that the control of the related compositions could modulate the interfacial charge carrier dynamics of MAPbBr(3)/g-C3N4 NCs. An increase in the charge transfer rate constant (ket) for MAPbBr(3)/g-C3N4 NCs was discovered when the constituent ratio of p-g-C3N4 was enhanced. Furthermore, we utilized MAPbBr(3)/p-g-C3N4 NCs as a photocatalyst to carry out the photocatalytic reduction of pnitrophenol (PNP) under visible-light irradiation. A significant photoreduction rate (kPNP) of PNP was observed in the photocatalytic reaction, which indicated the great potential of MAPbBr(3)/p-g-C3N4 NCs to convert solar energy into chemical energy. In particular, the present investigation opens a new field for organolead bromide perovskites in applications in photocatalysis, as well as related photoelectric conversion.
机译:我们证明了在质子化石墨碳氮化物(P-G-C3N4)片上的甲胺铅溴(Mapbbr(3),MA:CH3NH3 +)钙钛矿纳米颗粒的装饰,首次形成纳米复合材料(NCS)。 MAPBBR(3)/ P-G-C3N4 NCS的内在II型带结构导致显着的电荷分离性能,这对于光电转换中的相关应用有很大利益。通过时间分辨的光致发光(TRPL)光谱和奇异值分解全局拟合(SVD-GF)分析MAPBBBR(3)/ PG-C3N4 NCS的界面电荷转移行为,其显示导通带中的光透射电子(CB )MAPBBR(3)的浅陷阱(ST)态可以转移到G-C3N4的CB中。 TrPL迹线的拟合结果表明,相关组合物的控制可以调节MAPBBR(3)/ G-C3N4 NCS的界面电荷载体动态。当提高P-G-C3N4的组分比时发现了MAPBBR(3)/ g-C3N4 NCS的电荷转移速率常数(KET)的增加。此外,我们利用MAPBBBR(3)/ p-G-C3N4NCS作为光催化剂,以在可见光照射下进行苯硝基苯酚(PNP)的光催化还原。在光催化反应中观察到PNP的显着的光电计速(KPNP),这表明MAPBBR(3)/ P-G-C3N4 NC的巨大潜力将太阳能转化为化学能。特别地,本研究调查在光催化在光催化中的应用中开启了有机溴化物钙酸盐的新场,以及相关的光电转换。

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