Investigate the Function and Structure of (Fe,Cr) La2Ti2O7 Photocatalyst Calcined under the Nitrogen Atmosphere

Hussanai Luangthanarak, R. Supruangnet, W. Tanthanuch, Sukasem Watcharamaisakul
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Abstract

Extensive research has been conducted on enhancing the photocatalytic activity of Lanthanum titanium oxide (La2Ti2O7) based photocatalysts. However, these photocatalysts were found to be inactive under visible light. To address this limitation, a modification was developed by co-doping Fe and Cr on La2Ti2O7 to enable visible light driven photocatalytic response. The calcination of (Fe,Cr) La2Ti2O7 was carried out under nitrogen atmosphere at various temperatures for 24 h. The results showed that the (Fe,Cr)-La2Ti2O7 calcined at 1250 °C for 24 h exhibited the highest methylene blue degradation under visible light. Synchrotron X-ray absorption spectroscopy indicated that Fe and Cr were substitutionally located adjacent to the Ti atom within the La2Ti2O7 structure. This metal  substitutionally facilitated electron transfer and perturbed the p-d hybridization by modifying the local electronic structure of the surrounding oxygen atoms and transition metal ions, thereby reducing the band gap energy and enhancing the photocatalytic capability. Copyright © 2023 by Authors, Published by BCREC Group. This is an open access article under the CC BY-SA License (https://creativecommons.org/licenses/by-sa/4.0). 
氮气氛下煅烧(Fe,Cr) La2Ti2O7光催化剂的结构与功能研究
在提高氧化镧(La2Ti2O7)基光催化剂的光催化活性方面进行了大量的研究。然而,这些光催化剂在可见光下是无活性的。为了解决这一限制,研究人员通过在La2Ti2O7上共掺杂Fe和Cr来实现可见光驱动的光催化反应。在氮气气氛下,对(Fe,Cr) La2Ti2O7在不同温度下煅烧24 h,结果表明,(Fe,Cr)-La2Ti2O7在1250℃下煅烧24 h,在可见光下亚甲基蓝降解效果最好。同步加速器x射线吸收光谱表明,在La2Ti2O7结构中,Fe和Cr取代位于Ti原子附近。这种金属通过改变周围氧原子和过渡金属离子的局部电子结构,取代性地促进了电子转移,扰乱了p-d杂化,从而降低了带隙能量,增强了光催化能力。版权所有©2023作者,BCREC集团出版。这是一篇基于CC BY-SA许可(https://creativecommons.org/licenses/by-sa/4.0)的开放获取文章。
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