Wang Zhigang, Yu Hongliang, Liu Zhuoyuan
School of Chemistry and Chemical Engineering, Hubei Polytechnic University, Huangshi 435003, China.
Molecules. 2023 Jul 31;28(15):5792. doi: 10.3390/molecules28155792.
A novel and efficient technique has been designed for the creation of oxygen vacancies on LaTiO (LTO) nanosheets. This is achieved via a controlled solid-state reaction between NaBH and LTO nanosheets. Transmission electron microscopy (TEM) analyses expose that these processed LTO specimens possess a unique crystalline core/amorphous shell structure, represented as LaTiO@LaTiO. According to X-ray photoelectron spectroscopy (XPS) observations, there is a notable correlation between the reaction time, temperature, and the concentration of oxygen vacancies. The concentration of these vacancies tends to increase along with the reaction time and temperature. Concurrently, UV-Visible spectra and photocatalytic tests reveal a significant impact of oxygen vacancies on the LTO surface on both light absorption and photocatalytic functionality. Most notably, the LTO nanosheets with engineered oxygen vacancies have demonstrated an exceptional photocatalytic capacity for hydrogen production under visible light. The maximal activity recorded was an impressive 149 μmol g h, which is noticeably superior to the performance of the pristine LaTiO.
一种新颖且高效的技术已被设计用于在钛酸镧(LTO)纳米片上产生氧空位。这是通过硼氢化钠(NaBH)与LTO纳米片之间的可控固态反应实现的。透射电子显微镜(TEM)分析表明,这些经过处理的LTO样品具有独特的晶核/非晶壳结构,表示为LaTiO@LaTiO。根据X射线光电子能谱(XPS)观察,反应时间、温度与氧空位浓度之间存在显著相关性。这些空位的浓度倾向于随着反应时间和温度的增加而增加。同时,紫外可见光谱和光催化测试表明,LTO表面的氧空位对光吸收和光催化功能都有显著影响。最值得注意的是,具有工程化氧空位的LTO纳米片在可见光下表现出了卓越的光催化产氢能力。记录到的最大活性为令人印象深刻的149 μmol g⁻¹ h⁻¹,明显优于原始LaTiO的性能。