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Perovskite Oxynitride Solid Solutions of LaTaON

机译:钙钛矿氧氮化物固体溶液的拉伸

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摘要

The search for solar‐driven photocatalysts for overall water splitting has been actively pursued. Although metal oxynitrides with metal d0/d10‐closed shell configuration are very promising candidates in terms of their visible light absorption, they usually suffer from serious photo‐generated charge recombination and thus, little photoactivity. Here, by forming their solid solutions of LaTaON2 and CaTaO2N, which are traditionally considered to be inorganic yellow‐red pigments but have poor photocatalytic activity, a class of promising solar‐driven photocatalysts La1‐xCaxTaO1+yN2‐y (0 ≤ x, y ≤ 1) are explored. In particular, the optimal photocatalyst with x = 0.9 has the ability of realizing overall water splitting with stoichiometric H2/O2 ratio under the illumination of both AM1.5 simulated solar light and visible light. The modulated key parameters including band structure, Ta bonding environment, defects concentration, and band edge alignments revealed in La0.1Ca0.9TaO1+yN2‐y have substantially promoted the separation of photogenerated charge carriers with sufficient energetics for water oxidation and reduction reactions. The results obtained in this study provide an important candidate for designing efficient solar‐driven photocatalysts for overall water splitting.
机译:正在积极寻求寻找用于整体水分裂的太阳能光催化剂。尽管具有金属D0 / D10封闭壳体配置的金属氧氮化是在其可见光吸收方面具有非常有前途的候选者,但它们通常遭受严重的光产生电荷重组,因此较少的照片。在此,通过形成LataOn2和CataO 2n的固体溶液,传统上被认为是无机的黄色颜料,但具有差的光催化活性,一类有前景的太阳能触发光催化剂La1-Xcaxtao1 + Yn2-探索y(0≤x,y≤1)。特别地,具有X = 0.9的最佳光催化剂具有在AM1.5模拟太阳能光和可见光的照明下实现具有化学计量H2 / O2比的总水分的能力。在La0.1ca0.9tao1 +中显示包括带结构,ta键合环境,缺陷浓度和带边缘对齐的调制关键参数。YN2-Y基本上促进了具有足够的能量氧化和还原反应的充满活力的光生电载体的分离。本研究中获得的结果提供了一种用于设计高效的太阳能驱动光催化剂的重要候选者,用于整体水分裂。

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