首页> 外文期刊>Applied Catalysis, B. Environmental: An International Journal Devoted to Catalytic Science and Its Applications >Heterostructured Er~(3+) doped BiVO4 with exceptional photocatalytic performance by cooperative electronic and luminescence sensitization mechanism
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Heterostructured Er~(3+) doped BiVO4 with exceptional photocatalytic performance by cooperative electronic and luminescence sensitization mechanism

机译:杂化结构的Er〜(3+)掺杂BiVO4通过协同的电子和发光敏化机理具有出色的光催化性能

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摘要

Er-BiVO4 has been synthesized by means of mw-assisted hydrothermal method having good photoacti-vity under sun-like excitation. It is stated that the precursor addition sequence plays a critical role which determine the further structural feature of BiVO4. From the structural and morphological characterization, it can be demonstrated that the presence of Er~(3+) would induce the stabilization of the tetragonal phase probably due to the formation of tetragonal-ErVO4 seeds previous to BiVO4 formation. The best photocatalytic performance is attained for the sample with 0.75 at% Er~(3+) content At this dopant loading a mixture of tetragonal and monoclinic phase (70% tetragonal) is obtained. The dramatic increase in the photocatalytic activity for 0.75 at% Er-BiVO4 is related to the occurrence of such heterostructure. For this system, the MB degradation rate constant appears drastically higher as bare m-BiVO4. Furthermore, activities of photocatalysts for visible-light-driven O2 evolution have been evaluated, demonstrating that the photocatalytic activity of this Er-doped system (O2 evolution rate, 1014 μmol g~(-1) h~(-1)) is 20 times as that of undoped m-BiVO4 (O2 evolution rate, 54 μmol g~(-1) h~(-1)). From the obtained results, the cooperative conjunction of electronic and luminescence mechanism involved in the reaction is proposed to be the origin of the enhanced photocatalytic efficiencies of such systems.
机译:Er-BiVO4是通过MW辅助水热法合成的,在太阳光激发下具有良好的光活性。据指出,前体添加序列起决定BiVO4进一步结构特征的关键作用。从结构和形态特征可以证明,Er〜(3+)的存在将诱导四方相的稳定,这可能是由于在BiVO4形成之前形成了四方ErVO4种子。对于具有0.75 at%Er〜(3+)含量的样品,可以获得最佳的光催化性能。在该掺杂剂负载下,获得了四方相和单斜相(70%四方相)的混合物。 0.75at%的Er-BiVO4的光催化活性的急剧增加与这种异质结构的发生有关。对于该系统,MB降解速率常数与裸m-BiVO4相比显得更高。此外,已经评估了可见光驱动的O2分解的光催化剂活性,表明该掺Er体系的光催化活性(O2分解速率为1014μmolg〜(-1)h〜(-1))为20。是未掺杂的m-BiVO4的2倍(O2释放速率为54μmolg〜(-1)h〜(-1))。从获得的结果,反应中涉及的电子和发光机理的协同结合被认为是这种系统提高的光催化效率的起源。

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