控制 Bi2MoO6 微球的结晶度以提高光催化氧进化能力

IF 4.1 3区 化学 Q2 CHEMISTRY, PHYSICAL Journal of Photochemistry and Photobiology A-chemistry Pub Date : 2024-08-29 DOI:10.1016/j.jphotochem.2024.115996
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引用次数: 0

摘要

光催化剂的结晶度对其反应活性有着深远的影响。本文采用溶热法合成了花状 Bi2MoO6 微球,随后在不同温度下进行煅烧,以调节其结晶度和粒径。与原始 Bi2MoO6 相比,经过热处理的样品表现出更强的光催化氧进化能力。煅烧温度越高,形成的结晶越大,从而显著提高了活性。我们证明,结晶度而非表面积对 Bi2MoO6 的光催化性能起着更为重要的作用。提高结晶度可以增厚空间电荷层(SCL),从而产生更大的带弯曲,促进电子-空穴对的分离。反之,结晶度低会导致大量表面和块体缺陷,促进电子-空穴重组。总之,高效的电荷分离和抑制的重组使煅烧后的 Bi2MoO6 具有更高的水氧化效率。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Crystallinity control on Bi2MoO6 microspheres for improved photocatalytic oxygen evolution

Crystallinity of the photocatalyst has a profound impact on its reactivity. Here, flower-like Bi2MoO6 microspheres were synthesized via a solvothermal method and subsequently calcined at varying temperatures to regulate the crystallinity and particle size. The thermally treated samples exhibited enhanced photocatalytic oxygen evolution compared to the pristine Bi2MoO6. Higher calcination temperatures led to the formation of larger crystallites, significantly boosting the activity. We demonstrate that crystallinity, rather than surface area, plays a more vital role in governing the photocatalytic performance of Bi2MoO6. Improved crystallinity can thicken the space charge layer (SCL), resulting in a greater band bending that facilitates the separation of electron-hole pairs. Conversely, poor crystallinity leads to an abundance of surface and bulk defects, promoting electron-hole recombination. Overall, efficient charge separation and suppressed recombination endow the calcined Bi2MoO6 with enhanced water oxidation efficiency.

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来源期刊
CiteScore
7.90
自引率
7.00%
发文量
580
审稿时长
48 days
期刊介绍: JPPA publishes the results of fundamental studies on all aspects of chemical phenomena induced by interactions between light and molecules/matter of all kinds. All systems capable of being described at the molecular or integrated multimolecular level are appropriate for the journal. This includes all molecular chemical species as well as biomolecular, supramolecular, polymer and other macromolecular systems, as well as solid state photochemistry. In addition, the journal publishes studies of semiconductor and other photoactive organic and inorganic materials, photocatalysis (organic, inorganic, supramolecular and superconductor). The scope includes condensed and gas phase photochemistry, as well as synchrotron radiation chemistry. A broad range of processes and techniques in photochemistry are covered such as light induced energy, electron and proton transfer; nonlinear photochemical behavior; mechanistic investigation of photochemical reactions and identification of the products of photochemical reactions; quantum yield determinations and measurements of rate constants for primary and secondary photochemical processes; steady-state and time-resolved emission, ultrafast spectroscopic methods, single molecule spectroscopy, time resolved X-ray diffraction, luminescence microscopy, and scattering spectroscopy applied to photochemistry. Papers in emerging and applied areas such as luminescent sensors, electroluminescence, solar energy conversion, atmospheric photochemistry, environmental remediation, and related photocatalytic chemistry are also welcome.
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