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Design of Fe-MOF-bpdc deposited with cobalt oxide (CoOx) nanoparticles for enhanced visible-light-promoted water oxidation reaction

机译:用氧化钴(CoOX)纳米粒子沉积Fe-Mof-BPDC,用于增强可见光促进水氧化反应

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摘要

This work spotlights the facile method to deposit cobalt oxide (CoOx) nanoparticles as a cocatalyst on Fe-MOF-bpdc to enhance its photocatalytic activity for water oxidation reaction (WOR) under visible light irradiation to evolve gaseous O-2. Due to the soft conditions needed for the process developed, the framework structure of Fe-MOF-bpdc was maintained even after the deposition of CoOx. The optimized CoOx@Fe-MOF-bpdc composite showed enhanced activity towards visible-light-driven WOR as compared to pristine Fe-MOF-bpdc, the amount of evolved O-2 being increased by about 2 times at the maximum with CoOx loading of 2 wt% as Co metal. Investigations on the wavelength dependence of visible-light-driven WOR on CoOx@Fe-MOF-bpdc revealed that the direct photo-excitation of Fe-oxo clusters within Fe-MOF-bpdc plays an important role to initiate the reaction. Furthermore, it was found that the rate of 2-propanol oxidation reaction, which is a typical two-electron oxidation reaction, was hardly affected by CoOx deposition, suggesting that CoOx acts as a unique hole trapping site and more preferentially catalyse the four-electron oxidation reactions like WOR than the two-electron oxidation reaction.
机译:这项工作占据了Fe-Mof-BPDC上作为助催化剂将氧化钴(COOO)纳米颗粒的容易载体纳米粒子沉积,以增强其在可见光辐照下的水氧化反应(WOR)的光催化活性,以演变气态O-2。由于开发过程所需的柔软条件,即使在COOO沉积之后,也保持Fe-Mof-BPDC的骨架结构。与原始Fe-Mof-BPDC相比,优化的CoOX @ Fe-Mof-BPDC复合材料显示出可见光驱动的效果的增强活性,并且在最大值增加的情况下,进化的O-2增加了约2次2 wt%作为金属。对CoOX @ Fe-Mof-BPDC在CoOX @ Fe-Mof-BPDC上的波长依赖性的研究表明,Fe-Mof-BPDC内的Fe-Oxo簇的直接照片激发起源起动反应。此外,发现2-丙醇氧化反应的速率,这是一种典型的双电子氧化反应,几乎不受CoOX沉积的影响,表明CoOx作为独特的孔捕获部位,更优先催化四电子氧化反应与双电子氧化反应一样。

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