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Photocatalyzed Hydrogen Evolution from Water by a Composite Catalyst of NH2 -MIL-125(Ti) and Surface Nickel(II) Species

机译:通过NH2 -MIL-125(Ti)和表面镍(II)物种的复合催化剂从水的光催化氢化

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摘要

A composite of the metal–organic framework (MOF) NH2-MIL-125(Ti) and molecular and ionic nickel(II) species, catalyzed hydrogen evolution from water under UV light. In 95 v/v¿% aqueous conditions the composite produced hydrogen in quantities two orders of magnitude higher than that of the virgin framework and an order of magnitude greater than that of the molecular catalyst. In a 2 v/v¿% water and acetonitrile mixture, the composite demonstrated a TOF of 28 mol H2 g(Ni)-1 h-1 and remained active for up to 50 h, sustaining catalysis for three times longer and yielding 20-fold the amount of hydrogen. Appraisal of physical mixtures of the MOF and each of the nickel species under identical photocatalytic conditions suggest that similar surface localized light sensitization and proton reduction processes operate in the composite catalyst. Both nickel species contribute to catalytic conversion, although different activation behaviors are observed.
机译:金属 - 有机骨架(MOF)NH2-MIL-125(TI)和分子和离子镍(II)物种的复合物,催化来自紫外光下的水的氢逸出。在95V / V +%水条件下,复合材料以比原处框架的量高的两个数量级和大于分子催化剂的数量级。在2V / V +%的水和乙腈混合物中,复合材料证明了28mol H 2 G(Ni)-1 H-1的TOF,并且保持活性至多50小时,维持催化三倍,并产生20-折叠氢气量。在相同的光催化条件下对MOF的物理混合物和每种镍种类的评估表明,在复合催化剂中,相似的表面局部光敏和质子还原过程。镍种类均有助于催化转化,尽管观察到不同的活化行为。

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