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Unique cation surroundings in the structure of Ag_3PW_(12)O_(40) salt

机译:Ag_3PW_(12)O_(40)盐结构中独特的阳离子环境

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The Ag_3PW_(12)O_(40).3H_2O salt forms two different structures: the first one, existing at temperature up to 473 K, contains one water molecule hydrating each silver cation, whereas the other one appears above 573 K after the loss of the water molecule. It results in the shortening of the lattice parameter a from 1193 to 11.70 A. This dehydration-hydration process of silver salt is reversible. In the structure at 473 K, the [Ag(H_2O)]~+ complex is centered in the octahedral space between the Keggin anions. Each silver cation is bonded to two terminal oxygens of different Keggin anions while water molecule forms weak hydrogen bonds with other two Keggin anions. Unexpectedly, in dehydrated structure existing at 573 K, Ag~+ cations are not centered in the octahedral space between Keggin anions and are connected to two terminal oxygens of Keggin anions only. Probably, the formation of two various structures of silver tungstophosphate influences its catalytic activity with changing temperature.
机译:Ag_3PW_(12)O_(40).3H_2O盐​​形成两种不同的结构:第一种结构存在于最高473 K的温度下,包含一个水分子使每个银阳离子水合,而另一种在573 K损失后出现在573 K以上。水分子。这导致晶格参数a从1193 A缩短到11.70A。银盐的脱水-脱水过程是可逆的。在473 K的结构中,[Ag(H_2O)]〜+络合物位于Keggin阴离子之间的八面体空间的中心。每个银阳离子键合到不同Keggin阴离子的两个末端氧上,而水分子与其他两个Keggin阴离子形成弱氢键。出乎意料的是,在存在于573 K的脱水结构中,Ag〜+阳离子不在Keggin阴离子之间的八面体空间中居中,仅与Keggin阴离子的两个末端氧连接。钨磷酸盐磷的两种不同结构的形成可能会随着温度的变化影响其催化活性。

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