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In-situ Raman spectroscopic insight into charge delocalization-improved electrical conductivity in metal–cyanide frameworks

机译:原位拉曼光谱洞察金属-氰化物骨架中电荷离域的电导率

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Porous crystalline materials (PCMs) have attracted widespread attention due to their high porosity and chemical tunability. To solve the problem of the low electrical conductivity of traditional PCMs, a guest-promoted approach has been developed to impart electrical conductivity, whereas microscopic understanding of this process from experiments is largely lacking. Here we use in-situ electrochemical surface-enhanced Raman spectroscopy (EC-SERS) to investigate the microscopic mechanism of the enhanced electrical conductivity in metal–cyanide frameworks, in Prussian Blue (PB), induced by alkali metal ions. The EC-SERS result demonstrates that the charge is localized around the iron atom in PB and becomes delocalized on the CN bond after insertion of the alkali metal ions, verified by density functional theory (DFT) calculations. The enhanced electrical conductivity of PCMs promoted by the guest via the through-bond mechanism instead of the through-space hopping mechanism in pristine PB, offers a new approach to develop conductive PCMs.
机译:多孔晶体材料(潜热)吸引了广泛的关注由于其高孔隙度和化学的可调性。传统的低导电率吸附,guest-promoted方法开发赋予导电性,而微观的理解这个过程从实验中主要是缺乏。原位电化学表面增强拉曼光谱学(EC-SERS)调查的微观机制增强电在功率超声电导框架,普鲁士蓝(PB),由碱金属离子。EC-SERS结果表明电荷本地化在铁原子在PB和变得离域在CN债券插入的碱金属离子,验证了密度泛函理论(DFT)计算。增强导电性的个pcm都提升客人通过通过债券机制而不是通过空间跳跃机制原始PB,提供了一种新的方法来培养导电吸附。

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