论文标题

跨单原子电极的照片加速水解离

Photo-accelerated water dissociation across one-atom-thick electrodes

论文作者

Cai, J., Griffin, E., Guarochico-Moreira, V., Barry, D., Xin, B., Huang, S., Geim, A. K., Peeters, F. M., Lozada-Hidalgo, M.

论文摘要

最近的实验表明,界面水解离(H2O = H + + OH-)可以通过施加到石墨烯电极的电场呈指数加速,这是与Wien效应相关的现象。在这里,我们报告了可见光照明下的界面水解离反应的加速顺序加速。该过程伴随着质子和氢氧化物离子在一个原子厚的石墨烯之间的空间分离,并通过强界面电场增强。发现的照片效应归因于石墨烯相对于质子的完美选择性的组合,从而防止质子羟化质子重组,以及通过维也纳效应的质子转运加速,这与水分离反应同步。我们的发现提供了对原子质蛋白质选择界面附近离子动力学的基本见解,并表明强大的界面场可以增强和调整非常快速的离子过程,这与在光学分析和设计可重新配置材料中的应用相关。

Recent experiments demonstrated that interfacial water dissociation (H2O = H+ + OH-) could be accelerated exponentially by an electric field applied to graphene electrodes, a phenomenon related to the Wien effect. Here we report an order-of-magnitude acceleration of the interfacial water dissociation reaction under visible-light illumination. This process is accompanied by spatial separation of protons and hydroxide ions across one-atom-thick graphene and enhanced by strong interfacial electric fields. The found photo-effect is attributed to the combination of graphene's perfect selectivity with respect to protons, which prevents proton-hydroxide recombination, and to proton transport acceleration by the Wien effect, which occurs in synchrony with the water dissociation reaction. Our findings provide fundamental insights into ion dynamics near atomically-thin proton-selective interfaces and suggest that strong interfacial fields can enhance and tune very fast ionic processes, which is of relevance for applications in photo-catalysis and designing reconfigurable materials.

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