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J Phys Chem B. 2018 Nov 21;122(46):10600-10606. doi: 10.1021/acs.jpcb.8b10325. Epub 2018 Nov 7.

Disorder in Aqueous Solutions and Peak Broadening in X-ray Photoelectron Spectroscopy.

Liu J1,2, Zhang H2, Li Y1,2, Liu Z1,2.

Author information

1
School of Physical Science and Technology , ShanghaiTech University , Shanghai 201210 , China.
2
State Key Laboratory of Functional Materials for Informatics, Shanghai Institute of Microsystem and Information Technology , Chinese Academy of Sciences , Shanghai 200050 , China.

Abstract

The microscopic structure and photoelectron spectra of an aqueous solution are investigated with ab initio molecular dynamics simulations and ambient pressure X-ray photoelectron spectroscopy (AP-XPS). The simulation results show that the structural fluctuations in an aqueous solution can lead to remarkable peak broadening (∼1 eV) of ionic species, which is in good agreement with the results from AP-XPS experiments. We find that this broadening of the XPS peaks can be directly correlated with the local structural fluctuations in the aqueous solution, such as the evolution of solvation shells. This work demonstrates that the rich dynamics of solvation shells in aqueous solutions can be revealed by combining advanced simulations with in situ AP-XPS, and may stimulate new developments in the in situ XPS characterization of complex electrochemical reactions.

PMID:
30359023
DOI:
10.1021/acs.jpcb.8b10325

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