期刊
JOURNAL OF PHYSICAL CHEMISTRY LETTERS
卷 7, 期 19, 页码 3882-3885出版社
AMER CHEMICAL SOC
DOI: 10.1021/acs.jpclett.6b01931
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- Office of Basic Energy Sciences, Office of Science, U.S. Department of Energy (DOE) through the Chemical Sciences Division of the Lawrence Berkeley National Laboratory (LBNL) [DE-AC02-05CH11231]
The behavior of ions at aqueous interfaces influences vital processes in many fields but has long remained a subject of controversy. Over the past decade, counterintuitive surface concentration enhancement of several ions in aqueous solution has been demonstrated via nonlinear laser spectroscopy and mass spectrometry. While the evidence for significant ion enhancement at the air water interface is convincing, the mechanism remains incompletely understood. Toward this end, we present the full broadband DUV-SFG spectrum of the charge-transfer-to-solvent (CTTS) band of interfacial aqueous iodide measured in a single laser shot with a newly developed broadband deep UV-SFG technique, clearly revealing a similar to 8 nm redshift and a significant linewidthr narrowing relative to bulk solution spectra. KI and NaI solutions yield indistinguishable results. Additionally, we observe a dramatic change in the relative intensities of the J = 3/2 and 1/2 CTTS transitions.
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