Impact of electrolyte on the structure and orientation of water at air/water-polyethylene glycol polymer interface

被引:0
|
作者
Bandyopadhyay, Anisha [1 ]
Mondal, Jahur Alam [1 ]
机构
[1] Homi Bhabha Natl Inst, Bhabha Atom Res Ctr, Radiat & Photochem Div, Trombay, Mumbai 400085, India
来源
JOURNAL OF CHEMICAL PHYSICS | 2024年 / 161卷 / 17期
关键词
SUM-FREQUENCY GENERATION; HYDRATION; SURFACES; PRECIPITATION; CONFORMATION; PHASE; MODEL; BULK; PEG;
D O I
10.1063/5.0231332
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Polyethylene glycol (PEG) is a water soluble, non-ionic polymer with applications in drug delivery, protein precipitation, anti-biofouling, water-splitting, Li-ion batteries, and fuel cells. The interaction of PEG with water and electrolytes plays pivotal roles in such applications. Using interface-selective spectroscopy, heterodyne-detected vibrational sum frequency generation, and Raman difference spectroscopy with simultaneous curve fitting analysis, we show that water adopts different structures and orientations at the air/water-PEG interface, which depends on the molar mass of the PEG. At the air/water-PEG4000 (MW 4000u) interface, water is H-up oriented (i.e., water Hs are pointed away from the aqueous bulk) around 3200 cm(-1) and H-down oriented (i.e., water Hs are pointed toward the aqueous bulk) around 3470 cm(-1). Variation of the bulk concentration of PEG4000 does not change the dual orientation of interfacial water. The presence of an electrolyte (1.0M NaCl) selectively reduces the H-up oriented water without affecting the H-down oriented water at the air/water-PEG4000 interface. The selective reorganization of the interfacial water is assigned to the disruption of the asymmetric hydration around ether-oxygen of the surface-adsorbed PEG4000 by the Na+ ion of the electrolyte. Interestingly, in the case of low molar mass PEG (air/water-PEG200), the interfacial water neither shows the dual orientation nor is affected by 1.0M NaCl.
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页数:9
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