Fourier transform infrared spectroscopy investigation of water microenvironments in polyelectrolyte multilayers at varying temperatures

Tutkimustuotos: Lehtiartikkelivertaisarvioitu

Tutkijat

  • Chikaodinaka I. Eneh
  • Matthew J. Bolen
  • Pilar C. Suarez-Martinez
  • Adam L. Bachmann
  • Tawanda J. Zimudzi
  • Michael A. Hickner
  • Piotr Batys
  • Maria Sammalkorpi
  • Jodie L. Lutkenhaus

Organisaatiot

  • Texas A and M University
  • North Carolina State University
  • Pennsylvania State University
  • Polish Academy of Sciences

Kuvaus

Polyelectrolyte multilayers (PEMs) are thin films formed by the alternating deposition of oppositely charged polyelectrolytes. Water plays an important role in influencing the physical properties of PEMs, as it can act both as a plasticizer and swelling agent. However, the way in which water molecules distribute around and hydrate ion pairs has not been fully quantified with respect to both temperature and ionic strength. Here, we examine the effects of temperature and ionic strength on the hydration microenvironments of fully immersed poly(diallyldimethylammonium)/polystyrene sulfonate (PDADMA/PSS) PEMs. This is accomplished by tracking the OD stretch peak using attenuated total reflectance Fourier transform infrared (ATR-FTIR) spectroscopy at 0.25-1.5 M NaCl and 35-70 °C. The OD stretch peak is deconvoluted into three peaks: (1) high frequency water, which represents a tightly bound microenvironment, (2) low frequency water, which represents a loosely bound microenvironment, and (3) bulk water. In general, the majority of water absorbed into the PEM exists in a bound state, with little-to-no bulk water observed. Increasing temperature slightly reduces the amount of absorbed water, while addition of salt increases the amount of absorbed water. Finally, a van't Hoff analysis is applied to estimate the enthalpy (11-22 kJ mol-1) and entropy (48-79 kJ mol-1 K-1) of water exchanging from low to high frequency states.

Yksityiskohdat

AlkuperäiskieliEnglanti
Sivut2291-2300
Sivumäärä10
JulkaisuSoft Matter
Vuosikerta16
Numero9
TilaJulkaistu - 7 maaliskuuta 2020
OKM-julkaisutyyppiA1 Julkaistu artikkeli, soviteltu

ID: 41816481