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Peer-reviewedCC BYLangmuir : the ACS journal of surfaces and colloids

Hydrogen Bonding is Required for Continuous Polyvinylpyrrolidone Adhesive Films.

  1. 1Chemistry Department, Carr Laboratory, Mount Holyoke College, 50 College Street, South Hadley, Massachusetts01075, United States.

Abstract

The versatility of polyvinylpyrrolidone (PVP) as a dispersing and adhesive agent lies in its amphiphilicity and hydrogen bonding capability. In this study, silicon wafers (SiO2) were silanized with N-(2-aminoethyl)-3-aminopropyltriethoxysilane (AEAPTES), (N,N-dimethylamino)trimethylsilane (TMS), and n-octyldimethylchlorosilane (C8) to construct four substrates with varying fractions of hydrogen bonding sites and hydrophobic groups. PVP thin films were fabricated on the substrates using both static adsorption and spin coating methods. PVP spontaneously adsorbs to and results in 1 nm-thick films on all the substrates, demonstrating the polymer's capability as a universal adhesive. The continuity of the dried PVP films at the nanoscopic and micron scales was imaged using atomic force and optical microscopy, respectively. The film stability was correlated to the fraction of substrate hydrogen bonding sites. The films are stable on SiO2 with 100% hydrogen bonding sites, unstable on TMS with 100% hydrophobic groups, and metastable on AEAPTES and C8 with a mixture of hydrogen bonding sites and hydrophobic groups.

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BibTeX
@article{mim2026hydrogen,
  title = {{Hydrogen Bonding is Required for Continuous Polyvinylpyrrolidone Adhesive Films.}},
  author = {Mahira Mim and An C N Nguyen and Mamie Mulder and Hanae Takahashi and Mackenzie Windus and Wei Chen},
  journal = {Langmuir : the ACS journal of surfaces and colloids},
  year = {2026},
  month = oct,
  doi = {10.1021/acs.langmuir.6c04951},
  url = {https://europepmc.org/article/MED/42899871},
  note = {CC BY},
}
RIS
TY  - JOUR
TI  - Hydrogen Bonding is Required for Continuous Polyvinylpyrrolidone Adhesive Films.
AU  - Mahira Mim
AU  - An C N Nguyen
AU  - Mamie Mulder
AU  - Hanae Takahashi
AU  - Mackenzie Windus
AU  - Wei Chen
PY  - 2026
DA  - 2026/10/01
JO  - Langmuir : the ACS journal of surfaces and colloids
DO  - 10.1021/acs.langmuir.6c04951
UR  - https://europepmc.org/article/MED/42899871
AB  - The versatility of polyvinylpyrrolidone (PVP) as a dispersing and adhesive agent lies in its amphiphilicity and hydrogen bonding capability. In this study, silicon wafers (SiO2) were silanized with N-(2-aminoethyl)-3-aminopropyltriethoxysilane (AEAPTES), (N,N-dimethylamino)trimethylsilane (TMS), and n-octyldimethylchlorosilane (C8) to construct four substrates with varying fractions of hydrogen bonding sites and hydrophobic groups. PVP thin films were fabricated on the substrates using both static adsorption and spin coating methods. PVP spontaneously adsorbs to and results in 1 nm-thick films on all the substrates, demonstrating the polymer's capability as a universal adhesive. The continuity of the dried PVP films at the nanoscopic and micron scales was imaged using atomic force and optical microscopy, respectively. The film stability was correlated to the fraction of substrate hydrogen bonding sites. The films are stable on SiO2 with 100% hydrogen bonding sites, unstable on TMS with 100% hydrophobic groups, and metastable on AEAPTES and C8 with a mixture of hydrogen bonding sites and hydrophobic groups.
SN  - 0743-7463
SN  - 1520-5827
ER  -