# Quantifying hydrogen bonding using electrically tunable nanoconfined water

https://mdr.nims.go.jp/datasets/0f346be1-84ab-4ae0-ac16-c16890716673

## File

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## Id

0f346be1-84ab-4ae0-ac16-c16890716673

## Local identifier



## Visibility

open_to_public

## State

published

## Created at

2026-05-17T00:48:35.879575Z

## Updated at

2026-05-18T01:24:25.262040Z

## Published at

2026-05-18T03:23:09.240347Z

## Doi



## First published url

https://doi.org/10.1038/s41467-025-58608-6

## Date published

2025-04-15

## Recorded date published



## Resource type

journal_article

## Manuscript type

vor

## Collection



## Title

- title: Quantifying hydrogen bonding using electrically tunable nanoconfined water
  title_type: original
  lang: en

## Description

- description: Unique properties of water in liquid and solid phases are largely attributed
    to hydrogen bonding (HB)1. Traditional analysis of HB typically involves vibrational
    spectroscopy, where shift of the stretching frequency of covalent O-H bond correlates
    with the strength of HB2. However, the underlying mechanisms of this phenomenon
    are still debated3-5. Here we introduce a simple approximation based on an elastic
    dipole in external electric field, which captures a wide range of phenomena regarding
    HB in water systems. To this end, we use gypsum, with crystalline water embedded
    in heterostructure, to calibrate the HB strength through externally applied electric
    field. Our approach provided a coherent description on both HB and dielectric
    behaviour of nanoconfined water reported in the literature. In particular, it
    quantitatively reproduces the properties of confined water in various systems,
    rationalising behaviour like the reduced static permittivity observed in nanoconfined
    water6,7, enhancing our understanding of the importance of confined water in biological
    and technological systems. Finally, our work introduces hydrogen bond heterostructures
    (HBHs) as a new class of materials, offering electrical and chemical tunability,
    and a stronger, more directional bonding than that of van der Waals heterostructures.
  description_type: abstract
  lang: und

## Creator

- name: Ziwei Wang
  role: author
- name: Anupam Bhattacharya
  role: author
- name: Mehmet Yagmurcukardes
  role: author
- name: Vasyl Kravets
  role: author
- name: Pablo Díaz-Núñez
  role: author
- name: Ciaran Mullan
  role: author
- name: Ivan Timokhin
  role: author
- name: Takashi Taniguchi
  role: author
  orcid: https://orcid.org/0000-0002-1467-3105
  organization: National Institute for Materials Science
- name: Kenji Watanabe
  role: author
  orcid: https://orcid.org/0000-0003-3701-8119
  organization: National Institute for Materials Science
- name: Alexander N. Grigorenko
  role: author
- name: Francois Peeters
  role: author
- name: Kostya S. Novoselov
  role: author
- name: Qian Yang
  role: author
- name: Artem Mishchenko
  role: author

## Contact agent



## Publisher

organization: Springer Science and Business Media LLC

## Managing organization



## Keyword

- subject: hydrogen bonding
  schema: not_defined
- subject: 'nanoconfined water     '
  schema: not_defined
- subject: electric field tuning
  schema: not_defined

## Rights

- identifier: https://creativecommons.org/licenses/by/4.0/
  date_licensed: 2025-04-15

## Other identifier(s)



## Data origin

- data_origin_type: other

## Embargo



## Journal

- title: Nature Communications
  issn: '20411723'
  volume: '16'
  issue: '1'
  article_number: '3447'

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## Fileset

- id: a574057a-c009-4d02-b52e-a0cf3e23acd8
  filename: s41467-025-58608-6.pdf
  content_type: application/pdf
  size: 2753829
  md5: 3478a8981d331b4d260db4eb5738eab8

## Thumbnail

fileset_id: a574057a-c009-4d02-b52e-a0cf3e23acd8
filename: s41467-025-58608-6.pdf