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A reconfigurable piezo-ionotropic polymer membrane for sustainable multi-resonance acoustic sensing

Author

Listed:
  • Wu Bin Ying

    (Hanyang University
    School of Electrical Engineering, Korea Advanced Institute of Science and Technology (KAIST))

  • Joo Sung Kim

    (Hanyang University)

  • Zhengyang Kong

    (Hanyang University)

  • Zhe Yu

    (Chinese Academy of Sciences
    East China Normal University)

  • Elvis K. Boahen

    (Hanyang University)

  • Fenglong Li

    (Chinese Academy of Sciences)

  • Chao Chen

    (Chinese Academy of Sciences)

  • Ying Tian

    (Hanyang University
    Chinese Academy of Sciences)

  • Ji Hong Kim

    (Hanyang University)

  • Hanbin Choi

    (Hanyang University)

  • Jung-Yong Lee

    (School of Electrical Engineering, Korea Advanced Institute of Science and Technology (KAIST))

  • Jin Zhu

    (Chinese Academy of Sciences)

  • Do Hwan Kim

    (Hanyang University
    Hanyang University
    Hanyang University)

Abstract

Sensorineural hearing loss is the most common form of deafness, typically resulting from the loss of sensory cells on the basilar membrane, which cannot regenerate and thus lose sensitivity to sound vibrations. Here, we report a reconfigurable piezo-ionotropic polymer membrane engineered for biomimetic sustainable multi-resonance acoustic sensing, offering exceptional sensitivity (530 kPa-1) and broadband frequency discrimination (20 Hz to 3300 Hz) while remaining resistant to “dying”. The acoustic sensing capability is driven by an ion hitching-in cage effect intrinsic to the ion gel combined with fluorinated polyurethane. In this platform, the engineered ionotropic polymer stretches under acoustic vibrations, allowing cations to penetrate the widened hard segments and engage in strong ion-dipole interactions (cation···F), thereby restricting ion flux and amplifying impedance changes. Additionally, the sensor’s sustainability is ensured through its self-healing properties and hydrophobic components, which enable effective self-repair in both conventional and aqueous environments without ion leakage, achieving a room-temperature healing speed of 0.3–0.4 μm/min. This sustainable acoustic sensing technology enables the devices to reliably identify specific sounds in everyday environments (e.g., human voices, piano notes), demonstrating their potential application as artificial basilar membranes.

Suggested Citation

  • Wu Bin Ying & Joo Sung Kim & Zhengyang Kong & Zhe Yu & Elvis K. Boahen & Fenglong Li & Chao Chen & Ying Tian & Ji Hong Kim & Hanbin Choi & Jung-Yong Lee & Jin Zhu & Do Hwan Kim, 2025. "A reconfigurable piezo-ionotropic polymer membrane for sustainable multi-resonance acoustic sensing," Nature Communications, Nature, vol. 16(1), pages 1-13, December.
  • Handle: RePEc:nat:natcom:v:16:y:2025:i:1:d:10.1038_s41467-025-63643-4
    DOI: 10.1038/s41467-025-63643-4
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    References listed on IDEAS

    as
    1. Tianpei Xu & Long Jin & Yong Ao & Jieling Zhang & Yue Sun & Shenglong Wang & Yuanxiao Qu & Longchao Huang & Tao Yang & Weili Deng & Weiqing Yang, 2024. "All-polymer piezo-ionic-electric electronics," Nature Communications, Nature, vol. 15(1), pages 1-11, December.
    2. Zhengyang Kong & Elvis K. Boahen & Dong Jun Kim & Fenglong Li & Joo Sung Kim & Hyukmin Kweon & So Young Kim & Hanbin Choi & Jin Zhu & Wu Ying & Do Hwan Kim, 2024. "Ultrafast underwater self-healing piezo-ionic elastomer via dynamic hydrophobic-hydrolytic domains," Nature Communications, Nature, vol. 15(1), pages 1-12, December.
    3. Vipin Amoli & Joo Sung Kim & Eunsong Jee & Yoon Sun Chung & So Young Kim & Jehyoung Koo & Hanbin Choi & Yunah Kim & Do Hwan Kim, 2019. "A bioinspired hydrogen bond-triggered ultrasensitive ionic mechanoreceptor skin," Nature Communications, Nature, vol. 10(1), pages 1-13, December.
    4. Siyoung Lee & Junsoo Kim & Inyeol Yun & Geun Yeol Bae & Daegun Kim & Sangsik Park & Il-Min Yi & Wonkyu Moon & Yoonyoung Chung & Kilwon Cho, 2019. "An ultrathin conformable vibration-responsive electronic skin for quantitative vocal recognition," Nature Communications, Nature, vol. 10(1), pages 1-11, December.
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