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| Main Authors: | , , , , , |
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| Format: | Preprint |
| Published: |
2024
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| Subjects: | |
| Online Access: | https://arxiv.org/abs/2411.12975 |
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| _version_ | 1866916488702590976 |
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| author | Hwang, Jonggeun Shin, Dongha Deveney, Brendan T. Lee, Manhee Zhang, Xingcai Jhe, Wonho |
| author_facet | Hwang, Jonggeun Shin, Dongha Deveney, Brendan T. Lee, Manhee Zhang, Xingcai Jhe, Wonho |
| contents | The hydrogen bond (HB) network of water under confinement has been predicted to have distinct structures from that of bulk water. However, direct measurement of the structure has not been achieved. Here, we present experimental evidence of confinement-induced ice formation in water. We directly probe the HB network of a water nano-meniscus formed and confined between a mica substrate and a precisely-controlled-plasmonically active silver tip. By employing tip-enhanced Raman spectroscopy (TERS), we observe a novel double donor-double acceptor (DDAA) peak that emerges in the OH stretching band of water molecules at room temperature and at sub-nanometer confinement. This Raman peak indicates the presence of a solid phase of water, namely ice-VII with the body-centered cubic (bcc) unit. Interestingly, we observe a structural transition from bcc DDAA (ice-VII) to tetrahedral DDAA as the confinement is weakened. Moreover, by identifying the spatial distribution of the HB network, we find that the bcc DDAA network of ice-VII is predominantly present within the interior of the confined water, rather than at air/water or at solid/water interfaces. This suggest the possibility that the appearance of ice-VII in the strongly confined space could be a general characteristic of water under extreme confinement. |
| format | Preprint |
| id |
arxiv_https___arxiv_org_abs_2411_12975 |
| institution | arXiv |
| publishDate | 2024 |
| record_format | arxiv |
| spellingShingle | Nano-confinement induced nucleation of ice-VII at room temperature Hwang, Jonggeun Shin, Dongha Deveney, Brendan T. Lee, Manhee Zhang, Xingcai Jhe, Wonho Soft Condensed Matter The hydrogen bond (HB) network of water under confinement has been predicted to have distinct structures from that of bulk water. However, direct measurement of the structure has not been achieved. Here, we present experimental evidence of confinement-induced ice formation in water. We directly probe the HB network of a water nano-meniscus formed and confined between a mica substrate and a precisely-controlled-plasmonically active silver tip. By employing tip-enhanced Raman spectroscopy (TERS), we observe a novel double donor-double acceptor (DDAA) peak that emerges in the OH stretching band of water molecules at room temperature and at sub-nanometer confinement. This Raman peak indicates the presence of a solid phase of water, namely ice-VII with the body-centered cubic (bcc) unit. Interestingly, we observe a structural transition from bcc DDAA (ice-VII) to tetrahedral DDAA as the confinement is weakened. Moreover, by identifying the spatial distribution of the HB network, we find that the bcc DDAA network of ice-VII is predominantly present within the interior of the confined water, rather than at air/water or at solid/water interfaces. This suggest the possibility that the appearance of ice-VII in the strongly confined space could be a general characteristic of water under extreme confinement. |
| title | Nano-confinement induced nucleation of ice-VII at room temperature |
| topic | Soft Condensed Matter |
| url | https://arxiv.org/abs/2411.12975 |