Interfaces Govern Structure of Angstrom-scale Confined Water
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arXiv
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| Natura: | Preprint |
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2023
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| _version_ | 1866910447438921728 |
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| author | Wang, Yongkang Tang, Fujie Yu, Xiaoqing Chiang, Kuo-Yang Yu, Chun-Chieh Ohto, Tatsuhiko Chen, Yunfei Nagata, Yuki Bonn, Mischa |
| author_facet | Wang, Yongkang Tang, Fujie Yu, Xiaoqing Chiang, Kuo-Yang Yu, Chun-Chieh Ohto, Tatsuhiko Chen, Yunfei Nagata, Yuki Bonn, Mischa |
| contents | Water plays a crucial role in geological, biological, and technological processes. Nanoscale water confinement occurs in many of these settings, including sedimentary rocks, water channel proteins, and applications like desalination and water purification membranes. The structure and properties of water in nanoconfinement can differ significantly from bulk water, exhibiting, for instance, modified hydrogen bonds, dielectric constant, and phase transitions. Despite the importance of strongly nanoconfined water, experimentally elucidating the nanoconfinement effect on water, such as its orientation and hydrogen bond (H-bond) network, has remained challenging. Here, we study two-dimensionally nanoconfined aqueous electrolyte solutions with tunable confinement from nanoscale to angstrom-scale sandwiched between a graphene sheet and CaF2. We employ heterodyne-detection sum-frequency generation (HD-SFG) spectroscopy, a surface-specific vibrational spectroscopy capable of directly and selective probing water orientation and H-bond environment at interfaces and under confinement. Remarkably, the vibrational spectra of the nanoscale confined water can be described quantitatively by the sum of the individual water surface signals from the CaF2/water and water/graphene interfaces until the confinement reduces to angstrom-scale (< ~8 Å). Ab initio molecular dynamics simulations confirm our experimental observation. These results manifest that interfacial, rather than nanoconfinement effects, dominate the water structure until angstrom-level confinement. |
| format | Preprint |
| id |
arxiv_https___arxiv_org_abs_2310_10354 |
| institution | arXiv |
| publishDate | 2023 |
| record_format | arxiv |
| spellingShingle | Interfaces Govern Structure of Angstrom-scale Confined Water Wang, Yongkang Tang, Fujie Yu, Xiaoqing Chiang, Kuo-Yang Yu, Chun-Chieh Ohto, Tatsuhiko Chen, Yunfei Nagata, Yuki Bonn, Mischa Chemical Physics Water plays a crucial role in geological, biological, and technological processes. Nanoscale water confinement occurs in many of these settings, including sedimentary rocks, water channel proteins, and applications like desalination and water purification membranes. The structure and properties of water in nanoconfinement can differ significantly from bulk water, exhibiting, for instance, modified hydrogen bonds, dielectric constant, and phase transitions. Despite the importance of strongly nanoconfined water, experimentally elucidating the nanoconfinement effect on water, such as its orientation and hydrogen bond (H-bond) network, has remained challenging. Here, we study two-dimensionally nanoconfined aqueous electrolyte solutions with tunable confinement from nanoscale to angstrom-scale sandwiched between a graphene sheet and CaF2. We employ heterodyne-detection sum-frequency generation (HD-SFG) spectroscopy, a surface-specific vibrational spectroscopy capable of directly and selective probing water orientation and H-bond environment at interfaces and under confinement. Remarkably, the vibrational spectra of the nanoscale confined water can be described quantitatively by the sum of the individual water surface signals from the CaF2/water and water/graphene interfaces until the confinement reduces to angstrom-scale (< ~8 Å). Ab initio molecular dynamics simulations confirm our experimental observation. These results manifest that interfacial, rather than nanoconfinement effects, dominate the water structure until angstrom-level confinement. |
| title | Interfaces Govern Structure of Angstrom-scale Confined Water |
| topic | Chemical Physics |
| url | https://arxiv.org/abs/2310.10354 |