Atomistic insights into hydrogen bonds of water around detonation nanodiamonds: effects of surface chemistry and dissolved ions
Farshad Saberi-Movahed, Donald W Brenner

TL;DR
This study uses molecular dynamics to explore how surface chemistry and dissolved ions affect hydrogen bonding of water around detonation nanodiamonds, revealing complex dependencies on charge and ion type.
Contribution
It distinguishes among different hydrogen bond types and examines the effects of surface functionalization and various salts on water's hydrogen bonding near nanodiamonds.
Findings
Charged nanodiamonds induce stronger hydration layer hydrogen bonds.
Surface functional groups influence hydrogen bond strength in water.
Divalent cations like Mg²⁺ and Ca²⁺ enhance hydrogen bonding around charged nanodiamonds.
Abstract
Prior studies on the effects of surface chemistry of detonation nanodiamonds (DNDs) on Hydrogen Bonds (HBs) of water have not unambiguously distinguished among three broad categories of HBs: water-site HBs (HB), water-water HBs in hydration layers of DNDs (HB), and water-water HBs in the bulk region (HB). Furthermore, the effects of dissolved ions in the solution on the aforementioned HBs have not been studied yet. In this study, we addressed these issues via Molecular Dynamics simulations. Each system under study contained a single DND that was functionalized either with purely -H or with a mixture of -H and one of -NH, -COOH, or -OH groups. Then, the product was dissolved in 0.1M aqueous solution of any of KCl, NaCl, CaCl, or MgCl salts. All DNDs except for DND-OH, which was charge neutral, existed as either a charged or a neutral particle in the…
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Taxonomy
TopicsDiamond and Carbon-based Materials Research · Carbon Nanotubes in Composites · High-pressure geophysics and materials
