Scholarlink

Context <p>Based on density functional theory (DFT), this study investigated the interfacial interactions between pristine graphene (Gr), Gr with single-vacancy (SV), double-vacancy (DV), and Stone–Wales (SW) defects, as well as graphene oxide (GO) modified with different oxygen-containing functional groups, and representative units of calcium silicate hydrate (C-S-H) gel. The results show that the adsorption strength of Si(OH)<sub>4</sub> on pristine Gr/GO surfaces is mainly controlled by the polarity of the functional groups, following the order of GO-COOH &gt; GO-OH &gt; GO-O &gt; Gr. The SW defect can enhance the adsorption on Gr and GO-OH, but weakens the short-range interaction between GO-COOH and Si(OH)<sub>4</sub>. For negatively charged SiO(OH)<sub>3</sub><sup>−</sup>, the SV defect can significantly promote interfacial charge redistribution. The adsorption energy of GO-OH-SV reaches −1.907&#xa0;eV, accompanied by proton transfer and local structural reconstruction. The introduction of Ca<sup>2+</sup> and OH<sup>−</sup> can further improve adsorption stability through coordination bridging, charge compensation, and the synergistic effect between defects and functional groups. Among them, the adsorption energy of Si(OH)<sub>4</sub> on Gr-DV decreases to −3.902&#xa0;eV, while that of SiO(OH)<sub>3</sub><sup>−</sup> on GO-O-SV decreases to −4.974&#xa0;eV. The interaction between pristine Gr and the silicate chain is mainly characterized by weak van der Waals interactions, whereas hydroxyl and carboxyl groups can form specific bonding with the dangling oxygen atoms of the silicate chain through active hydrogen atoms and enhance charge transfer. In the Ca<sup>2+</sup>/OH<sup>−</sup> environment, oxygen-containing functional groups and defect sites jointly construct multiple adsorption centers, further strengthening the interfacial bonding between Gr/GO and C-S-H gel units.</p> Methods <p>Density functional theory (DFT) calculations were carried out using the CASTEP module in Materials Studio software. The GGA-PBE functional, ultrasoft pseudopotential, DFT-D dispersion correction, and Monkhorst–Pack <i>k</i>-point sampling were used for geometry optimization and energy calculations. Adsorption energy, formation energy, and charge density difference were calculated to evaluate the interaction between Gr/GO and C-S-H gel units.</p>

错误：搜索内容不能为空，请输入英文关键词
错误：关键词超出字数限制，请精简
高级检索

First-principles study on the interaction between Gr/GO and C-S-H gel units

  • 期刊论文

  • 发表日期：

    2026年7月21日

查看全文
  • Jianlin He,
  • Chunwei Zhang

摘要

Context

Based on density functional theory (DFT), this study investigated the interfacial interactions between pristine graphene (Gr), Gr with single-vacancy (SV), double-vacancy (DV), and Stone–Wales (SW) defects, as well as graphene oxide (GO) modified with different oxygen-containing functional groups, and representative units of calcium silicate hydrate (C-S-H) gel. The results show that the adsorption strength of Si(OH)4 on pristine Gr/GO surfaces is mainly controlled by the polarity of the functional groups, following the order of GO-COOH > GO-OH > GO-O > Gr. The SW defect can enhance the adsorption on Gr and GO-OH, but weakens the short-range interaction between GO-COOH and Si(OH)4. For negatively charged SiO(OH)3−, the SV defect can significantly promote interfacial charge redistribution. The adsorption energy of GO-OH-SV reaches −1.907 eV, accompanied by proton transfer and local structural reconstruction. The introduction of Ca2+ and OH− can further improve adsorption stability through coordination bridging, charge compensation, and the synergistic effect between defects and functional groups. Among them, the adsorption energy of Si(OH)4 on Gr-DV decreases to −3.902 eV, while that of SiO(OH)3− on GO-O-SV decreases to −4.974 eV. The interaction between pristine Gr and the silicate chain is mainly characterized by weak van der Waals interactions, whereas hydroxyl and carboxyl groups can form specific bonding with the dangling oxygen atoms of the silicate chain through active hydrogen atoms and enhance charge transfer. In the Ca2+/OH− environment, oxygen-containing functional groups and defect sites jointly construct multiple adsorption centers, further strengthening the interfacial bonding between Gr/GO and C-S-H gel units.

Methods

Density functional theory (DFT) calculations were carried out using the CASTEP module in Materials Studio software. The GGA-PBE functional, ultrasoft pseudopotential, DFT-D dispersion correction, and Monkhorst–Pack k-point sampling were used for geometry optimization and energy calculations. Adsorption energy, formation energy, and charge density difference were calculated to evaluate the interaction between Gr/GO and C-S-H gel units.