石墨烯
生物分子
氧化物
吸附
化学物理
材料科学
氧气
分子
共价键
分子动力学
氢键
密度泛函理论
从头算
氢
化学工程
纳米技术
计算化学
化学
物理化学
有机化学
工程类
冶金
作者
Yusong Tu,Liang Zhao,Jiajia Sun,Yi Wu,Xiaojie Zhou,Liang Chen,Xiaoling Lei,Haiping Fang,Guosheng Shi
标识
DOI:10.1088/0256-307x/37/6/066803
摘要
We theoretically and experimentally show that, with water being adsorbed, the graphene oxide (GO) is converted to a spontaneously dynamic covalent material under ambient conditions, where the dominated epoxy and hydroxyl groups are mediated by water molecules to spontaneously break/reform their C–O bonds to achieve dynamic oxygen migration. This dynamic material presents structural adaptivity for response to biomolecule adsorption. Both density functional theory calculations and ab initio molecular dynamics simulations demonstrate that this spontaneously dynamic characteristics is attributed to the adsorption of water molecules, which sharply reduces the barriers of these oxygen migration reactions on GO to the level less than or comparable to the hydrogen bonding energy in liquid water .
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