Chin. Phys. Lett.  2020, Vol. 37 Issue (6): 066803    DOI: 10.1088/0256-307X/37/6/066803
CONDENSED MATTER: STRUCTURE, MECHANICAL AND THERMAL PROPERTIES |
Water-Mediated Spontaneously Dynamic Oxygen Migration on Graphene Oxide with Structural Adaptivity for Biomolecule Adsorption
Yusong Tu1,2**, Liang Zhao1, Jiajia Sun1, Yuanyan Wu1, Xiaojie Zhou3, Liang Chen4, Xiaoling Lei5,6, Haiping Fang5,6, Guosheng Shi7**
1College of Physics Science and Technology, Yangzhou University, Jiangsu 225009, China
2Key Laboratory of Polar Materials and Devices (Ministry of Education), Department of Optoelectronics, East China Normal University, Shanghai 200062, China
3National Facility for Protein Science in Shanghai, Shanghai Advanced Research Institute, Chinese Academy of Sciences, Shanghai 201210, China
4Department of Optical Engineering, Zhejiang A&F University, Lin'an 311300, China
5Department of Physics, East China University of Science and Technology, Shanghai 200237, China
6Division of Interfacial Water and Key Laboratory of Interfacial Physics and Technology, Shanghai Institute of Applied Physics, Chinese Academy of Sciences, Shanghai 201800, China
7Shanghai Applied Radiation Institute, Shanghai University, Shanghai 200444, China
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Yusong Tu, Liang Zhao, Jiajia Sun et al  2020 Chin. Phys. Lett. 37 066803
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Abstract 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.
Received: 07 May 2020      Published: 29 May 2020
PACS:  68.37.-d (Microscopy of surfaces, interfaces, and thin films)  
  68.90.+g (Other topics in structure, and nonelectronic properties of surfaces and interfaces; thin films and low-dimensional structures)  
  61.48.Gh (Structure of graphene)  
  87.90.+y (Other topics in biological and medical physics)  
Fund: *Supported by the National Natural Science Foundation of China (Grant Nos. 11675138, 11705160, 11605151, U1832150, U1932123 and 11974366), the National Science Fund for Outstanding Young Scholars (Grant No. 11722548), the Key Research Program of Chinese Academy of Sciences (Grant No. QYZDJ-SSW-SLH053), the Fundamental Research Funds for the Central Universities, the Special Program for Applied Research on Supercomputation of the NSFC-Guangdong Joint Fund (the second stage), Supercomputer Center of CAS, and the BL01B Beamline of NFPS at SSRF.
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http://cpl.iphy.ac.cn/10.1088/0256-307X/37/6/066803       OR      http://cpl.iphy.ac.cn/Y2020/V37/I6/066803
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Yusong Tu
Liang Zhao
Jiajia Sun
Yuanyan Wu
Xiaojie Zhou
Liang Chen
Xiaoling Lei
Haiping Fang
Guosheng Shi
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