Time Evolution of the Wettability of Supported Graphene under Ambient Air Exposure

被引:123
作者
Aria, Adrianus I. [1 ]
Kidambi, Piran R. [1 ,3 ]
Weatherup, Robert S. [1 ,4 ]
Xiao, Long [1 ]
Williams, John A. [2 ]
Hofmann, Stephan [1 ]
机构
[1] Univ Cambridge, Dept Engn, Div Elect Engn, Cambridge CB2 1PZ, England
[2] Univ Cambridge, Dept Engn, Div Mech Mat & Design, Cambridge CB2 1PZ, England
[3] MIT, Dept Mech Engn, Cambridge, MA 02139 USA
[4] Univ Calif Berkeley, Lawrence Berkeley Natl Lab, Div Mat Sci, Berkeley, CA 94720 USA
基金
英国工程与自然科学研究理事会;
关键词
CHEMICAL-VAPOR-DEPOSITION; IN-SITU OBSERVATIONS; SOLID-SURFACES; WATER WETTABILITY; METAL; ADSORPTION; CONTAMINANTS; MECHANISMS; FRICTION; KINETICS;
D O I
10.1021/acs.jpcc.5b10492
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The wettability of graphene is both fundamental and crucial for interfacing in most applications, but a detailed understanding of its time evolution remains elusive. Here we systematically investigate the wettability of metal-supported, chemical vapor deposited graphene films as a function of ambient air exposure time using water and various other test liquids with widely different surface tensions. The wettability of graphene is not constant, but varies with substrate interactions and air exposure time. The substrate interactions affect the initial graphene wettability, where, for instance, water contact angles of, similar to 85 and, similar to 61 degrees were measured for Ni and Cu supported graphene, respectively, after just minutes of air exposure. Analysis of the surface free energy components indicates that the substrate interactions strongly influence the Lewis acid-base component of supported graphene, which is considerably weaker for Ni supported graphene than for Cu supported graphene, suggesting that the classical van der Waals interaction theory alone is insufficient to describe the wettability of graphene. For prolonged air exposure, the effect of physisorption of airborne contaminants becomes increasingly dominant, resulting in an increase of water contact angle that follows a universal linear logarithmic relationship with exposure time, until saturating at a maximum value of 92-98 degrees. The adsorbed contaminants render all supported graphene samples increasingly nonpolar, although their total surface free energy decreases only by 10-16% to about 37-41 mJ/m(2). Our finding shows that failure to account for the air exposure time may lead to widely different wettability values and contradicting arguments about the wetting transparency of graphene.
引用
收藏
页码:2215 / 2224
页数:10
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