Ion transport in graphene nanofluidic channels

被引:32
作者
Xie, Quan [1 ]
Xin, Fang [2 ]
Park, Hyung Gyu [3 ]
Duan, Chuanhua [1 ]
机构
[1] Boston Univ, Dept Mech Engn, Boston, MA 02215 USA
[2] Tsinghua Univ, Sch Aerosp Engn, Beijing 100084, Peoples R China
[3] Eidgenoss Tech Hsch ETH Zurich, Dept Mech & Proc Engn, CH-8092 Zurich, Switzerland
基金
瑞士国家科学基金会;
关键词
CARBON NANOTUBE MEMBRANES; FAST WATER TRANSPORT; OXIDE MEMBRANES; PROTON CONDUCTION; SILICA GLASSES; DESALINATION; ENERGY; NANOCHANNELS; SEPARATION; INTERFACE;
D O I
10.1039/c6nr06977k
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Carbon nanofluidic structures made of carbon nanotubes or graphene/graphene oxide have shown great promise in energy and environment applications due to the newly discovered fast and selective mass transport. However, they have yet to be utilized in nanofluidic devices for lab-on-a-chip applications because of great challenges in their fabrication and integration. Herein we report the fabrication of two-dimensional planar graphene nanochannel devices and the study of ion transport inside a graphene nanochannel array. A MEMS fabrication process that includes controlled nanochannel etching, graphene wet transfer, and vacuum anodic bonding is developed to fabricate graphene nanochannels where graphene conformally coats the channel surfaces. We observe higher ionic conductance inside the graphene nanochannels compared with silica nanochannels with the same geometries at low electrolyte concentrations (10(-6) M-10(-2) M). Enhanced electroosmotic flow due to the boundary slip at graphene surfaces is attributed to the measured higher conductance in the graphene nanochannels. Our results also suggest that the surface charge on the graphene surface, originating from the dissociation of oxygen-containing functional groups, is crucial to the enhanced electroosmotic flow inside the nanochannels.
引用
收藏
页码:19527 / 19535
页数:9
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