Proton transport in electrochemically reduced graphene oxide: Enhancing H+/H2O selectivity

被引:15
作者
Chernova, E. A. [1 ]
Brotsman, V. A. [2 ]
Gurianov, K. E. [1 ]
Eliseev, Ar. A. [2 ]
Valeev, R. G. [3 ]
Kolesnik, I. V. [1 ]
Chumakov, A. P. [4 ]
Petukhov, D. I. [1 ,2 ]
Eliseev, An. A. [1 ,2 ]
机构
[1] Lomonosov Moscow State Univ, Dept Mat Sci, 1-73 Leninskiye Gory, Moscow 119991, Russia
[2] Lomonosov Moscow State Univ, Dept Chem, 1-3 Leninskiye Gory, Moscow 119991, Russia
[3] Russian Acad Sci UdmFRC UB RAS, Ural Brunch, Udmurt Fed Res Ctr, St Them Tatiana Baramzina 34, Izhevsk 426067, Russia
[4] European Synchrotron Radiat Facil, 71 Av Martyrs, F-38042 Grenoble, France
基金
俄罗斯科学基金会;
关键词
Graphene oxide membranes; Protons transport; Diffusion coefficients; H plus; H2O selectivity; Fuel cells; REDUCTION; MEMBRANES; WATER;
D O I
10.1016/j.carbon.2023.118288
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
Proton-selective membranes are prepared by electrochemical reduction of graphene oxide films in aqueous electrolytes. Rapid kinetics of oxygenated groups reduction was revealed by complementary FTIR- and XPSspectroscopy giving rise to a partially reduced graphene oxide with C/O ratio in the range of 2-4. The reduction is accompanied by interstitial water loss and shrinkage of d-spacing from 1.15 nm, typical for graphene oxide, to graphene-like -0.36 nm as revealed by X-ray diffraction analysis. The presence of remaining oxygen groups in reduced graphene oxide enables fast transport of protons with Grotthuss hopping mechanism and diffusion coefficients in the range of 3-7 & BULL;10  11 m2 s  1 at 25 degrees C. At the same time, the reduction of GO layers hinders dramatically the transport of H2O molecules due to suppression of capillary condensation of water in the oxygen-deficient channels of the reduced graphene oxide providing the H+/H2O selectivity of up to 1400 upon electrochemical reduction. The suggested approach opens the avenue for the performance enhancement of carbon-based membranes for proton-selective transport in fuel cells and electrolyzers.
引用
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页数:10
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