New insights into the surface properties of hard-templated ordered mesoporous carbons

被引:27
作者
Li, Xiaoan [1 ,2 ]
Forouzandeh, Farisa [1 ]
Frstenhaupt, Tobias [3 ]
Banham, Dustin [1 ,4 ]
Feng, Fangxia [1 ]
Ye, Siyu [4 ]
Kwok, Daniel Y. [2 ]
Birss, Viola [1 ]
机构
[1] Univ Calgary, Dept Chem, 2500 Univ Dr NW, Calgary, AB T2N 1N4, Canada
[2] Univ Calgary, Dept Mech & Mfg Engn, 2500 Univ Dr NW, Calgary, AB T2N 1N4, Canada
[3] Univ Calgary, Microscopy & Imaging Facil, Hlth Sci Ctr B129,3330 Hosp Dr NW, Calgary, AB T2N 4N1, Canada
[4] Ballard Power Syst, 9000 Glenlyon Pkwy, Burnaby, BC V5J 5J8, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
CARBIDE-DERIVED-CARBON; INTRINSIC WATER WETTABILITY; PEM FUEL-CELLS; ELECTROCHEMICAL PERFORMANCE; ALKALINE ELECTROLYTE; NANOPOROUS CARBON; FUNCTIONAL-GROUPS; CATALYST SUPPORT; ADSORPTION; NANOPARTICLES;
D O I
10.1016/j.carbon.2017.11.049
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
Although hard-templated ordered mesoporous carbons (OMCs) have been widely studied in the past decades, their surface properties, especially surface wettability, have not been investigated in detail. This study shows that as-synthesized hard-templated OMCs (sucrose-and anthracene-derived OMCs, i.e., OMC-S and OMC-A, respectively, formed using the identical hexagonal mesoporous silica template) have very different surface characteristics, with OMC-S being significantly more hydrophobic than OMC-A. This is attributed to the presence of a thin, hydrophobic, microporous carbon shell layer surrounding the mesoporous core of the OMC-S particles, seen here for the first time by transmission electron microscope tomography and confirmed by the slower water uptake and slower electrochemical kinetics of OMC-S vs. OMC-A. At the same time, the mesopores within both OMC-S and OMC-A remain hydrophilic, as shown primarily by water vapor sorption measurements, due to the high density of surface oxygen groups inside the pores, as also confirmed by cyclic voltammetry. These oxygen groups are proposed to have been derived from C-O-Si bonds that formed at the carbon/silica interface during the carbonization process, leaving C-OH groups behind after removal of the silica template. These findings are relevant to a broad range of nanoporous carbon surfaces prepared with hard templates. (C) 2017 Elsevier Ltd. All rights reserved.
引用
收藏
页码:707 / 717
页数:11
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