Effects of oxygen functional groups on the enhancement of the hydrogen spillover of Pd-doped activated carbon

被引:49
作者
Chung, Tsui-Yun [1 ]
Tsao, Cheng-Si [1 ]
Tseng, Hui-Ping [1 ]
Chen, Chien-Hung [1 ]
Yu, Ming-Sheng [1 ]
机构
[1] Inst Nucl Energy Res, Taoyuan 32546, Taiwan
关键词
Adsorption; Microporous materials; Surface properties; Hydrogen spillover; CATALYTIC-PROPERTIES; SURFACE-CHEMISTRY; STORAGE BEHAVIORS; ADSORPTION; NANOFIBERS; PALLADIUM; MECHANISM; CAPACITY;
D O I
10.1016/j.jcis.2014.10.062
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 hydrogen storage performance of Pd-doped oxidized activated carbon (Pd/AC-ox) with various oxygen contents or functional groups was investigated. The surface chemistry of the Pd/AC-ox sample was modified by treatment with hydrogen gas. Temperature-programmed desorption was performed to characterize the oxygen functional groups in each sample. In this study, low- and high-pressure hydrogen adsorption isotherm experiments were conducted using a static volumetric measurement at room temperature (RT) and pressures of up to 8 MPa. The results showed that increasing the oxygen content and functional groups on the surface of the Pd/AC-ox significantly improved the reversible RT hydrogen storage capacity due to the spillover effect. The hydrogen spillover enhancement factors at 0.12 MPa were greater than 100% for all samples. The hydrogen uptake of Pd/AC-ox1 at RT and 8 MPa with an oxygen content of 8.94 wt.% was 0.37 wt.%, which was 48% greater than that of Pd-free AC-ox (0.25 wt.%). In addition, the hydrogen uptake of Pd/AC-ox3 with lower oxygen contents demonstrates that the hydrogen spillover enhancement gradually disappears when the pressure is increased to more than 2 MPa (i.e., a transition from spillover to physisorption). The surface diffusion, or reversible adsorption, of the spiltover H atoms, which is enhanced by oxygen functional groups, was affected by a threshold amount of oxygen groups (such as hydroxyl groups). (C) 2014 Elsevier Inc. All rights reserved.
引用
收藏
页码:98 / 105
页数:8
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