Enhanced hydrogen storage and CO2 capture capacities on carbon aerogels from Ni-N co-doping

被引:42
作者
Cheng, Jiahao [1 ,2 ]
Cheng, Xingxing [1 ,2 ]
Wang, Zhiqiang [1 ,2 ]
Jen, Tien-Chien [3 ]
机构
[1] Shandong Univ, Sch Energy & Power Engn, Jinan 250061, Peoples R China
[2] Natl Engn Lab Reducing Emiss Coal Combust, Jinan 250061, Peoples R China
[3] Univ Johannesburg, Mech Engn Dept, ZA-2006 Johannesburg, South Africa
关键词
Carbon aerogels; Hydrogen storage; CO2; capture; Surface functionalization; Hydrogen spillover; HIGH-SURFACE-AREA; ACTIVATED CARBON; ANODE MATERIALS; STEP SYNTHESIS; ADSORPTION; SPILLOVER; PERFORMANCE; COMPOSITES; GRAPHENE;
D O I
10.1016/j.fuel.2024.132271
中图分类号
TE [石油、天然气工业]; TK [能源与动力工程];
学科分类号
0807 ; 0820 ;
摘要
Carbon aerogels (CAs) has been a promising candidate for gas adsorption due to their unique attributes, but the poor surface properties and temperature reliance limit the application range. Investigations have proven that surface modification can enhance the adsorption performance. Thus, nickel and nitrogen co-doped cellulosebased carbon aerogels were synthesized by introducing nanoparticles. The outcomes demonstrate the excellent adsorption capacity and reversible adsorption/desorption features. Nickel particles improved the dissociation of hydrogen by "hydrogen spillover" effect, and interacted electrostatically with CO2 enhanced the capture performance. Nitrogen particles enhanced the unsaturation of Ni active sites and the surface basicity, resulting a stronger interaction force with adsorbed gases. Ultimately, despite a slightly decrease in specific surface area and micropore volume, the sample exhibit the hydrogen storage capacity of 0.79 wt.% (298 K) and 7.4 wt.% (77 K), and the CO2 capture of 17.1 mmol/g (298 K). Unique design strategy of co-doping reduced the reliance on surface area and temperature changes, and is expected to be a regular means of industrial modification of carbon materials.
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页数:8
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