沸石
微型多孔材料
碳纤维
吸附
化学工程
材料科学
化学气相沉积
分子筛
纳米技术
化学
催化作用
有机化学
复合材料
复合数
工程类
作者
Seokin Choi,Hyeonbin Kim,Songhyun Lee,Yuguo Wang,Cemal Ercan,Rashid Othman,Minkee Choi
标识
DOI:10.1016/j.cej.2015.06.055
摘要
Zeolite-templated carbons (ZTCs) possess extra-large surface areas (⩾2000 m2 g−1) and micropore volumes (⩾1.0 cm3 g−1), which allow superior electrochemical performances and gas adsorption properties compared with conventional activated carbons. Unfortunately, ZTCs have been mostly synthesized at a small laboratory-scale due to the limited reproducibility of carbon structures at a large-scale synthesis. The biggest challenge in the carbon replication of zeolites is the deposition of dense carbon layers at the external surface of zeolite crystallites before the complete zeolite micropore filling with carbon. The formation of external carbon layers hinders a faithful carbon replication of zeolite structure, and also significantly limits the adsorption properties of the resultant template-free ZTCs. Here, we demonstrate that acetylene chemical vapor deposition (CVD) at a relatively mild temperature (823 K), followed by thermal treatment at 1073 K, can selectively deposit carbons in the micropores of zeolites, regardless of the synthesis batch size. By combining the mild CVD condition and the use of a rotary tubular furnace, which allows the continuous agitation of zeolites during the synthesis, 50 g NaX and BEA zeolite could be faithfully replicated to ZTCs with a high BET surface area (>2700 m2 g−1) and micropore volume (>1.10 cm3 g−1) without depositing nonporous external carbon layers that significantly hinder the bulky molecular diffusion.
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