TY - JOUR
T1 - The synthesis and characterization of a super-activated carbon containing substitutional boron (BCx) and its applications in hydrogen storage
AU - Jeong, Youmi
AU - Mike Chung, T. C.
N1 - Funding Information:
The authors would like to thank the US Department of Energy and the Hydrogen Sorption Center of Excellent (lead: National Renewable Energy Laboratory) for their financial support. The authors would also like to thank NIST (Drs. Craig Brown and Dan Neumann) and Air Products Co. (Drs. Alan Cooper) for their assistance in prompt gamma ray activation analysis (PGAA) and hydrogen adsorption isotherm measurements.
PY - 2010/8
Y1 - 2010/8
N2 - A new family of porous boron-substituted carbon (BCx) materials with controlled structure is investigated. The chemistry involves a B-precursor polymer, i.e., poly(borachlorophenyldiacetylene), containing inorganic additives (templates). At pyrolysis <400 °C, the B-precursor engages in easy inter-chain reactions to form dark solid with high yield (>85%). Above 600 °C, the amorphous carbon-like BCx materials containing up to 12% B have been prepared, which show an extended fused hexagonal ring structure with B-puckered curvature. This out of planar B moiety maintains its electron deficiency, due to limited π-electron delocalization, and exhibits super-activated properties to enhance H2 binding energy (20-10 kJ/mol) and adsorption capacity. After removing the inorganic additives by water-washing, the resulting porous BCx shows a surface area 500-800 m2/g. Evidently, the pore size distribution is directly related to melting temperature and distribution of the inorganic salts. As the temperature increases to >1400 °C, the distorted ring structure gradually flatten out to form a multi-layer (crystalline) BCx structure. The resulting planar graphitic layer only can accommodate a reduced B content (<3% at 1800 °C) and low surface area. The B moieties also lose their acidity due to the extensive π-electron delocalization.
AB - A new family of porous boron-substituted carbon (BCx) materials with controlled structure is investigated. The chemistry involves a B-precursor polymer, i.e., poly(borachlorophenyldiacetylene), containing inorganic additives (templates). At pyrolysis <400 °C, the B-precursor engages in easy inter-chain reactions to form dark solid with high yield (>85%). Above 600 °C, the amorphous carbon-like BCx materials containing up to 12% B have been prepared, which show an extended fused hexagonal ring structure with B-puckered curvature. This out of planar B moiety maintains its electron deficiency, due to limited π-electron delocalization, and exhibits super-activated properties to enhance H2 binding energy (20-10 kJ/mol) and adsorption capacity. After removing the inorganic additives by water-washing, the resulting porous BCx shows a surface area 500-800 m2/g. Evidently, the pore size distribution is directly related to melting temperature and distribution of the inorganic salts. As the temperature increases to >1400 °C, the distorted ring structure gradually flatten out to form a multi-layer (crystalline) BCx structure. The resulting planar graphitic layer only can accommodate a reduced B content (<3% at 1800 °C) and low surface area. The B moieties also lose their acidity due to the extensive π-electron delocalization.
UR - http://www.scopus.com/inward/record.url?scp=77955227589&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=77955227589&partnerID=8YFLogxK
U2 - 10.1016/j.carbon.2010.03.029
DO - 10.1016/j.carbon.2010.03.029
M3 - Article
AN - SCOPUS:77955227589
SN - 0008-6223
VL - 48
SP - 2526
EP - 2537
JO - Carbon
JF - Carbon
IS - 9
ER -