TY - JOUR
T1 - Chemisorption of CO2on Nitrogen-Doped Graphitic Carbons
AU - Shibuya, Riku
AU - Takeyasu, Kotaro
AU - Guo, Donghui
AU - Kondo, Takahiro
AU - Nakamura, Junji
N1 - Funding Information:
The authors thank Akinori Okonogi, Shunsuke Saji, and Chisato Akiba for their experimental assistance. This work is partly supported by JST PRESTO (JPMJPR1296) and ENEOS hydrogen trust fund (2015). We thank Editage ( www.editage.com ) for English language editing.
Publisher Copyright:
© 2022 American Chemical Society. All rights reserved.
PY - 2022/11/29
Y1 - 2022/11/29
N2 - The adsorption of CO2on nitrogen-doped graphitic carbon materials, such as graphene nanosheet (GNS) powder and highly oriented pyrolytic graphite (HOPG), was comparatively studied using temperature-programmed desorption (TPD) and X-ray photoelectron spectroscopy (XPS). Desorption of CO2was observed at approximately 380 K for both pyridinic-nitrogen (pyri-N)-doped GNS and pyri-N-doped HOPG samples in the TPD experiments, whereas no CO2desorption was observed for graphitic nitrogen-doped HOPG. This indicated that only pyri-N species create identical CO2adsorption sites on any graphitic carbon surface. The adsorption energies of CO2on pyri-N-doped carbons were estimated between 101 and 108 kJ mol-1, indicating that chemisorption, rather than physisorption, took place. The CO2adsorption/desorption process was reproducible in repeated measurements, and no CO2dissociation occurred during the process, suggesting that it is a promising CO2capturing material. The O 1s peak of the adsorbed CO2clearly appeared at 531.5-532 eV in the XPS measurements. The N 1s peak of pyri-N did not change with CO2adsorption, indicating that CO2is not directly bound to pyri-N but is adsorbed on a carbon atom near the pyridinic nitrogen via the nonbonding pzorbital of the carbon atom.
AB - The adsorption of CO2on nitrogen-doped graphitic carbon materials, such as graphene nanosheet (GNS) powder and highly oriented pyrolytic graphite (HOPG), was comparatively studied using temperature-programmed desorption (TPD) and X-ray photoelectron spectroscopy (XPS). Desorption of CO2was observed at approximately 380 K for both pyridinic-nitrogen (pyri-N)-doped GNS and pyri-N-doped HOPG samples in the TPD experiments, whereas no CO2desorption was observed for graphitic nitrogen-doped HOPG. This indicated that only pyri-N species create identical CO2adsorption sites on any graphitic carbon surface. The adsorption energies of CO2on pyri-N-doped carbons were estimated between 101 and 108 kJ mol-1, indicating that chemisorption, rather than physisorption, took place. The CO2adsorption/desorption process was reproducible in repeated measurements, and no CO2dissociation occurred during the process, suggesting that it is a promising CO2capturing material. The O 1s peak of the adsorbed CO2clearly appeared at 531.5-532 eV in the XPS measurements. The N 1s peak of pyri-N did not change with CO2adsorption, indicating that CO2is not directly bound to pyri-N but is adsorbed on a carbon atom near the pyridinic nitrogen via the nonbonding pzorbital of the carbon atom.
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U2 - 10.1021/acs.langmuir.2c01987
DO - 10.1021/acs.langmuir.2c01987
M3 - Article
C2 - 36377773
AN - SCOPUS:85141961118
SN - 0743-7463
VL - 38
SP - 14430
EP - 14438
JO - Langmuir
JF - Langmuir
IS - 47
ER -