TY - JOUR
T1 - Spray pyrolysis-assisted synthesis of hollow cobalt nitrogen-doped carbon catalyst for the performance enhancement of membraneless fuel cells
AU - Ji, Jungyeon
AU - Im, Kyungmin
AU - An, Heeyeon
AU - Yoo, Sung Jong
AU - Chung, Yongjin
AU - Kim, Jinsoo
AU - Kwon, Yongchai
N1 - Publisher Copyright:
© 2021 John Wiley & Sons Ltd.
PY - 2022/2
Y1 - 2022/2
N2 - Hollow cobalt nitrogen-doped carbon (H-CoNC) is suggested for use in the membraneless hydrogen peroxide fuel cell (HPFC) and enzymatic biofuel cell (EBC) as anodic catalyst boosting hydrogen peroxide oxidation reaction (HPOR). For fabricating H-CoNCs, a facile spray pyrolysis-assisted process is used, and such produced H-CoNCs show a porous and hollow-shell structure, while they include a large amount of isolated Co atoms and coordinate bonds with Co and nitrogen (Co-N4). This structure promotes mass transfer to the active site and excellent catalytic activity for HPOR. With these benefits of H-CoNCs, the current density of the bioanode consisting of H-CoNC, carbon nanotube, and glucose oxidase (H-CoNC/CNT/GOx) observed at 0.3 V under 150 mM glucose is 315.5 μA cm−2, which is 2.1 times higher than that of a conventionally synthesized catalyst using Co-doped carbon nanoparticles (CoNC-NPs) (CoNC-NPs/CNT/GOx, 146.2 μA cm−2). With this superior catalytic activity for HPOR, maximum power density (MPD) of membraneless EBC using H-CoNC/CNT/GOx is 33.8 ± 4.52 μW cm−2, which is 52% higher than that of CoNP-NPs/CNT/GOx. In addition, a membraneless HPFC using H-CoNC/CNT demonstrates 4.87 times higher MPD (231.3 ± 11.3 μW cm−2) than that using CoNC-NPs/CNT, proving that H-CoNC improves the performance of fuel cells by its excellent catalytic activity.
AB - Hollow cobalt nitrogen-doped carbon (H-CoNC) is suggested for use in the membraneless hydrogen peroxide fuel cell (HPFC) and enzymatic biofuel cell (EBC) as anodic catalyst boosting hydrogen peroxide oxidation reaction (HPOR). For fabricating H-CoNCs, a facile spray pyrolysis-assisted process is used, and such produced H-CoNCs show a porous and hollow-shell structure, while they include a large amount of isolated Co atoms and coordinate bonds with Co and nitrogen (Co-N4). This structure promotes mass transfer to the active site and excellent catalytic activity for HPOR. With these benefits of H-CoNCs, the current density of the bioanode consisting of H-CoNC, carbon nanotube, and glucose oxidase (H-CoNC/CNT/GOx) observed at 0.3 V under 150 mM glucose is 315.5 μA cm−2, which is 2.1 times higher than that of a conventionally synthesized catalyst using Co-doped carbon nanoparticles (CoNC-NPs) (CoNC-NPs/CNT/GOx, 146.2 μA cm−2). With this superior catalytic activity for HPOR, maximum power density (MPD) of membraneless EBC using H-CoNC/CNT/GOx is 33.8 ± 4.52 μW cm−2, which is 52% higher than that of CoNP-NPs/CNT/GOx. In addition, a membraneless HPFC using H-CoNC/CNT demonstrates 4.87 times higher MPD (231.3 ± 11.3 μW cm−2) than that using CoNC-NPs/CNT, proving that H-CoNC improves the performance of fuel cells by its excellent catalytic activity.
UR - https://www.scopus.com/pages/publications/85113291829
U2 - 10.1002/er.7200
DO - 10.1002/er.7200
M3 - Article
AN - SCOPUS:85113291829
SN - 0363-907X
VL - 46
SP - 760
EP - 773
JO - International Journal of Energy Research
JF - International Journal of Energy Research
IS - 2
ER -