TY - JOUR
T1 - Pore-controlled carbon nanotube sheet anodes for proton/anion-exchange membrane water electrolyzers
AU - Eun Park, Ji
AU - Na, Geumbi
AU - Yeom, Kyungbeen
AU - Park, Sung Bin
AU - Jun Sim, Hyeon
AU - Sung, Yung Eun
AU - Choi, Changsoon
N1 - Publisher Copyright:
© 2023 Elsevier B.V.
PY - 2023/3/1
Y1 - 2023/3/1
N2 - The commercialization of proton/anion-exchange membrane water electrolyzers (PEMWEs/AEMWEs) requires the development of high-performance and durable anodes. Herein, pore-controlled electrodes (C@PCEs) that incorporate carbon nanotube sheets with square pores and catalyst nanoparticles are designed. Ir and NiFe catalysts, which promote the oxygen evolution reaction under acidic and alkaline conditions, respectively, are applied in PEMWEs and AEMWEs. The C@PCEs have higher catalytic activities than the corresponding conventional densely packed electrodes (C@DPEs). Additionally, the PEMWEs and AEMWEs with C@PCEs exhibit improved performance with reduced overpotentials compared to those with C@DPEs. This enhancement in performance is ascribed to the pore structure of the C@PCEs, in which the electrocatalyst is well dispersed without agglomeration, thus increasing the electrochemical surface area. In addition, the highly conductive and porous carbon nanotube framework promotes electron and mass transfer. These results demonstrate that the C@PCE design is promising for anodes in both PEMWEs and AEMWEs.
AB - The commercialization of proton/anion-exchange membrane water electrolyzers (PEMWEs/AEMWEs) requires the development of high-performance and durable anodes. Herein, pore-controlled electrodes (C@PCEs) that incorporate carbon nanotube sheets with square pores and catalyst nanoparticles are designed. Ir and NiFe catalysts, which promote the oxygen evolution reaction under acidic and alkaline conditions, respectively, are applied in PEMWEs and AEMWEs. The C@PCEs have higher catalytic activities than the corresponding conventional densely packed electrodes (C@DPEs). Additionally, the PEMWEs and AEMWEs with C@PCEs exhibit improved performance with reduced overpotentials compared to those with C@DPEs. This enhancement in performance is ascribed to the pore structure of the C@PCEs, in which the electrocatalyst is well dispersed without agglomeration, thus increasing the electrochemical surface area. In addition, the highly conductive and porous carbon nanotube framework promotes electron and mass transfer. These results demonstrate that the C@PCE design is promising for anodes in both PEMWEs and AEMWEs.
KW - Anion-exchange membrane water electrolyzers
KW - Anode
KW - Oxygen evolution reactions
KW - Pore-controlled carbon nanotube electrodes
KW - Proton-exchange membrane water electrolyzers
UR - http://www.scopus.com/inward/record.url?scp=85147559622&partnerID=8YFLogxK
U2 - 10.1016/j.cej.2023.141671
DO - 10.1016/j.cej.2023.141671
M3 - Article
AN - SCOPUS:85147559622
SN - 1385-8947
VL - 459
JO - Chemical Engineering Journal
JF - Chemical Engineering Journal
M1 - 141671
ER -