TY - JOUR
T1 - Plasma-enhanced alternating atomic layer deposition of nickel and copper oxide on wood-derived monolithic carbon electrode for robust oxygen evolution reaction
AU - Zhang, Bin
AU - Ye, Wenkai
AU - Hu, Jiahao
AU - Ji, Tuo
AU - Lin, Han
AU - Mu, Liwen
AU - Lu, Xiaohua
AU - Zhu, Jiahua
N1 - Publisher Copyright:
© 2025
PY - 2024/3/18
Y1 - 2024/3/18
N2 - The oxygen evolution reaction (OER) is a critical half-reaction that occurs at the anode for water electrolysis, along with sluggish kinetics and high overpotential owing to its four-electron transfer process. Iridium-based electrocatalysts are recognized as the superior OER performance, but are limited by high cost and shortage reserves. Hence, we report a monolithic electrode with Ni doped Cu2-xO growth on the carbonized wood (CW) surface by an alternating plasma-enhanced atomic layer deposition (PEALD) strategy. The alternating deposition of Ni and Cu2-xO ensures uniform doping of Ni and facilitates the electron transfer from d-orbital of Cu2⁺ to the Ni site. This electron transfer reduces electron repulsion among the p-orbitals of the coordinated O atoms, enhancing the local metal-oxygen bonding strength and adjusting the charge at the Cu site. Consequently, the electronic structure of the catalyst is optimized, leading to exceptional OER performance with an overpotential of 110.2 mV at 10 mA cm−2 and significantly enhanced stability of 75 h.
AB - The oxygen evolution reaction (OER) is a critical half-reaction that occurs at the anode for water electrolysis, along with sluggish kinetics and high overpotential owing to its four-electron transfer process. Iridium-based electrocatalysts are recognized as the superior OER performance, but are limited by high cost and shortage reserves. Hence, we report a monolithic electrode with Ni doped Cu2-xO growth on the carbonized wood (CW) surface by an alternating plasma-enhanced atomic layer deposition (PEALD) strategy. The alternating deposition of Ni and Cu2-xO ensures uniform doping of Ni and facilitates the electron transfer from d-orbital of Cu2⁺ to the Ni site. This electron transfer reduces electron repulsion among the p-orbitals of the coordinated O atoms, enhancing the local metal-oxygen bonding strength and adjusting the charge at the Cu site. Consequently, the electronic structure of the catalyst is optimized, leading to exceptional OER performance with an overpotential of 110.2 mV at 10 mA cm−2 and significantly enhanced stability of 75 h.
KW - Atomic layer deposition
KW - Monolithic catalysts
KW - Ni-doped CuO
KW - OER
UR - http://www.scopus.com/inward/record.url?scp=85217955251&partnerID=8YFLogxK
U2 - 10.1016/j.ijhydene.2025.02.226
DO - 10.1016/j.ijhydene.2025.02.226
M3 - 文章
AN - SCOPUS:85217955251
SN - 0360-3199
VL - 110
SP - 83
EP - 89
JO - International Journal of Hydrogen Energy
JF - International Journal of Hydrogen Energy
ER -