TY - JOUR
T1 - Y and Fe co-doped LaNiO3 perovskite as a novel bifunctional electrocatalyst for rechargeable zinc-air batteries
AU - Lu, Zeming
AU - Zhou, Hang
AU - Qian, Bin
AU - Wang, Shun
AU - Zheng, Yifeng
AU - Ge, Lin
AU - Chen, Han
N1 - Publisher Copyright:
© 2022 Hydrogen Energy Publications LLC
PY - 2023/3/12
Y1 - 2023/3/12
N2 - Perovskite oxides are widely regarded as the promising air electrode catalytic materials for zinc-air batteries (ZABs). In the present work, A-site Y and B-site Fe co-doped La0.85Y0.15Ni0.7Fe0.3O3 perovskite catalyst was prepared by self-propagating high-temperature synthesis, and this material was evaluated as a bifunctional electrocatalyst for ZABs. The effect of co-doping on crystal structure and reaction activities, which can promote oxygen reduction reaction (ORR) and oxygen evolution reaction (OER), was investigated. Results show that Y and Fe co-doping substantially improved the ORR and OER of LaNiO3. In comparison with LaNiO3, the ORR performance of La0.85Y0.15Ni0.7Fe0.3O3 exhibited a higher limiting current density (3.8 mA cm−2 at 0.4 V vs. RHE) and more positive onset potential (0.75 V vs. RHE) at 1600 rpm. It also had an excellent OER performance of 1.74 V vs. RHE at 10 mA cm−2. When La0.85Y0.15Ni0.7Fe0.3O3 was used as an air electrode catalyst for ZABs, it exhibited a high power density of 93.6 mW cm−2, which increased by 84.8% compared with that of LaNiO3. Moreover, the full cell with La0.85Y0.15Ni0.7Fe0.3O3 air electrode catalyst was operated for more than 80 h, maintaining good stability. Therefore, La0.85Y0.15Ni0.7Fe0.3O3 can be used as a promising bifunctional air electrode catalyst for ZABs. The characterization analysis reveals that A-site Y and B-site Fe co-doped catalyst transforms crystal structure from trigonal system to cubic system, retain the valence state of Ni3+ and increases the contents of O22−/O−, and these properties are more conducive for LaNiO3 catalysis.
AB - Perovskite oxides are widely regarded as the promising air electrode catalytic materials for zinc-air batteries (ZABs). In the present work, A-site Y and B-site Fe co-doped La0.85Y0.15Ni0.7Fe0.3O3 perovskite catalyst was prepared by self-propagating high-temperature synthesis, and this material was evaluated as a bifunctional electrocatalyst for ZABs. The effect of co-doping on crystal structure and reaction activities, which can promote oxygen reduction reaction (ORR) and oxygen evolution reaction (OER), was investigated. Results show that Y and Fe co-doping substantially improved the ORR and OER of LaNiO3. In comparison with LaNiO3, the ORR performance of La0.85Y0.15Ni0.7Fe0.3O3 exhibited a higher limiting current density (3.8 mA cm−2 at 0.4 V vs. RHE) and more positive onset potential (0.75 V vs. RHE) at 1600 rpm. It also had an excellent OER performance of 1.74 V vs. RHE at 10 mA cm−2. When La0.85Y0.15Ni0.7Fe0.3O3 was used as an air electrode catalyst for ZABs, it exhibited a high power density of 93.6 mW cm−2, which increased by 84.8% compared with that of LaNiO3. Moreover, the full cell with La0.85Y0.15Ni0.7Fe0.3O3 air electrode catalyst was operated for more than 80 h, maintaining good stability. Therefore, La0.85Y0.15Ni0.7Fe0.3O3 can be used as a promising bifunctional air electrode catalyst for ZABs. The characterization analysis reveals that A-site Y and B-site Fe co-doped catalyst transforms crystal structure from trigonal system to cubic system, retain the valence state of Ni3+ and increases the contents of O22−/O−, and these properties are more conducive for LaNiO3 catalysis.
KW - Bifunctional catalyst
KW - Oxygen evolution reaction
KW - Oxygen reduction reaction
KW - Perovskite
KW - Zinc-air battery
UR - http://www.scopus.com/inward/record.url?scp=85144953319&partnerID=8YFLogxK
U2 - 10.1016/j.ijhydene.2022.11.228
DO - 10.1016/j.ijhydene.2022.11.228
M3 - 文章
AN - SCOPUS:85144953319
SN - 0360-3199
VL - 48
SP - 8082
EP - 8092
JO - International Journal of Hydrogen Energy
JF - International Journal of Hydrogen Energy
IS - 22
ER -