2021
DOI: 10.1016/j.jechem.2020.11.033
|View full text |Cite
|
Sign up to set email alerts
|

Oxygen vacancies engineering by coordinating oxygen-buffering CeO2 with CoO nanorods as efficient bifunctional oxygen electrode electrocatalyst

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
2
1

Citation Types

1
31
0

Year Published

2021
2021
2024
2024

Publication Types

Select...
6
1

Relationship

0
7

Authors

Journals

citations
Cited by 63 publications
(32 citation statements)
references
References 79 publications
1
31
0
Order By: Relevance
“…Therefore, researchers focus on increasing the active sites by either doping foreign elements (Fe-doped NiO coupled with Ni clusters), creating heterostructures to enhance electron transfer (NiO/NiCo 2 O 4 ), or designing various morphologies (nanosheets or nanoflakes) that provide more active sites . On the other hand, recently, the electrochemical activity of the most abundant lanthanum oxide, that is, CeO 2 , is being extensively studied in bifunctional OER/ORR catalysis due to its reversible shuttling between Ce 3+ and Ce 4+ states and intrinsic oxygen vacancy defects. In the CeO 2 fluorite lattice, when an oxygen vacancy is created, one Ce 4+ is replaced by two Ce 3+ ions to balance the charge. Thus, CeO 2 can act as an oxygen buffer, which can supply or store oxygen in O 2 -deficient or O 2 -rich conditions, respectively .…”
Section: Introductionmentioning
confidence: 99%
“…Therefore, researchers focus on increasing the active sites by either doping foreign elements (Fe-doped NiO coupled with Ni clusters), creating heterostructures to enhance electron transfer (NiO/NiCo 2 O 4 ), or designing various morphologies (nanosheets or nanoflakes) that provide more active sites . On the other hand, recently, the electrochemical activity of the most abundant lanthanum oxide, that is, CeO 2 , is being extensively studied in bifunctional OER/ORR catalysis due to its reversible shuttling between Ce 3+ and Ce 4+ states and intrinsic oxygen vacancy defects. In the CeO 2 fluorite lattice, when an oxygen vacancy is created, one Ce 4+ is replaced by two Ce 3+ ions to balance the charge. Thus, CeO 2 can act as an oxygen buffer, which can supply or store oxygen in O 2 -deficient or O 2 -rich conditions, respectively .…”
Section: Introductionmentioning
confidence: 99%
“…Compared with that before the reaction, the peaks of Co 2p spectrum for Co(CO 3 ) 0.5 OH@CC negatively shift, which suggested that Co 2+ had a tendency to transform like Co 3+ during the OER process. The Co 3+ species may be assigned to the Co species in CoOOH, suggesting CoOOH may serve as active site for the OER (Zhong et al, 2021). Furthermore, the morphology of Co(CO 3 ) 0.5 OH@CC is maintained well apart from the slight surface corrosion (Figures 5C,D).…”
Section: Resultsmentioning
confidence: 93%
“…Peaks at 780.5 eV and 795.4 eV correspond to Co 3+ , and two peaks at 782.2 eV and 797.6 eV correlate to Co 2+ . These Co species can be assigned as CoN x or Co oxide [50,51] . The presence of oxides is generally associated with oxygen vacancies.…”
Section: Resultsmentioning
confidence: 99%