2022
DOI: 10.1016/j.cclet.2021.10.034
|View full text |Cite
|
Sign up to set email alerts
|

Recent advances of two-dimensional CoFe layered-double-hydroxides for electrocatalytic water oxidation

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
4
1

Citation Types

0
12
0

Year Published

2022
2022
2024
2024

Publication Types

Select...
8
1

Relationship

1
8

Authors

Journals

citations
Cited by 26 publications
(12 citation statements)
references
References 88 publications
0
12
0
Order By: Relevance
“…Because of these advantages, LDH with anion intercalation always exhibits an excellent activity and stability in water splitting. The layer distance between LDH materials can be also easily tuned by the organic small molecules, in which the organic small molecules efficiently weaken the interlayer interaction of LDH materials, thus leading to the enhanced electrocatalytic activity [122][123][124]. Gao's group reported that CoFe-LDH materials with a large interlayer distance of 0.6 nm were prepared in the ethanol solution using ammonium bicarbonate (NH4HCO3) as a pH regulator [122].…”
Section: Gu Et Al Realized the Preparation Of Intercalation-induced P...mentioning
confidence: 99%
“…Because of these advantages, LDH with anion intercalation always exhibits an excellent activity and stability in water splitting. The layer distance between LDH materials can be also easily tuned by the organic small molecules, in which the organic small molecules efficiently weaken the interlayer interaction of LDH materials, thus leading to the enhanced electrocatalytic activity [122][123][124]. Gao's group reported that CoFe-LDH materials with a large interlayer distance of 0.6 nm were prepared in the ethanol solution using ammonium bicarbonate (NH4HCO3) as a pH regulator [122].…”
Section: Gu Et Al Realized the Preparation Of Intercalation-induced P...mentioning
confidence: 99%
“…9 However, it is still difficult to manipulate such dynamic evolution and the in situ-formed active surface species because of the sluggish reconfiguration of the electrolyte-nonpermeable solid surface. 10,11 To promote the in situ formation of active (oxy)hydroxides toward the reaction-preferred surface, an effective activation of transitionmetal electrocatalysts via tuning surface/interfacial interactions is highly desired. 12−14 Ceria (CeO 2 ) with the flexible transition between Ce 3+ and Ce 4+ oxidation states can serve as the promoter for a variety of electrocatalysis because its good electronic/ionic conductivity and rich oxygen defects in lattices enable the strong interactions and available synergies with the host surface.…”
Section: Introductionmentioning
confidence: 99%
“…The oxidation-driven reconstruction in situ generates the corresponding (oxy)­hydroxides as actual active species, showing a positive correlation of activity with the oxidation current prior to OER occurrence . However, it is still difficult to manipulate such dynamic evolution and the in situ -formed active surface species because of the sluggish reconfiguration of the electrolyte-nonpermeable solid surface. , To promote the in situ formation of active (oxy)­hydroxides toward the reaction-preferred surface, an effective activation of transition-metal electrocatalysts via tuning surface/interfacial interactions is highly desired. …”
Section: Introductionmentioning
confidence: 99%
“…Transition-metal (e.g., Co, Fe and Ni) layered double hydroxides (LDH) have emerged as promising electrocatalysts for OER because of their flexible open layer structures, tunable chemical composition, and cost effectiveness [4][5][6]. In particular, the OER activity of bimetallic CoFe LDH is dramatically improved compared to the individual Co and Fe components due to the modulated electronic structures, enhanced charge transfer, and synergistic interactions between Co and Fe [7,8]. However, the bulk CoFe LDH still suffers from both intrinsically weak electronic conductivity and serious aggregation problems.…”
Section: Introductionmentioning
confidence: 99%