2021
DOI: 10.1016/j.colsurfa.2021.127404
|View full text |Cite
|
Sign up to set email alerts
|

Bimetallic PdAg nanoparticles for enhanced electrocatalysis of ethanol oxidation reaction

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
4
1

Citation Types

0
5
0

Year Published

2021
2021
2024
2024

Publication Types

Select...
8

Relationship

1
7

Authors

Journals

citations
Cited by 18 publications
(6 citation statements)
references
References 51 publications
0
5
0
Order By: Relevance
“…Several in-situ Infrared spectroscopy (IR) and in-situ Raman spectroscopy measurements are reported that the generated oxygen-containing or carbon-containing C 2 intermediates species would poison electrocatalysts, thereby capturing the exposed reaction sites on the surface of electrocatalysts. [14][15][16][17] So, developing efficient electrocatalysts has become more urgent.…”
Section: Introductionmentioning
confidence: 99%
“…Several in-situ Infrared spectroscopy (IR) and in-situ Raman spectroscopy measurements are reported that the generated oxygen-containing or carbon-containing C 2 intermediates species would poison electrocatalysts, thereby capturing the exposed reaction sites on the surface of electrocatalysts. [14][15][16][17] So, developing efficient electrocatalysts has become more urgent.…”
Section: Introductionmentioning
confidence: 99%
“…41 The lower intensity of O K-edge features in the Pd/Co 1 Fe 3 − LDH/NF catalyst indicated crystal structure distortion of 6a), evidencing the reduction reaction of oxidized PdO into metallic Pd. 42 It could be seen that Pd/Co 1 Fe 3 −LDH/NF exhibited the highest intensities and active areas than Pd/NF, suggesting that Pd/Co 1 Fe 3 − LDH/NF had more active sites and higher utilization efficiency. This was due to the homogeneous dispersion of Pd nanoparticles on Co 1 Fe 3 −LDH/NF with a high specific surface area structure, which could remarkably facilitate electron and mass transfer between the electrolyte and the catalyst.…”
Section: Resultsmentioning
confidence: 92%
“…The electrocatalytic activity of Pd/Co 1 Fe 3 –LDH/NF was evaluated in a N 2 -saturated KOH (1.0 M) solution, while Pd/NF, Pd/C (20%), Pt/C (20%), Co 1 Fe 3 –LDH/NF, and NF were applied as comparison samples. The cyclic voltammograms (CV) of Pd/Co 1 Fe 3 –LDH/NF and Pd/NF electrodes each exhibited two pronounced cathode peaks ranging from −0.6 to −0.25 V (Figure a), evidencing the reduction reaction of oxidized PdO into metallic Pd . It could be seen that Pd/Co 1 Fe 3 –LDH/NF exhibited the highest intensities and active areas than Pd/NF, suggesting that Pd/Co 1 Fe 3 –LDH/NF had more active sites and higher utilization efficiency.…”
Section: Resultsmentioning
confidence: 99%
“…To further analyze the crystal structure of Pd 62 Ag 38 PNWs, XRD measurement was performed on Pd 62 Ag 38 PNWs. Figure E shows that the XRD peak of Pd 62 Ag 38 PNWs is located between the standard XRD peaks of Pd (PDF# 46-1043) and Ag (PDF# 04-0783), indicating that Pd and Ag form an alloy phase. , Figure G is the HRTEM image of Pd 62 Ag 38 PNWs, which shows that the lattice width of Pd 62 Ag 38 PNWs is 0.233 nm, corresponding to the (111) plane of the PdAg alloy. , In summary, Pd 62 Ag 38 PNWs form a PdAg alloy phase. The surface composition and element valence of Pd 62 Ag 38 PNWs were measured by XPS. , The results are shown in Figure S4.…”
Section: Resultsmentioning
confidence: 99%