2013
DOI: 10.1016/j.elecom.2012.11.016
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Lightweight, flexible, nanorod electrode with high electrocatalytic activity

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Cited by 10 publications
(13 citation statements)
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“…Silver paste was from Dupont (Dupont 4929 N, DuPont Corporation, Wilmington, DE, USA). Aqueous CNT solutions (1 mg ml À 1 ) with sodium dodecylbenzenesulphonate (SDBS) (1:10 in quality ratio) as a surfactant were prepared according to the Hu et al 40 Gold nanorods were synthesized in accordance with our previous work 41 ).…”
Section: Methodsmentioning
confidence: 99%
“…Silver paste was from Dupont (Dupont 4929 N, DuPont Corporation, Wilmington, DE, USA). Aqueous CNT solutions (1 mg ml À 1 ) with sodium dodecylbenzenesulphonate (SDBS) (1:10 in quality ratio) as a surfactant were prepared according to the Hu et al 40 Gold nanorods were synthesized in accordance with our previous work 41 ).…”
Section: Methodsmentioning
confidence: 99%
“…In comparison with other Pd catalysts33 and Pt‐based alloy catalysts,34 the EASA of Pd nanotubes with 150 nm wall thickness is even better. It is also about four times that of gold nanorod electrodes 35…”
Section: Resultsmentioning
confidence: 91%
“…The EASAs of Pd nanotubes with 77, 101, and 150 nm wall thickness are 6.5, 10.6, and 83.2 m 2 g À1 ,r espectively.T he thicker wall probably makes the tube surfacer ougher, and therefore enables them to have ab iggerE ASA. [35] The electrochemical stability of Pd nanotubes for C 2 H 5 OH electrooxidation wasi nvestigated by chronoamperometric experiments at À0.1 Vv ersus SCE in as olution containing C 2 H 5 OH (1.0 m) andK OH (1.0 m) at room temperature (Figure 4b). [35] The electrochemical stability of Pd nanotubes for C 2 H 5 OH electrooxidation wasi nvestigated by chronoamperometric experiments at À0.1 Vv ersus SCE in as olution containing C 2 H 5 OH (1.0 m) andK OH (1.0 m) at room temperature (Figure 4b).…”
Section: Electrocatalytic Performance Of Pd Nanotubesmentioning
confidence: 99%
“…The oxidation peak current density for tail‐side exposed electrode is also found to be much higher than head‐side exposed electrode (Figure F), and both of them exhibited a good linear relationship between the oxidation peak current densities and scan rate, indicating that the reactions for C 2 H 5 OH electro‐oxidation on these two kinds of electrodes are surface‐controlled processes . In addition, the ratio of anodic oxidation peak current density to cathodic reduction peak current density ( I pa / I pc ) for both electrodes decreased upon increasing of scan rate (Figure S2, Supporting Information), while the ratio for head‐side exposed electrode is significantly smaller than that of tail‐side exposed electrode, confirming that both two electrodes have good electro‐oxidation abilities, and surface Au oxides contributed mainly to the oxidation of C 2 H 5 OH …”
mentioning
confidence: 90%