An Electrochemical Method for CuO Thin Film Deposition from Aqueous Solution

Poizot, Philippe; Hung, Chen-Jen; Nikiforov, Maxim P.; Bohannan, Eric W.; Switzer, Jay A.

doi:10.1149/1.1535753

Cited by 93 publications

(87 citation statements)

References 36 publications

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“…Since the potential region 0.9-1 V is more positive than the formal oxidation potential of the Ni(II)/Ni(III) redox transition [16], the Ni(II) formed from the NiEDTA complex decomposition is immediately oxidized to Ni(III) and/ or Ni(IV) species (i.e., NiOOH and/or NiO 2 insoluble compounds). In the negative scan, the nickel in high oxidation states is reduced back to Ni(II) as Ni(OH) 2 causing the redox waves centred at about 0.4 V. A similar electrochemical mechanism for the anodic electrodeposition of cobalt-based oxides from alkaline medium containing tartrate complexing species has recently been reported [17]. The initial formation (nucleation) of nickel oxyhydroxide on the electrode surface is slow, but the initially formed film accelerated its growth markedly.…”

Section: Electrodeposition Of Nickel Oxyhydroxide From Edta Alkaline supporting

confidence: 55%

Electrochemical deposition of nickel and nickel–thallium composite oxides films from EDTA alkaline solutions

Casella

Spera

2005

Journal of Electroanalytical Chemistry

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Section: Electrodeposition Of Nickel Oxyhydroxide From Edta Alkaline supporting

confidence: 55%

Electrochemical deposition of nickel and nickel–thallium composite oxides films from EDTA alkaline solutions

Casella

Spera

2005

Journal of Electroanalytical Chemistry

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“…Since Switzer and co-workers [19,20] introduced an electrochemical method for the first time as a synthetic route to ceramic films as well as polycrystalline CeO 2 powders, nano-sized metal oxides prepared by an electrochemical method have been an active research area. A number of metal oxides thin films, including ZnO [21,22], zirconium oxide [23], tungsten oxide [24], bismuth oxide [25], Cu 2 O [26] and CuO [27][28][29], have been synthesized via an electrochemical method. Reetz and co-workers [30][31][32][33] proposed a sacrificial anode electrochemical route to synthesize nanometal clusters.…”

Section: Introductionmentioning

confidence: 99%

Shape- and size-controlled electrochemical synthesis of cupric oxide nanocrystals

Yuan

Jiang

Lin

et al. 2007

Journal of Crystal Growth

117

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“…In contrast to previous work, 38,44 where epitaxial Cu 2 O layers were electrodeposited onto substrates relatively inert against oxidation, the systems Cu 2 O/Si and Cu 2 O/InP represent prototypes for epitaxial electrodeposition on substrates that are very susceptible to oxidation. Nevertheless, Cu 2 O layers can be grown on Si and InP substrates epitaxially and with high structural quality 17,19,20,24,25,45–49 …”

Section: Introductionmentioning

confidence: 99%

Epitaxial Growth of Cuprous Oxide Electrodeposited onto Semiconductor and Metal Substrates

Oba

Ernst

et al. 2005

Journal of the American Ceramic Society

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It is demonstrated that cuprous oxide (Cu2O) can be electrodeposited epitaxially onto silicon (Si) and indium phosphide (InP) (001) single‐crystalline substrates from aqueous solution. Epitaxial electrodeposition under these conditions is remarkable considering the strong driving force for the formation of amorphous native oxide layers on Si and InP substrates. To elucidate the growth mechanisms, the microstructure of the interfaces between the Cu2O layer and the two different substrates was investigated by TEM (transmission electron microscopy) in conjunction with XEDS (X‐ray energy‐dispersive spectroscopy) and EELS (electron energy‐loss spectroscopy). In both heteroepitaxial systems, the Cu2O layers have a unique but non‐trivial crystallographic orientation relationship (OR) with the substrate, which can be described as a 45° rotation around the common [001] axis representing the substrate normal. We show that this relationship minimizes the overall misfit between corresponding interatomic spacings of the two adjacent crystals. In apparent contradiction to the unique OR, TEM revealed that in both hetero‐systems the Cu2O layer is separated from the substrate by an amorphous interlayer. The thickness of the interlayer typically is a few nanometers. The presence of an amorphous interlayer contrasts with our experimental results on electrodeposited Cu2O on Au (001) single‐crystal substrates, also included in this article, where TEM shows the Cu2O epilayer in direct contact with the substrate. XEDS and EELS analysis of the chemical composition and bonding at Cu2O/Si and Cu2O/InP interfaces in the as‐grown state as well as after tempering revealed that the interlayer is mainly composed of SiO2 and InPO4, respectively. Most likely, the observed epitaxial layers on top of an amorphous interlayer evolve by nucleation of epitaxial Cu2O directly on the substrate. While simultaneous oxidation of the substrate leads to the formation of an amorphous layer, the epitaxial nuclei can laterally overgrow the oxide. Consequently, the local composition of the amorphous layer varies with the nature of the substrate.

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An Electrochemical Method for CuO Thin Film Deposition from Aqueous Solution

Cited by 93 publications

References 36 publications

Electrochemical deposition of nickel and nickel–thallium composite oxides films from EDTA alkaline solutions

Electrochemical deposition of nickel and nickel–thallium composite oxides films from EDTA alkaline solutions

Shape- and size-controlled electrochemical synthesis of cupric oxide nanocrystals

Epitaxial Growth of Cuprous Oxide Electrodeposited onto Semiconductor and Metal Substrates

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