2015
DOI: 10.1039/c5nr01493j
|View full text |Cite
|
Sign up to set email alerts
|

Constructing Fe2O3/TiO2 core–shell photoelectrodes for efficient photoelectrochemical water splitting

Abstract: In this study, plasma enhanced chemical vapor deposition (PECVD) was utilized to co-axially modify hydrothermally grown Fe2O3 nanorod arrays by depositing a TiO2 overlayer to create Fe2O3/TiO2 core-shell photoelectrodes. Comprehensive structural (XRD, SEM, TEM) and compositional (XPS) analyses were performed to understand the effects of the TiO2 shell on the PEC activities of the Fe2O3 core. It was revealed that the heterojunction structure formed between TiO2 and Fe2O3, significantly improved the separation e… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
2

Citation Types

1
30
0

Year Published

2015
2015
2022
2022

Publication Types

Select...
5
3

Relationship

2
6

Authors

Journals

citations
Cited by 73 publications
(31 citation statements)
references
References 57 publications
(56 reference statements)
1
30
0
Order By: Relevance
“…In Figure S5b (Supporting Information), the Co 2p 3/2 and Co 2p 1/2 orbits with a splitting of 15.4 eV are observed at 779.2 and 794.6 eV along with two shakeup satellites, revealing the coexistence of Co 3+ and Co 2+ in Co 3 O 4 . Furthermore, as shown in Figure S5c (Supporting Information), Fe 2p 3/2 and Fe 2p 1/2 orbits with a splitting of 13.4 eV were observed at 711 and 724.6 eV, which confirm the presence of Fe 3+ . Figure S6a (Supporting Information) shows the O 1s spectra of NiO/Co 3 O 4 microcubes, the peak of O1 at 529.2 eV represents the typical metal–oxygen bond, the peak of O2 at 531.1 eV corresponds to the hydroxyl group (OH) on the surfaces of NiO/Co 3 O 4 , and the peak of O3 at 532.5 eV can be ascribed to chemically and physically adsorbed water on the material surface .…”
Section: Resultssupporting
confidence: 75%
“…In Figure S5b (Supporting Information), the Co 2p 3/2 and Co 2p 1/2 orbits with a splitting of 15.4 eV are observed at 779.2 and 794.6 eV along with two shakeup satellites, revealing the coexistence of Co 3+ and Co 2+ in Co 3 O 4 . Furthermore, as shown in Figure S5c (Supporting Information), Fe 2p 3/2 and Fe 2p 1/2 orbits with a splitting of 13.4 eV were observed at 711 and 724.6 eV, which confirm the presence of Fe 3+ . Figure S6a (Supporting Information) shows the O 1s spectra of NiO/Co 3 O 4 microcubes, the peak of O1 at 529.2 eV represents the typical metal–oxygen bond, the peak of O2 at 531.1 eV corresponds to the hydroxyl group (OH) on the surfaces of NiO/Co 3 O 4 , and the peak of O3 at 532.5 eV can be ascribed to chemically and physically adsorbed water on the material surface .…”
Section: Resultssupporting
confidence: 75%
“…In Figure S13 (Supporting Information), the LSV and I-t curves under chopped illumination of the photoanode are provided. [57] As for the TiO 2 /BaTiO 3 and Fe 2 O 3 /TiO 2 core/shell structures, [58,59] the photocurrent of 1.25 and 0.9 mA cm −2 at 1.23 V (vs RHE) in 1 m NaOH is reported. It is worth pointing out that the photocurrent density of the MOFs-derived Co 3 O 4 /TiO 2 /Si NR in both alkaline and neutral electrolyte, to our best of knowledge, is comparable to or even better than previously reported on the TiO 2 -based photoanodes (Table S2, Supporting Information).…”
Section: Resultsmentioning
confidence: 99%
“…Considering the above‐mentioned issues with hematite, the requirement for an overpotential, which arises due to the sluggish oxygen evolving reaction (OER) kinetics and the presence of surface trap states, is of particular interest. To overcome these drawbacks and improve the PEC performance, surface modification with oxygen evolution catalysts (OEC) to overcome the OER kinetics issue have been employed, while surface passivation by various treatments have been shown to reduce the density of surface traps . Ruthenium oxide (RuO 2 ) and iridium oxide (IrO 2 ) have been demonstrated as cocatalysts with hematite to improve the OER activity, but Ru and Ir are precious metals with moderate OER activity, thus limiting their commercial potential .…”
mentioning
confidence: 99%