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Review
. 2016;8(1):1-12.
doi: 10.1007/s40820-015-0063-3. Epub 2015 Oct 28.

Recent Advances in Visible-Light-Driven Photoelectrochemical Water Splitting: Catalyst Nanostructures and Reaction Systems

Affiliations
Review

Recent Advances in Visible-Light-Driven Photoelectrochemical Water Splitting: Catalyst Nanostructures and Reaction Systems

Xiaoping Chen et al. Nanomicro Lett. 2016.

Abstract

Photoelectrochemical (PEC) water splitting using solar energy has attracted great attention for generation of renewable hydrogen with less carbon footprint, while there are enormous challenges that still remain for improving solar energy water splitting efficiency, due to limited light harvesting, energy loss associated to fast recombination of photogenerated charge carriers, as well as electrode degradation. This overview focuses on the recent development about catalyst nanomaterials and nanostructures in different PEC water splitting systems. As photoanode, Au nanoparticle-decorated TiO2 nanowire electrodes exhibited enhanced photoactivity in both the UV and the visible regions due to surface plasmon resonance of Au and showed the largest photocurrent generation of up to 710 nm. Pt/CdS/CGSe electrodes were developed as photocathode. With the role of p-n heterojunction, the photoelectrode showed high stability and evolved hydrogen continuously for more than 10 days. Further, in the Z-scheme system (Bi2S3/TNA as photoanode and Pt/SiPVC as photocathode at the same time), a self-bias (open-circuit voltage V oc = 0.766 V) was formed between two photoelectrodes, which could facilitate photogenerated charge transfers and enhance the photoelectrochemical performance, and which might provide new hints for PEC water splitting. Meanwhile, the existing problems and prospective solutions have also been reviewed.

Keywords: Heterojuction; Hybrid systems; Nanostructures; Photoelectrochemical water splitting; Reaction system.

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Figures

Fig. 1
Fig. 1
The schematic setup of PEC water splitting system
Fig. 2
Fig. 2
Semiconductors coated on substrate as photoanode for PEC water splitting [15]
Fig. 3
Fig. 3
SEM images of titanium dioxide arrays [29, 34]
Fig. 4
Fig. 4
The overlapping in band gaps between two different photocatalysts and the electron-trap mechanism
Fig. 5
Fig. 5
Schematic interfacial electron transfer between TiO2 and Bi2WO6 [47]
Fig. 6
Fig. 6
The diagram of BiVO4/WO3 heterojunction and electron transport process [58]
Fig. 7
Fig. 7
FeOOH as photoanode for photoelectrochemical water splitting [60]
Fig. 8
Fig. 8
The scheme of the nanostructure of the CdS/TiO2 nanoarrays and charge-transfer mechanism [68]
Fig. 9
Fig. 9
Semiconductors coated on substrates as photocathode for PEC water splitting [15]
Fig. 10
Fig. 10
SEM image of a p–n Cu2O homojunction [78]
Fig. 11
Fig. 11
Schematic representation of the electrode structure of the surface-protected Cu2O electrode [80]
Fig. 12
Fig. 12
EDX mapping of CdS/CuGaSe2 sample with chemical bath deposition for 1 min [18]
Fig. 13
Fig. 13
n-type and p-type semiconductors coated on substrates as photoanode and photocathode, respectively, for PEC water splitting (Z-scheme) [15]
Fig. 14
Fig. 14
Reaction and band model in photovoltaic cell using p-type CaFe2O4 and n-type TiO2 semiconductor electrodes [83]
Fig. 15
Fig. 15
The energy-level diagram of the self-biasing PEC cell assembled with Bi2S3/TNA photoanode and Pt/SiPVC photocathode under short-circuit situation [19]

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