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. 2024 Feb 27;4(5):2300318.
doi: 10.1002/smsc.202300318. eCollection 2024 May.

Boosting the Solar Water Oxidation Performance of Fe2O3 Photoanode via Embedding Laser-Generated Pt Nanocrystals

Affiliations

Boosting the Solar Water Oxidation Performance of Fe2O3 Photoanode via Embedding Laser-Generated Pt Nanocrystals

Fan Li et al. Small Sci. .

Abstract

α-Fe2O3 with suitable band structure, good chemical stability, and easy preparation, is a potential photoanode material. However, the key to enhance the performance of α-Fe2O3 photoanode is to improve the transport characteristics of bulk carriers. It is expected to form a Schottky barrier to improve the carrier separation efficiency by embedding metal nanoparticles into the matrix, but the process is still challenging. Herein, a strategy of forming the Schottky barrier is shown to improve bulk carrier transport dynamics by embedding laser-generated Pt nanocrystals in α-Fe2O3 photoanode, which achieves photocurrent densities of up to 1.16 mA cm-2 at 1.23 VRHE (from original 0.21 mA cm-2). This work provides another way to promote the carrier transfer and separation of α-Fe2O3, which is of great significance to improve the photoelectrochemical water splitting performance.

Keywords: composite Fe2O3@Pt; nanocrystals embedding; nanoporous α‐Fe2O3; photoanodes; photoelectrochemical water splitting.

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Conflict of interest statement

The authors declare no conflict of interest.

Figures

Figure 1
Figure 1
a) Schematic illustration of Pt nanocrystals generated by PLIL. b) TEM image and c) HRTEM image of Pt nanocrystals. d) Size distribution of Pt nanocrystals (insert: photographs of Pt solution before and after PLIL).
Figure 2
Figure 2
a) Surface SEM images of Fe2O3 and b) Fe2O3@Pt‐2 films. c) Cross‐section SEM images of Fe2O3 and d) Fe2O3@Pt‐2 films. e) Optical microscopies of the Fe2O3 precursor and f) Fe2O3@Pt‐2 precursor. g) TEM and h) HRTEM images of Fe2O3@Pt‐2 film.
Figure 3
Figure 3
a) Schematic illustration of Fe2O3@Pt films. b) J–V curve of Fe2O3 and different Fe2O3@Pt films. c) Transient photocurrent measurements of Fe2O3 and Fe2O3@Pt‐2 films. d) IPCE spectra. e) ABPE spectra. f) Electrochemical impedance spectra (EIS) curves under irradiation of Fe2O3 and Fe2O3@Pt‐2 film.
Figure 4
Figure 4
a) The calculated current density flux and integrated current density (J abs) of Fe2O3 and Fe2O3@ Pt‐2 films. b) Surface charge injection efficiency (η inj) of Fe2O3 and Fe2O3@ Pt‐2 films. c) Bulk charge separation efficiency (η sep) of Fe2O3 and Fe2O3@ Pt‐2 films. d) Open‐circuit potential of Fe2O3 and Fe2O3@Pt‐2 films. Schematic diagram of band structures of Fe2O3 and Fe2O3@Pt‐2 films: e) before and f) after contacting with the electrolytes.
Figure 5
Figure 5
a) TEM image of Au nanocrystals (insert: HRTEM image). b) HRTEM images of Fe2O3@Au films. c) J–V curve of Fe2O3 and Fe2O3@Au films. d) IPCE spectra. e) EIS curves under irradiation of Fe2O3 and Fe2O3@Au film. f) Open‐circuit potential of Fe2O3 and Fe2O3@Au films.

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