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APPLIED SURFACE SCIENCE · 2017 · IF 3.387

Boosting photoelectrochemical performance of hematite photoanode with TiO2 underlayer by extremely rapid high temperature annealing

Dan Wang,Ying Chen,Yang Zhang,Xintong Zhang,Norihiro Suzuki,Chiaki Terashima

Extremely rapid high temperature annealing (ER-HTA) was used to boost the photoelectrochemical (PEC) performance of hematite thin film deposited on a TiO 2 nanosheet-modified SnO 2 :F substrate (FTO-TN-HM). The PEC performance of FTO-TN-HM photoanodes were strongly enhanced with increasing ER-HTA temperatures from 700 to 820   °C with a holding time as short as 30   s. The photocurrent density of FTO-TN-HM photoanode treated by ER-HTA at 800   °C was 0.49   mA   cm -2 and interfacial hole transfer efficiency of 32% was achieved at 1.23   V vs. RHE, which were 18.8 and 16 times as great as FTO-TN-HM photoanodes annealed at 500   °C for 30   min, respectively. The effect of ER-HTA on the PEC performance of FTO-TN-HM photoanodes were studied comparatively, which suggested that the improved crystallinity, decreased recombination through surface states, and enhanced interfacial Ti 4+ diffusion all contributed to their advanced PEC performance. Our studies confirm that the ER-HTA treatment is an effective method to improve the PEC properties of hematite photoanodes with TiO 2 underlayer and might be applicable for other semiconducting photoelectrodes to get better PEC performance.

研究领域: 材料科学 · 能源科学
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Advanced Materials Interfaces · 2020 ·Vol. 7 ·期 6 ·1901947 · IF 4.948

Ion Sputtering–Assisted Double-Side Interfacial Engineering for CdIn2S4 Photoanode toward Improved Photoelectrochemical Water Splitting

Weiwei Xu,Wei Tian,Linxing Meng,Fengren Cao,Liang Li

Due to its suitable band energy level and small band gap, CdIn 2 S 4 is a promising photoanode for photoelectrochemical (PEC) water splitting. Nevertheless, the serious charge recombination at the back contact and photoelectrode/electrolyte interface severely hinders its PEC activity. Herein, a facile magnetron ion-sputtering strategy is adopted to fabricate TiO 2 underlayer and NiO overlayer to modify both sides of CdIn 2 S 4 photoanode. The TiO 2 underlayer serves as an electron transport layer to promote electrons transfer from CdIn 2 S 4 to fluorine-doped tin oxide substrate and hinder holes' transportation, thus suppressing the charge recombination at the back contact. NiO, as a p-type semiconductor, forms a p-n heterojunction with CdIn 2 S 4 , inducing a built-in electric field to facilitate charge transport. Meanwhile, NiO overlayer acts as a co-catalyst to enhance surface reaction kinetics, and thereby improves the carrier injection efficiency at photoelectrode/electrolyte interface. As a result, the optimum TiO 2 /CdIn 2 S 4 /NiO photoanode exhibits photocurrent as high as 0.6 mA cm −2 at 1.23 V versus reversible hydrogen electrode, which is about 2.3 times that of bare CdIn 2 S 4 . This work provides an effective strategy to manipulate the charge carrier dynamics to improve the PEC activity of photoanode.

研究领域: 材料科学 · 能源科学
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