Fabrication of CuFe2O4/α-Fe2O3 Composite Thin Films on FTO Coated Glass and 3-D Nanospike Structures for Efficient Photoelectrochemical Water Splitting

材料科学 制作 复合数 薄膜 纳米技术 复合材料 化学工程 医学 工程类 病理 替代医学
作者
Shabeeb Hussain,Shazia Hussain,Aashir Waleed,Mohammad Mahdi Tavakoli,Zilong Wang,Shihe Yang,Zhiyong Fan,Muhammad Arif Nadeem
出处
期刊:ACS Applied Materials & Interfaces [American Chemical Society]
卷期号:8 (51): 35315-35322 被引量:80
标识
DOI:10.1021/acsami.6b12460
摘要

Recently, photoelectrochemical conversion (PEC) of water into fuel is attracting great attention of researchers due to its outstanding benefits. Herein, a systematic study on PEC of water using CuFe2O4/ α-Fe2O3 composite thin films is presented. CuFe2O4/ α-Fe2O3 composite thin films were deposited on two different substrates; (1) planner FTO glass and (2) 3-dimensional nanospike (NSP). The films on both substrates were characterized and tested as anode material for photoelectrochemical water splitting reaction. During PEC studies, it was observed that the ratio between two components of composite is crucial and highest PEC activity results were achieved by 1:1 component ratio (CF-1) of CuFe2O4 and α-Fe2O3. The CF-1 ratio sample deposited on planar FTO substrate provided a photocurrent density of 1.22 mA/cm2 at 1.23 VRHE which is 1.9 times higher than bare α-Fe2O3 sample. A significant PEC activity outperformance was observed when CF-1 ratio composite thin films were deposited on 3D NSP. The highest photocurrent density of 2.26 mA/cm2 at 1.23 VRHE was achieved for 3D NSP sample which is around 3.6 times higher than photocurrent density generated by α-Fe2O3 thin film only. The higher photocurrent densities of 3D nanostructured devices compared to planar one are attributed to the enhanced light trapping and increased surface area for photoelectrochemical water oxidation on the surface. The difference between valence and conduction bands of CuFe2O4 and α-Fe2O3 allows better separation of photogenerated electrons and holes at the CuFe2O4/ α-Fe2O3 interface which makes it more active for photoelectrochemical water splitting.
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