Zhou Yanhong, Zhang Yiran, Jing Boyang, Liu Xiaoyuan, Wang Debao
Key Laboratory of Inorganic Synthetic and Applied Chemistry, College of Chemistry and Molecular Engineering, Qingdao University of Science and Technology, Qingdao 266042, China.
Nanomaterials (Basel). 2025 May 20;15(10):767. doi: 10.3390/nano15100767.
Hematite (FeO) has been accepted as a promising and potential photo(electro)catalyst. However, its poor carrier separation and transfer efficiency has limited its application for photoelectrocatalytic (PEC) water oxidation. Herein, a S-doped FeOOH (S:FeOOH) layer was rationally designed and grown on FeO to construct a S:FeOOH/FeO composite photoanode. The obtained S:FeOOH/FeO photoanodes were fully characterized. The surface injection efficiency for FeO was then significantly increased with a high η value of 92.8%, which increases to 2.98 times for FeO and 2.16 times for FeOOH/FeO, respectively. With 2.43 mA cm at 1.23 V, the optimized S:FeOOH/FeO photoanode was entrusted with a higher photocurrent density. The onset potential for S:FeOOH/FeO cathodically shifts 70 mV over FeO. The improved PEC performance suggests that the S:FeOOH layer acts as ultrafast transport channels for holes at the photoanode/electrolyte interface, suppressing surface charge recombination. A Z-scheme band alignment between FeO and S:FeOOH was deduced from the UV-Vis and UPS spectra to promote charge transfer. This method provides an alternative for the construction of photoanodes with enhanced PEC water splitting performance.
赤铁矿(FeO)已被公认为一种有前景的潜在光(电)催化剂。然而,其较差的载流子分离和转移效率限制了其在光电催化(PEC)水氧化中的应用。在此,合理设计并在FeO上生长了一层硫掺杂的FeOOH(S:FeOOH),以构建S:FeOOH/FeO复合光阳极。对所得的S:FeOOH/FeO光阳极进行了全面表征。FeO的表面注入效率随后显著提高,η值高达92.8%,分别是FeO的2.98倍和FeOOH/FeO的2.16倍。在1.23 V下,优化后的S:FeOOH/FeO光阳极具有2.43 mA cm的光电流密度。S:FeOOH/FeO的起始电位相对于FeO向阴极方向移动了70 mV。PEC性能的改善表明,S:FeOOH层在光阳极/电解质界面充当空穴的超快传输通道,抑制表面电荷复合。通过紫外-可见光谱和紫外光电子能谱推断出FeO和S:FeOOH之间的Z型能带排列,以促进电荷转移。该方法为构建具有增强PEC水分解性能的光阳极提供了一种替代方案。