Zhi Yin, Leng Xueyang, Wang Dutong, Xu Lingling
Key Laboratory of Photonic and Electronic Bandgap Materials, Ministry of Education, School of Physics and Electronic Engineering, Harbin Normal University, Harbin 150025, China.
ACS Appl Mater Interfaces. 2024 Oct 9;16(40):54058-54066. doi: 10.1021/acsami.4c14137. Epub 2024 Sep 30.
α-FeO is a very attractive photoanode for photoelectrochemical (PEC) water decomposition. However, its short diffusion length, poor conductivity, and fast charge-carrier recombination severely limit device efficiency. Here, coloading an AlO passivation layer and a CoO cocatalyst onto Ti-doped α-FeO was carried out to promote PEC water oxidation by improving charge separation and transfer at the electrode/electrolyte interface and inhibiting photocarrier recombination. The optimized Ti:FeO/AlO/CoO photoanode shows a large photocurrent density of 1.41 mA cm at 1.23 V vs reversible hydrogen electrode, which is 47 times greater than that of a pristine Ti:FeO photoanode. The dual modifications with a combined passivation layer and cocatalyst on the photoanode verify a valuable way for solar energy conversion in PEC water oxidation.
α-FeO是一种极具吸引力的用于光电化学(PEC)水分解的光阳极。然而,其短扩散长度、低电导率以及快速的电荷载流子复合严重限制了器件效率。在此,通过在掺钛α-FeO上共负载AlO钝化层和CoO助催化剂,以改善电极/电解质界面处的电荷分离和转移并抑制光载流子复合,从而促进PEC水氧化。优化后的Ti:FeO/AlO/CoO光阳极在相对于可逆氢电极1.23 V时显示出1.41 mA cm的大光电流密度,这比原始Ti:FeO光阳极的光电流密度大47倍。在光阳极上采用钝化层和助催化剂的双重改性验证了PEC水氧化中太阳能转换的一种有价值的方法。