Qin Dong-Dong, He Cai-Hua, Li Yang, Trammel Antonio C, Gu Jing, Chen Jing, Yan Yong, Shan Duo-Liang, Wang Qiu-Hong, Quan Jing-Jing, Tao Chun-Lan, Lu Xiao-Quan
Key Lab of Bioelectrochemistry and Environmental Analysis of Gansu, College of Chemistry and Chemical Engineering, Northwest Normal University, Lanzhou, 730070, P. R. China.
Department of Chemistry & Biochemistry, San Diego State University, San Diego, CA, 92182, USA.
ChemSusChem. 2017 Jul 10;10(13):2796-2804. doi: 10.1002/cssc.201700501. Epub 2017 Jun 1.
Zinc oxide is regarded as a promising candidate for application in photoelectrochemical water oxidation due to its higher electron mobility. However, its instability under alkaline conditions limits its application in a practical setting. Herein, we demonstrate an easily achieved wet-chemical route to chemically stabilize ZnO nanowires (NWs) by protecting them with a thin layer Fe O shell. This shell, in which the thickness can be tuned by varying reaction times, forms an intact interface with ZnO NWs, thus protecting ZnO from corrosion in a basic solution. The reverse energetic heterojunction nanowires are subsequently activated by introducing an amorphous iron phosphate, which substantially suppressed surface recombination as a passivation layer and improved photoelectrochemical performance as a potential catalyst. Compared with pure ZnO NWs (0.4 mA cm ), a maximal photocurrent of 1.0 mA cm is achieved with ZnO/Fe O core-shell NWs and 2.3 mA cm was achieved for the PH -treated NWs at 1.23 V versus RHE. The PH low-temperature treatment creates a dual function, passivation and catalyst layer (Fe PO ), examined by X-ray photoelectron spectroscopy, TEM, photoelectrochemical characterization, and impedance measurements. Such a nano-composition design offers great promise to improve the overall performance of the photoanode material.
由于具有较高的电子迁移率,氧化锌被认为是一种有前途的光电化学水氧化应用候选材料。然而,其在碱性条件下的不稳定性限制了它在实际应用中的使用。在此,我们展示了一种易于实现的湿化学路线,通过用一层薄的FeO壳层保护氧化锌纳米线(NWs)来对其进行化学稳定。该壳层的厚度可以通过改变反应时间来调节,它与氧化锌纳米线形成了一个完整的界面,从而保护氧化锌在碱性溶液中不被腐蚀。随后,通过引入非晶态磷酸铁来激活反向能量异质结纳米线,其作为钝化层可大幅抑制表面复合,并作为潜在催化剂提高光电化学性能。与纯氧化锌纳米线(0.4 mA cm)相比, 氧化锌/FeO核壳纳米线在相对于可逆氢电极(RHE)为1.23 V时实现了最大光电流1.0 mA cm,而经过PH处理的纳米线则达到了2.3 mA cm。通过X射线光电子能谱、透射电子显微镜、光电化学表征和阻抗测量研究发现,PH低温处理产生了钝化和催化剂层(FePO)的双重功能。这种纳米复合设计为提高光阳极材料的整体性能带来了巨大希望。