Mor Gopal K, Prakasam Haripriya E, Varghese Oomman K, Shankar Karthik, Grimes Craig A
Department of Electrical Engineering and Materials Research Institute, The Pennsylvania State University, University Park, Pennsylvania 16802, USA.
Nano Lett. 2007 Aug;7(8):2356-64. doi: 10.1021/nl0710046. Epub 2007 Jul 3.
In an effort to obtain a material architecture suitable for high-efficiency visible spectrum water photoelectrolysis, herein we report on the fabrication and visible spectrum (380-650 nm) photoelectrochemical properties of self-aligned, vertically oriented Ti-Fe-O nanotube array films. Ti-Fe metal films of variable composition, iron content ranging from 69% to 3.5%, co-sputtered onto FTO-coated glass are anodized in an ethylene glycol + NH4F electrolyte. The resulting amorphous samples are annealed in oxygen at 500 degrees C, resulting in nanotubes composed of a mixed Ti-Fe-O oxide. Some of the iron goes into the titanium lattice substituting titanium ions, and the rest either forms alpha-Fe2O3 crystallites or remains in the amorphous state. Depending upon the Fe content, the band gap of the resulting films ranges from about 380 to 570 nm. The Ti-Fe oxide nanotube array films are utilized in solar spectrum water photoelectrolysis, demonstrating 2 mA/cm2 under AM 1.5 illumination with a sustained, time-energy normalized hydrogen evolution rate by water splitting of 7.1 mL/W.hr in a 1 M KOH solution with a platinum counter electrode under an applied bias of 0.7 V. The surface morphology, structure, elemental analysis, optical, and photoelectrochemical properties of the Ti-Fe oxide nanotube array films are considered.
为了获得适合高效可见光谱水光电解的材料结构,在此我们报告自对准、垂直取向的Ti-Fe-O纳米管阵列薄膜的制备及其可见光谱(380-650nm)光电化学性质。将铁含量在69%至3.5%之间的不同成分的Ti-Fe金属薄膜共溅射在涂有FTO的玻璃上,然后在乙二醇+NH4F电解液中进行阳极氧化。所得非晶样品在500℃的氧气中退火,得到由Ti-Fe-O混合氧化物组成的纳米管。部分铁进入钛晶格取代钛离子,其余的则形成α-Fe2O3微晶或保持非晶态。根据铁含量的不同,所得薄膜的带隙范围约为380至570nm。Ti-Fe氧化物纳米管阵列薄膜用于太阳光谱水光电解,在0.7V的外加偏压下,以铂对电极在1M KOH溶液中,AM 1.5光照下显示出2mA/cm2的电流密度,通过水分解的持续时间-能量归一化析氢速率为7.1mL/W·hr。我们还研究了Ti-Fe氧化物纳米管阵列薄膜的表面形貌、结构、元素分析、光学和光电化学性质。