赤铁矿
化学气相沉积
微晶
材料科学
纳米棒
纹理(宇宙学)
各向异性
微观结构
基质(水族馆)
磁各向异性
磁电阻
薄膜
化学工程
磁场
纳米技术
矿物学
化学
磁化
复合材料
冶金
光学
地质学
工程类
人工智能
计算机科学
图像(数学)
海洋学
物理
量子力学
作者
Daniel Stadler,Thomas Brede,Danny Schwarzbach,Fernando Maccari,Thomas Fischer,Oliver Gutfleisch,Cynthia A. Volkert,Sanjay Mathur
出处
期刊:Nanoscale advances
[Royal Society of Chemistry]
日期:2019-01-01
卷期号:1 (11): 4290-4295
被引量:5
摘要
Chemical vapor deposition of iron pentacarbonyl (Fe(CO)5) in an external magnetic field (B = 1.00 T) was found to significantly affect the microstructure and anisotropy of as-deposited iron crystallites that could be transformed into anisotropic hematite (α-Fe2O3) nanorods by aerobic oxidation. The deterministic influence of external magnetic fields on CVD deposits was found to be substrate-independent as demonstrated by the growth of anisotropic α-Fe columns on FTO (F:SnO2) and Si (100), whereas the films deposited in the absence of the magnetic field were constituted by isotropic grains. TEM images revealed gradual increase in average crystallite size in correlation to the increasing field strength and orientation, which indicates the potential of magnetic field-assisted chemical vapor deposition (mfCVD) in controlling the texture of the CVD grown thin films. Given the facet-dependent activity of hematite in forming surface-oxygenated intermediates, exposure of crystalline facets and planes with high atomic density and electron mobilities is crucial for oxygen evolution reactions. The field-induced anisotropy in iron nanocolumns acting as templates for growing textured hematite pillars resulted in two-fold higher photoelectrochemical efficiency for hematite films grown under external magnetic fields (J = 0.050 mA cm-2), when compared to films grown in zero field (J = 0.027 mA cm-2). The dark current measurements indicated faster surface kinetics as the origin of the increased catalytic activity.
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