Growth and Characterization of Epitaxial FeWO4 Thin Films with Controlled Oxygen Stoichiometry

IF 7 2区 材料科学 Q2 CHEMISTRY, PHYSICAL
John G. Hylak, , , Thomas T. Tran, , , Andriy Zakutayev, , and , Harry A. Atwater*, 
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Abstract

We report the growth of single-phase epitaxial FeWO4 thin films, using plasma-assisted molecular beam epitaxy, and investigate structural, optical, and electronic properties. The FeWO4 films grow in (100) orientation on c-plane sapphire (0001) substrates and exhibit 3 rotational twin variants where FeWO4 [001] is aligned to sapphire [100] equivalent in-plane directions. X-ray diffraction measurements indicate that the epitaxial FeWO4 (100) structure is optimized when 80–100 W of rf power is applied to an atomic oxygen source during growth, yielding films with minimal strain and impurity phases or other orientations. In films grown with 120 W of rf power, FeWO4 crystallites develop inhomogeneous and homogeneous strains and are potentially contaminated with Fe3+ oxide phase impurities. In films grown with 60 W of rf power, FeWO4 crystallites do not form fully epitaxial layers. X-ray photoelectron spectroscopy indicates that the structural changes are correlated with the Fe3+/Fe2+ oxidation state ratio increasing from 0.6–1.4 with rf power from 60–120 W. X-ray fluorescence spectroscopy indicates that the Fe/W composition ratio is also increasing from 1.1–1.8 with rf power from 60–120 W. Ultraviolet and visible optical absorption spectra indicate a 1.8 ± 0.1 eV band gap with an additional interband absorption feature at 3.1 ± 0.1 eV in the 80–100 W films, with similar onsets observed in the 60 W films. In the 120 W films, the higher lying transition is shifted to 2.7 ± 0.1 eV due to the Fe3+ enrichment. Electrical resistivity decreases over 2 orders of magnitude with oxidation from 104–105 Ω cm in 60 W films to 120 ± 10 Ω cm in 120 W films. Thermopower measurements show p-type to n-type conductivity conversion when oxidation states shift from Fe2+ majority in the 100 W films to Fe3+ majority in the 120 W films. We conclude that electron polaron hopping driven by Fe3+ is a dominant transport mechanism and a source of n-type conductivity in overoxidized FeWO4 films.

Abstract Image

控制氧化学计量法制备外延FeWO4薄膜
我们报道了利用等离子体辅助分子束外延生长的单相外延FeWO4薄膜,并研究了其结构、光学和电子特性。FeWO4薄膜在c面蓝宝石(0001)衬底上以(100)取向生长,并表现出3个旋转孪晶变体,其中FeWO4[001]与蓝宝石[100]在等效平面方向上对齐。x射线衍射测量表明,在生长过程中,在原子氧源上施加80-100 W的射频功率,FeWO4(100)外延结构得到优化,得到应变最小、杂质相或其他取向的薄膜。在120w的rf功率下生长的薄膜中,FeWO4晶体发育为非均匀和均匀的菌株,并且可能被Fe3+氧化物相杂质污染。在60 W射频功率下生长的薄膜中,FeWO4晶体不能形成完全外延层。x射线光电子能谱分析表明,Fe3+/Fe2+的氧化态比在60 ~ 120 W范围内从0.6 ~ 1.4增加与结构变化有关。x射线荧光光谱分析表明,当射频功率为60 ~ 120 W时,Fe/W组成比也从1.1 ~ 1.8增加。紫外和可见光吸收光谱表明,在80-100 W的薄膜中存在1.8±0.1 eV的带隙和3.1±0.1 eV的带间吸收特征,在60 W的薄膜中也观察到类似的现象。在120w的薄膜中,由于Fe3+的富集,高压电跃迁到2.7±0.1 eV。电阻率随着氧化从60w薄膜的104-105 Ω cm降低到120w薄膜的120±10 Ω cm,降低了2个数量级。当氧化态从100 W薄膜中的Fe2+为主转变为120 W薄膜中的Fe3+为主时,热功率测量显示了p型到n型的电导率转换。我们得出结论,Fe3+驱动的电子极化子跳变是过度氧化FeWO4薄膜的主要输运机制和n型电导率的来源。
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来源期刊
Chemistry of Materials
Chemistry of Materials 工程技术-材料科学:综合
CiteScore
14.10
自引率
5.80%
发文量
929
审稿时长
1.5 months
期刊介绍: The journal Chemistry of Materials focuses on publishing original research at the intersection of materials science and chemistry. The studies published in the journal involve chemistry as a prominent component and explore topics such as the design, synthesis, characterization, processing, understanding, and application of functional or potentially functional materials. The journal covers various areas of interest, including inorganic and organic solid-state chemistry, nanomaterials, biomaterials, thin films and polymers, and composite/hybrid materials. The journal particularly seeks papers that highlight the creation or development of innovative materials with novel optical, electrical, magnetic, catalytic, or mechanical properties. It is essential that manuscripts on these topics have a primary focus on the chemistry of materials and represent a significant advancement compared to prior research. Before external reviews are sought, submitted manuscripts undergo a review process by a minimum of two editors to ensure their appropriateness for the journal and the presence of sufficient evidence of a significant advance that will be of broad interest to the materials chemistry community.
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