Hoye Robert L Z, Muñoz-Rojas David, Musselman Kevin P, Vaynzof Yana, MacManus-Driscoll Judith L
†Department of Materials Science and Metallurgy, University of Cambridge, 27 Charles Babbage Road, Cambridge CB3 0FS, U.K.
‡LMGP, University Grenoble-Alpes, CNRS, F-38000 Grenoble, France.
ACS Appl Mater Interfaces. 2015 May 27;7(20):10684-94. doi: 10.1021/am5073589. Epub 2015 May 15.
A close-proximity atmospheric pressure chemical vapor deposition (AP-CVD) reactor is developed for synthesizing high quality multicomponent metal oxides for electronics. This combines the advantages of a mechanically controllable substrate-manifold spacing and vertical gas flows. As a result, our AP-CVD reactor can rapidly grow uniform crystalline films on a variety of substrate types at low temperatures without requiring plasma enhancements or low pressures. To demonstrate this, we take the zinc magnesium oxide (Zn(1-x)Mg(x)O) system as an example. By introducing the precursor gases vertically and uniformly to the substrate across the gas manifold, we show that films can be produced with only 3% variation in thickness over a 375 mm(2) deposition area. These thicknesses are significantly more uniform than for films from previous AP-CVD reactors. Our films are also compact, pinhole-free, and have a thickness that is linearly controllable by the number of oscillations of the substrate beneath the gas manifold. Using photoluminescence and X-ray diffraction measurements, we show that for Mg contents below 46 at. %, single phase Zn(1-x)Mg(x)O was produced. To further optimize the growth conditions, we developed a model relating the composition of a ternary oxide with the bubbling rates through the metal precursors. We fitted this model to the X-ray photoelectron spectroscopy measured compositions with an error of Δx = 0.0005. This model showed that the incorporation of Mg into ZnO can be maximized by using the maximum bubbling rate through the Mg precursor for each bubbling rate ratio. When applied to poly(3-hexylthiophene-2,5-diyl) hybrid solar cells, our films yielded an open-circuit voltage increase of over 100% by controlling the Mg content. Such films were deposited in short times (under 2 min over 4 cm(2)).
一种用于电子领域高质量多组分金属氧化物合成的近距常压化学气相沉积(AP-CVD)反应器被开发出来。它结合了机械可控的衬底-歧管间距和垂直气流的优点。因此,我们的AP-CVD反应器能够在低温下在各种衬底类型上快速生长均匀的晶体薄膜,而无需等离子体增强或低压条件。为了证明这一点,我们以锌镁氧化物(Zn(1-x)Mg(x)O)体系为例。通过将前驱体气体垂直且均匀地通过气体歧管引入到衬底上,我们展示了在375 mm²的沉积区域内,薄膜厚度变化仅为3%。这些厚度比之前的AP-CVD反应器所制备的薄膜要均匀得多。我们的薄膜还致密、无针孔,并且其厚度可通过气体歧管下方衬底的振荡次数线性控制。利用光致发光和X射线衍射测量,我们表明当Mg含量低于46原子%时,可制备出单相Zn(1-x)Mg(x)O。为了进一步优化生长条件,我们开发了一个将三元氧化物的组成与通过金属前驱体的鼓泡速率相关联的模型。我们将该模型与X射线光电子能谱测量的组成进行拟合,误差为Δx = 0.0005。该模型表明,对于每种鼓泡速率比,通过Mg前驱体的最大鼓泡速率可使Mg掺入ZnO的量最大化。当应用于聚(3-己基噻吩-2,5-二亚基)混合太阳能电池时,通过控制Mg含量,我们的薄膜使开路电压提高了100%以上。此类薄膜在短时间内(4 cm²面积上不到2分钟)即可沉积完成。