ELECTROCHEMICAL HYDROGENIZATION OF THE FRONTAL SURFACE OF SOLAR CELLS AND THEIR RESEARCH BY MASS SPECTROSCOPY

V. Yerokhov, A. Druzhinin, I. Skrypnyk
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Abstract

Purpose. Texturing of the silicon surface, both by chemical and electrochemical etching, is an integral part of the technology of modern high-performance silicon solar cells. The texture on the front surface of the solar cells not only reduces reflection losses, but also helps to capture long-wave light in the SC structure, thereby expanding its operating spectral range and increasing the short-circuit current. In this regard, the study of the PSi layer in a nanotexture by mass-spectroscopy on the functional properties of the frontal silicon surface, which was pre-textured, is of particular interest. Methodology. The study of all stages of formation of hydrogenated porous structure and identification of technological patterns that affect the characteristics of the obtained nano-, meso-, macropores are very important, because most of the porous parameters are laid at the stage of formation of nucleation (seed) centers. In order to improve the passivating properties of PSi layers used in solar cells, the process of electrochemical hydrogenation of PSi as on p - type silicon substrates with a resistivity of 0.1 ÷ 10 Ohmsm also on substrates with a formed emitter junction n+- p of conductivity was studied. Various solutions were used as the electrolyte, such as (HF: C2H5OH=1: 1), (HF: C2H5OH=1:2) and so on. The current density and anodizing time varied over a wide range of values, which allowed the formation of PSi layers with different porosity and thickness. A solution of HF: C2H5OH = 1: 1 was used as the electrolyte. The anodizing current and time varied over a wide range of values to obtain PSi layers with different porosity and thickness. To determine the conditions of the process of electrochemical hydrogenation of PSi during its cathodic polarization, potentiostatic current-voltage curves of the system Pt (anode)-electrolyte-porous silicon/ silicon (cathode) for electrolytes with different chemical composition were taken. Finding. Comparison of the surface appearance of Baysix type multicrystalline silicon samples before and after hydrogen hydrogenation in an electrolyte based on hydrofluoric acid ((HF: C2H5OH=10:1), (HF:C2H5OH=10:2) and so on), both in the secondary ion Spectra and in the image of the distribution of elements over the surface (mass spectral ion microscope and Ion microzond mode). Originality. We get a 2D image (size 200x200 microns) of the surface of the current of secondary ions H+ hydrogen and 2D image of the secondary ion current of molecular SiH2+ the surface of a Baysix type multicrystalline substrate passivated with hydrogen by hydrogenation, which is comparable to the optical image of a pure silicon surface that has been hydrogenated. From the form of 2D-ion images, as well as their individual parts, it can be seen that all the difference in the current intensity of the secondary ions is due to the topography of the surface of the samples. Practical value. The prospects of creating efficient solar cells using multifunctional multi-textures of porous silicon are shown. References 24, figures 6.
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太阳能电池正面电化学加氢及其质谱研究
目的。通过化学和电化学蚀刻对硅表面进行变形是现代高性能硅太阳能电池技术的重要组成部分。太阳能电池前表面的纹理不仅减少了反射损耗,而且有助于SC结构中的长波光捕获,从而扩大了其工作光谱范围,增加了短路电流。在这方面,用质谱法研究纳米织构中的PSi层对预织构硅正面表面的功能特性是特别有趣的。方法。研究氢化多孔结构形成的各个阶段以及确定影响所获得的纳米、中、大孔特性的工艺模式是非常重要的,因为大多数多孔参数都是在成核(种子)中心形成阶段确定的。为了提高太阳能电池用PSi层的钝化性能,研究了在电阻率为0.1 ÷ 10欧姆的p型硅衬底上PSi的电化学加氢过程,以及在形成电导率为n+- p的发射极结的衬底上PSi的电化学加氢过程。电解液采用了(HF: C2H5OH= 1:1)、(HF: C2H5OH=1:2)等不同的溶液。电流密度和阳极氧化时间在很大范围内变化,这使得形成具有不同孔隙率和厚度的PSi层成为可能。采用HF: C2H5OH = 1:1的溶液作为电解液。阳极氧化电流和时间在很大范围内变化,以获得具有不同孔隙率和厚度的PSi层。为了确定PSi阴极极化过程中电化学加氢的条件,采用Pt(阳极)-电解质-多孔硅/硅(阴极)体系对不同化学成分电解质的恒电位电流-电压曲线。发现。贝六型多晶硅样品在氢氟酸(HF:C2H5OH= 10:1)、(HF:C2H5OH=10:2)等电解质中加氢前后表面形貌的比较,包括二次离子光谱和表面元素分布图像(质谱离子显微镜和离子微区模式)。创意。我们得到了经氢钝化的Baysix型多晶衬底表面二次离子H+氢电流的二维图像(尺寸为200x200微米)和分子SiH2+二次离子电流的二维图像,与经过氢化处理的纯硅表面光学图像相当。从2d离子图像的形式,以及它们各自的部分可以看出,二次离子电流强度的所有差异都是由于样品表面的地形。实用价值。展望了利用多孔硅的多功能复合结构制造高效太阳能电池的前景。参考文献24,图6。
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