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Thin film Sn_2S_3 via chemical deposition and controlled heating - Its prospects as a solar cell absorber

机译:通过化学沉积和受控加热的薄膜Sn_2S_3-其作为太阳能电池吸收剂的前景

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As a semiconductor of "earth-abundant" elements, Sn2S3 with a bandgap (E-g) close to 1 eV merits attention, but a method to prepare phase-pure thin film remains elusive. We report the formation of Sn2S3 thin film of 360 nm in thickness by heating chemically deposited tin sulfide thin films at 450 degrees C during 30-45 min in presence of sulfur at a pressure, 75 Torr of nitrogen. Energy dispersive x-ray emission spectra and grazing incidence x-ray diffraction established a reaction route for this conversion of SnS completely to Sn2S3 via an intermediate phase, SnS2. The optical bandgap of the material is 1.25 eV (indirect) and 1.75 eV (direct, forbidden). The optical absorption suggests a light-generated current density of 30 mA/cm(2) for the Sn2S3 film (360 nm) as a solar cell absorber. Thin film Sn2S3 formed in 30 min heating has a p-type electrical conductivity in the dark of 1 x 10(-4) Omega(-1) cm(-1), which increases to 3 x 10(-4) Omega(-1) cm(-1) in 0.2 s under 800 W/m(2) tungsten-halogen illumination. An estimate made for its mobility-lifetime product is, 6 x 10(-6) cm(2) V-1. We discuss the prospects of this material for solar cells.
机译:带隙(E-g)接近1 eV的Sn2S3作为“富含地球”元素的半导体值得关注,但是制备纯相薄膜的方法仍然难以捉摸。我们报告了通过在30到45分钟内在75托氮气压力下在硫的存在下在450摄氏度下加热化学沉积的硫化锡薄膜,形成360纳米厚的Sn2S3薄膜的过程。能量色散x射线发射光谱和掠入射x射线衍射建立了一条途径,使SnS通过中间相SnS2完全转化为Sn2S3。该材料的光学带隙为1.25 eV(间接)和1.75 eV(直接,禁止)。光吸收表明,作为太阳能电池吸收剂的Sn2S3膜(360 nm)的光产生电流密度为30 mA / cm(2)。在30分钟的加热中形成的薄膜Sn2S3在黑暗中具有1 x 10(-4)Omega(-1)cm(-1)的p型电导率,该电导率增加到3 x 10(-4)Omega(- 1)在800 W / m(2)卤钨钨灯下在0.2 s内的cm(-1)。其移动寿命产品的估计值为6 x 10(-6)cm(2)V-1。我们讨论了这种材料用于太阳能电池的前景。

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