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首页> 外文期刊>Journal of Alloys and Compounds: An Interdisciplinary Journal of Materials Science and Solid-state Chemistry and Physics >Nanoscale charge transport and local surface potential distribution to probe the defect passivation in Cr-substituted earth abundant CZTS absorber layer
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Nanoscale charge transport and local surface potential distribution to probe the defect passivation in Cr-substituted earth abundant CZTS absorber layer

机译:纳米级电荷运输和局部表面电位分布探测CR替代土坯的缺陷钝化丰富的CZTS吸收层

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The non-stochiometric deviations in CZTS often results in certain detrimental point defects that act as trap centers causing non-radiative recombination and potential fluctuations, eventually results in large open circuit voltage (V-OC) deficit in CZTS solar cells. Cationic substitution in CZTS layer is one of the leading approaches to capture the great potential of kesterite solar cells for future cost-effective photovoltaic technology. Here, chromium incorporation in CZTS is studied for cationic substitution in CZTS layer, as it renders multiple chemical states including +1, +2 and + 4 of Cu, Zn and Sn cations in CZTS. The CZTS films determine to have good crystallinity and morphology with no significant disparity among pristine and Cr-doped CZTS films, apart from slight shift of XRD (112) peak indicating partial cation substitution by smaller Cr atoms. However, the Zn content is found to be decreased with increasing Cr content in CZTS layer. Substantial enhancement in the absorption of Cr-doped CZTS films indicate intermediate band (IB) within the band gap. Photoluminescence (PL) emission spectra strongly suggests reduced non-radiative recombination and potential fluctuations in Cr-CZTS films. X-ray photoelectron spectroscopy investigations reveal Zn substitution by Cr in CZTS crystal geometry. Using nanoscale Kelvin Probe Force Microscopy (KPFM) and Conducting Atomic Force Microscopy (CAFM), we verify the surface potential variation and nanoscale electrical conductivity in pristine and Cr-CZTS films. Additionally, Zn substitution by Cr eventually lead to suppression of Zn-sn deep level defects segregated at grain boundaries (GBs). CAFM strongly confirms the GB passivation in Cr-CZTS films. This work widens the opportunity of exploring potential cationic substitution in CZTS for developing high efficiency CZTS solar cells. (C) 2020 Elsevier B.V. All rights reserved.
机译:CZT中的非化学计量偏差通常会导致某些有害点缺陷,这些缺陷充当陷阱中心,导致非辐射复合和潜在波动,最终导致CZT太阳能电池中的大开路电压(V-OC)缺陷。CZTS层中的阳离子替代是获取未来成本效益光伏技术中的巨大潜力的主要方法之一。在这里,研究了CZTS中铬的掺入对CZTS层中阳离子取代的影响,因为它使CZTS中的铜、锌和锡阳离子呈现出多种化学状态,包括+1、+2和+4。CZTS薄膜具有良好的结晶度和形貌,在原始和掺铬CZTS薄膜中没有显著差异,除了XRD(112)峰的轻微移动表明较小的Cr原子部分取代了阳离子。但是,随着CZTS层中Cr含量的增加,Zn含量降低。Cr掺杂CZTS薄膜的吸收显著增强表明带隙内存在中间带(IB)。光致发光(PL)发射光谱强烈表明,Cr CZTS薄膜中的非辐射复合和潜在波动减少。X射线光电子能谱研究表明,CZTS晶体中的锌被铬取代。利用纳米开尔文探针力显微镜(KPFM)和导电原子力显微镜(CAFM),我们验证了原始和Cr CZTS薄膜的表面电位变化和纳米级电导率。此外,铬取代锌最终会抑制晶界(GBs)分离的Zn-sn深能级缺陷。CAFM强烈证实了Cr CZTS薄膜中的GB钝化。这项工作拓宽了在CZTS中探索潜在阳离子替代物以开发高效CZTS太阳能电池的机会。(C) 2020爱思唯尔B.V.版权所有。

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