通过本征缓冲层改性优化p型聚siox钝化触点界面性能

IF 6.6 2区 材料科学 Q2 ENERGY & FUELS Solar Energy Materials and Solar Cells Pub Date : 2025-04-01 Epub Date: 2025-01-18 DOI:10.1016/j.solmat.2025.113418
Yingwen Zhao , Paul Procel Moya , Yifeng Zhao , Zhirong Yao , Jin Yan , Hiroki Nakajima , Engin Özkol , Miro Zeman , Luana Mazzarella , Olindo Isabella
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引用次数: 0

摘要

多晶硅(poly-Si)载流子选择性钝化触点(cspc)具有较高的光转换效率(PCE)和成本效益,已成为高效晶体硅(c-Si)太阳能电池的一种有前途的方法。为了最大限度地减少掺杂多晶硅窗口层引起的寄生吸收损失,开发了宽带隙氧合金多晶硅(poly-SiOx)层。然而,对于掺杂硼的聚siox接触堆来说,实现良好的表面钝化仍然存在挑战,这可能是由于退火过程中硼的扩散以及氧含量增加导致结晶度降低导致掺杂浓度降低所致。在本研究中,我们研究了等离子体增强化学气相沉积(PECVD)沉积的10 nm厚的具有不同氧含量(a- si (Ox):H)的本构氢化非晶硅缓冲层,并将其置于隧道氧化硅(SiOx)和聚SiOx (p+)之间,对钝化接触结构和太阳能电池性能的影响。经过加氢步骤后,无氧a-Si:H缓冲层抛光表面的隐含开路电压(iVoc)为728.3 mV,接触电阻率(ρc)为59.18 mΩ cm2,钝化质量高。这些改进可归因于适当的隧道氧化物厚度,并通过透射电子显微镜(TEM)图像证实,缓冲层的结晶度更高,这有助于在缓冲层中更有效地掺杂。能量色散x射线能谱(EDX)和x射线光电子能谱(XPS)结果证明了这一点。在器件层面,在n型c-Si晶片上制备正面有纹、背面扁平、后结的poly-SiOx/poly-SiOx太阳能电池,效率从无PECVD缓冲层的3.55%提高到无氧a- si:H PECVD缓冲层的18.9%。通过部署10 nm厚的LPCVD缓冲层,进一步证明了缓冲层结晶度对电池性能的影响,在相同的器件结构下,缓冲层的效率达到21.15%。
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Optimization of interface properties in p-type poly-SiOx passivating contacts through intrinsic buffer layer modification
Polycrystalline silicon (poly-Si) carrier-selective passivating contacts (CSPCs), featuring high photoconversion efficiency (PCE) and cost-effectiveness, have emerged as a promising approach for high-efficiency crystalline silicon (c-Si) solar cells. To minimize parasitic absorption losses induced by doped poly-Si window layers, wide bandgap oxygen-alloyed poly-Si (poly-SiOx) layers are developed. However, challenges persist in achieving excellent surface passivation for boron-doped poly-SiOx contact stacks, likely caused by boron diffusion during annealing and the reduced doping concentration resulting from lower crystallinity as oxygen content increases. In this study, we investigate the impact on the passivating contact structure and solar cell performance of a 10-nm thick intrinsic hydrogenated amorphous silicon buffer layer with varying oxygen content (a-Si (Ox):H) deposited by plasma-enhanced chemical vapor deposition (PECVD), and placed between the tunneling silicon oxide (SiOx) and the poly-SiOx (p+). After the hydrogenation step, we obtain both high passivation quality with implied open circuit voltage (iVoc) of 728.3 mV and low contact resistivity (ρc) of 59.18 mΩ cm2 on polished surface for oxygen-free a-Si:H buffer layer. These improvements can be attributed to the appropriate thickness of the tunnel oxide and confirmed by transmission electron microscopy (TEM) images, to higher crystallinity of the buffer layer, which facilitates more efficient doping in the buffer layer. This is evidenced by energy dispersive X-ray spectroscopy (EDX), and X-ray photoelectron spectroscopy (XPS) results. At the device level, a front-side textured, rear-side flat, rear junction poly-SiOx/poly-SiOx solar cell on n-type c-Si wafer, an efficiency improvement can be observed from 3.55 % without a PECVD buffer layer to 18.9 % with an oxygen-free a-Si:H PECVD buffer layer. The impact of the buffer layer crystallinity on cell performance is further demonstrated by deploying a 10-nm thick LPCVD buffer layer, which facilitates an efficiency of 21.15 % for the same device structure.
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来源期刊
Solar Energy Materials and Solar Cells
Solar Energy Materials and Solar Cells 工程技术-材料科学:综合
CiteScore
12.60
自引率
11.60%
发文量
513
审稿时长
47 days
期刊介绍: Solar Energy Materials & Solar Cells is intended as a vehicle for the dissemination of research results on materials science and technology related to photovoltaic, photothermal and photoelectrochemical solar energy conversion. Materials science is taken in the broadest possible sense and encompasses physics, chemistry, optics, materials fabrication and analysis for all types of materials.
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