Oxide-nitride nanolayer stacks for enhanced passivation of p-type surfaces in silicon solar cells

IF 6.3 2区 材料科学 Q2 ENERGY & FUELS
Xinya Niu , Anastasia Soeriyadi , Guanze He , Shona McNab , Sergio Lozano-Perez , Ruy S. Bonilla
{"title":"Oxide-nitride nanolayer stacks for enhanced passivation of p-type surfaces in silicon solar cells","authors":"Xinya Niu ,&nbsp;Anastasia Soeriyadi ,&nbsp;Guanze He ,&nbsp;Shona McNab ,&nbsp;Sergio Lozano-Perez ,&nbsp;Ruy S. Bonilla","doi":"10.1016/j.solmat.2024.113231","DOIUrl":null,"url":null,"abstract":"<div><div>In the quest for ultra-high-efficiency silicon solar cells, optimising surface passivation has emerged as a critical pathway to minimise losses and enhance device performance. Recent breakthroughs in aluminium oxide (AlO<sub>x</sub>) passivation show an interface to Si with low interface defect density and high negative charge density after activation annealing at 400–450 °C, enabling low surface recombination velocities. The formation of an interfacial SiO<sub>x</sub> layer has been recognised as a key factor. In this study, we present an in-depth investigation of a SiO<sub>x</sub>/AlO<sub>x</sub>/SiN<sub>x</sub> nanolayer stack interface with Si, where the SiO<sub>x</sub> is wet chemically grown. By varying the AlO<sub>x</sub> deposition from 5 to 40 ALD cycles, we observed a reduction in interface defect density, indicating the presence of negatively charged hydrogen in the AlO<sub>x</sub> layer. We reveal a distinctly different interface between Si and nanolayer stacks with or without AlO<sub>x</sub>. Activation annealing significantly reduced recombination losses for stacks with AlO<sub>x</sub>, attributed to increased charge density and decreased carrier capture velocity at the valence band-tail. We find lower electron capture rates in nanolayer stacks containing AlO<sub>x</sub>, suggesting effective passivation of donor states by negatively charged hydrogen. Additionally, the formation of new acceptor states was detected by an increase in hole capture velocity at the interface after annealing. Electron energy loss spectroscopy (EELS) identified an Al:SiO<sub>x</sub>N<sub>y</sub> layer of ∼2.5 nm thick with excess oxygen content and a mixture of tetrahedral and octahedral coordinated Al, likely contributing to the formation of acceptor defects and suggest an intrinsic link between the chemical and field-effect passivation.</div></div>","PeriodicalId":429,"journal":{"name":"Solar Energy Materials and Solar Cells","volume":"280 ","pages":"Article 113231"},"PeriodicalIF":6.3000,"publicationDate":"2024-11-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Solar Energy Materials and Solar Cells","FirstCategoryId":"88","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0927024824005439","RegionNum":2,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"ENERGY & FUELS","Score":null,"Total":0}
引用次数: 0

Abstract

In the quest for ultra-high-efficiency silicon solar cells, optimising surface passivation has emerged as a critical pathway to minimise losses and enhance device performance. Recent breakthroughs in aluminium oxide (AlOx) passivation show an interface to Si with low interface defect density and high negative charge density after activation annealing at 400–450 °C, enabling low surface recombination velocities. The formation of an interfacial SiOx layer has been recognised as a key factor. In this study, we present an in-depth investigation of a SiOx/AlOx/SiNx nanolayer stack interface with Si, where the SiOx is wet chemically grown. By varying the AlOx deposition from 5 to 40 ALD cycles, we observed a reduction in interface defect density, indicating the presence of negatively charged hydrogen in the AlOx layer. We reveal a distinctly different interface between Si and nanolayer stacks with or without AlOx. Activation annealing significantly reduced recombination losses for stacks with AlOx, attributed to increased charge density and decreased carrier capture velocity at the valence band-tail. We find lower electron capture rates in nanolayer stacks containing AlOx, suggesting effective passivation of donor states by negatively charged hydrogen. Additionally, the formation of new acceptor states was detected by an increase in hole capture velocity at the interface after annealing. Electron energy loss spectroscopy (EELS) identified an Al:SiOxNy layer of ∼2.5 nm thick with excess oxygen content and a mixture of tetrahedral and octahedral coordinated Al, likely contributing to the formation of acceptor defects and suggest an intrinsic link between the chemical and field-effect passivation.

Abstract Image

用于增强硅太阳能电池 p 型表面钝化的氧化物-氮化物纳米层堆
在追求超高效硅太阳能电池的过程中,优化表面钝化已成为最大限度减少损耗和提高器件性能的关键途径。最近在氧化铝(AlOx)钝化方面取得的突破表明,在 400-450 °C 下活化退火后,硅的界面缺陷密度低,负电荷密度高,从而实现了较低的表面重组速度。界面氧化硅层的形成被认为是一个关键因素。在本研究中,我们对 SiOx/AlOx/SiNx 纳米层堆叠与 Si 的界面进行了深入研究,其中 SiOx 是湿化学生长的。通过改变 5 至 40 个 ALD 周期的氧化铝沉积,我们观察到界面缺陷密度降低,这表明氧化铝层中存在带负电荷的氢。我们揭示了有无氧化铝的硅和纳米层堆栈之间截然不同的界面。活化退火显著降低了带氧化铝的堆栈的重组损耗,这归因于电荷密度的增加和价带尾处载流子捕获速度的降低。我们发现在含有氧化铝的纳米层堆栈中电子捕获率较低,这表明带负电的氢有效地钝化了供体态。此外,退火后界面处空穴捕获速度的增加也检测到了新受体态的形成。电子能量损失光谱(EELS)确定了一个厚度为 2.5 纳米的 Al:SiOxNy 层,该层氧含量过高,并混合了四面体和八面体配位的铝,这可能有助于形成受体缺陷,并表明化学钝化和场效应钝化之间存在内在联系。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
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.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信