首页 > 最新文献

2014 IEEE 40th Photovoltaic Specialist Conference (PVSC)最新文献

英文 中文
Modeling nonuniform irradiance and chromatic aberration effects in a four junction solar cell using SPICE 用SPICE模拟四结太阳能电池的非均匀辐照度和色差效应
Pub Date : 2014-06-08 DOI: 10.1109/PVSC.2014.6925639
Pratibha Sharma, M. Wilkins, H. Schriemer, K. Hinzer
A two-dimensional, distributed resistance model for a four junction solar cell is implemented in SPICE. Efficiency estimates for Gaussian irradiance profiles with different peak-to-average ratios (PAR) are determined via grid optimization at concentrations of 500, 1000 and 2000 suns. Optimizing finger spacing for a PAR of 6 improves cell efficiency by 1.8% (absolute) at 2000 suns compared to that observed from finger spacing optimized for a uniform illumination. To address the impact of chromatic aberration on cell efficiency, a CPV system is modeled in Zemax for a geometric concentration of 1250X. Using a finger spacing optimized for uniform irradiance at the average optical efficiency of 82%, the neglect of chromatic aberration was found to overstate system efficiency by 3% (absolute).
在SPICE中实现了四结太阳能电池的二维分布电阻模型。在500、1000和2000个太阳的浓度下,通过网格优化确定了具有不同峰均比(PAR)的高斯辐射剖面的效率估计。在PAR为6时优化手指间距,与在均匀光照下优化手指间距观察到的结果相比,在2000个太阳下电池效率提高了1.8%(绝对)。为了解决色差对电池效率的影响,在Zemax中模拟了一个几何浓度为1250X的CPV系统。在平均光学效率为82%的情况下,使用优化均匀辐照度的手指间距,发现忽略色差会使系统效率夸大3%(绝对)。
{"title":"Modeling nonuniform irradiance and chromatic aberration effects in a four junction solar cell using SPICE","authors":"Pratibha Sharma, M. Wilkins, H. Schriemer, K. Hinzer","doi":"10.1109/PVSC.2014.6925639","DOIUrl":"https://doi.org/10.1109/PVSC.2014.6925639","url":null,"abstract":"A two-dimensional, distributed resistance model for a four junction solar cell is implemented in SPICE. Efficiency estimates for Gaussian irradiance profiles with different peak-to-average ratios (PAR) are determined via grid optimization at concentrations of 500, 1000 and 2000 suns. Optimizing finger spacing for a PAR of 6 improves cell efficiency by 1.8% (absolute) at 2000 suns compared to that observed from finger spacing optimized for a uniform illumination. To address the impact of chromatic aberration on cell efficiency, a CPV system is modeled in Zemax for a geometric concentration of 1250X. Using a finger spacing optimized for uniform irradiance at the average optical efficiency of 82%, the neglect of chromatic aberration was found to overstate system efficiency by 3% (absolute).","PeriodicalId":6649,"journal":{"name":"2014 IEEE 40th Photovoltaic Specialist Conference (PVSC)","volume":"18 1","pages":"3293-3297"},"PeriodicalIF":0.0,"publicationDate":"2014-06-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"84584261","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 13
High-performance hetero-junction crystalline silicon photovoltaic technology 高性能异质结晶体硅光伏技术
Pub Date : 2014-06-08 DOI: 10.1109/PVSC.2014.6925134
J. Levrat, C. Allébe, N. Badel, L. Barraud, M. Bonnet-eymard, J. Champliaud, F. Debrot, A. Descoeudres, A. Faes, A. Lachowicz, S. Nicolay, L. Sansonnens, C. Ballif, J. Geissbühler, S. D. Wolf, M. Despeisse
Silicon heterojunction solar cell technology (HJT) takes advantage of ultra-thin amorphous silicon layers deposited on both sides of monocrystalline silicon wafers, enabling excellent silicon wafer surface passivation resulting in high device power output and in addition to efficient use of thin wafers. A full cell processing platform was developed in our laboratory, enabling to achieve > 22 % cell efficiency. Advanced concepts for metallization and interconnection are under study, from fine-line printing combined with SmartWire interconnection to Copper plating. Importantly, we show that the HJT technology intrinsically enables high bifaciality of the cells (> 95 %), and further demonstrates a low thermal coefficient (<; 0.2 - 0.3 %/°C). The high performance of heterojunction cells and SmartWire interconnection based modules allow for very low cost of electricity for Heterojunction based solar systems, with a potential below 6 Euro cents per kWh in Europe, bringing photovoltaics as a very competitive electricity source. It further provides upgrade potential towards 24 % cell efficiency.
硅异质结太阳能电池技术(HJT)利用沉积在单晶硅片两侧的超薄非晶硅层,实现优异的硅片表面钝化,从而提高器件功率输出,并有效利用薄晶片。在我们的实验室开发了一个完整的电池处理平台,使电池效率达到bbbb22 %。金属化和互连的先进概念正在研究中,从细线印刷结合SmartWire互连到镀铜。重要的是,我们证明了HJT技术本质上实现了电池的高双面性(> 95%),并进一步证明了低热系数(<;0.2 - 0.3% /°c)。高性能的异质结电池和基于SmartWire互连的模块使得基于异质结的太阳能系统的电力成本非常低,在欧洲每千瓦时的潜在成本低于6欧分,使光伏发电成为非常有竞争力的电力来源。它进一步提供了向24%的电池效率升级的潜力。
{"title":"High-performance hetero-junction crystalline silicon photovoltaic technology","authors":"J. Levrat, C. Allébe, N. Badel, L. Barraud, M. Bonnet-eymard, J. Champliaud, F. Debrot, A. Descoeudres, A. Faes, A. Lachowicz, S. Nicolay, L. Sansonnens, C. Ballif, J. Geissbühler, S. D. Wolf, M. Despeisse","doi":"10.1109/PVSC.2014.6925134","DOIUrl":"https://doi.org/10.1109/PVSC.2014.6925134","url":null,"abstract":"Silicon heterojunction solar cell technology (HJT) takes advantage of ultra-thin amorphous silicon layers deposited on both sides of monocrystalline silicon wafers, enabling excellent silicon wafer surface passivation resulting in high device power output and in addition to efficient use of thin wafers. A full cell processing platform was developed in our laboratory, enabling to achieve > 22 % cell efficiency. Advanced concepts for metallization and interconnection are under study, from fine-line printing combined with SmartWire interconnection to Copper plating. Importantly, we show that the HJT technology intrinsically enables high bifaciality of the cells (> 95 %), and further demonstrates a low thermal coefficient (<; 0.2 - 0.3 %/°C). The high performance of heterojunction cells and SmartWire interconnection based modules allow for very low cost of electricity for Heterojunction based solar systems, with a potential below 6 Euro cents per kWh in Europe, bringing photovoltaics as a very competitive electricity source. It further provides upgrade potential towards 24 % cell efficiency.","PeriodicalId":6649,"journal":{"name":"2014 IEEE 40th Photovoltaic Specialist Conference (PVSC)","volume":"62 1","pages":"1218-1222"},"PeriodicalIF":0.0,"publicationDate":"2014-06-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"84928815","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 7
The application of a magnetic field to improve polymer: Fullerence solar cell performance 应用磁场改善聚合物:太阳能电池的充盈性能
Pub Date : 2014-06-08 DOI: 10.1109/PVSC.2014.6925259
F. Hsu, Chiang-Ting Chen, Cheng-Hung Li, C. Chen, Y. Chen
Charge transport in a percolated network resulted from the mixing of donor (polymer) and acceptor materials is one of the important issues in improving the performance of polymer solar cells. We demonstrate a simple approach to enhance the performance of polymer solar cells based on poly(3-hexythiophene) (P3HT):fullerene blend incorporating a small amount of magnetic FePt-nanowires (FePt-NWs) as an additive. The photoactive film was prepared under the application of a magnetic field perpendicular to the substrate during solvent drying process. The power conversion efficiency has been improved up to ~ 60% for the treated cells. The improved device performance can be attributed to the overall improvement of polymer crystallinity.
由供体(聚合物)和受体材料混合产生的渗透网络中的电荷传输是提高聚合物太阳能电池性能的重要问题之一。我们展示了一种简单的方法来增强基于聚(3-己噻吩)(P3HT):富勒烯共混物的聚合物太阳能电池的性能,并加入少量磁性fept纳米线(FePt-NWs)作为添加剂。在溶剂干燥过程中,在垂直于基材的磁场作用下制备光活性膜。经过处理的电池的功率转换效率提高了约60%。器件性能的提高可归因于聚合物结晶度的整体提高。
{"title":"The application of a magnetic field to improve polymer: Fullerence solar cell performance","authors":"F. Hsu, Chiang-Ting Chen, Cheng-Hung Li, C. Chen, Y. Chen","doi":"10.1109/PVSC.2014.6925259","DOIUrl":"https://doi.org/10.1109/PVSC.2014.6925259","url":null,"abstract":"Charge transport in a percolated network resulted from the mixing of donor (polymer) and acceptor materials is one of the important issues in improving the performance of polymer solar cells. We demonstrate a simple approach to enhance the performance of polymer solar cells based on poly(3-hexythiophene) (P3HT):fullerene blend incorporating a small amount of magnetic FePt-nanowires (FePt-NWs) as an additive. The photoactive film was prepared under the application of a magnetic field perpendicular to the substrate during solvent drying process. The power conversion efficiency has been improved up to ~ 60% for the treated cells. The improved device performance can be attributed to the overall improvement of polymer crystallinity.","PeriodicalId":6649,"journal":{"name":"2014 IEEE 40th Photovoltaic Specialist Conference (PVSC)","volume":"503 1","pages":"1750-1753"},"PeriodicalIF":0.0,"publicationDate":"2014-06-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"85626638","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 1
Minority carrier lifetimes in 1.0-eV p-In0.27Ga0.73As layers grown on GaAs substrates 在GaAs衬底上生长的1.0 ev p-In0.27Ga0.73As层的少数载流子寿命
Pub Date : 2014-06-08 DOI: 10.1109/PVSC.2014.6925664
R. Tatavarti, K. Ban, A. Wibowo, D. Kuciauskas, H. Guthrey, K. Jones, S. Johnston, A. Norman, D. Levi, M. Al‐Jassim
Time-resolved photoluminescence (TRPL) measurements indicated minority carrier lifetimes of 15 ns for electrons in 2-μm thick layers of 1.0-eV p-In0.27Ga0.73As grown on 6-inch GaAs wafers. Electron lifetimes increased from 10 ns to 15 ns as the thickness of 1.0-eV p-In0.27Ga0.73As was increased from 0.5 μm to 2 μm. The electron lifetimes decreased from 15 ns for a p-InxGa1-xAs with a doping density of 1×1017 cm-3 to 5 ns for a doping density of 5×1017 cmq̑3. Cathodoluminescence imaging measurements indicated dislocation densities of 7.9×105 cm-2 for a 1.0-μm thick layer of p-In0.27Ga0.73As (1.0eV) at the center of the wafer and 1.4×106 cm-2 towards the edge. Cross-section transmission electron microscopy studies were performed to study dislocation blocking and threading dislocation propagation through the metamorphic graded AllnGaAs layers.
时间分辨光致发光(TRPL)测量表明,在6英寸GaAs晶圆上生长的1.0 ev p-In0.27Ga0.73As的2 μm厚层中,电子的少数载流子寿命为15 ns。当1.0 ev p-In0.27Ga0.73As厚度从0.5 μm增加到2 μm时,电子寿命从10 ns增加到15 ns。当掺杂密度为1×1017 cm-3时,p-InxGa1-xAs的电子寿命从15 ns降至5×1017 cmq -3时的5 ns。阴极发光成像测量表明,在晶圆中心和边缘的1.0 μm厚p-In0.27Ga0.73As (1.0 ev)层位错密度分别为7.9×105 cm-2和1.4×106 cm-2。通过透射电镜研究了位错在变质梯度AllnGaAs层中的阻滞和穿线位错传播。
{"title":"Minority carrier lifetimes in 1.0-eV p-In0.27Ga0.73As layers grown on GaAs substrates","authors":"R. Tatavarti, K. Ban, A. Wibowo, D. Kuciauskas, H. Guthrey, K. Jones, S. Johnston, A. Norman, D. Levi, M. Al‐Jassim","doi":"10.1109/PVSC.2014.6925664","DOIUrl":"https://doi.org/10.1109/PVSC.2014.6925664","url":null,"abstract":"Time-resolved photoluminescence (TRPL) measurements indicated minority carrier lifetimes of 15 ns for electrons in 2-μm thick layers of 1.0-eV p-In<sub>0.27</sub>Ga<sub>0.73</sub>As grown on 6-inch GaAs wafers. Electron lifetimes increased from 10 ns to 15 ns as the thickness of 1.0-eV p-In<sub>0.27</sub>Ga<sub>0.73</sub>As was increased from 0.5 μm to 2 μm. The electron lifetimes decreased from 15 ns for a p-In<sub>x</sub>Ga<sub>1-x</sub>As with a doping density of 1×10<sup>17</sup> cm<sup>-3</sup> to 5 ns for a doping density of 5×10<sup>17</sup> cm<sup>q̑3</sup>. Cathodoluminescence imaging measurements indicated dislocation densities of 7.9×10<sup>5</sup> cm<sup>-2</sup> for a 1.0-μm thick layer of p-In<sub>0.27</sub>Ga<sub>0.73</sub>As (1.0eV) at the center of the wafer and 1.4×10<sup>6</sup> cm<sup>-2</sup> towards the edge. Cross-section transmission electron microscopy studies were performed to study dislocation blocking and threading dislocation propagation through the metamorphic graded AllnGaAs layers.","PeriodicalId":6649,"journal":{"name":"2014 IEEE 40th Photovoltaic Specialist Conference (PVSC)","volume":"51 1","pages":"3414-3416"},"PeriodicalIF":0.0,"publicationDate":"2014-06-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"85665528","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Analysis of GaAs solar cells at High MOCVD growth rates 高MOCVD生长速率下GaAs太阳能电池的分析
Pub Date : 2014-06-08 DOI: 10.1109/PVSC.2014.6925345
K. Schmieder, M. Yakes, C. Bailey, Z. Pulwin, M. Lumb, L. Hirst, M. González, S. Hubbard, C. Ebert, R. Walters
Single junction GaAs solar cells grown by MOCVD are fabricated over a range of growth rates targeting up to 56 μm/hr in order to evaluate the effect on photovoltaic device performance. MOCVD recipe conditions are provided. Dopant incorporation efficiency is found to increase at high growth rates, potentially due to reduced Zn desorption as the time required to deposit a monolayer of GaAs is reduced. Device results are characterized by light and dark-IV as well as external quantum efficiency and verified against bulk minority carrier lifetime data from time-resolved photoluminescence. High growth rate solar cells degrade less than 4% relative to baseline devices with Voc and Jsc losses of 1% and 3%, respectively. The comparison suggests that both bulk Shockley Read Hall (SRH) lifetime and surface recombination velocity (SRV) are affected by growth rate and contribute to a reduction in performance.
为了评估MOCVD对光伏器件性能的影响,在高达56 μm/hr的生长速率范围内制备了MOCVD生长的单结GaAs太阳能电池。提供了MOCVD的配方条件。研究发现,在高生长速率下,掺杂剂的掺入效率会增加,这可能是由于沉积单层砷化镓所需的时间减少了Zn的脱附。器件结果具有光和暗iv以及外部量子效率的特征,并与时间分辨光致发光的大量少数载流子寿命数据进行了验证。与Voc和Jsc损失分别为1%和3%的基准器件相比,高生长速率太阳能电池的降解率低于4%。对比表明,体积肖克利-里德-霍尔(SRH)寿命和表面复合速度(SRV)都受到生长速率的影响,并导致性能下降。
{"title":"Analysis of GaAs solar cells at High MOCVD growth rates","authors":"K. Schmieder, M. Yakes, C. Bailey, Z. Pulwin, M. Lumb, L. Hirst, M. González, S. Hubbard, C. Ebert, R. Walters","doi":"10.1109/PVSC.2014.6925345","DOIUrl":"https://doi.org/10.1109/PVSC.2014.6925345","url":null,"abstract":"Single junction GaAs solar cells grown by MOCVD are fabricated over a range of growth rates targeting up to 56 μm/hr in order to evaluate the effect on photovoltaic device performance. MOCVD recipe conditions are provided. Dopant incorporation efficiency is found to increase at high growth rates, potentially due to reduced Zn desorption as the time required to deposit a monolayer of GaAs is reduced. Device results are characterized by light and dark-IV as well as external quantum efficiency and verified against bulk minority carrier lifetime data from time-resolved photoluminescence. High growth rate solar cells degrade less than 4% relative to baseline devices with Voc and Jsc losses of 1% and 3%, respectively. The comparison suggests that both bulk Shockley Read Hall (SRH) lifetime and surface recombination velocity (SRV) are affected by growth rate and contribute to a reduction in performance.","PeriodicalId":6649,"journal":{"name":"2014 IEEE 40th Photovoltaic Specialist Conference (PVSC)","volume":"69 1","pages":"2130-2133"},"PeriodicalIF":0.0,"publicationDate":"2014-06-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"85732926","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 13
Hierarchical modeling of electron and hole transport in nanoparticle thin films: From ab initio to Monte Carlo 纳米粒子薄膜中电子和空穴输运的分层建模:从从头算到蒙特卡罗
Pub Date : 2014-06-08 DOI: 10.1109/PVSC.2014.6925113
G. Zimányi, M. Voros, I. Carbone, S. Carter
Nanoparticle solar cells show the promise of enhancing the efficiency of solar cells over the Shockley-Queisser limit due to the quantum-confinement-enhanced charge multiplication process. A fundamental challenge of nanoparticle solar cells, however, is that the same quantum confinement that enhances charge multiplication also tends to localize the carriers and thus hinders charge transport. To create a roadmap for overcoming this challenge, we developed a multi-scale transport modeling scheme that starts with ab initio modeling of individual nanoparticles, continues with extracting a few summary parameters that best characterize the physics of these nanoparticles, such as charging energies and size dependent energy levels, and finally feeds this information into a kinetic Monte Carlo hopping transport framework to simulate electron and hole transport across realistically modeled nanoparticle films and devices. We demonstrate the power of this hierarchical modeling by exploring the carrier mobilities of PbSe nanoparticle films as a function of composition, disorder and temperature, where comparison of our results with experiments is possible.
由于量子约束增强的电荷倍增过程,纳米粒子太阳能电池显示出提高太阳能电池效率超过Shockley-Queisser极限的希望。然而,纳米粒子太阳能电池的一个基本挑战是,增强电荷倍增的量子限制也倾向于使载流子局部化,从而阻碍电荷传输。为了创建克服这一挑战的路线图,我们开发了一个多尺度输运建模方案,该方案从单个纳米粒子的从头开始建模,继续提取一些最能表征这些纳米粒子物理特性的摘要参数,如充电能量和尺寸相关的能级,最后将这些信息输入到动态蒙特卡罗跳跃输运框架中,以模拟电子和空穴在真实模拟的纳米颗粒薄膜和器件之间的输运。我们通过探索PbSe纳米颗粒薄膜的载流子迁移率作为成分、无序性和温度的函数来证明这种分层建模的力量,其中我们的结果与实验的比较是可能的。
{"title":"Hierarchical modeling of electron and hole transport in nanoparticle thin films: From ab initio to Monte Carlo","authors":"G. Zimányi, M. Voros, I. Carbone, S. Carter","doi":"10.1109/PVSC.2014.6925113","DOIUrl":"https://doi.org/10.1109/PVSC.2014.6925113","url":null,"abstract":"Nanoparticle solar cells show the promise of enhancing the efficiency of solar cells over the Shockley-Queisser limit due to the quantum-confinement-enhanced charge multiplication process. A fundamental challenge of nanoparticle solar cells, however, is that the same quantum confinement that enhances charge multiplication also tends to localize the carriers and thus hinders charge transport. To create a roadmap for overcoming this challenge, we developed a multi-scale transport modeling scheme that starts with ab initio modeling of individual nanoparticles, continues with extracting a few summary parameters that best characterize the physics of these nanoparticles, such as charging energies and size dependent energy levels, and finally feeds this information into a kinetic Monte Carlo hopping transport framework to simulate electron and hole transport across realistically modeled nanoparticle films and devices. We demonstrate the power of this hierarchical modeling by exploring the carrier mobilities of PbSe nanoparticle films as a function of composition, disorder and temperature, where comparison of our results with experiments is possible.","PeriodicalId":6649,"journal":{"name":"2014 IEEE 40th Photovoltaic Specialist Conference (PVSC)","volume":"49 1","pages":"1124-1126"},"PeriodicalIF":0.0,"publicationDate":"2014-06-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"85745045","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Arc fault risk assessment and degradation model development for photovoltaic connectors 光伏连接器电弧故障风险评估及退化模型开发
Pub Date : 2014-06-08 DOI: 10.1109/PVSC.2014.6924875
B. Yang, Kenneth Armijo, R. K. Harrison, Kara E. Thomas, Jay Johnson, Jason M. Taylor, N. R. Sorensen
This work investigates balance of systems (BOS) connector reliability from the perspective of arc fault risk. Accelerated tests were performed on connectors for future development of a reliability model. Thousands of hours of damp heat and atmospheric corrosion tests found BOS connectors to be resilient to corrosion-related degradation. A procedure was also developed to evaluate new and aged connectors for arc fault risk. The measurements show that arc fault risk is dependent on a combination of materials composition as well as design geometry. Thermal measurements as well as optical emission spectroscopy were also performed to further characterize the arc plasma. Together, the degradation model, arc fault risk assessment technique, and characterization methods can provide operators of photovoltaic installations information necessary to develop a data-driven plan for BOS connector maintenance as well as identify opportunities for arc fault prognostics.
本文从电弧故障风险的角度研究了平衡系统(BOS)连接器的可靠性。为了将来开发可靠性模型,对连接器进行了加速测试。数千小时的湿热和大气腐蚀测试发现,BOS连接器具有抗腐蚀相关降解的弹性。还开发了一种程序来评估新的和旧的连接器的电弧故障风险。测量结果表明,电弧故障风险取决于材料组成和设计几何形状的组合。热测量和光学发射光谱也进行了进一步表征电弧等离子体。退化模型、电弧故障风险评估技术和表征方法可以为光伏设备运营商提供必要的信息,以制定BOS连接器维护的数据驱动计划,并确定电弧故障预测的机会。
{"title":"Arc fault risk assessment and degradation model development for photovoltaic connectors","authors":"B. Yang, Kenneth Armijo, R. K. Harrison, Kara E. Thomas, Jay Johnson, Jason M. Taylor, N. R. Sorensen","doi":"10.1109/PVSC.2014.6924875","DOIUrl":"https://doi.org/10.1109/PVSC.2014.6924875","url":null,"abstract":"This work investigates balance of systems (BOS) connector reliability from the perspective of arc fault risk. Accelerated tests were performed on connectors for future development of a reliability model. Thousands of hours of damp heat and atmospheric corrosion tests found BOS connectors to be resilient to corrosion-related degradation. A procedure was also developed to evaluate new and aged connectors for arc fault risk. The measurements show that arc fault risk is dependent on a combination of materials composition as well as design geometry. Thermal measurements as well as optical emission spectroscopy were also performed to further characterize the arc plasma. Together, the degradation model, arc fault risk assessment technique, and characterization methods can provide operators of photovoltaic installations information necessary to develop a data-driven plan for BOS connector maintenance as well as identify opportunities for arc fault prognostics.","PeriodicalId":6649,"journal":{"name":"2014 IEEE 40th Photovoltaic Specialist Conference (PVSC)","volume":"5 1","pages":"3549-3555"},"PeriodicalIF":0.0,"publicationDate":"2014-06-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"80971645","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 4
Thin film Iron Pyrite synthesized by sulfurization of Iron Oxide for application in photovoltaics 氧化铁硫化法制备薄膜硫铁矿在光伏中的应用
Pub Date : 2014-06-08 DOI: 10.1109/PVSC.2014.6925411
Pravakar P. Rajbhandari, T. Dhakal, C. Westgate
Iron Pyrite (FeS2) is considered as a promising candidate for photovoltaic application because of its suitable band-gap, very high light absorption coefficient and the abundance of the component elements in the earth's crust. The problem however is that Iron Sulfide has several coexisting phases. Even with the same stoichiometry, it may have two different phases such as pyrite and marcasite. In this report, a phase pure iron pyrite is fabricated on a plain glass and molybdenum coated glass in an atmospheric pressure chemical vapor deposition system (APCVD) by annealing sputtered iron oxide (Fe2O3) in sulfur environment (elemental sulfur) at temperatures higher than 350°C. X-ray Diffraction measurement showed only pyrite phase and energy dispersive spectroscopy (EDS) showed 1:2 ratio for iron to sulfur. Depth profile using X-ray Photoelectron Spectroscopy showed a full conversion of iron oxide into pyrite. Increasing the temperature beyond 350°C, grain size got bigger, but pyrrhotite phase with very low resistivity started to appear.
铁黄铁矿(FeS2)因其具有合适的带隙、很高的光吸收系数和地壳中丰富的组成元素而被认为是光伏应用的有前途的候选者。然而,问题是硫化铁有几个共存的相。即使在相同的化学计量下,它也可能有两种不同的相,如黄铁矿和黄铁矿。在常压化学气相沉积系统(APCVD)中,将溅射氧化铁(Fe2O3)在高于350℃的硫环境(单质硫)中退火,制备出相纯的黄铁矿。x射线衍射测定显示为黄铁矿相,能谱分析显示铁与硫的比例为1:2。x射线光电子能谱深度剖面显示氧化铁完全转化为黄铁矿。当温度超过350℃时,晶粒尺寸变大,但开始出现电阻率极低的磁黄铁矿相。
{"title":"Thin film Iron Pyrite synthesized by sulfurization of Iron Oxide for application in photovoltaics","authors":"Pravakar P. Rajbhandari, T. Dhakal, C. Westgate","doi":"10.1109/PVSC.2014.6925411","DOIUrl":"https://doi.org/10.1109/PVSC.2014.6925411","url":null,"abstract":"Iron Pyrite (FeS2) is considered as a promising candidate for photovoltaic application because of its suitable band-gap, very high light absorption coefficient and the abundance of the component elements in the earth's crust. The problem however is that Iron Sulfide has several coexisting phases. Even with the same stoichiometry, it may have two different phases such as pyrite and marcasite. In this report, a phase pure iron pyrite is fabricated on a plain glass and molybdenum coated glass in an atmospheric pressure chemical vapor deposition system (APCVD) by annealing sputtered iron oxide (Fe2O3) in sulfur environment (elemental sulfur) at temperatures higher than 350°C. X-ray Diffraction measurement showed only pyrite phase and energy dispersive spectroscopy (EDS) showed 1:2 ratio for iron to sulfur. Depth profile using X-ray Photoelectron Spectroscopy showed a full conversion of iron oxide into pyrite. Increasing the temperature beyond 350°C, grain size got bigger, but pyrrhotite phase with very low resistivity started to appear.","PeriodicalId":6649,"journal":{"name":"2014 IEEE 40th Photovoltaic Specialist Conference (PVSC)","volume":"33 1","pages":"2400-2403"},"PeriodicalIF":0.0,"publicationDate":"2014-06-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"78562535","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Study of the passivation mechanism of c-Si by Al2O3 using in situ infrared spectroscopy 用原位红外光谱研究Al2O3钝化c-Si的机理
Pub Date : 2014-06-08 DOI: 10.1109/PVSC.2014.6924988
Rohan P. Chaukulkar, W. Nemeth, A. Dameron, P. Stradins, S. Agarwal
We present an in situ attenuated total reflection Fourier transform infrared (ATR-FTIR) spectroscopy study of the passivation mechanism in the surface passivation of Si solar cells by Al2O3 thin films deposited via atomic layer deposition (ALD) using TMA and O3 as precursors. The IR measurements suggest that during the annealing stage, the Si-H bonding near the interface decreases. We have used D-terminated c-Si internal-reflection crystals to differentiate the residual H atoms that may migrate from ALD Al2O3 films versus the residual D atoms present at the Al2O3/c-Si interface after ALD. Within the sensitivity of the ATR-FTIR spectroscopy setup of ~1012 cm-2 for Si-H bonds, we do not detect any migration of H from Al2O3 to the c-Si interface. Therefore, we conclude that the migration of O, and the subsequent restructuring of the interface during the annealing step, primarily contributes toward the chemical passivation of the Al2O3/c-Si interface.
本文采用原位衰减全反射傅立叶变换红外(ATR-FTIR)光谱研究了以TMA和O3为前驱体,通过原子层沉积(ALD)沉积Al2O3薄膜对硅太阳能电池表面钝化的机理。红外测量表明,在退火阶段,界面附近的Si-H键减少。我们使用D端c-Si内反射晶体来区分ALD Al2O3薄膜中可能迁移的残余H原子与ALD后Al2O3/c-Si界面上存在的残余D原子。在ATR-FTIR光谱设置的~1012 cm-2的Si-H键灵敏度范围内,我们没有检测到H从Al2O3到c-Si界面的任何迁移。因此,我们得出结论,O的迁移以及随后在退火步骤中界面的重组是导致Al2O3/c-Si界面化学钝化的主要原因。
{"title":"Study of the passivation mechanism of c-Si by Al2O3 using in situ infrared spectroscopy","authors":"Rohan P. Chaukulkar, W. Nemeth, A. Dameron, P. Stradins, S. Agarwal","doi":"10.1109/PVSC.2014.6924988","DOIUrl":"https://doi.org/10.1109/PVSC.2014.6924988","url":null,"abstract":"We present an in situ attenuated total reflection Fourier transform infrared (ATR-FTIR) spectroscopy study of the passivation mechanism in the surface passivation of Si solar cells by Al<sub>2</sub>O<sub>3</sub> thin films deposited via atomic layer deposition (ALD) using TMA and O<sub>3</sub> as precursors. The IR measurements suggest that during the annealing stage, the Si-H bonding near the interface decreases. We have used D-terminated c-Si internal-reflection crystals to differentiate the residual H atoms that may migrate from ALD Al<sub>2</sub>O<sub>3</sub> films versus the residual D atoms present at the Al<sub>2</sub>O<sub>3</sub>/c-Si interface after ALD. Within the sensitivity of the ATR-FTIR spectroscopy setup of ~10<sup>12</sup> cm<sup>-2</sup> for Si-H bonds, we do not detect any migration of H from Al<sub>2</sub>O<sub>3</sub> to the c-Si interface. Therefore, we conclude that the migration of O, and the subsequent restructuring of the interface during the annealing step, primarily contributes toward the chemical passivation of the Al<sub>2</sub>O<sub>3</sub>/c-Si interface.","PeriodicalId":6649,"journal":{"name":"2014 IEEE 40th Photovoltaic Specialist Conference (PVSC)","volume":"126 1","pages":"0582-0585"},"PeriodicalIF":0.0,"publicationDate":"2014-06-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"85399556","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 1
Defect creation in low lattice-mismatched epitaxial structures 低晶格错配外延结构的缺陷产生
Pub Date : 2014-06-08 DOI: 10.1109/PVSC.2014.6924969
A. Maros, N. Faleev, C. Honsberg
The formation of crystalline defects is studied as a function of the epitaxial layer thickness in InGaAs and GaAsSb material systems grown by molecular beam epitaxy on (001) GaAs wafers. The Sb and In composition is roughly 8% in both sets of samples while the nominal thicknesses are respectively 50, 125, 250nm and 500nm for the InGaAs structures and 100, 250 and 500nm for the GaAsSb structures. High-resolution x-ray diffraction results show that similar partial relaxation is obtained in both systems for nearly the same thickness. Consistent structural transformation of point defects into dislocation loops related to the thickness of ternary layers is revealed. This resulted in a partial relaxation of 42 and 46% in the 250 nm thick GaAsSb and InGaAs layers respectively due to a density of secondary 60° dislocation loops of ~ 1 × 109 cm-2. The relaxation increased to 64% in the 500nm thick InGaAs and to 68% for the 500nm thick GaAsSb films even though the density of 60° dislocation loops in the volume was reduced due to intersections of these dislocation loops. Explanation of revealed structural features is suggested.
研究了分子束外延生长在(001)GaAs晶片上的InGaAs和GaAsSb材料体系中晶体缺陷的形成与外延层厚度的关系。两组样品中Sb和In的含量约为8%,InGaAs结构的标称厚度分别为50、125、250nm和500nm, GaAsSb结构的标称厚度分别为100、250和500nm。高分辨率x射线衍射结果表明,两种体系在几乎相同的厚度下获得了相似的部分弛豫。揭示了与三元层厚度相关的点缺陷向位错环的一致结构转变。在250 nm厚的GaAsSb和InGaAs层中,由于60°位错环的密度为~ 1 × 109 cm-2,导致部分弛豫分别为42%和46%。在500nm厚的InGaAs薄膜中,弛豫率增加到64%,而在500nm厚的GaAsSb薄膜中,弛豫率增加到68%,尽管由于这些位错环的交叉,体积中60°位错环的密度降低了。对揭示的构造特征提出了解释。
{"title":"Defect creation in low lattice-mismatched epitaxial structures","authors":"A. Maros, N. Faleev, C. Honsberg","doi":"10.1109/PVSC.2014.6924969","DOIUrl":"https://doi.org/10.1109/PVSC.2014.6924969","url":null,"abstract":"The formation of crystalline defects is studied as a function of the epitaxial layer thickness in InGaAs and GaAsSb material systems grown by molecular beam epitaxy on (001) GaAs wafers. The Sb and In composition is roughly 8% in both sets of samples while the nominal thicknesses are respectively 50, 125, 250nm and 500nm for the InGaAs structures and 100, 250 and 500nm for the GaAsSb structures. High-resolution x-ray diffraction results show that similar partial relaxation is obtained in both systems for nearly the same thickness. Consistent structural transformation of point defects into dislocation loops related to the thickness of ternary layers is revealed. This resulted in a partial relaxation of 42 and 46% in the 250 nm thick GaAsSb and InGaAs layers respectively due to a density of secondary 60° dislocation loops of ~ 1 × 109 cm-2. The relaxation increased to 64% in the 500nm thick InGaAs and to 68% for the 500nm thick GaAsSb films even though the density of 60° dislocation loops in the volume was reduced due to intersections of these dislocation loops. Explanation of revealed structural features is suggested.","PeriodicalId":6649,"journal":{"name":"2014 IEEE 40th Photovoltaic Specialist Conference (PVSC)","volume":"2 1","pages":"0499-0504"},"PeriodicalIF":0.0,"publicationDate":"2014-06-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"85798935","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 1
期刊
2014 IEEE 40th Photovoltaic Specialist Conference (PVSC)
全部 Acc. Chem. Res. ACS Applied Bio Materials ACS Appl. Electron. Mater. ACS Appl. Energy Mater. ACS Appl. Mater. Interfaces ACS Appl. Nano Mater. ACS Appl. Polym. Mater. ACS BIOMATER-SCI ENG ACS Catal. ACS Cent. Sci. ACS Chem. Biol. ACS Chemical Health & Safety ACS Chem. Neurosci. ACS Comb. Sci. ACS Earth Space Chem. ACS Energy Lett. ACS Infect. Dis. ACS Macro Lett. ACS Mater. Lett. ACS Med. Chem. Lett. ACS Nano ACS Omega ACS Photonics ACS Sens. ACS Sustainable Chem. Eng. ACS Synth. Biol. Anal. Chem. BIOCHEMISTRY-US Bioconjugate Chem. BIOMACROMOLECULES Chem. Res. Toxicol. Chem. Rev. Chem. Mater. CRYST GROWTH DES ENERG FUEL Environ. Sci. Technol. Environ. Sci. Technol. Lett. Eur. J. Inorg. Chem. IND ENG CHEM RES Inorg. Chem. J. Agric. Food. Chem. J. Chem. Eng. Data J. Chem. Educ. J. Chem. Inf. Model. J. Chem. Theory Comput. J. Med. Chem. J. Nat. Prod. J PROTEOME RES J. Am. Chem. Soc. LANGMUIR MACROMOLECULES Mol. Pharmaceutics Nano Lett. Org. Lett. ORG PROCESS RES DEV ORGANOMETALLICS J. Org. Chem. J. Phys. Chem. J. Phys. Chem. A J. Phys. Chem. B J. Phys. Chem. C J. Phys. Chem. Lett. Analyst Anal. Methods Biomater. Sci. Catal. Sci. Technol. Chem. Commun. Chem. Soc. Rev. CHEM EDUC RES PRACT CRYSTENGCOMM Dalton Trans. Energy Environ. Sci. ENVIRON SCI-NANO ENVIRON SCI-PROC IMP ENVIRON SCI-WAT RES Faraday Discuss. Food Funct. Green Chem. Inorg. Chem. Front. Integr. Biol. J. Anal. At. Spectrom. J. Mater. Chem. A J. Mater. Chem. B J. Mater. Chem. C Lab Chip Mater. Chem. Front. Mater. Horiz. MEDCHEMCOMM Metallomics Mol. Biosyst. Mol. Syst. Des. Eng. Nanoscale Nanoscale Horiz. Nat. Prod. Rep. New J. Chem. Org. Biomol. Chem. Org. Chem. Front. PHOTOCH PHOTOBIO SCI PCCP Polym. Chem.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
×
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
现在去查看 取消
×
提示
确定
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 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 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1