Corrosion of novel reactive silver ink and commercial silver-based metallizations in diluted acetic acid

被引:15
作者
Jeffries, April M. [2 ]
Nietzold, Tara [2 ]
Schelhas, Laura T. [3 ,4 ]
Bertoni, Mariana, I [1 ]
机构
[1] Arizona State Univ, Sch Elect Comp & Energy Engn, Tempe, AZ 85281 USA
[2] Arizona State Univ, Sch Engn Matter Transport & Energy, Tempe, AZ 85281 USA
[3] SLAC Natl Lab Accelerator, Menlo Pk, CA 94025 USA
[4] Natl Renewable Energy Lab, Golden, CO 80401 USA
关键词
Metallization; Corrosion pathways; Silver reactive inks; Cell degradation; RAMAN-SPECTROSCOPY; ACETATE; DEGRADATION; FEATURES; PHENOL; LEAD;
D O I
10.1016/j.solmat.2020.110900
中图分类号
TE [石油、天然气工业]; TK [能源与动力工程];
学科分类号
0807 ; 0820 ;
摘要
Silver-based metallizations in photovoltaic modules are susceptible to corrosion by acetic acid generated in ethylene vinyl acetate encapsulated modules, resulting in power losses over time. Here, three silver-based metallizations are exposed to diluted acetic acid, in concentrations representative of that found in field-exposed modules. Compositional, morphological, and structural changes of the metallizations are studied over 3000 h of exposure to diluted acetic acid using Raman spectroscopy mapping, X-ray diffraction, and scanning electron microscopy. The three metallizations studied are: 1) a commercial high-temperature fire-through Ag paste, commonly used for Si diffused junction solar cells; 2) a commercial low-temperature paste normally used for silicon heterojunction cells; and 3) a novel low-temperature reactive silver ink shown to be suitable for photovoltaic applications. We find distinct corrosion rates for the high-temperature silver paste and reactive silver ink in the presence of diluted acetic acid. On the other hand, the low-temperature silver paste appears to be more corrosion resistant, likely due to a polymer layer that protects the silver particles.
引用
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页数:8
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