High-powered thermal gel degradation evaluation on board-level HFCBGA subjected to reliability tests

HFCBGA is a thermally enhanced FCBGA with its heat spreader extending the heat conduction area by connecting itself to the rear side of the silicon die. A thermal interface material plays an important role as a heat conduction path. The thermal performance should not only be checked at time zero, and several reliability tests have to be undertaken to uncover the field conditions faced by end users. A temperature cycling test, highly-accelerated temperature and humidity stress test and multiple reflows are utilized to investigate the thermal resistance of junction to case of a selected thermal gel.     

Layer by layer characterisation of the degradation process in PCDTBT:PC71BM based normal architecture polymer solar cells

This work demonstrates the stability and degradation of OSCs based on poly[N-9′-heptadecanyl-2,7-carbazole-alt-5,5-(4′,7′-di-2-thienyl-2′,1′,3′ benzothiadiazole)] (PCDTBT): (6,6)-Phenyl C₇₁ butyric acid methyl ester (PC₇₁BM) photoactive blend layers as a function of ageing time in air. Analysis of the stability and degradation process for the OSCs was conducted under ambient air by using current-voltage (I-V) measurements and x-ray photoelectron spectroscopy (XPS). The interface between photoactive layer and HTL (PEDOT:PSS) was also investigated. Device stability was investigated by calculating decay in power conversion efficiency (PCE) as a function of ageing time in the air. The PCE of devices decrease from 5.17 to 3.61% in one week of fabrication, which is attributed to indium and oxygen migration into the PEDOT:PSS and PCDTBT:PC₇₁BM layer. Further, after aging for 1000 h, XPS spectra confirm the significant diffusion of oxygen into the HTL and photoactive layer which increased from 3.0 and 23.3% to 20.4 and 35.7% in photoactive layer and HTL, respectively. Similarly, the indium content reached to 17.9% on PEDOT:PSS surface and 0.4% on PCDTBT:PC₇₁BM surface in 1000 h. Core-level spectra of active layer indicate the oxidation of carbon atoms in the fullerene cage, oxidation of nitrogen present in the polymer matrix and formation of In₂O₃ due to indium diffusion. We also observed a steady fall in the optical absorption of the active layer during ageing in ambient air and it reduced to 76.5% of initial value in 1000 h. On the basis of these experimental results, we discussed key parameters that account for the degradation process and stability of OSCs in order to improve the device performance.     

Dielectric function and degradation process of poly(triarylamine) (PTAA)

We investigated the optical properties and the degradation process of the organic p-type semiconductor poly(triarylamine) (PTAA) in the mid infrared region. The dielectric function of PTAA was determined in the spectral region of 700 up to 6000 cm⁻¹ by modeling ellipsometric measurements. Due to degradation at 65 °C, PTAA thin films developed carbonyl and hydroxyl features in the infrared spectra. Degradation under 85% RH additionally led to absorption signals of water. A degradation of the bare gold substrates was also observed. For bare gold films, morphology changed upon degradation and adsorption of hydrocarbons from the ambience took place.     

微波器件失效率快速试验方法研究

介绍了微波低噪声GaAs FET恒定应力加速寿命试验结果,沟道温度T_(ch)为145℃时,平均寿命MTTF为9.64×10~6h,最主要的失效模式是源漏饱和电流I_(DSS)退化降低。建立了表征GaAs FET稳定性的敏感参数I_(DSS)的退化模型InP=a+blnt,分析了I_(DSS)退化与温度应力的加速关系。提出了快速推断器件可靠性的建议。     

Diffusion and influence of Cu on properties of CdTe thin films and CdTe/CdS cells

The effective diffusion coefficients of Cu for thermal and photodiffusion in the CdTe films have been estimated from resistivity versus duration of thermal or photoannealing curves. In the temperature range 60–200°C the effective coefficient of thermal diffusion (D_t) and photodiffusion (D_ph) are described as D_t=7.3×10⁻⁷exp(−0.33/kT) and D_ph=4.7×10⁻⁸exp(−0.20/kT).It is found that the diffusion doping of CdTe thin films by Cu at 400°C results in a sharp decrease of resistivity up to 7 orders of magnitude of p-type material, depending on thickness of Cu film. The comparative study of performance of CdTe(Cu)/CdS and CdTe/CdS cells has been studied. It is shown that the diffusion doping of CdTe film by Cu increases efficiency of CdTe(Cu)/CdS cells from 0.9% to 6.8%. The degradation of photovoltaic parameters of CdTe(Cu)/CdS cell, during testing under forward and reverse bias at room temperature, proceeds at a larger rate than those of CdTe/CdS cell without Cu. The degradation of performance of CdTe(Cu)/CdS cells is tentatively assigned to electrodiffusion of Cu in CdTe, resulting in redistribution of concentration of Cu-related centers in CdTe film and heterojunction region.     

Investigation of thermal and electrochemical degradation of fuel cell catalysts

A significant problem hindering large-scale implementation of proton exchange membrane (PEM) fuel cell technology is the loss of performance during extended operation and automotive cycling. Recent investigations of the deterioration of cell performance have revealed that a considerable part of the performance loss is due to the degradation of the electrocatalyst. In this study, an attempt is made to experimentally simulate the degradation processes such as carbon corrosion and platinum (Pt) surface area loss using an accelerated thermal sintering protocol. Two types of Tanaka fuel cell catalyst samples were heat-treated at 250 °C in humidified helium (He) gas streams and several oxygen (O₂) concentrations. The catalysts were then cycled electrochemically in pellet electrodes to determine the hydrogen adsorption (HAD) area and its evolution in subsequent electrochemical cycling. Samples that had undergone different degrees of carbon corrosion and Pt sintering were characterized for changes in carbon mass, active Pt surface area, BET (Brunauer, Emmett and Teller) surface area, and Pt crystallite size. Studies of the effect of oxygen and water concentration on two Tanaka catalysts, dispersed on carbon supports with varying BET areas, revealed that carbon oxidation in the presence of Pt follows two pathways: an oxygen pathway that leads to mass loss due to formation of gaseous products, and a water pathway that results in mass gains, especially for high BET area supports. These processes may be assisted by the formation of highly reactive OH and OOH type radicals. Platinum surface area loss, measured at varying oxygen concentrations and as a function of sintering time using X-ray diffraction (XRD), CO chemisorption, and electrochemical hydrogen adsorption, reveal an important role for carbon corrosion rather than an increase in Pt particle size for the surface area loss. Platinum surface area loss during 10 h of thermal degradation was equivalent to electrochemical degradation observed over 500 cycles for a Tanaka Pt/Vulcan electrode cycled between 0 and 1.2 V (normal hydrogen electrode-NHE). Carbon mass loss observed for 5 h of thermal degradation was comparable to that obtained during a potential hold for 86 h at 1.2 V (NHE) and 95 °C for the same catalysts.     

Efficiency and degradation of a copper indium diselenide photovoltaic module and yearly output at a sunny site in Jordan

The present work mainly deals with the testing and modeling of a commercially-available copper indium diselenide (CIS) ST40 module from the former Siemens Solar Industries (SSI). For this purpose, a large quantity of current/voltage characteristics were measured in the Paul Scherrer Institute (PSI)’s photovoltaic test-facility under different cell temperatures, solar irradiation and air mass, AM, conditions. They were used to develop a semi-empirical efficiency model to correlate all measured data sets. The goal was to make available a model, allowing quick and accurate calculation of the performance of the CIS module under all relevant operating conditions.

For the undegraded state of the module, the efficiency model allowed us to deduce the efficiency at Standard Test Conditions, STC, and its temperature coefficient at STC, which were 11.58% and minus 0.050%/°C, respectively. The output of the undegraded module under STC was found to be 42.4 W, i.e., 6% higher than specified by the manufacturer (40 W). Furthermore, the efficiency does not decrease with increasing air mass. At a cell temperature of 25 °C and a relative air mass of 1.5, the module has a maximum in efficiency of 12.0% at an irradiance of about 650 W/m². This indicates that the series-resistance losses become significant at higher irradiances. Hence, improving the transparent conducting oxide (TCO) electrode on the front side of the cells might lead to a higher output at high irradiances.

Identical testing and modeling were repeated after having exposed the module to real weather conditions for one year. We found that the STC efficiency was reduced by 9.0%, from 11.58 down to 10.54%. The temperature coefficient of the efficiency had changed from minus 0.050 %/°C to minus 0.039%/°C. These results indicate possible chemical changes in the semiconductor film. The output of the module at STC was reduced by 9.0% from 42.4 W down to 38.6 W.

Using meteorological data from a sunny site in the South of Jordan (Al Qauwairah) and the efficiency model presented here allows us to predict the yearly electricity yield of the CIS module in that area. Prior to degradation, the yield was found to be 362 kWh/m² for the Sun-tracked module; and 265 kWh/m² for the fix-installed module (South-oriented, at an inclination angle of 30°). After degradation the corresponding yields were found to be 334 and 241 kWh/m²; meaning losses of 8.4% and 9.5%, respectively. (Note: all units of energy, kWh, are referred to the active cell area.) Having available efficiency models for other module types, similar predictions of the yield can be made, facilitating the comparisons of the yearly yields of different module types at the same site. This in turn allows selecting the best module type for a particular site.     

悬架双筒液压充气减振器的基本结构和工作原理

该文对双筒液压充气减振器的基本结构和工作原理进行了分析，指出双筒液压充气减振器由于提高了减振器的临界速度，从而增强了外特性的抗畸变能力。提供了国产夏利（ＴＪ７１００）微轿车前减振器充气前后的试验外特性。     

Stability of Polymer Electrolyte Membranes In Fuel Cells: Initial Attempts To Bridge Physical And Chemical Degradation Modes

In recent years, research on coupled degradation of Nafion^® membrane in polymer electrolyte fuel cell has generated huge interest among the scientific community. The coupled phenomenon behind the premature failure of fuel cell membranes in terms of its degradation is not well established. As the researches on this are in its adolescence, we try to provide some significant answers to the degradation phenomenon in terms of mechanically stimulated chemical degradation of the membrane. While the basic concept heavily relies on accurately modeling the membrane for its mechanical response to obtain molecular chain stretch, the results are utilized by the modified chemical rate equation for unzipping degradation mechanism. This article addresses significant degradation issues such as localized membrane thinning and pinhole formation, and inhomogeneous damage patterns in membrane electrode assembly in terms of mechanically induced accelerated chemical degradation of the membrane.     

甲苯的复合氧化反应动力学及其降解的研究

在停止流动光谱仪反应器中研究了污水中的甲苯在3种氧化剂H2O2、O3和O3/H2O2、温度298K及pH=3~11时的氧化反应动力学及其降解过程。实验结果表明,甲苯在H2O2中氧化速率很慢,在O3中的氧化速率较快,当两种强氧化剂H2O2与O3耦合,构成高级氧化过程(AOP),甲苯的氧化速率最快。随着pH值增加,甲苯在O3和O3/H2O2中的氧化速率进一步加快。通过理论分析,初步探讨了有机污染物降解过程的机理;通过对实验数据的回归分析,获得了反应动力学常数。