Effect of Electromigration on the Mechanical Performance of Sn-3.5Ag Solder Joints with Ni and Ni-P Metallizations

The effect of moderate electric current density (1 × 10³ to 3 × 10³ A/cm²) on the mechanical properties of Ni-P/Sn-3.5Ag/Ni-P and Ni/Sn-3.5Ag/Ni solder joints was investigated using a microtensile test. Thermal aging was carried out at 160°C for 100 h while the current was passed. The interfacial microstructure and intermetallic compound (IMC) growth were analyzed. It was found that, at these levels of current density, there were no observable voids or hillocks. Samples aged at 160°C without current stressing failed mostly inside the bulk solder with significant prior plastic deformation. The passage of current was found to cause brittle failure of the solder joints and this tendency for brittle failure increased with increasing current density. Fractographic analysis showed that, in most of the electrically stressed samples, fracture occurred at the interface region between the solder and the joining metals. The critical current density that caused brittle fracture was about 2 × 10³ A/cm². Once brittle fracture occurred, the tensile toughness, defined as the energy per unit fractured area, was usually lower than ~5 kJ/m², compared with the case of ductile fracture where this value was typically greater than ~9 kJ/m². When comparing the two types of joint, the brittle failure was found to be more severe with the Ni than with the Ni-P joint. This work also found that the passage of electric current affects the IMC growth rate more significantly in the Ni than in the Ni-P joint. In the case of the Ni joint, the Ni₃Sn₄ IMC at the anode side was appreciably thicker than that formed at the cathode side. However, in the case of electroless Ni-P metallization, this difference was much smaller.     

A New Method for Blocking Probability Evaluation in OBS/OPS Networks With Deflection Routing

In this paper, we present a new method for the estimation of blocking probabilities in bufferless optical burst or packet switched networks. In such networks, deflection routing is used to reduce blocking probability. However, it requires certain wastage due to trunk reservation that must be used to avoid instability. We provide a wide range of simulation and numerical results to validate our new approximation method and demonstrate various effects on blocking probability and utilization, such as network size, trunk size, the maximal number of allowable deflections, and burst/packet length.     

Optimal resource allocation in uplink SC-FDMA systems

We present algorithms for resource allocation in Single Carrier Frequency Division Multiple Access (SC-FDMA) systems, which is the uplink multiple access scheme considered in the Third Generation Partnership Project-Long Term Evolution (3GPP-LTE) standard. Unlike the well-studied problem of Orthogonal Frequency Division Multiple Access (OFDMA) resource allocation, the "subchannel adjacency" restriction, whereby users can only be assigned multiple subchannels that are adjacent to each other, makes the problem much harder to solve. We present a novel reformulation of this problem as a pure binary-integer program called the set partitioning problem, which is a well studied problem in operations research. We also present a greedy heuristic algorithm that approaches the optimal performance in cases of practical interest. We present simulation results for 3GPP-LTE uplink scenarios.     

Hole mobilities of thermally polymerized triaryldiamine derivatives and their application as hole-transport materials in organic light-emitting diodes (OLEDs)

This paper describes the synthesis of three triaryldiamine derivatives presenting two thermally polymerizable trifluorovinyl ether groups that can be polymerized through thermal curing to form perfluorocyclobutyl (PFCB) polymers. These PFCB polymers, studied using time-of-flight techniques for the first time, exhibited remarkable non-dispersive hole-transport properties, with values of μ_h of ca. 10^?4 cm² V^?1 s^?1. When we employed these thermally polymerized polymers as hole-transport layers (HTLs) in electroluminescence devices containing tris(8-hydroxyquinolate) aluminum (Alq₃) as the emission layer, we obtained high current densities (ca. 3400 mA cm^?2), impressive brightnesses (5 × 10⁴ cd m^?2), and high external quantum efficiencies (EQEs = 1.43%). These devices exhibited the same turn-on voltage, but higher EQEs, relative to those incorporating the vacuum-processed model compound N,N′-di(1-naphthyl)-N,N′-diphenylbenzidine (α-NPD) (EQE = 1.37%) as the HTL under the same device structure.     

The characteristics of carbon nanotube‐reinforced poly(phenylene sulfide) nanocomposites

Multiwall carbon nanotube reinforced poly (phenylene sulfide) (PPS) nanocomposites were successfully fabricated through melt compounding. Structural, electrical, thermal, rheological, and mechanical properties of the nanocomposites were systematically studied as a function of carbon nanotube (CNT) fraction. Electrical conductivity of the polymer was dramatically enhanced at low loading level of the nanotubes; the electrical percolation threshold lay between 1 and 2 wt % of the CNTs. Rheological properties of the PPS nanocomposites also showed a sudden change with the CNT fraction; the percolation threshold was in the range of 0–0.5 wt % of CNTs. The difference in electrical and rheological percolation threshold was mainly due to the different requirements needed in the carbon nanotube network in different stages. The crystallization and melting behavior of CNT‐filled PPS nanocomposites were studied with differential scanning calorimetry; no new crystalline form of PPS was observed in the nanocomposites, but the crystallization rate was reduced. The thermal and mechanical properties of the nanocomposites were also investigated, and both of them showed significant increase with CNT fraction. For 5 wt % of CNT‐filled PPS composite, the onset of degradation temperature increased by about 13.5°C, the modulus increased by about 33%, and tensile strength increased by about 172%. © 2009 Wiley Periodicals, Inc. J Appl Polym Sci, 2009     

Double Hysteresis Loop and Aging Effect in K0.5Na0.5NbO3–K5.4Cu1.3Ta10O9 Lead-Free Ceramics

In this work, the double-loop-like characteristics of K_0.5Na_0.5NbO₃+ x mol% K_5.4Cu_1.3Ta₁₀O₉ ceramic and its relationships with the transition temperature, aging, and switching have been investigated. Our results reveal that the phase transition temperature is an important parameter determining the aging requirement for the ceramics to exhibit the double-loop-like characteristics. For a ceramic with a high transition temperature, e.g. the ceramic with x =0.75 (tetragonal–orthorhombic phase temperature ∼206°C), the vacancies can migrate during the crystal transformation and settle in a distribution with the same symmetry as the crystal after the transformation. As a result, defect dipoles along the polarization direction are formed and provide restoring forces to reverse the switched polarizations, and thus producing a double polarization hysteresis ( P – E ) loop. On the other hand, aging is required for a ceramic with a low transition temperature, e.g. aging at 80°C for 30 days is required for the ceramic with x =1.5 (transition temperature ∼175°C). Our results also reveal that the defect dipoles can be switched under a slow-switching electric field (<1 Hz) or at high temperatures (>100°C), thus leading to an opening of the double P – E loop.     

Ionic double layer of atomically flat gold formed on mica templates

Electrical impedance spectroscopy characterisations of gold surfaces formed on mica templates in contact with potassium chloride electrolytes were performed at the electric potential of zero charge over a frequency range of 6 × 10⁻³ to 100 × 10³ Hz. They revealed constant-phase-angle (CPA) behaviour with a frequency exponent value of 0.96 for surfaces that were also characterised as atomically flat using atomic force microscopy (AFM). As the frequency exponent value was only marginally less than unity, the CPA behaviour yielded a realistic estimate for the capacitance of the ionic double layer. The retention of the CPA behaviour was attributed to specific adsorption of chloride ions which was detected as an adsorption conductance element in parallel with the CPA impedance element. Significant variations in the ionic double layer capacitance as well as the adsorption conductance were observed for electrolyte concentrations ranging from 33 μM to 100 mM, but neither of these variations correlated with concentration. This is consistent with the electrical properties of the interface deriving principally from the inner or Stern region of the double layer.     

X-ray diffraction studies of electrochemical graphite intercalation compounds of ionic liquids

Electrochemical intercalation studies are used to characterize a series of ionic liquids composed of a variety of cationic and anionic species. Electrochemically, the ionic liquids are characterized by cyclic voltammograms and charge–discharge experiments for the intercalation and de-intercalation of the various cationic and anionic species into graphite. X-ray structure analysis is also performed to determine the relationship between the electrochemical behaviour of the ionic liquids, and the formation of intercalated graphitic compounds. Two different types of imidazolium cations are studied, specifically the di- and trisubstituted imidazolium. These cations are paired with the following anions: tetrafluoroborate, hexafluorophosphate, bis(trifluoromethanesulfonyl)imide, bis(perfluoroethanesulfonyl)imide, nitrate and hydrogen sulfate. Results indicate stronger intercalation chemistry for the trisubstituted imidazoliums, correlating with the greater charge–discharge efficiencies found for these types of ionic liquids. Many of the anions exhibit very poor charge–discharge efficiencies, correlating to very poorly formed graphite intercalates. The exception to this is the hydrogen sulfate intercalate, which had low charge–discharge efficiencies but formed a well defined graphite intercalate. Only the imide based anions exhibited both high charge–discharge efficiencies and the formation of a clearly defined graphite intercalate.     

An evaluation model for indoor environmental quality (IEQ) acceptance in residential buildings

The indoor environmental quality (IEQ) in residential buildings is examined from the prospect of an occupant's acceptance in four aspects: thermal comfort, indoor air quality, noise level and illumination level. Based on the evaluations by 125 occupants living in 32 typical residential apartments in Hong Kong, this study proposes empirical expressions to approximate the overall IEQ acceptance with respect to four contributors, namely operative temperature, carbon dioxide concentration, equivalent noise level and illumination level, via a multivariate logistic regression model. A range of IEQ acceptances for regular residential conditions is determined and the dependence of the predicted overall IEQ acceptance on the variations of the contributors is discussed. The proposed overall IEQ acceptance can be used as a quantitative assessment criterion for similar residential environments where an occupant's evaluation is expected.     

2-羟基-3-氯丙磺酸钠的合成及结构表征

以环氧氟丙烷为原料,以亚硫酸氢钠和亚硫酸钠为混合磺化剂合成2-羟基-3-氯丙磺酸钠,探讨了磺化剂种类及摩尔比、反应温度,反应时间对产率的影响.结果表明,最佳反应条件为:NaHSO_3与环氧氯丙烷的摩尔比为1:15:1,磺化剂Na_2SO_3与NaHSO_3的摩尔比为0.20:0.62,反应2 h,产率70.8%.产物的熔点为253～254℃.并通过红外光谱、核磁、质谱等方法对产物进行了结构表征.