Effect of mass transport along interfaces and grain boundaries on copper interconnect degradation

2004 ◽  
Vol 812 ◽  
Author(s):  
Ehrenfried Zschech ◽  
Moritz A. Meyer ◽  
Eckhard Langer

AbstractIn-situ SEM electromigration studies were performed at fully embedded via/line interconnect structures to visualize the time-dependent void evolution in inlaid copper interconnects. Void formation, growth and movement, and consequently interconnect degradation, depend on both interface bonding and copper microstructure. Two phases are distinguished for the electromigration-induced interconnect degradation process: In the first phase, agglomerations of vacancies and voids are formed at interfaces and grain boundaries, and voids move along weak interfaces. In the second phase of the degradation process, they merge into a larger void which subsequently grows into the via and eventually causes the interconnect failure. Void movement along the copper line and void growth in the via are discontinuous processes, whereas their step-like behavior is caused by the copper microstructure. Directed mass transport along inner surfaces depends strongly on the crystallographic orientation of the copper grains. Electromigration lifetime can be drastically increased by changing the copper/capping layer interface. Both an additional CoWP coating and a local copper alloying with aluminum increase the bonding strength of the top interface of the copper interconnect line, and consequently, electromigration-induced mass transport and degradation processes are reduced significantly.

2000 ◽  
Vol 6 (S2) ◽  
pp. 386-387
Author(s):  
N. Ravishankar ◽  
M.T. Johnson ◽  
C. Barry Carter

The migration of grain boundaries in polycrystalline materials can occur under a variety of driving forces. Grain growth in a single-phase material and Ostwald ripening of a second phase are two common processes involving boundary migration. The mass transport in each of these cases can be related to a chemical potential difference across the grains; due to curvature in the former case and due to a difference in the chemistry in the latter case. The mass transport across grains controls the densification process during sintering. In the case of liquid-phase sintering (LPS), a liquid film may be present at the grain boundaries which results in an enhanced mass transport between grains leading to faster densification. Hence, in LPS, it is important to understand mass transport across and along a boundary containing a liquid film. The use of bicrystals and tricrystals with glass layers in the boundary can provide a controlled geometry by which to study this phenomenon.


2014 ◽  
Vol 70 (a1) ◽  
pp. C32-C32
Author(s):  
Peter Rudolph

The quality of single crystals, epitaxial layers and devices made there from are very sensitively influenced by structural and atomistic deficiencies generated during the crystal growth. Crystalline imperfections comprise point defects, dislocations, grain boundaries, second-phase particles. Over more than a half-century of the development of crystal growth, most of the important defect-forming mechanisms have become well understood [1-2]. As a result, the present state of technology makes it possible to produce crystals of remarkably high quality. However, that is not to say that all problems are already solved. For instance, in comparison with silicon the point defect dynamics in semiconductor and oxide compounds is not nearly as well understood. The density of equivalent defect types and antisites in each sub-lattice is determined by deviation from stoichiometry. Their charge state depends on the Fermi level position leading via interaction with dopants to certain compensation level and complex formation. One measure proves to be the in situ control of stoichiometry. Due to high-temperature dislocation dynamics heterogeneous dislocation substructures are formed. Both, acting thermo-mechanical stress and given point defect situation force the dislocation to glide and climb. In the course of enthalpy minimization the long-range character of dislocation interaction produces agglomerates and patterns with polygonized cell walls, i.e. small angle grain boundaries [3]. Thanks to the rules of correspondence of Taylor and Kuhlmann-Wilsdorf one is able to estimate the interaction between shear stress, dislocation density and cell diameter (Fig.). In epitaxy the Nye tensor, describing dislocation distribution inhomogeneity, affects the layer stress considerably. The growth under minimum stress, solution hardening and in situ stoichiometry control are effective counteracting methods. One of the most serious consequences during cooling down of as-grown crystals is the point defect condensation in precipitates and micro-voids decorating dislocation patterns or inducing high mechanical misfit stress that generates dislocation loops. It proves to be favourable to anneal the crystal a few degrees below the melting point in order to dissolve the particles and re-diffuse their into the crystal matrix.


2013 ◽  
Vol 753 ◽  
pp. 221-224 ◽  
Author(s):  
Krzysztof Sztwiertnia ◽  
Magdalena Bieda ◽  
Anna Korneva

In situ orientation mapping using TEM and calorimetric measurements were carried out to investigate the annealing behavior of cold-rolled 6013 aluminum alloy. The recrystallization of the material can be considered to be a number of processes that correspond to two separate stored energy release peaks. In the temperature range of the peak 1, the deformation zones around the large second-phase particles acted as sites for particle-stimulated nucleation. In the matrix, at the same time, some elongation of grains occurred. The elongated matrix grains appeared because of the reduction of the dislocation density and the annihilation of some low-angle grain boundaries between chains of subgrains lying in layers parallel to the sheet plane. The matrix processes in this temperatures range can be considered forms of continuous recrystallization. The matrix high-angle grain boundaries started to migrate at the temperature range of the peak 2. They moved mostly in the direction normal to the sheet plane. Heating of the sample for an appropriate time at those temperatures resulted in the complete discontinuous recrystallization of the material. The recrystallized microstructure was dominated now by elongated grains, which were a few times thicker than those obtained by annealing at the temperatures of the peak 1.


1989 ◽  
Vol 257 (4) ◽  
pp. G539-G547
Author(s):  
S. J. Hersey ◽  
A. Perez ◽  
S. Matheravidathu ◽  
G. Sachs

Gastric glands, isolated from rabbit, were permeabilized with digitonin to permit measurement of H+-K+-adenosinetriphosphatase (ATPase) activity and proton transport in situ. Measurement of proton gradient formation using acridine orange fluorescence showed two phases of ATP-driven proton accumulation; one phase occurs spontaneously in KCl medium and one phase requires the K+ ionophore valinomycin. Valinomycin was found to increase H+-K+-ATPase activity, indicating that the second phase is because of increased proton transport rather than a decrease in proton leak rate. The acid-activated, irreversible inhibitor, omeprazole, was used to selectively eliminate the H+-K+-ATPase molecules associated with the spontaneous component of proton transport. After omeprazole treatment a residual, valinomycin-dependent component of proton transport could be demonstrated. These results are interpreted as evidence for two compartments of H+-K+-ATPase, separated by a barrier that prevents K+ diffusion and pH equilibration. The two compartments may be separated also on the basis of anion selectivity. The spontaneously active compartment was found to be functional with various anions, including sulfate and isethionate, whereas the valinomycin-dependent component is highly selective for chloride. The proportion of H+-K+-ATPase that exists in each compartment was quantitated by measuring the fraction of total ATPase activity that could be inhibited by omeprazole in the absence and presence of valinomycin. For glands that were preconditioned with cimetidine, approximately 30% of the inhibitable enzyme was found associated with the spontaneous compartment, and this fraction increased to approximately 70% with histamine preconditioning.(ABSTRACT TRUNCATED AT 250 WORDS)


2005 ◽  
Vol 71 (5) ◽  
pp. 2520-2529 ◽  
Author(s):  
Satoshi Okabe ◽  
Tsukasa Ito ◽  
Kenichi Sugita ◽  
Hisashi Satoh

ABSTRACT The succession of sulfur-oxidizing bacterial (SOB) community structure and the complex internal sulfur cycle occurring in wastewater biofilms growing under microaerophilic conditions was analyzed by using a polyphasic approach that employed 16S rRNA gene-cloning analysis combined with fluorescence in situ hybridization, microelectrode measurements, and standard batch and reactor experiments. A complete sulfur cycle was established via S0 accumulation within 80 days in the biofilms in replicate. This development was generally split into two phases, (i) a sulfur-accumulating phase and (ii) a sulfate-producing phase. In the first phase (until about 40 days), since the sulfide production rate (sulfate-reducing activity) exceeded the maximum sulfide-oxidizing capacity of SOB in the biofilms, H2S was only partially oxidized to S0 by mainly Thiomicrospira denitirificans with NO3 − as an electron acceptor, leading to significant accumulation of S0 in the biofilms. In the second phase, the SOB populations developed further and diversified with time. In particular, S0 accumulation promoted the growth of a novel strain, strain SO07, which predominantly carried out the oxidation of S0 to SO4 2− under oxic conditions, and Thiothrix sp. strain CT3. In situ hybridization analysis revealed that the dense populations of Thiothrix (ca. 109 cells cm−3) and strain SO07 (ca. 108 cells cm−3) were found at the sulfur-rich surface (100 μm), while the population of Thiomicrospira denitirificans was distributed throughout the biofilms with a density of ca. 107 to 108 cells cm−3. Microelectrode measurements revealed that active sulfide-oxidizing zones overlapped the spatial distributions of different phylogenetic SOB groups in the biofilms. As a consequence, the sulfide-oxidizing capacities of the biofilms became high enough to completely oxidize all H2S produced by SRB to SO4 2− in the second phase, indicating establishment of the complete sulfur cycle in the biofilms.


2006 ◽  
Vol 914 ◽  
Author(s):  
Zung-Sun Choi ◽  
Reiner Mönig ◽  
Carl V. Thompson ◽  
Michael Burns

AbstractWe have observed the real-time behavior of electomigration-induced voids in both passivated and unpassivated copper interconnects in a Scanning Electron Microscope (SEM), and correlated void nucleation, growth, drift and stagnation with post-electromigration crystallographic microanalyses carried out using Electron Back-Scattered Diffraction (EBSD) analysis. Voids that nucleate at various locations along the interconnects often drift toward the cathode, where they grow, coalesce, and eventually cause electrical failure. In-situ SEM observations allowed for the tracking of void shapes and drift rates over long (multi-grain) distances. Changes in the size and the velocity of the voids were observed when the voids passed through different grains. These changes are attributed to the difference in diffusivity for different grain orientations. In passivated lines, voids were often trapped at individual grain boundaries, where they grew to cause failure, or de-trapped to continue to drift toward the cathode. In unpassivated lines, voids did not drift, but instead always nucleated and grew and grain boundaries. Locations at which voids grew in unpassivated lines, or at which voids were trapped and grew in passivated lines, were correlated with the crystallographic orientations of “upwind” and “downwind” grains. From these analyses, we find that the average electromigration interface diffusivities (z*D) as a function of grain orientation are ordered according to {100} > {111} > {110}. Quantitative analysis of void dynamics, correlated with crystallographic microanalyses, provides important data for modeling of electromigration-induced failure, and for process-optimization for improved reliability.


2012 ◽  
Vol 2012 ◽  
pp. 1-7 ◽  
Author(s):  
E. Moncada ◽  
R. Quijada ◽  
P. Zapata

The nanocomposites formation byin situpolymerization used a metallocene catalyst (butyl-2-cyclopentadienyl zirconium 2-chlorines) and a hectorite synthetic clay type which is discussed. This research was carried out in two phases. The first phase consisted of mixing the components of the metallocenic polymerization reaction (metallocene-methylaluminoxane-ethylene) with clay in a reactor. In the second phase, the metallocenic catalytic system was supported by clay particles and then a polymerization reaction was made. In this second phase, the clay particles were modified using a sol-gel reaction with different pH values: pH = 3, pH = 8, and pH = 12. The results were compared in terms of the catalytic activity in the different systems (phase 1 and phase 2) and the nanoparticle morphology of nanocomposites generated in this study.


2021 ◽  
Vol 12 (1) ◽  
Author(s):  
Bushra Jabar ◽  
Fu Li ◽  
Zhuanghao Zheng ◽  
Adil Mansoor ◽  
Yongbin Zhu ◽  
...  

AbstractNanocomposite engineering decouples the transport of phonons and electrons. This usually involves the in-situ formation or ex-situ addition of nanoparticles to a material matrix with hetero-composition and hetero-structure (heC-heS) interfaces or hetero-composition and homo-structure (heC-hoS) interfaces. Herein, a quasi homo-composition and hetero-structure (hoC-heS) nanocomposite consisting of Pnma Bi2SeS2 - Pnnm Bi2SeS2 is obtained through a Br dopant-induced phase transition, providing a coherent interface between the Pnma matrix and Pnnm second phase due to the slight structural difference between the two phases. This hoC-heS nanocomposite demonstrates a significant reduction in lattice thermal conductivity (~0.40 W m−1 K−1) and an enhanced power factor (7.39 μW cm−1 K−2). Consequently, a record high figure-of-merit ZTmax = 1.12 (at 773 K) and a high average figure-of-merit ZTave = 0.72 (in the range of 323–773 K) are achieved. This work provides a general strategy for synergistically tuning electrical and thermal transport properties by designing hoC-heS nanocomposites through a dopant-induced phase transition.


2016 ◽  
Author(s):  
Jan Eichler ◽  
Ina Kleitz ◽  
Maddalena Bayer ◽  
Daniela Jansen ◽  
Sepp Kipfstuhl ◽  
...  

Abstract. Impurities control a variety of physical properties of polar ice. Their impact can be observed at all scales – from the microstructure (e.g., grain size and orientation) to the ice sheet flow behavior (e.g., borehole tilting and closure). Most impurities are likely to form micrometer-sized second phase inclusions. It has been suggested that these particles control the grain size of polycrystalline ice by the pinning of grain boundaries (Zener pinning), which should be reflected in the distribution of the inclusions in relation to the grain boundary network. We used an optical microscope to generate high-resolution large-scale maps (3 μm pix−1, 8 × 2 cm2) of the distribution of micro-inclusions in four samples from the EDML (Antarctica) and NEEM (Greenland) polar ice cores. The in-situ positions of more than 5000 μ-inclusions have been determined. A Raman microscope was used to confirm the extrinsic nature of a sample proportion of the mapped inclusions. A superposition of the 2D grain boundary network and μ-inclusion distributions show no significant correlations between grain boundaries and μ-inclusions. In particular, no signs could be found of grain boundaries harvesting μ-inclusions, no evidence of μ-inclusions inhibiting grain boundary migration by slow mode pinning could be detected. Consequences for our understanding of the impurity effect on ice microstructure and rheology are discussed.


2020 ◽  
Vol 321 ◽  
pp. 12043
Author(s):  
Nicholas E. Byres ◽  
João Quinta da Fonseca ◽  
Benjamin Dod ◽  
Jack Donoghue ◽  
Alec Davis ◽  
...  

The ß-annealing of Titanium-6Al-4V (Ti64) wrought aerospace components can lead to the development of abnormal grain structures (AGS) that jeopardise material performance. Therefore, an in-depth understanding into the origins of AGS will help in the design of processing routes that can avoid the conditions that lead to their development. This research demonstrates the application of novel concurrent in-situ heating and electron back scatter diffraction (EBSD) techniques to help elucidate possible mechanisms for the development of AGS. It was found that primary-a (ap) may play a key role, acting as a second phase particle, in pinning the ß-phase grain boundaries during recrystallisation. The strengthening of a large area cube component texture macrozone, consisting of predominantly low angle grain boundaries, is also a prerequisite for the development of AGS.


Sign in / Sign up

Export Citation Format

Share Document