Evaluation of Cu/Sn-Cu Bump Bonding Processes for 3D Integration Using a Fluxing Adhesive

2010 ◽  
Vol 2010 (DPC) ◽  
pp. 001726-001742
Author(s):  
Alan Huffman ◽  
Jason Reed ◽  
Matthew Lueck ◽  
Christopher Gregory ◽  
Dorota Temple ◽  
...  

The study of copper-based bump structures for interconnects in 3D integration applications has been ongoing for several years. Typically, an array of Cu bumps is bonded to an array of Sn-capped Cu bumps or another Cu bump array using a thermocompression bonding process. These processes rely on high pressures and temperatures to facilitate bonding between the bump arrays. In order for this bonding to take place, some method of oxide removal is normally required for the Cu and/or Cu/Sn bump surfaces before bonding. A number of different methods have been investigated by a number of groups, including chemical cleaning, plasma cleaning, self-assembled monolayers, and no-flow underfill (NUF) materials. The use of NUFs is particularly intriguing, since these materials can be formulated with fluxing agents which could reduce surface oxides on Cu and Sn and can be deposited immediately prior to the thermocompression bonding process. In addition, the material provides a protective encapsulant to the interconnect array, protecting it from environmental damage and adding mechanical strength to the assembly. We will present the results of a study to evaluate new fluxing NUF materials in thermocompression bonding processes on full area array test devices with 25 micron bump pitch. The test devices are fabricated with either Cu or Cu/Sn bumps to provide two different bonding options (Cu to Cu or Cu/Sn to Cu). We will compare the NUF bonding process and resulting bonded interfaces to assemblies fabricated using our standard bonding processes, which rely on both chemical and plasma pretreatment processes to prepare the bump arrays before bonding. Mechanical and electrical data will be used to compare the two bonding processes, as well as SEM cross-section analysis of the bonded interfaces.

2014 ◽  
Vol 553 ◽  
pp. 35-40
Author(s):  
Leyla Ramin ◽  
Ahmad Jabbarzadeh

Molecular dynamics simulation was used to study the effect of pressure on self-assembled monolayers (SAM) of n-alkanethiols [(CH3(CH2) n-1, n=14, 15] on Au (111) for dry systems and in the presence of water. The stress-strain behavior and effects of compression on structural characteristics under various normal pressures have been investigated. We found the effect of compression on tilt and tilt orientation angles for dry and hydrated SAM system. Furthermore, a comparison of the results obtained for tilt and tilt orientation angles for hydrated C14 and C15 indicates a more stable structure for C15 (an odd system) under high pressures. We also found excellent elastic recovery of SAM monolayers with and without water is evidence of their exceptional potential to be used under compression in various conditions. Young’s moduli are calculated for various systems under uniaxial compression.


2007 ◽  
Vol 91 (6) ◽  
pp. 061913 ◽  
Author(s):  
X. F. Ang ◽  
F. Y. Li ◽  
W. L. Tan ◽  
Z. Chen ◽  
C. C. Wong ◽  
...  

2007 ◽  
Vol 990 ◽  
Author(s):  
Xiaofang Ang ◽  
Li Cheong Chin ◽  
Guo Ge Zhang ◽  
Jun Wei ◽  
Zhong Chen ◽  
...  

ABSTRACTElevated bonding temperature for interconnection deteriorates the reliability of both the device and the interconnect; hence the imperative for developing low temperature bonding methods. This study investigates the feasibility of using self-assembled monolayers (SAMs) to assist direct gold-gold bonding. This involves a simple molecular self-assembly process whereby a monolayer of alkyl chains with a sulfur end group is attached to the gold surface prior to thermocompression bonding. Using this method, we have achieved gold to gold bonding at a bonding temperature below 100°C, a significant reduction compared to the conventional bonding temperatures of above 150 °C. We attribute this temperature reduction to two properties of SAMs - (1) surface passivation of the Au surface that precludes adsorption of surface contaminants, and (2) The easy displacement of SAMs through thermal desorption just before bonding occurs. This SAMs-assisted bonding mechanism is supported by X-ray photoelectron spectroscopy (XPS) and surface plasmon resonance (SPR) results.


Langmuir ◽  
2014 ◽  
Vol 30 (13) ◽  
pp. 3832-3844 ◽  
Author(s):  
Yiting Sun ◽  
Mikhail Krishtab ◽  
Herbert Struyf ◽  
Patrick Verdonck ◽  
Steven De Feyter ◽  
...  

1998 ◽  
Vol 95 (6) ◽  
pp. 1339-1342 ◽  
Author(s):  
R. Michalitsch ◽  
A. El Kassmi ◽  
P. Lang ◽  
A. Yassar ◽  
F. Garnier

2003 ◽  
Vol 104 ◽  
pp. 459-462 ◽  
Author(s):  
R. Klauser ◽  
M. Zharnikov ◽  
I.-H. Hong ◽  
S.-C. Wang ◽  
A. Gölzhäuser ◽  
...  

2020 ◽  
Author(s):  
Clément Dulong ◽  
Bruno Madebène ◽  
Susanna Monti ◽  
Johannes Richardi

<div><div><div><p>A new reactive force field based on the ReaxFF formalism is effectively parametrized against an extended training set of quantum chemistry data (containing more than 120 different structures) to describe accurately silver- and silver-thiolate systems. The results obtained with this novel representation demonstrate that the novel ReaxFF paradigm is a powerful methodology to reproduce more appropriately average geometric and energetic properties of metal clusters and slabs when compared to the earlier ReaxFF parametrizations dealing with silver and gold. ReaxFF cannot describe adequately specific geometrical features such as the observed shorter distances between the under-coordinated atoms at the cluster edges. Geometric and energetic properties of thiolates adsorbed on a silver Ag20 pyramid are correctly represented by the new ReaxFF and compared with results for gold. The simulation of self-assembled monolayers of thiolates on a silver (111) surface does not indicate the formation of staples in contrast to the results for gold-thiolate systems.</p></div></div></div>


2020 ◽  
Author(s):  
Xinkai Qiu ◽  
Sylvia Rousseva ◽  
Gang Ye ◽  
Jan C. Hummelen ◽  
Ryan Chiechi

This paper describes the reconfiguration of molecular tunneling junctions during operation via the self-assembly of bilayers of glycol ethers. We use well-established functional groups to modulate the magnitude and direction of rectification in assembled tunneling junctions by exposing them to solutions containing different glycol ethers. Variable-temperature measurements establish that rectification occurs by a bias-dependent tunneling-hopping mechanism and that glycol ethers, beside being an unusually efficient tunneling medium, behave identically to alkanes. We fabricated memory bits from crossbar junctions prepared by injecting eutectic Ga-In into microfluidic channels. Two 8-bit registers were able to perform logical AND operations on bit strings encoded into chemical packets as microfluidic droplets that alter the composition of the crossbar junctions through self-assembly to effect memristor-like properties. This proof of concept work demonstrates the potential for fieldable molecular-electronic devices based on tunneling junctions of self-assembled monolayers and bilayers.


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