Wet Chemical Processing with Megasonics Assist for the Removal of Bumping Process Photomasks

2014 ◽  
Vol 2014 (DPC) ◽  
pp. 001966-001981 ◽  
Author(s):  
Sohn Hong Seong ◽  
John Tracy

A new generation of negative tone resists by TOK, JSR, and Dow Chemical is gaining momentum in advanced packaging applications. Resist thickness requirements are actually increasing to the 50-100 um range as Cu pillars are adopted to accommodate the tighter pitches required in advanced packaging. In order to form pillars the resist must be thicker to contain the entire bump structure. Thick, negative tone resists are more transparent to exposure light wavelengths than positive tone resists and can be exposed by the lithography process much faster (~1 x 104 cross-linking chemical events are driven by 1 photochemical event vs. 100 – 1000 for positive tone resist).1 Therefore exposure times can be shorter, post-exposure bake steps can be shorter, and delay before or after exposure is not necessary, saving photolithography time and CoO. And, due to more complete cross-linking throughout the resist, the resist mask profiles are truer (from Flack et.al, “A Comparison of New Thick Photoresists for Solder Bumping”, SPIE 2005).1 The major drawback to negative tone resists is that the solvent strip times of the highly cross-linked resist masks are much longer than for positive tone. Flack et.al. noted resist strip times of 5 minutes for two positive resists used in their experiments vs. 50 minutes for the AZ-100nXT negative tone resist, using AZ400T at 80°C (most likely in an immersion tool). Long strip times or special stripping requirements are noted on the data sheets of the other majority suppliers of negative resists as well. Akrion engineers have developed a novel, single-wafer, negative PR strip processes using organic solvents plus Goldfinger megasonics, to provide 30 - 70% reductions in process times and the associated chemical consumption when compared to processes that do not utilize a megasonics assist. The multi-step process can be accomplished in a single process chamber, with each step optimized for time and temperature based on the resist thickness and solvent stripping chemistry used. In the Akrion process, a period of solvent exposure at low wafer spin speed is used initially to begin swelling and dissolving the thick photoresist layer. This is followed by a second solvent exposure step using aggressive frontside megasonic energy to promote polymer chain scission throughout the bulk of the photoresist layer. Following this step A DI water rinse and spin dry step are sufficient to completely remove the solvent, dissolved photoresist and any polymer residues. This paper reviews the development of the Akrion process and several examples of improvement in stripping time and results from work with customers.

2014 ◽  
Vol 219 ◽  
pp. 225-229
Author(s):  
Hong Seong Sohn ◽  
Tan Kuam Hua ◽  
Ding Liang ◽  
Steven Lee Hou Jang ◽  
Loh Woon Leng ◽  
...  

A new generation of negative tone and chemically amplified positive tone photoresists by TOK, JSR, Dow Chemical and others has gained momentum for advanced packaging applications. Resist thickness requirements are increasing to the 40-100 μm range as Cu pillars and micro-bumps are adopted, to accommodate the tighter pitches required in the newest multi-chip package designs. In order to form the pillars, the resist mask must be thicker than the height of the pillars to contain the entire bump structure.


2014 ◽  
Author(s):  
Richard A. Lawson ◽  
Jun Sung Chun ◽  
Mark Neisser ◽  
Laren M. Tolbert ◽  
Clifford L. Henderson
Keyword(s):  

2016 ◽  
Vol 89 (4) ◽  
pp. 671-688 ◽  
Author(s):  
M. A. L. Verbruggen ◽  
L. van der Does ◽  
W. K. Dierkes ◽  
J. W. M. Noordermeer

ABSTRACT The theoretical model developed by Charlesby to quantify the balance between cross-links creation of polymers and chain scission during radiation cross-linking and further modifications by Horikx to describe network breakdown from aging were merged to characterize the balance of both types of scission on the development of the sol content during de-vulcanization of rubber networks. There are, however, disturbing factors in these theoretical considerations vis-à-vis practical reality. Sulfur- and peroxide-cured NR and EPDM vulcanizates were de-vulcanized under conditions of selective cross-link and random main-chain scissions. Cross-link scission was obtained using thiol-amine reagents for selective cleavage of sulfur cross-links. Random main-chain scission was achieved by heating peroxide vulcanizates of NR with diphenyldisulfide, a method commonly employed for NR reclaiming. An important factor in the analyses of these experiments is the cross-linking index. Its value must be calculated using the sol fraction of the cross-linked network before de-vulcanization to obtain reliable results. The values for the cross-linking index calculated with sol-gel data before de-vulcanization appear to fit the experimentally determined modes of network scission during de-vulcanization very well. This study confirms that the treatment of de-vulcanization data with the merged Charlesby and Horikx models can be used satisfactorily to characterize the de-vulcanization of NR and EPDM vulcanizates.


Polymers ◽  
2019 ◽  
Vol 11 (8) ◽  
pp. 1280 ◽  
Author(s):  
Zaghdoudi ◽  
Kömmling ◽  
Jaunich ◽  
Wolff

Elastomers are susceptible to chemical ageing, i.e., scission and cross-linking, at high temperatures. This thermally driven ageing process affects their mechanical properties and leads to limited operating time. Continuous and intermittent stress relaxation measurements were conducted on ethylene propylene diene rubber (EPDM) and hydrogenated nitrile butadiene rubber (HNBR) samples for different ageing times and an ageing temperature of 125 °C. The contributions of chain scission and cross-linking were analysed for both materials at different ageing states, elucidating the respective ageing mechanisms. Furthermore, compression set experiments were performed under various test conditions. Adopting the two-network model, compression set values were calculated and compared to the measured data. The additional effect of physical processes to scission and cross-linking during a long-term thermal exposure is quantified through the compression set analysis. The characteristic times relative to the degradation processes are also determined.


1953 ◽  
Vol 26 (3) ◽  
pp. 643-654 ◽  
Author(s):  
J. Reid Shelton ◽  
William L. Cox

Abstract The over-all rate of deterioration of physical properties increases with the oxygen concentration, as would be expected from the increased rate of oxygen absorption: The nature of the deterioration resulting from a given amount of oxygen absorbed is influenced also by changes in the partial pressure of oxygen in the aging atmosphere. It appears that chain scission is favored at higher oxygen concentrations, while cross-linking becomes of greater relative importance at lower oxygen concentrations. These data suggest that R⋅ radicals are more effective than RO2⋅ radicals in reacting with double bonds to form crosslinks. Heat aging in the absence of oxygen, as observed by heating a vulcanizate in lamp-grade nitrogen, results in considerable stiffening, particularly in the case of a GR-S black stock. This effect is observed primarily in the first few hours of heating, and may account for some of the erratic behavior observed in the early stages of aging when changes in physical properties are compared on the basis of amount of oxygen absorbed. Higher oxygen concentration brings about a more rapid oxidation, and also results in a higher proportion of chain scission compared to cross-linking for a given amount of oxygen absorbed. As tensile decay is the most evident sign of deterioration of Hevea stocks, it follows that the aging behavior of natural rubber in air at normal storage temperatures will be better than that predicted by high temperature testing in oxygen. In the case of GR-S stocks, on the other hand, oxidative hardening is the most serious result of aging, and consequently, the aging behavior of GR-S stocks in air at normal storage temperatures is poorer than would be expected on the basis of comparative tests in oxygen at higher temperatures.


COSMOS ◽  
2013 ◽  
Vol 09 (01) ◽  
pp. 37-46 ◽  
Author(s):  
S. M. P. KALAISELVI ◽  
T. L. TAN ◽  
R. S. RAWAT ◽  
P. LEE ◽  
S. P. HEUSSLER ◽  
...  

The usage of chemically-amplified, negative tone SU-8 photoresist is numerous, spanning industrial, scientific and medical fields. Hence, in this study, some preliminary studies were conducted to understand the dosage and heat treatment requirements of the SU-8 photoresist essential for pattern generation using X-ray lithography. In this work, using Synchrotron as the X-ray source, SU-8 photoresist was characterized for X-ray lithography in terms of its process parameters such as X-ray exposure dose, post exposure bake (PEB) time and temperature for various photoresist thicknesses which is considered worthwhile in view of applications of SU-8 for the fabrication of very high aspect ratio micro structures. The process parameters were varied and the resultant cross linking of the molecular chains of the photoresist was accurately monitored using a Fourier Transform Infra-Red (FTIR) spectrometer and the results are discussed. The infrared absorption peak at 914 cm-1 in the spectrum of the SU-8 photoresist was found to be a useful indicator for the completion of cross linking in the SU-8 photoresist. Results show that the cross linking of the SU-8 photoresist is at a higher rate from 0 J/cm3 to 30 J/cm3 after which the peak almost saturates regardless of the PEB time. It is a good evidence for the validation of dosage requirement of SU-8 photoresist for effective completion of cross linking, which in turn is a requirement for efficient fabrication of micro and nano structures. An analogous behavior was also observed between the extent of cross linking and the PEB time and temperature. The rate of cross linking declines after a certain period of PEB time regardless of PEB temperature. The obtained results also show a definite relation between variation of the absorbance area of the peak at 914 cm-1 and the X-ray exposure dose.


2006 ◽  
Vol 16 (9) ◽  
pp. 1841-1846 ◽  
Author(s):  
Vempati Srinivasa Rao ◽  
Vaidyanathan Kripesh ◽  
Seung Wook Yoon ◽  
Andrew A O Tay

2015 ◽  
Author(s):  
Richard A. Lawson ◽  
Hannah Narcross ◽  
Brandon Sharp ◽  
Jun Sung Chun ◽  
Mark Neisser ◽  
...  
Keyword(s):  

2018 ◽  
Vol 2018 (1) ◽  
pp. 000361-000364
Author(s):  
Keith Best ◽  
Ognian Dimov ◽  
Sudmun Habib ◽  
Sanjay Malik

Abstract This paper presents a new dielectric material capable of resolving 2 to 3μm features that are required for high density advanced packaging applications. The material is applied in dry film format to be conducive to panel-level processing. The material can be processed at temperatures below 170°C and total thermal shrinkage is below 5%, resulting in exceptionally low stress of 11 MPa. The film is thermally stable at temperatures up to 350°C. Mechanical and electrical properties of the material are state of the art. As the demand for high density packages increases, so will the pressure to lower the cost of manufacturing. Migrating from wafers to large non-circular panels offers several key cost advantages. There are multiple technical challenges that need to be addressed before commercial viability of panel scale manufacturing can be established. A new class of novel dielectric materials will be needed that can be processed at low temperatures and demonstrate low shrinkage to minimize warpage. In this study, 2 to 3μm patterns were successfully formed using i-line stepper exposure conditions. The process started by laminating a 510mm × 515mm panel with highly photosensitive dielectric film. The laminated panels were exposed at a nominal dose of 125 mJ/cm2. Fine negative tone patterns were created after development. For the metallization of the layer, the seed layer was deposited with titanium-copper sputtering. After the seed formation, trenches were filled with copper by an electrolytic plating process.


2014 ◽  
Vol 47 (9) ◽  
pp. 2891-2898 ◽  
Author(s):  
Jeongwoo Lee ◽  
Murthy V. S. N. Maddipatla ◽  
Abraham Joy ◽  
Bryan D. Vogt

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