Ultra-high refractive index polymers in the visible wavelength for nanoimprint lithography

Author(s):  
Carlos A. Pina-Hernandez ◽  
Adam Legacy ◽  
Stefano Cabrini ◽  
Keiko Munechika
2020 ◽  
Vol 31 (1) ◽  
pp. 256-260 ◽  
Author(s):  
Yunhui Tang ◽  
Stefano Cabrini ◽  
Jun Nie ◽  
Carlos Pina-Hernandez

2016 ◽  
Vol 41 (15) ◽  
pp. 3423 ◽  
Author(s):  
Alexander Koshelev ◽  
Giuseppe Calafiore ◽  
Carlos Piña-Hernandez ◽  
Frances I. Allen ◽  
Scott Dhuey ◽  
...  

Author(s):  
Junlun Qiu ◽  
Getian Hu ◽  
Yuqiao Wang ◽  
Yurui Wang ◽  
Ming Luo ◽  
...  

This paper demonstrates a novel resist with high refractive index for UV-curing nanoimprint lithography based on o-phenoxyphenyl acrylated polytitanoxane oligomer. The oligomer is synthesized by hydrolysis and condensation of Ti-OEt...


Author(s):  
E. Zanchetta ◽  
G. Della Giustina ◽  
A. Gandin ◽  
V. Auzelyte ◽  
G. Brusatin

AbstractDirect printing of spin-on functional films is probably the most efficient method to develop low-cost novel photonic nanodevices, such as diffraction gratings, planar waveguides, nano- lasers, and antireflective coatings. For these applications high refractive index transparent materials are demanded; however, this class of materials generally requires inorganic oxides, well known for their hardness, typical of ceramic materials, and so incompatible with a soft character of printable resins. Herein, inorganic high refractive index TiO2 micro- and nano- structures, with unusual depth up to 600 nm and aspect ratio larger than 5, are obtained by combining thermal nanoimprint lithography (NIL) with UV curing. To achieve printed patterns, a hybrid organic-inorganic spin-on film is deposited at low-temperature by sol–gel processing. Two distinct bottom-up synthetic approaches are used, called in situ and ex situ, using titanium isopropoxide (90%) or TiO2 anatase nanoparticles (70%), respectively, and adding a silica sol modified by organic moieties. The two syntheses were optimized to obtain, after patterning by thermal imprint, amorphous or crystalline titania crack-free micro- and nano- patterns for in situ and ex situ, respectively. The further UV irradiation converts imprinted films to totally inorganic patterns, through the titania photocatalytic effect, allowing refractive indexes up to 1.82 at 632 nm to be achieved. This novel strategy of combining thermal imprint with UV exposure allows inorganic deep patterns to be fabricated without a calcination step, which is generally needed for inorganic resists processing. Eventually, a thermal treatment only at 300 °C can be applied to achieve a final refractive index of 2 at 632 nm.


2019 ◽  
Author(s):  
Mohammad Atif Faiz Afzal ◽  
Mojtaba Haghighatlari ◽  
Sai Prasad Ganesh ◽  
Chong Cheng ◽  
Johannes Hachmann

<div>We present a high-throughput computational study to identify novel polyimides (PIs) with exceptional refractive index (RI) values for use as optic or optoelectronic materials. Our study utilizes an RI prediction protocol based on a combination of first-principles and data modeling developed in previous work, which we employ on a large-scale PI candidate library generated with the ChemLG code. We deploy the virtual screening software ChemHTPS to automate the assessment of this extensive pool of PI structures in order to determine the performance potential of each candidate. This rapid and efficient approach yields a number of highly promising leads compounds. Using the data mining and machine learning program package ChemML, we analyze the top candidates with respect to prevalent structural features and feature combinations that distinguish them from less promising ones. In particular, we explore the utility of various strategies that introduce highly polarizable moieties into the PI backbone to increase its RI yield. The derived insights provide a foundation for rational and targeted design that goes beyond traditional trial-and-error searches.</div>


2013 ◽  
Vol 28 (6) ◽  
pp. 671-676 ◽  
Author(s):  
Yu-Qing ZHANG ◽  
Li-Li ZHAO ◽  
Shi-Long XU ◽  
Chao ZHANG ◽  
Xiao-Ying CHEN ◽  
...  

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