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Brian J. Rodriguez

Researcher at University College Dublin

Publications -  251
Citations -  9953

Brian J. Rodriguez is an academic researcher from University College Dublin. The author has contributed to research in topics: Piezoresponse force microscopy & Ferroelectricity. The author has an hindex of 53, co-authored 236 publications receiving 8711 citations. Previous affiliations of Brian J. Rodriguez include National University of Ireland & Max Planck Society.

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Biocompatibility of ferroelectric lithium niobate and the influence of polarization charge on osteoblast proliferation and function.

TL;DR: The cells showed enhanced proliferation rates and improved osteoblast function through mineral formation on the positively and negatively charged LN surfaces compared to electrostatically neutral x-cut LN and a glass cover slip control, highlighting the potential of LN as a template for investigating the role of charge on cellular processes.
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Piezoresponse force microscopy for piezoelectric measurements of III-nitride materials

TL;DR: In this article, piezoresponse force microscopy (PFM) was used to investigate the polarity distribution of GaN-based lateral polarity heterostructures with nanometer scale spatial resolution.
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Plasmon enhanced Raman from Ag nanopatterns made using periodically poled lithium niobate and periodically proton exchanged template methods

TL;DR: In this paper, the plasmon active properties of Ag nanopattern arrays formed using ferroelectric lithography based on two separate approaches, i.e., periodically poled lithium niobate (PPLN) and periodically proton exchanged (PPE) template methods, were investigated.
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Accelerated Development of Supramolecular Corneal Stromal-Like Assemblies from Corneal Fibroblasts in the Presence of Macromolecular Crowders.

TL;DR: The influence of macromolecular crowding (MMC)/excluding volume effect, a biophysical phenomenon that accelerates thermodynamic activities and biological processes by several orders of magnitude, in human corneal fibroblast (HCF) culture, indicates that MMC may be suitable not only for clinical translation and commercialization of tissue engineering by self-assembly therapies, but also for the development of in vitro pathophysiology models.