dc.contributor.advisor | Ghosh, Ambarish | |
dc.contributor.advisor | Jayaprakash, Balaji | |
dc.contributor.advisor | Sikdar, Sujit K | |
dc.contributor.author | Yadav, Saumitra | |
dc.date.accessioned | 2020-07-27T10:51:17Z | |
dc.date.available | 2020-07-27T10:51:17Z | |
dc.date.submitted | 2018 | |
dc.identifier.uri | https://etd.iisc.ac.in/handle/2005/4511 | |
dc.description.abstract | Neuroscience is at crossroads. Several interdisciplinary optical developments centred around
nonlinear optical processes helps in better understanding of brain function at sub-micron and
millisecond precision. Traditional neurophysiological approaches measure the activities from
one or group of neurons at a time. Multi-Photon microscopy paves the way towards network
level understanding of brain circuit in slices and also in behaving animals. The technological
advancement in the field of nonlinear microscopy and a rich toolkit provided by developments
in nanoscience and nanotechnology (Rubinov 2015) now enable us to record activity of
thousands of neurons.
Given the importance of two-photon microscopy and repertoire of nanofabricated devices due
to advancement in nanoscience and engineering, we investigate the application of custom-built
multi-photon microscopy which can be used to understand synaptic and network level
physiology and characterization of nanofabricated devices with future application in the field
of neuroscience. The work presented in this thesis was divided into two main parts. In my first
part of study we begin with the development of two photon microscope which can perform
submicron structure (spine) imaging in a neural tissue. In addition, we combined the two photon
imaging set-up with the whole cell patch clamp recording to perform simultaneous
patch clamp recording and two photon calcium imaging. The realized electro-optic setup can
help in understanding of single or interaction of group of neurons in a network under a
physiological condition like in slices or in live mice brain.
Two-photon uncaging combined with calcium imaging is a critical experimental tool to
investigate synaptic plasticity rules in a spatiotemporal scheme. To perform simultaneous
uncaging and imaging, typically ultrafast laser pulses from two separate laser systems are used
in conjunction with two independent sets of galvanometric mirrors. However, such a setup is
instrument intensive and requires synchronized operation of two laser systems making it
relatively tedious to operate and maintain. Here, in this section we report a single ultrafast laser
system based optical setup that uses a single set of galvanometric mirrors based regular
scanning assembly to perform simultaneous two photon uncaging and calcium imaging in a
hippocampal neuron. A fast operating optical shutter operating along with our delay line optics
and galvanometric mirror is used to generate patterned uncaging excitation. Spatial control of
uncaging is measured and shown to be close to the optical resolution. The accuracy and
synchrony are shown to be within few microseconds. We put to use the good control of
uncaging location in these experiments to investigate the cooperative and associative plasticity.
However, multi-photon microscopy despites its extensive application in the field of
neuroscience also enable the researchers to perform the characterization of nanofabricated
devices. My second part of study catered on characterization of nanofabricated devices using
the above custom built two-photon optical set-up. One such application was the photo response
characterization of in-house developed light detectors using state-of-the-art nanofabrication
techniques to each mode locked pulses from ultrafast laser using phase locked techniques. We
used the modified two photon optical set-up to measure the frequency response of the photo
detector using high-speed sampling scope. The 3dB cut off frequency is estimated from the
9
relation, f3dB = 0.45/FWHM, where FWHM is full width at half maximum of time response
of photo detector. The highest bandwidth of 15.5 GHz corresponding to FWHM of 29 ps is
obtained at 10V reverse bias. At lower reverse bias voltages broadening of the pulse response
(FWHM) indicates the photodetector bandwidth is transit time limited. At 20 V reverse bias
pulse response broadens slightly due to impact ionization build up time in the photo detector.
In short, we have successfully demonstrated an integrated lateral silicon pin photo detector on
SiN-SOI platform using the two-photon imaging set-up. We obtained the highest responsivity
of 0.44 A/W at 25 V bias and estimated the best 3dB cut off frequency of 15.5 GHz at 10 V
reverse bias. To the best of our knowledge, this is the highest ever reported bandwidth of a
waveguide integrated Silicon photo detector at 850 nm wavelength band.
Another application was the investigation of the circular differential two photon luminescence
response from a three-dimensional chiral metamaterial, comprising a system of achiral
(spherical) metal nanoparticles arranged on a chiral (helical) dielectric template. The enhanced
dipolar response of the individual particles arising from their strong electromagnetic coupling
resulted in strong photoluminescence under peak illumination intensities as low as 2
×103 W/cm2. The strong chiro-optical effect observed in these experiments may be relevant to
technologies related to nonlinear plasmonics, in particular imaging applications where control
over the polarization state of the imaged photons may be desirable. | en_US |
dc.language.iso | en_US | en_US |
dc.relation.ispartofseries | G29604 | |
dc.rights | I grant Indian Institute of Science the right to archive and to make available my thesis or dissertation in whole or in part in all forms of media, now hereafter known. I retain all proprietary rights, such as patent rights. I also retain the right to use in future works (such as articles or books) all or part
of this thesis or dissertation | en_US |
dc.subject | photon luminescence | en_US |
dc.subject | imaging in a neural tissue | en_US |
dc.subject.classification | Research Subject Categories::TECHNOLOGY::Other technology::Medical engineering | en_US |
dc.title | Development and application of multi-photon microscopy in neuroscience and nanoscience | en_US |
dc.type | Thesis | en_US |
dc.degree.name | PhD | en_US |
dc.degree.level | Doctoral | en_US |
dc.degree.grantor | Indian Institute of Science | en_US |
dc.degree.discipline | Engineering | en_US |