Dear group:
We are seeking a part-time temporary employee (20-25 hours/week) to work in
our office in for approximately 3 months beginning on May 18th or 26th.
If you know of a professional that is reliable, has the skills, and is able
to work in a fast-paced office environment, please forward and have them
send us their CV.
I've attached the role and qualifications.
Thanks,
Marlon.
---------------
Marlon G. Cummings
Lab Manager, Aspuru-Guzik Group
Mallinckrodt M136
Department of Chemistry and Chemical Biology
Harvard University
12 Oxford Street
Cambridge, MA 02138
617-496-9964
617-496-9411 (fax)
http://aspuru.chem.harvard.edu/
Hi QIP community,
I have prevailed upon EECS to let me offer 6.453, Quantum Optical Communication, in Fall 2015, whereas previously its next offering would have been in Fall 2016. I have attached an extract from the Fall 2015 on-line subject listing that describes the subject. Anyone potentially interested in taking the class who wants more information about it should contact me.
Best regards,
Jeff Shapiro
************************************************
Jeffrey H. Shapiro
Julius A. Stratton Professor
of Electrical Engineering
Massachusetts Institute of Technology
Room 36-517
Cambridge, MA 02139-4307
Phone: 617-253-4179
Fax: 617-324-3633
email: jhs(a)mit.edu<mailto:jhs@mit.edu>
************************************************
_______________________________________________
qip mailing list
qip(a)mit.edu
http://mailman.mit.edu/mailman/listinfo/qip
Hi everyone,
This week, on May 7th, we have a special group meeting given by Dr. Justin
Caram from MIT. Please see below for the title and abstract of his talk.
Cheers,
Jennifer
------------------------------
Title: Long-Range Excitonic Transport in Double-Walled J-Aggregates/
Ensemble Methods in Single Molecule Microscopy
I will discuss two different topics: 1) Creating circuit elements which
conduct excitons instead of charge, and 2) using the intrinsic coherence
length of light to study spectral dynamics.
1) Due to their long-range order, large domain sizes and high oscillator
strengths, one-dimensional tubular J-Aggregates can be used as the
excitonic equivalent of a wire. However, photochemical instability has
hindered the study of these materials and their implementation in practical
devices. In this talk, I demonstrate cyanine based J-aggregates which are
stabilized against photobleaching and cryogenic damage in a sugar-based
matrix. I probe the temperature dependent absorption and emission of these
aggregates, and signatures of exciton-exciton annihilation at low photon
fluxes. I demonstrate micron scale one-dimensional exciton diffusion
lengths at room temperature, and band-like transport as we tune dynamic
disorder in the system. This distance is among the longest exciton
diffusion distances ever measured for an organic supramolecular system.
2) Colloidal nanostructures show size, shape and surface heterogeneity.
This structural diversity leads to significant variation in optical and
photochemical properties, such as blinking, lifetimes, and
exciton/biexciton dynamics — even within a single colloidal preparation.
Both ensemble and single molecule spectroscopic approaches can elucidate
this heterogeneity but often rely on selective data acquisition and
modeling. We have developed new approaches to study single quantum dot
properties under very weak excitation conditions, and in solution,
extracting single dot spectral lineshapes, and exciton/biexciton
interactions. To accomplish this, we combine the fluorescent correlation
spectroscopy (FCS) with Fourier Spectroscopy, utilizing the intrinsic
coherence length of emission to encode an FCS trace with spectral
information. We use Solution Photon Correlation Fourier Spectroscopy
(S-PCFS), probes the intrinsic linewidths of a variety of new materials and
structures, including colloidal quantum rods, nanoplatelets and quantum
confined NIR emitting nanocrystals, elucidating new spectral dynamics in
these systems. This work can then inform the synthetic community on how
best to optimize these properties. I will present new results about PbS
nanoparticle lineshapes in solution, which describe how these systems can
be optimized and how to use them for photochemical and photovoltaic
applications.
This looks like a lot, but the each topic should be about 20 minutes.
_______________________________________________
Aspuru-meetings-list mailing list
Aspuru-meetings-list(a)lists.fas.harvard.edu
https://lists.fas.harvard.edu/mailman/listinfo/aspuru-meetings-list
TODAY!
Please post and forward to your group(s).
Joint Seminar: Physical Chemistry and Center for Excitonics
Navigating Space-Time with Ultrafast Exciton Photolithography or Scintillating Near-fields to Follow Dynamic Processes in Molecular Materials
May 5, 2015 at 4:30pm/ rm: 4-370
Naomi Ginsberg
University of California/Department of Chemistry and Physics
[nsginsberg]
abstract:
A cross-cutting theme in my research group is to examine dynamic processes in spatially-heterogeneous condensed phase molecular materials over a wide range of time scales. I will share recent results in multiple areas, all underpinned by the strong correlation between physical structure and the optical properties of materials. Our investigations often require tailoring the spatial and temporal resolution of our measurement approaches. I will explain how by measuring the ultrafast electronic properties of heterogeneous, ‘printed’ semiconducting films of small organic molecules we infer the much slower dynamics by which complex nanoscale structural motifs in the films emerge when they self-assemble in an evaporating solvent. These studies reveal the generation of non-equilibrium nanoscale structures that arise from coupling the dynamics of fundamental phase transformation processes of solute crystallization with solvent evaporation. They also pinpoint the challenges associated with developing high carrier mobility materials for printed plastic electronics.
The migration of Frenkel excitons, tightly-bound electron-hole pairs, in organic and hybrid organic-inorganic semiconducting films is critical to the function of many next generation optoelectronic devices. While these materials can exhibit a high degree of structural heterogeneity on the nanoscale, traditional measurements of exciton diffusion lengths are performed on bulk samples. Since both the characteristic length scales of structural heterogeneity and the reported bulk diffusion lengths are typically smaller than the optical diffraction limit, I will describe how we adapt far-field super-resolution fluorescence imaging to determine in-situ exciton diffusivities and to uncover the correlations between the structural and energetic landscapes that the excitons explore. Motivated by the need to observe the dynamics of biomolecular interactions on their characteristic length scales, I will also show how we have appropriated the nanoscale resolution of electron microscopy and the near-field luminescence properties of scintillating oxide films to non-invasively image soft materials that cannot be interrogated directly with a damaging electron beam. In addition to focusing on soft materials in organic electronics and biology, I will also demonstrate this new imaging modality applied to plasmonic nanostructures.
bio:
Naomi Ginsberg received a B. A. Sc. from the University of Toronto (Engineering Science) (2000) and a Ph.D. from Harvard University with the Physics – Hau group (2007). From 2007 – 2010, she was a Postdoctoral Fellow in the Physical Biosciences Division-Fleming group at the Lawrence Berkeley National Laboratory. Awards include UC Berkeley Department of Chemistry Teaching Award (2013), DARPA Young Faculty Awardee (2012), Packard Fellow for Science and Engineering (2011), and Cupola Era Endowed Chair in the College of Chemistry (2010-2012). Her group focuses on visualizing ultrafast energy flow in natural and artificial light harvesting systems and on combining electron and optical microscopies to facilitate high-resolution studies of living things and molecular interactions in solution. Naomi’s background in chemistry, physics, and engineering has led her to observe coherent and previously obscured energy transfer in light harvesting complexes from plants, to develop polarization techniques in ultrafast multidimensional spectroscopy to extract structure from electronically-coupled systems, to slow, stop, and store light pulses in some of the coldest atom clouds on Earth, and to discover, follow, and understand the interactions of superfluid nonlinear excitations.
Please post and forward to your group(s).
Joint Seminar: Physical Chemistry and Center for Excitonics
Navigating Space-Time with Ultrafast Exciton Photolithography or Scintillating Near-fields to Follow Dynamic Processes in Molecular Materials
May 5, 2015 at 4:30pm/ rm: 4-370
Naomi Ginsberg
University of California/Department of Chemistry and Physics
[nsginsberg]
abstract:
A cross-cutting theme in my research group is to examine dynamic processes in spatially-heterogeneous condensed phase molecular materials over a wide range of time scales. I will share recent results in multiple areas, all underpinned by the strong correlation between physical structure and the optical properties of materials. Our investigations often require tailoring the spatial and temporal resolution of our measurement approaches. I will explain how by measuring the ultrafast electronic properties of heterogeneous, ‘printed’ semiconducting films of small organic molecules we infer the much slower dynamics by which complex nanoscale structural motifs in the films emerge when they self-assemble in an evaporating solvent. These studies reveal the generation of non-equilibrium nanoscale structures that arise from coupling the dynamics of fundamental phase transformation processes of solute crystallization with solvent evaporation. They also pinpoint the challenges associated with developing high carrier mobility materials for printed plastic electronics.
The migration of Frenkel excitons, tightly-bound electron-hole pairs, in organic and hybrid organic-inorganic semiconducting films is critical to the function of many next generation optoelectronic devices. While these materials can exhibit a high degree of structural heterogeneity on the nanoscale, traditional measurements of exciton diffusion lengths are performed on bulk samples. Since both the characteristic length scales of structural heterogeneity and the reported bulk diffusion lengths are typically smaller than the optical diffraction limit, I will describe how we adapt far-field super-resolution fluorescence imaging to determine in-situ exciton diffusivities and to uncover the correlations between the structural and energetic landscapes that the excitons explore. Motivated by the need to observe the dynamics of biomolecular interactions on their characteristic length scales, I will also show how we have appropriated the nanoscale resolution of electron microscopy and the near-field luminescence properties of scintillating oxide films to non-invasively image soft materials that cannot be interrogated directly with a damaging electron beam. In addition to focusing on soft materials in organic electronics and biology, I will also demonstrate this new imaging modality applied to plasmonic nanostructures.
bio:
Naomi Ginsberg received a B. A. Sc. from the University of Toronto (Engineering Science) (2000) and a Ph.D. from Harvard University with the Physics – Hau group (2007). From 2007 – 2010, she was a Postdoctoral Fellow in the Physical Biosciences Division-Fleming group at the Lawrence Berkeley National Laboratory. Awards include UC Berkeley Department of Chemistry Teaching Award (2013), DARPA Young Faculty Awardee (2012), Packard Fellow for Science and Engineering (2011), and Cupola Era Endowed Chair in the College of Chemistry (2010-2012). Her group focuses on visualizing ultrafast energy flow in natural and artificial light harvesting systems and on combining electron and optical microscopies to facilitate high-resolution studies of living things and molecular interactions in solution. Naomi’s background in chemistry, physics, and engineering has led her to observe coherent and previously obscured energy transfer in light harvesting complexes from plants, to develop polarization techniques in ultrafast multidimensional spectroscopy to extract structure from electronically-coupled systems, to slow, stop, and store light pulses in some of the coldest atom clouds on Earth, and to discover, follow, and understand the interactions of superfluid nonlinear excitations.
There will be a Special HQOC Seminar on Wednesday, May 6, at 4 PM in Lyman 425. Rivka Bekenstein will be visiting from Technion, Israel Institute of Technology, and will present the following talk:
General Relativistic Phenomena in Optical Settings (see attached flyer for more details).
Rivka is also available for meetings and lab tours. Theorists, in particular, may be interested and can schedule appointments by signing up using the following link:
https://docs.google.com/a/g.harvard.edu/spreadsheets/d/1tAVgwJuPCdRvDUsq7Mr…
Karl
Karl Coleman
HQOC Laboratory Administrator
Faculty Assistant to Profs. Greiner and Lukin
Harvard University
Department of Physics
17 Oxford Street
Cambridge, MA 02138
P: (617) 496-2544
F: (617) 496-2545
Hello All,
Group pictures will happen after group meeting on Thursday as I received
minimal reasons to not do it this week. Please come to group meeting at
2:30 if you can, at your most photogenic and we'll start photographing at
roughly 3:30.
I'm sorry to those of you who won't be here; with a group this big, it's
virtually impossible to insure everyone will be at the same place any given
time :(
We're almost certainly going to go outside to take the picture, just FYI
Have a great week!
-Joey
Dear all,
Jacob and I have just signed up for a 5K. YOHOO.
If anybody wants to sign up, here is the link:
Saturday May 16th, 10 AM (Bib pickup 8.30-9.30 AM). It is in Millis, MA. I
imagine we could carpool there.
http://rcm.nu/1JKkdCm
It would be fun to have a group contingent. This is random 5K for a
Montessori School, so let's create a Harvard Contingent... We could try to
sign up for other 5Ks periodically. Sorry that it is not closer to the
campus, next time we will try to be in Cambridge, etc.
Alan
Alán Aspuru-Guzik | Professor of Chemistry and Chemical Biology
Harvard University | 12 Oxford Street, Room M113 | Cambridge, MA 02138
(617)-384-8188 | http://aspuru.chem.harvard.edu | http://about.me/aspuru