Professor Jenny Clark
School of Mathematical and Physical Sciences
Head of Materials and Biological Physics Research Cluster
Professor of Materials Physics
+44 114 222 3526
Full contact details
School of Mathematical and Physical Sciences
D16
Hicks Building
Hounsfield Road
葫芦影业
S3 7RH
- Profile
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My research interests involve understanding the photophysics of carbon-based materials such as biological materials, organic semiconductors and graphene.
I do this using a variety of spectroscopic techniques. For more information see my or contact me.
Research Experience
- 2009-2013 Royal Society Dorothy Hodgkin Fellow, Cambridge University, UK.
- 2009 Visiting Scholar, Hyderabad University, India.
- 2007-2009 Postdoctoral Research Fellow, Politecnico di Milano, Italy.
Supervisor: Prof. Guglielmo Lanzani
Fellowships and Awards
- 2014 University of 葫芦影业 Vice-Chancellor's Fellowship (5 years).
- 2010 Charles and Catherine Darwin Research Fellowship (3 years).
- 2009 Royal Society Dorothy Hodgkin Fellowship (4 years).
- 2004 European Materials Research Society (E-MRS) student award.
- 2003 EPSRC PhD studentship and Industrial Case Award (Seiko Epson UK, 3 years).
Career Breaks
- 2012 Maternity leave (9 months)
- 2013 Maternity leave (13 months)
- Qualifications
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- 2003-2007 PhD in Physics, Cambridge University, UK. Supervisor: Prof. C. Silva.
- 1999-2003 MSci in Physics with a Year in Europe, Imperial College, London, UK. (First Class Degree)
- Research interests
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New laser facility at 葫芦影业 university
葫芦影业 has a new laser facility that I help run. The facility is currently being built and will have several spectroscopy stations including:
- Pump-probe spectroscopy in the UV/VIs-NIR with 10fs resolution, capable of tracking excited-state dynamics up to 1ms.
- Time-resolved IR spectroscopy and 2D IR spectroscopy
- Time-resolved Raman
- Photoluminescence Up-Conversion
Ultrafast spectroscopy of carbon-based materials
To study organic semiconductors and biological samples, we mainly use transient absorption spectroscopy.
This technique uses laser pulses as short as 7 femtoseconds (7 millionths of a billionth of a second) to take snapshots of the electronic and vibrational state of the molecules after they have absorbed light.
By delaying the time at which the 'probe' pulse arrives to take a snapshot of the molecule, we can track the dynamics of the electrons in the molecule as a function of time.
- Publications
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Show: Featured publications All publications
Featured publications
Journal articles
All publications
Journal articles
- . J Phys Chem Lett, 6135-6142.
- . JACS Au, 1(12), 2188-2201.
- . Journal of Materials Chemistry C.
- . Nature Chemistry, 13(2), 163-171.
- . Nature Chemistry.
- . Journal of the American Chemical Society, 142(32), 13898-13907.
- . Journal of Materials Chemistry A.
- . Chemical Science, 11(2), 343-354.
- . Light: Science & Applications, 8(1).
- . The Journal of Chemical Physics, 151(4).
- . Annual Review of Physical Chemistry, 70(1), 323-351.
- . Optics Express, 26(3), 3320-3327.
- . Nature Communications, 8.
- . Journal of Materials Chemistry C, 5, 8380-8389.
- . Advanced Optical Materials, 4(10), 1615-1623.
- . Advanced Optical Materials, 4(10), 1614-1614.
- . Journal of the American Chemical Society, 137(15), 5130-5139.
- . Sensors and Actuators B: Chemical, 192, 565-571.
- . Advanced Materials, 26(6), 919-924.
- . Science, 343(6170), 512-516.
- . Journal of the American Chemical Society, 135(44), 16680-16688.
- . Journal of the American Chemical Society, 135(34), 12747-12754.
- . Journal of the American Chemical Society, 135(13), 5074-5083.
- . Nature Physics, 8(3), 225-231.
- . Nature Photonics, 5(9), 554-560.
- . Journal of the American Chemical Society, 133(31), 11830-11833.
- . Chemistry of Materials, 23(3), 805-809.
- . Journal of Polymer Science Part B: Polymer Physics, 49(1), 52-61.
- . Nature Photonics, 4(7), 438-446.
- . Frontiers of Optoelectronics in China, 3(1), 45-53.
- . Applied Optics, 48(31), G114-G114.
- . Applied Physics Letters, 94(16), 163306-163306.
- . The Journal of Chemical Physics, 130(7), 074904-074904.
- . Applied Physics Letters, 94(4), 041123-041123.
- . Journal of Applied Physics, 103(12), 124510-124510.
- . Journal of Nanophotonics, 2(1), 023504-023504.
- . Journal of the American Chemical Society.
- . Physical Chemistry Chemical Physics.
- . ACS Applied Optical Materials.
- . Faraday Discussions.
- . Physical Chemistry Chemical Physics.
- . Faraday Discussions.
- . Advanced Science, 2200366-2200366.
- . J. Mater. Chem., 20(3), 519-523.
- . Physical Review Letters, 98(20).
- . Physical Review B, 74(11).
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Chapters
Conference proceedings papers
- . Physical Chemistry of Semiconductor Materials and Interfaces XVII, 19 August 2018 - 23 August 2018.
- . 19th International Conference on Ultrafast Phenomena, 2014.
- . International Conference on Applications of Optics and Photonics
- . 2011 IEEE 61st Electronic Components and Technology Conference (ECTC), 31 May 2011 - 3 June 2011.
- . Metrology, Inspection, and Process Control for Microlithography XXIV
- . MRS Proceedings, Vol. 1270
- . International Conference on Ultrafast Phenomena, 2010.
- . 2009 International Symposium on Optomechatronic Technologies, 21 September 2009 - 23 September 2009.
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- . 2009 3rd ICTON Mediterranean Winter Conference (ICTON-MW), 10 December 2009 - 12 December 2009.
- . CLEO/Europe - EQEC 2009 - European Conference on Lasers and Electro-Optics and the European Quantum Electronics Conference, 14 June 2009 - 19 June 2009.
- . CLEO/Europe - EQEC 2009 - European Conference on Lasers and Electro-Optics and the European Quantum Electronics Conference, 14 June 2009 - 19 June 2009.
- . Conference on Lasers and Electro-Optics/International Quantum Electronics Conference, 2009.
- Ultrafast confocal microscope for time-resolved imaging of thin films. Optics InfoBase Conference Papers
- Microfluidic channels fabricated by femtosecond laser irradiation and chemical etching for optofluidic devices. Optics InfoBase Conference Papers
- Organic optofluidic devices produced by femtosecond laser micromachining. ISOT: 2009 INTERNATIONAL SYMPOSIUM ON OPTOMECHATRONIC TECHNOLOGIES (pp 404-408)
- . Organic Optoelectronics and Photonics III
- . Frontiers in Optics 2008/Laser Science XXIV/Plasmonics and Metamaterials/Optical Fabrication and Testing, 2008.
- Ultrafast photonics in polymers. Optics InfoBase Conference Papers
- Ultrafast resonant optical switching in organic materials doped in matrix. Materials Research Society Symposium Proceedings, Vol. 1003 (pp 142-146)
- . Advanced Materials, Vol. 22(28) (pp 3048-3051)
Preprints
- Research group
- Research highlights
In organic solar cells, absorption of light typically creates a tightly bound electron-hole pair. To collect the charges and produce current, the e-h pair must separate.
This happens at a junction between an electron accepting and an electron donating material. By directly tracking the separation of the charges, we showed that they separate to 4nm within 40fs thereby overcoming the electronic Coulomb potential between the electron and hole.
This fast separation occurs due to the wavelike nature of electrons which are governed by fundamental laws of quantum mechanics.
We were able to track the electron-hole separation using the electric field generated between them as they separate.
This electric field perturbs the spectra of the surrounding material and leads to an electro-absorption feature.
Measuring the evolution of the electroabsorption using transient absorption spectroscopy allowed us to track the charge separation in a polymer: PCBM blend and a small molecule: PCBM blend.
A single photon can alter the shape of a molecule. In the eye for example, a photon drives the cis-trans isomerisation which allows us to see.
Using a pump-push-probe technique, we showed that quantum effects can play an important role in this change leading to conformation relaxation rates hundreds of times faster than previously expected.
In general, conformational change occurs on a timescale defined by the energy of the main vibrational mode and the rate of energy dissipation.
Typically, for a conformational change such as a twist around the backbone of a conjugated molecule, this occurs on the tens of picoseconds timescale. However, we demonstrated experimentally that in certain circumstances the molecule, in this case an oligofluorene, can change conformation over two orders of magnitude faster (that is sub-100鈥塮s) in a manner analogous to inertial solvent reorganization demonstrated in the 1990s.
Theoretical simulations demonstrate that non-adiabatic transitions during internal conversion can efficiently convert electronic potential energy into torsional kinetic energy, providing the 鈥榢ick鈥 that prompts sub-100鈥塮s torsional reorganization.
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Ultrafast triplet formation: two for the price of one [3,4]
In general, photoexcitation leads to an excited state with spin-0 character known as a singlet exciton.
This can convert to a spin-1 excited state (a triplet exciton) through intersystem crossing. In systems made up entirely of Carbon, Nitrogen, Oxygen, Hydrogen or even Sulphur, intersystem crossing generally takes 10s of nanoseconds or more.
However, in certain systems, when the triplet energy is roughly half the singlet energy or less and there is enough space, the singlet can split into two triplet excitons.
The splitting process is known as singlet exciton fission. The ability to generate two excited states from one photon could be used in solar cells to dramatically improve their efficiency.
The fission process is still not fully understood. We have studied a range of materials with the aim of understanding - and one day hopefully controlling - singlet exciton fission.
In [3].
[4] and in carotenoid aggregates it ranges from 50-100fs depending on aggregate type [5].
Under intense laser excitation, thin films and suspensions of graphite and its nanostructure, including carbon black, nanotubes, few-layer graphenes and graphene oxides, exhibit induced transparency due to saturable absorption.
This switches to optical limiting only at very high fluences when induced breakdown gives rise to microbubbles and microplasmas that causes nonlinear scattering.
Here, we showed that dispersed graphenes, in contrast, can exhibit broadband nonlinear optical absorption at fluences well below this damage threshold with a strong matrix effect.
We obtained, for nanosecond visible and near-infrared pulses, a new benchmark for optical energy-limiting onset of 10 mJ cm鈭2 for a linear transmittance of 70%, with excellent output clamping in both heavy-atom solvents and polymer film matrices.
Nanosecond pump鈥損robe spectroscopy in chlorobenzene reveals that the nanographene domains switch from the usual broadband photo-induced bleaching to a novel reverse saturable absorption mechanism with increasing excitation densities across this threshold.
Strong solvent/matrix effect on the nonlinear optical properties of dispersed sub-GOx. a, Plot of output versus input fluence for a neat film of sub-GOx (T'=0.97), and sub-GOx in PMMA (T'=0.40) and in PC (T'=0.055). T 鈥 is the limiting differential transmittance.
The linear transmittance T is 0.73 for all films. b, Plot of output versus input fluence for sub-GOx dispersed in different solvents compared with C60 in TOL and single-walled CNT in THF, all in cells with 1.0 mm path length. NMP, N-methylpyrrolidinone; THF, tetrahydrofuran; ANS, anisole; MES, mesitylene; DFB, 1,3-difluorobenzene;
BN, benzonitrile; CB, chlorobenzene; BB, bromobenzene; DCB, 1,2-dichlorobenzene; TCB, 1,2,4-trichlorobenzene; TOL, toluene. T is 0.70.The large non-linear effect is due to the formation of localised exciton-like states which we attribute to triplet excitons due to the heavy-atom effect.
We speculate that the initial electron鈥揾ole gas condenses to triplet-like excitons when promoted by spin鈥搊rbit coupling with heavy atoms.
In contrast, in graphite or multilayer graphenes in which the inner layers are effectively isolated from the environment, the electron鈥揾ole gas cools and recombines rapidly.
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Ultrafast all-optical switching in plastic optical fibers [7]
The ability to switch light with sub-picosecond time-scales in an optical fiber network is important for improved signal data communication speed and potentially for optical computing.
We made a logical NOT gate using gain switching in isolated conjugated fluorene oligomers. We use the fact that charge absorption overlaps with stimulated emission and generate charges on the oligomers which recombine within a few tens of femtoseconds.
The change from amplification through stimulated emission to loss through charge absorption produces a large switching signal and the recombination allows for ultrafast sub 100fs switching.
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