arXiv subjects

Jacob J. Krich

Publications and source records attributed to Jacob J. Krich.

29 records · Page 2Linked to original sources

arXiv2016

Optimizations of GaAs Nanowire Solar Cells

The efficiency of GaAs nanowire solar cells can be significantly improved without any new processing steps or material requirements. We report coupled optoelectronic simulations of a GaAs nanowire (NW) solar cell with vertical p-i-n junction and high band gap AlInP passivating shell. Our frequency-dependent model facilitates calculation of quantum efficiency for the first time in NW solar cells. For passivated NWs, we find that short-wavelength photons can be most effectively harnessed by using a thin emitter while long-wavelength photons are best utilized by extending the intrinsic region to the nanowire/substrate interface, and using the substrate as a base. These two easily implemented changes, coupled with the increase of NW height to 3.5 um with realistic surface recombination in the presence of a passivation shell, result in a NW solar cell with greater than 19% efficiency.

cond-mat.mtrl-sci↗

arXiv2014

Practical Witness for Electronic Coherences

The origin of the coherences in two-dimensional spectroscopy of photosynthetic complexes remains disputed. Recently it has been shown that in the ultrashort-pulse limit, oscillations in a frequency-integrated pump-probe signal correspond exclusively to electronic coherences, and thus such experiments can be used to form a test for electronic vs. vibrational oscillations in such systems. Here we demonstrate a method for practically implementing such a test, whereby pump-probe signals are taken at several different pulse durations and used to extrapolate to the ultrashort-pulse limit. We present analytic and numerical results determining requirements for pulse durations and the optimal choice of pulse central frequency, which can be determined from an absorption spectrum. Our results suggest that for numerous systems the required experiment could be implemented by many ultrafast spectroscopy laboratories using pulses of tens of femtoseconds in duration. Such experiments could resolve the standing debate over the nature of coherences in photosynthetic complexes.

quant-ph↗

arXiv2013

Coherent exciton dynamics in supramolecular light-harvesting nanotubes revealed by ultrafast quantum process tomography

Long-lived exciton coherences have been recently observed in photosynthetic complexes via ultrafast spectroscopy, opening exciting possibilities for the study and design of coherent exciton transport. Yet, ambiguity in the spectroscopic signals has led to arguments for interpreting them in terms of the exciton dynamics, demanding more stringent tests. We propose a novel strategy, Quantum Process Tomography (QPT) for ultrafast spectroscopy, to reconstruct the evolving quantum state of excitons in double-walled supramolecular light-harvesting nanotubes at room temperature. The protocol calls for eight transient grating experiments with varied pulse spectra. Our analysis reveals unidirectional energy transfer from the outer to the inner wall excitons, absence of nonsecular processes, and an unexpected coherence between those two states lasting about 150 femtoseconds, indicating weak electronic coupling between the walls. Our work constitutes the first experimental QPT in a 'warm' and complex system, and provides an elegant scheme to maximize information from ultrafast spectroscopy experiments.

quant-ph↗

arXiv2013

Emergent percolation length and localization in random elastic networks

We study, theoretically and numerically, a minimal model for phonons in a disordered system. For sufficient disorder, the vibrational modes of this classical system can become Anderson localized, yet this problem has received significantly less attention than its electronic counterpart. We find rich behavior in the localization properties of the phonons as a function of the density, frequency and the spatial dimension. We use a percolation analysis to argue for a Debye spectrum at low frequencies for dimensions higher than one, and for a localization/delocalization transition (at a critical frequency) above two dimensions. We show that in contrast to the behavior in electronic systems, the transition exists for arbitrarily large disorder, albeit with an exponentially small critical frequency. The structure of the modes reflects a divergent percolation length that arises from the disorder in the springs without being explicitly present in the definition of our model. Within the percolation approach we calculate the speed-of-sound of the delocalized modes (phonons), which we corroborate with numerics. We find the critical frequency of the localization transition at a given density, and find good agreement of these predictions with numerical results using a recursive Green function method adapted for this problem. The connection of our results to recent experiments on amorphous solids are discussed.

cond-mat.dis-nn↗

arXiv2012

A witness for coherent electronic oscillations in ultrafast spectroscopy

We report a conceptually straightforward witness that isolates coherent electronic oscillations from their vibronic counterparts in nonlinear optical spectra of molecular aggregates: Coherent oscillations as a function of waiting time in broadband pump/broadband probe spectra correspond to coherent electronic oscillations. Oscillations in individual peaks of 2D electronic spectra do not necessarily yield this conclusion. Our witness is simpler to implement than quantum process tomography and potentially resolves a long-standing controversy on the character of oscillations in ultrafast spectra of photosynthetic light harvesting systems.

quant-ph↗

arXiv2011

Quantum State and Process Tomography of Energy Transfer Systems via Ultrafast Spectroscopy

The description of excited state dynamics in multichromophoric systems constitutes both a theoretical and experimental challenge in modern physical chemistry. An experimental protocol which can systematically characterize both coherent and dissipative processes at the level of the evolving quantum state of the chromophores is desired. In this article, we show that a carefully chosen set of polarization controlled two-color heterodyned photon-echo experiments can be used to reconstruct the time-evolving density matrix of the one-exciton manifold of a heterodimer. This possibility in turn allows for a complete description of the excited state dynamics via quantum process tomography (QPT). Calculations on the dimer show that QPT can reveal rich information about system-bath interactions, which otherwise appear nontrivially hidden in the polarization monitored in standard four-wave mixing experiments. Our study presents a novel method for analyzing condensed phase experiments with a quantum information processing perspective.

quant-ph↗

arXiv2011

Nonradiative lifetimes in intermediate band materials - absence of lifetime recovery

Intermediate band photovoltaics hold the promise of being highly efficient and cost effective photovoltaic cells. Intermediate states in the band gap, however, are known to facilitate nonradiative recombination. Much effort has been dedicated to producing metallic intermediate bands in hopes of producing lifetime recovery -- an increase in carrier lifetime as doping levels increase. We show that lifetime recovery induced by the insulator-to-metal transition will not occur, because the metallic extended states will be localised by phonons during the recombination process. Only trivial forms of lifetime recovery, e.g., from an overall shift in intermediate levels, are possible. Future work in intermediate band photovoltaics must focus on optimizing subgap optical absorption and minimizing recombination, but not via lifetime recovery.

cond-mat.mtrl-sci↗

arXiv2011

Scaling and localization lengths of a topologically disordered system

We consider a noninteracting disordered system designed to model particle diffusion, relaxation in glasses, and impurity bands of semiconductors. Disorder originates in the random spatial distribution of sites. We find strong numerical evidence that this model displays the same universal behavior as the standard Anderson model. We use finite-size-scaling to find the localization length as a function of energy and density, including localized states away from the delocalization transition. Results at many energies all fit onto the same universal scaling curve.

cond-mat.dis-nn↗

arXiv2009

Fluctuations of spin transport through chaotic quantum dots with spin-orbit coupling

As devices to control spin currents using the spin-orbit interaction are proposed and implemented, it is important to understand the fluctuations that spin-orbit coupling can impose on transmission through a quantum dot. Using random matrix theory, we estimate the typical scale of transmitted charge and spin currents when a spin current is injected into a chaotic quantum dot with strong spin-orbit coupling. These results have implications for the functioning of the spin transistor proposed by Schliemann, Egues, and Loss. We use a density matrix formalism appropriate for treating arbitrary input currents and indicate its connections to the widely used spin-conductance picture. We further consider the case of currents entangled between two leads, finding larger fluctuations.

cond-mat.mes-hall↗

arXiv2008

Spin polarized current generation from quantum dots without magnetic fields

An unpolarized charge current passing through a chaotic quantum dot with spin-orbit coupling can produce a spin polarized exit current without magnetic fields or ferromagnets. We use random matrix theory to estimate the typical spin polarization as a function of the number of channels in each lead in the limit of large spin-orbit coupling. We find rms spin polarizations up to 45% with one input channel and two output channels. Finite temperature and dephasing both suppress the effect, and we include dephasing effects using a new variation of the third lead model. If there is only one channel in the output lead, no spin polarization can be produced, but we show that dephasing lifts this restriction.

cond-mat.mes-hall↗

arXiv2007

Cubic Dresselhaus Spin-Orbit Coupling in 2D Electron Quantum Dots

We study effects of the oft-neglected cubic Dresselhaus spin-orbit coupling (i.e., $\propto p^3$) in GaAs/AlGaAs quantum dots. Using a semiclassical billiard model, we estimate the magnitude of the spin-orbit induced avoided crossings in a closed quantum dot in a Zeeman field. Using these results, together with previous analyses based on random matrix theory, we calculate corresponding effects on the conductance through an open quantum dot. Combining our results with an experiment on conductance through an 8 um^2 quantum dot [D M Zumbuhl et al., Phys. Rev. B 72, 081305 (2005)] suggests that 1) the GaAs Dresselhaus coupling constant, $γ$, is approximately 9 eVA^3, significantly less than the commonly cited value of 27.5 eVA^3 and 2) the majority of the spin-flip component of spin-orbit coupling can come from the cubic Dresselhaus term.

cond-mat.mes-hall↗