Passive Parity-Time Symmetry in Organic Thin Film Waveguides

Periodic media are fundamentally important for controlling the flow of light in photonics. Recently, the emerging field of non-Hermitian optics has generalized the notion of periodic media to include a new class of materials that obey parity-time (PT) symmetry, with real and imaginary refractive index variations that transform into one another upon spatial inversion, leading to a variety of unusual optical phenomena. Here, we introduce a simple approach based on interference lithography and oblique angle deposition to achieve PT-symmetric modulation in the effective index of large area organic thin film waveguides with the functional form Δ<i>ñ</i>_eff(<i>z</i>) ∼ <i>e</i>^<i>iqz</i>. Passive PT symmetry breaking is observed through asymmetry in the forward and backward diffraction of waveguided light that maximizes at the exceptional point, resulting in unidirectional reflectionless behavior that is visualized directly via leakage radiation microscopy. These results establish the basis for organic PT waveguide media that can be tuned for operation throughout the visible to near-infrared spectrum and provide a direct pathway to incorporate gain sufficient to achieve active PT symmetric lattices and gratings

The impact of physical performance and cognitive status on subsequent ADL disability in low-functioning older adults

We demonstrate that rectification ratios (RR) of ≳250 (≳1000) at biases of 0.5 V (1.2 V) are achievable at the two-molecule limit for donor–acceptor bilayers of pentacene on C₆₀ on Cu using scanning tunneling spectroscopy and microscopy. Using first-principles calculations, we show that the system behaves as a molecular Schottky diode with a tunneling transport mechanism from semiconducting pentacene to Cu-hybridized metallic C₆₀. Low-bias RRs vary by two orders-of-magnitude at the edge of these molecular heterojunctions due to increased Stark shifts and confinement effects

Nonimaging Optical Gain in Luminescent Concentration through Photonic Control of Emission Étendue

Luminescent and nonimaging optical concentration constitute two fundamentally different ways of collecting and intensifying light. Whereas nonimaging concentrators based on reflective, refractive, or diffractive optics operate most effectively for collimated light, luminescent concentrators (LCs) rely on absorption, re-emission, and waveguiding to concentrate diffuse light incident from any direction. LCs have been explored in many different shapes and sizes but have so far been unable to exploit the power of nonimaging optics to further increase their concentration ratio because their emission is angularly isotropic. Here, we use a luminescent thin film bilayer to create sharply directed conical emission in an LC and derive a nonimaging optical solution to leverage this directionality for secondary geometric gain ranging up to an order of magnitude or higher. We demonstrate this concept experimentally using a custom compound parabolic optical element index-matched to the LC surface and show that it delivers three times more luminescent power to an opposing GaAs photovoltaic cell when the emission profile is conically directed than when it is isotropic or the nonimaging optic is absent. These results open up a significant and general opportunity to improve LC performance for a variety of applications including photovoltaics, photobioreactors, and scintillator-based radiation detection

Direct Observation of Correlated Triplet Pair Dynamics during Singlet Fission Using Ultrafast Mid-IR Spectroscopy

Singlet fission is an exciton multiplication mechanism in organic materials whereby high energy singlet excitons can be converted into two triplet excitons with near unity quantum yields. As new singlet fission sensitizers are developed with properties tailored to specific applications, there is an increasing need for design rules to understand how the molecular structure and crystal packing arrangements influence the rate and yield with which spin-correlated intermediates known as correlated triplet pairs can be successfully separateda prerequisite for harvesting the multiplied triplets. Toward this end, we identify new electronic transitions in the mid-infrared spectral range that are distinct for both initially excited singlet states and correlated triplet pair intermediate states using ultrafast mid-infrared transient absorption spectroscopy of crystalline films of 6,13-bis­(triisopropylsilylethynyl) pentacene (TIPS-Pn). We show that the dissociation dynamics of the intermediates can be measured through the time evolution of the mid-infrared transitions. Combining the mid-infrared with visible transient absorption and photoluminescence methods, we track the dynamics of the relevant electronic states through their unique electronic signatures and find that complete dissociation of the intermediate states to form independent triplet excitons occurs on time scales ranging from 100 ps to 1 ns. Our findings reveal that relaxation processes competing with triplet harvesting or charge transfer may need to be controlled on time scales that are orders of magnitude longer than previously believed even in systems like TIPS-Pn where the primary singlet fission events occur on the sub-picosecond time scale