Sangita Baniya

Giant Rashba splitting in 2D organic-inorganic halide perovskites measured by transient spectroscopies

Transient and CW spectroscopies unravel giant Rashba splitting in 2D hybrid perovskite multilayers. Two-dimensional (2D) layered hybrid organic-inorganic halide perovskite semiconductors form natural “multiple quantum wells” that have strong spin-orbit coupling due to the heavy elements in their building blocks. This may lead to “Rashba splitting” close to the extrema in the electron bands. We have used a plethora of ultrafast transient, nonlinear optical spectroscopies and theoretical calculations to study the primary (excitons) and long-lived (free carriers) photoexcitations in thin films of 2D perovskite, namely, (C6H5C2H4NH3)2PbI4. The density functional theory calculation shows the occurrence of Rashba splitting in the plane perpendicular to the 2D barrier. From the electroabsorption spectrum and photoinduced absorption spectra from excitons and free carriers, we obtain a giant Rashba splitting in this compound, with energy splitting of (40 ± 5) meV and Rashba parameter of (1.6 ± 0.1) eV·Å, which are among the highest Rashba splitting size parameters reported so far. This finding shows that 2D hybrid perovskites have great promise for potential applications in spintronics.

Electroabsorption Spectroscopy Studies of (C4H9NH3)2PbI4 Organic–Inorganic Hybrid Perovskite Multiple Quantum Wells

Two-dimensional (2D) organic-inorganic hybrid perovskite multiple quantum wells that consist of multilayers of alternate organic and inorganic layers exhibit large exciton binding energies of order of 0.3 eV due to the dielectric confinement between the inorganic and organic layers. We have investigated the exciton characteristics of 2D butylammonium lead iodide, (C4H9NH3)2PbI4 using photoluminescence and UV-vis absorption in the temperature range of 10 K to 300 K, and electroabsorption spectroscopy. The evolution of an additional absorption/emission at low temperature indicates that this compound undergoes a phase transition at ≈250 K. We found that the electroabsorption spectrum of each structural phase contains contributions from both quantum confined exciton Stark effect and Franz-Keldysh oscillation of the continuum band, from which we could determine more accurately the 1s exciton, continuum band edge, and the exciton binding energy.

Colour selective control of terahertz radiation using two-dimensional hybrid organic inorganic lead-trihalide perovskites

Controlling and modulating terahertz signals is of fundamental importance to allow systems level applications. We demonstrate an innovative approach for controlling the propagation properties of terahertz (THz) radiation, through use of both the excitation optical wavelength (colour) and intensity. We accomplish this using two-dimensional (2D) layered hybrid trihalide perovskites that are deposited onto silicon substrates. The absorption properties of these materials in the visible range can be tuned by changing the number of inorganic atomic layers in between the organic cation layers. Optical absorption in 2D perovskites occurs over a broad spectral range above the bandgap, resulting in free carrier generation, as well as over a narrow spectral range near the bandedge due to exciton formation. We find that only the latter contribution gives rise to photo-induced THz absorption. By patterning multiple 2D perovskites with different optical absorption properties onto a single device, we demonstrate both colour selective modulation and focusing of THz radiation. These findings open new directions for creating active THz devices.All-optical approaches to modulate signals are of wide interest. Here the authors demonstrate the use of two-dimensional perovskites on silicon for optically controlling the propagation and attenuation of terahertz radiation in the visible by changing the number of atomic layers.

Optical studies of native defects in π-conjugated donor–acceptor copolymers

We used multiple spectroscopies such as photoinduced absorption (PIA), magneto photoinduced absorption, and doping induced absorption for studying native defects in π-conjugated donor–acceptor copolymer chains of benzodithio-phene fluorinated benzotriazole. The PIA spectrum contains characteristic photoinduced absorption bands that are due to polarons and triplet exciton species, whose strengths have different dependencies on the modulation frequency, temperature, and laser excitation, as well as magnetic field response. We found that the native defects in the copolymer chains serve as efficient traps that ionize the photoexcited excitons, thereby generating charge carriers whose characteristic optical properties are similar, but not equal to those of intrachain polarons formed by doping. The native defects density is of the order of 1017 cm−3 indicating that most of the copolymer chains contain native defects upon synthesis; however, this does not preclude their used-for photovoltaic applications.

Electronic and vibrational spectroscopy studies of PffBT4T π -conjugated donor-acceptor copolymer

Abstract. We used a variety of optical spectroscopies to investigate the charge excitations and correlated infrared (IR)-active and Raman-active vibrations in poly[(difluoro-benzothiadiazol-diyl)-alt-(di(2-octyldodecyl)-quaterthiophen-diyl)], PffBT4T, a π-conjugated donor–acceptor (DA) copolymer, which, when blended with fullerene PCBM molecules, serves as an active layer in high-performance photovoltaic solar cells. The applied optical spectroscopies in films of pristine PffBT4T and PffBT4T/PCBM blend include absorption, photoluminescence, electroabsorption, photoinduced absorption (PA), and resonant Raman scattering. We found that the PffBT4T copolymer chain contains 11 strongly coupled Raman-active vibrational modes, which are renormalized upon photogeneration of charge polarons onto the chain. As the lower energy polaron absorption band overlaps with the renormalized vibrational modes, they appear in the PA spectrum as antiresonance (AR) lines superposed onto the induced polaron absorption band. We show that the Raman scattering, doping induced, and photoinduced AR spectra in PffBT4T are well explained by the amplitude mode model (AMM), where a single vibrational propagator describes the renormalized Raman modes and their related photoinduced AR intensities in detail. Surprisingly, we found that two of the IR-active modes in the pristine copolymer must be included in the AMM propagator for explaining the complete photoinduced AR spectrum. This feature is unique to DA-copolymers and indicates that some intrachain C2v symmetry breaking occurs because of the different electron affinities of the donor and acceptor moieties.

Multiphoton Microscopy of π-Conjugated Copolymers and Copolymer/Fullerene Blends for Organic Photovoltaic Applications

Organic photovoltaic (OPV) cells based on π-conjugated copolymer/fullerene blends are devices with the highest power conversion efficiencies within the class of organic semiconductors. Although a number of image microscopies have been applied to films of π-conjugated copolymers and their fullerene blends, seldom have they been able to detect microscopic defects in the blend films. We have applied multiphoton microscopy (MPM) using a 65 fs laser at 1.56 μm for spectroscopy and mapping of films of various π-conjugated copolymers and their fullerene blends. All pristine copolymer films have shown third harmonic generation (THG) and two-photon or three-photon photoluminescence that could be used for mapping the films with micrometer spatial resolution. Since the fullerenes have much weaker THG efficiency than those of the copolymers, we could readily map the copolymer/fullerene blend films that showed interpenetrating micron-sized grains of the two constituents. In addition, we also found second harmonic generation from various micron-sized defects in the films that are formed during film deposition or light illumination at ambient conditions, which do not possess inversion symmetry. The MPM method is therefore beneficial for organic films and devices for investigating the properties and growth of copolymer/fullerene blends for OPV applications.

Magnetic field effect in organic light emitting diodes based on donor-acceptor exciplexes showing thermally activated delayed fluorescence

A new type of organic light-emitting diode (OLED) has emerged that shows enhanced operational stability and large internal quantum efficiency approaching 100%, which is based on exciplexes in donor-acceptor (D-A) blends having thermally activated delayed fluorescence (TADF) when doped with fluorescent emitters. We have investigated magnetoelectroluminescence (MEL) and magneto-conductivity in such TADF-based OLEDs, as well as magnetophotoluminescence (MPL) in thin films based on the OLEDs active layers, with various fluorescence emitters. We found that both MEL and MPL responses are thermally activated with substantially lower activation energy compared to that in the pristine undoped D-A exciplex host blend. In addition, both MPL and MEL steeply decrease with the emitters’ concentration. This indicates the existence of a loss mechanism, whereby the triplet charge-transfer state in the D-A exciplex host blend may directly decay to the lowest, non-emissive triplet state of the additive fluorescent emitter molecules.