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Mikko Linnolahti

Publications and source records attributed to Mikko Linnolahti.

3 recordsLinked to original sources

Enhanced Third-Order Optical Nonlinearity in a Dipolar Carbene-Metal-Amide Material with Two-Photon Excited Delayed Fluorescence

Advanced photonic materials showing two-photon absorption (2PA) have been widely explored to develop three-dimensional imaging, micro and nanofabrication, all-optical switching, lithography on a nanoscale and many other enabling technologies. These all require nonlinear absorption chromophores with intrinsic 2PA cross-sections and long-term photo-and thermal stability. Here, we disclose the very first example of the dipolar carbenemetal-amide (CMA) material showing a enhanced 2PA cross-section up to 105 GM. Overall molecular design considerations such as extended $π$-conjugation (to increase polarizability), minimizing the singlet-triplet energy gap ($Δ$E ST ), and using heavy metal atoms are the first design principles to obtain bright one-and two-photon excited thermally activated delayed fluorescence (TADF) material, showing one of the highest radiative rate of 2.18$\bullet$10 6 s -1 across CMA materials. Bright red CMA 2P-TADF material shows excellent photostability (LT 50 = 3 h) to 20 mW femtosecond pulsed laser excitation at 1000 nm, encouraging further CMA exploration for future applications in advanced photonic technologies requiring third-order nonlinear optical properties.

physics.chem-ph↗

Environmental Control of Triplet Emission in Donor-Bridge-Acceptor Organometallics

Carbene-metal-amides (CMAs) are a promising family of donor-bridge-acceptor molecular charge-transfer emitters for organic light-emitting diodes (OLEDs). Here a universal approach is introduced to tune the energy of their charge-transfer emission. A shift of up to 210 meV is achievable in the solid state via dilution in a polar host matrix. The origin of this shift has two components: constraint of thermally activated triplet diffusion, and electrostatic interactions between the guest molecules and the polar host. This allows the emission of mid-green CMA archetypes to be blue shifted without chemical modifications. Monte-Carlo simulations based on a Marcus-type transfer integral successfully reproduce the concentration- and temperature-dependent triplet diffusion process, and reveal a substantial shift in the ensemble density of states in polar hosts. In gold-bridged CMAs this substantial shift does not lead to a significant change in luminescence lifetime, thermal activation energy, reorganisation energy or intersystem crossing rate. These discoveries thus offer new experimental and theoretical insight in to the coupling between the singlet and triplet manifolds in these materials. Similar emission tuning can be achieved in related materials where chemical modification is used to modify the charge-transfer energy.

physics.app-ph↗

Highly efficient light-emitting diodes based on intramolecular rotation

The efficiency of an organic light-emitting diode (OLED) is fundamentally governed by the spin of recombining electron-hole pairs (singlet and triplet excitons), since triplets cannot usually emit light. The singlet-triplet energy gap, a key factor for efficient utilization of triplets, is normally positive. Here we show that in a family of materials with amide donor and carbene acceptor moieties linked by a metal, this energy gap for singlet and triplet excitons with charge-transfer character can be tuned from positive to negative values via the rotation of donor and acceptor about the metal-amide bond. When the gap is close to zero, facile intersystem crossing is possible, enabling efficient emission from singlet excitons. We demonstrate solution-processed LEDs with exceptionally high quantum efficiencies (near-100% internal and >27% external quantum efficiencies), and current and power efficiencies (87 cd/A and 75 lm/W) comparable to, or exceeding, those of state-of-the-art vacuum-processed OLEDs and quantum dot LEDs.

cond-mat.mtrl-sci↗