Probing the wave function and dynamics of the quintet multiexciton state with coherent control in a singlet fission material

High-spin states play a key role in chemical reactions found in nature. In artificial molecular systems, singlet fission produces a correlated triplet-pair state, a spin-bearing excited state that can be harnessed for more efficient solar-energy conversion and photocatalysis. In particular, triplet-pair states with overall quintet character (total spin S=2) have been discovered, but many of the fundamental properties of these biexciton states remain unexplored. The net spin of these pair states makes spin-sensitive probes attractive for their characterization. Combined with their surprisingly long spin coherence (of order microseconds), this opens up techniques relying on coherent spin control. Here we apply coherent manipulation of triplet-pair states to (i) isolate their spectral signatures from coexisting free triplets and (ii) selectively couple quintet and triplet states to specific nuclear spins. Using this approach, we separate quintet and triplet transitions and extract the relaxation dynamics and hyperfine couplings of the fission-borne spin states. Our results highlight the distinct properties of correlated and free triplet excitons and demonstrate optically induced nuclear spin polarization by singlet fission

Probing the wave function and dynamics of the quintet multiexciton state with coherent control in a singlet fission material

High-spin states play a key role in chemical reactions found in nature. In artificial molecular systems, singlet fission produces a correlated triplet-pair state, a spin-bearing excited state that can be harnessed for more efficient solar-energy conversion and photocatalysis. In particular, triplet-pair states with overall quintet character (total spin S = 2 ) have been discovered, but many of the fundamental properties of these biexciton states remain unexplored. The net spin of these pair states makes spin-sensitive probes attractive for their characterization. Combined with their surprisingly long spin coherence (of order microseconds), this opens up techniques relying on coherent spin control. Here we apply coherent manipulation of triplet-pair states to (i) isolate their spectral signatures from coexisting free triplets and (ii) selectively couple quintet and triplet states to specific nuclear spins. Using this approach, we separate quintet and triplet transitions and extract the relaxation dynamics and hyperfine couplings of the fission-borne spin states. Our results highlight the distinct properties of correlated and free triplet excitons and demonstrate optically induced nuclear spin polarization by singlet fission

Strongly exchange-coupled triplet pairs in an organic semiconductor

From biological complexes to devices based on organic semiconductors, spin interactions play a key role in the function of molecular systems. For instance, triplet-pair reactions impact operation of organic light-emitting diodes as well as photovoltaic devices. Conventional models for triplet pairs assume they interact only weakly. Here, using electron spin resonance, we observe long-lived, strongly-interacting triplet pairs in an organic semiconductor, generated via singlet fission. Using coherent spin-manipulation of these two-triplet states, we identify exchange-coupled (spin-2) quintet complexes co-existing with weakly coupled (spin-1) triplets. We measure strongly coupled pairs with a lifetime approaching 3 µs and a spin coherence time approaching 1 µs, at 10 K. Our results pave the way for the utilization of high-spin systems in organic semiconductors.Gates-Cambridge Trust, Winton Programme for the Physics of Sustainability, Freie Universität Berlin within the Excellence Initiative of the German Research Foundation, Engineering and Physical Sciences Research Council (Grant ID: EP/G060738/1)This is the author accepted manuscript. The final version is available from Nature Publishing Group at http://dx.doi.org/10.1038/nphys3908

Strongly exchange-coupled triplet pairs in an organic semiconductor

From biological complexes to devices based on organic semiconductors, spin interactions play a key role in the function of molecular systems. For instance, triplet-pair reactions impact operation of organic light-emitting diodes as well as photovoltaic devices. Conventional models for triplet pairs assume they interact only weakly. Here, using electron spin resonance, we observe long-lived, strongly-interacting triplet pairs in an organic semiconductor, generated via singlet fission. Using coherent spin-manipulation of these two-triplet states, we identify exchange-coupled (spin-2) quintet complexes co-existing with weakly coupled (spin-1) triplets. We measure strongly coupled pairs with a lifetime approaching 3 µs and a spin coherence time approaching 1 µs, at 10 K. Our results pave the way for the utilization of high-spin systems in organic semiconductors.Gates-Cambridge Trust, Winton Programme for the Physics of Sustainability, Freie Universität Berlin within the Excellence Initiative of the German Research Foundation, Engineering and Physical Sciences Research Council (Grant ID: EP/G060738/1)This is the author accepted manuscript. The final version is available from Nature Publishing Group at http://dx.doi.org/10.1038/nphys3908

Stable organic solar cells with Mg Ag contacts

Stable and efficient organic solar cells with Mg 20 at. Ag alloy cathodes and bulk heterojunction absorber layers from metal e.g., Cu, Zn phthalocyanine and C60 small molecules are demonstrated. Device efficiencies of 4.0 under an illumination of 100 mW cm2 at 25 C were achieved as a result of the fine adjustment of the cathode work function as well as of the absorber design. By combining low and high work function materials, the work function in both Mg Ag bilayer and Mg Ag alloy layer cathodes was adjusted for optimum photovoltaic parameters. The electric and photovoltaic properties of the devices are discussed with respect to the cathode layer structure. The formation of the absorber cathode interface was investigated by x ray photoelectron spectroscopy measurements XPS . The work function of the absorber and cathode layers were determined from the XPS high binding energy cutoff HBEC spectra. For optimized devices, the work function of the cathode at the side adjacent to the absorber layer equals 4.0 4.1 eV. While devices with Mg Ag bilayer contacts exhibit a 65 efficiency drop in the first month after the preparation, devices with Mg Ag alloy contacts demonstrate stable photovoltaic parameters within the time of the study of 1 yea

Detection of the electronic structure of iron III oxo oligomers forming in aqueous solutions

The nature of the small iron-oxo oligomers in iron-(III) aqueous solutions has a determining effect on the chemical processes that govern the formation of nanoparticles in aqueous phase. Here we report on a liquid-jet photoelectron-spectroscopy experiment for the investigation of the electronic structure of the occurring iron-oxo oligomers in FeCl₃ aqueous solutions. The only iron species in the as-prepared 0.75 M solution are Fe³⁺ monomers. Addition of NaOH initiates Fe³⁺ hydrolysis which is followed by the formation of iron-oxo oligomers. At small enough NaOH concentrations, corresponding to approximately [OH]/[Fe] = 0.2–0.25 ratio, the iron oligomers can be stabilized for several hours without engaging in further aggregation. Here, we apply a combination of non-resonant as well as iron 2p and oxygen 1s resonant photoelectron spectroscopy from a liquid microjet to detect the electronic structure of the occurring species. Specifically, the oxygen 1s partial electron yield X-ray absorption (PEY-XA) spectra are found to exhibit a peak well below the onset of liquid water and OH^- (aq) absorption. The iron 2p absorption gives rise to signal centered between the main absorption bands typical for aqueous Fe³⁺. Absorption bands in both PEY-XA spectra are found to correlate with an enhanced photoelectron peak near 20 eV binding energy, which demonstrates the sensitivity of resonant photoelectron (RPE) spectroscopy to mixing between iron and ligand orbitals. These various signals from the iron-oxo oligomers exhibit maximum intensity at [OH]/[Fe] = 0.25 ratio. For the same ratio, we observe changes in the pH as well as in complementary Raman spectra, which can be assigned to the transition from monomeric to oligomeric species. At approximately [OH]/[Fe] = 0.3 we begin to observe particles larger than 1 nm in radius, detected by small-angle X-ray scattering

Nanocasting of Superparamagnetic Iron Oxide Films with Ordered Mesoporosity

Maghemite and magnetite show superparamagnetic behavior when synthesized in a nanostructured form. The material s inducible magnetization enables applications ranging from contrast enhancing agents for magnetic resonance imaging to drug delivery systems, magnetic hyperthermia, and separation. Superparamagnetic iron oxides with templated porosity have been synthesized so far only in the form of hard templated powders, where silicon retained from the template severely degrades the material s magnetic properties. Here, for the first time, the synthesis of superparamagnetic iron oxides with soft templated mesopore structure is reported. The synthesis of nanostructured maghemite and magnetite films succeeds using micelles of amphiphilic block copolymers as templates. A thermal treatment of the initially formed mesoporous ferrihydrite in nitrogen produces maghemite, which can be partly reduced to magnetite via thermal treatment in hydrogen while retaining the templated mesopore structure. The resulting materials feature a unique combination of high surface area, controlled pore diameter, and tunable magnetic propertie