Intrinsic efficiency limits in low-bandgap non-fullerene acceptor organic solar cells. Nature Materials.

Large-conductance (BK type) Ca(2+)-dependent K(+) channels are essential for modulating muscle contraction and neuronal activities such as synaptic transmission and hearing. BK channels are activated by membrane depolarization and intracellular Ca(2+) and Mg(2+) (refs 6-10). The energy provided by voltage, Ca(2+) and Mg(2+) binding are additive in activating the channel, suggesting that these signals open the activation gate through independent pathways. Here we report a molecular investigation of a Mg(2+)-dependent activation mechanism. Using a combined site-directed mutagenesis and structural analysis, we demonstrate that a structurally new Mg(2+)-binding site in the RCK/Rossman fold domain -- an intracellular structural motif that immediately follows the activation gate S6 helix -- is responsible for Mg(2+)-dependent activation. Mutations that impair or abolish Mg(2+) sensitivity do not affect Ca(2+) sensitivity, and vice versa. These results indicate distinct structural pathways for Mg(2+)- and Ca(2+)-dependent activation and suggest a possible mechanism for the coupling between Mg(2+) binding and channel opening.

Self-assembled monolayers (SAMs) based on Br-2PACz ([2-(3,6dibromo-9H-carbazol-9-yl)ethyl]phosphonic acid) 2PACz ethyl]phosphonic acid) and ethyl]phosphonic acid) molecules were investigated as hole-extracting interlayers in organic photovoltaics (OPVs). The highest occupied molecular orbital (HOMO) energies of these SAMs were measured at À 6.01 and À 5.30 eV for Br-2PACz and MeO-2PACz, respectively, and found to induce significant changes in the work function (WF) of indium-tin-oxide (ITO) electrodes upon chemical functionalization. OPV cells based on PM6 (poly [(2,6-(4,8-bis(5-(2-ethylhexyl-3- ([6,6]-phenyl-C71-bu-tyric acid methyl ester) using ITO/Br-2PACz anodes exhibited a maximum power conversion efficiency (PCE) of 18.4 %, outperforming devices with ITO/MeO-2PACz (14.5 %) and ITO/poly (3,4-ethylenedioxythiophene):poly(styrene sulfonate) (PE-DOT : PSS) (17.5 %). The higher PCE was found to originate from the much higher WF of ITO/Br-2PACz (À 5.81 eV) compared to ITO/MeO-2PACz (4.58 eV) and ITO/PEDOT : PSS (4.9 eV), resulting in lower interface resistance, improved hole transport/extraction, lower trap-assisted recombination, and longer carrier lifetimes. Importantly, the ITO/Br-2PACz electrode was chemically stable, and after removal of the SAM it could be recycled and reused to construct fresh OPVs with equally impressive performance.

Slot-die (SD) coating is used to fabricate fully solution processed organic solar cells (OSCs) based on a blend of high performance donor polymer (PTB7-Th) and a non-fullerene acceptor (IEICO-4F) for stable devices over extended periods of operation. The optimization of a sequential deposition process of transport and active layers, under ambient conditions, enable high efficiency slot-die coated solar cells with remarkable power conversion efficiencies (PCE) > 11.0% to bridge the gap between lab-to-fab. Fully slot-die coated inverted OSCs are demonstrated with efficiencies reaching 11% along with 1 cm 2 devices, proving the scalability and reproducibility of the proposed technique. Further, replacing the evaporated Ag electrode with solution processed Ag nanowire (AgNW) electrodes shows the highest light utilization efficiency of 5.26% for semi-transparent OSC with a PCE of 9.07% and average visible transmission of 58%.

Advancing non-fullerene acceptor (NFA) organic photovoltaics requires the mitigation of the efficiency-limiting processes. Acceptor end-group and sidechain engineering are two handles to tune properties, and a better understanding of their specific impact on the photophysics could facilitate a more guided acceptor design. Here, the device performance, energetic landscape, and photophysics of rhodanine and dicyanovinyl end-capped IDT-based NFAs, namely, O-IDTBR and O-IDTBCN, in PCE10-based solar cells are compared by transient optical and electro-optical spectroscopy techniques and density functional theory calculations. It is revealed how the acceptors' quadrupole moments affect the interfacial energetic landscape, in turn causing differences in exciton quenching, charge dissociation efficiencies, and geminate versus non-geminate recombination losses. More precisely, it is found that the open circuit voltage (V OC ) is controlled by the acceptors' electron affinity (EA), while geminate and non-geminate recombination, and the field dependence of charge generation, rely on the acceptors' quadrupole moments. The kinetic parameters and yields of all processes are determined, and it is demonstrated that they can reproduce the performance differences of the devices' current-voltage characteristics in carrier drift-diffusion simulations. The results provide insight into the impact of the energetic landscape, specifically the role of the quadrupole moment of the acceptor, beyond trivial considerations of the donor-acceptor energy offsets.