The migration and accumulation of iodide ions create a modulation of the respective interfacial barriers causing the hysteresis in solar cells based on methylammonium lead iodide perovskites. Iodide ...ions are identified as the migrating species by measuring temperature dependent current‐transients and photoelectron spectroscopy. The involved changes in the built‐in potential due to ion migration are directly measured by electroabsorption spectroscopy.
Despite the central role of light absorption and the subsequent generation of free charge carriers in organic and hybrid organic-inorganic photovoltaics, the precise process of this initial ...photoconversion is still debated. We employ a novel broadband (UV-Vis-NIR) transient absorption spectroscopy setup to probe charge generation and recombination in the thin films of the recently suggested hybrid material combination poly(3-hexylthiophene)/silicon (P3HT/Si) with 40 fs time resolution. Our approach allows for monitoring the time evolution of the relevant transient species under various excitation intensities and excitation wavelengths. Both in regioregular (RR) and regiorandom (RRa) P3HT, we observe an instant (<40 fs) creation of singlet excitons, which subsequently dissociate to form polarons in 140 fs. The quantum yield of polaron formation through dissociation of delocalized excitons is significantly enhanced by adding Si as an electron acceptor, revealing ultrafast electron transfer from P3HT to Si. P3HT/Si films with aggregated RR-P3HT are found to provide free charge carriers in planar as well as in bulk heterojunctions, and losses are due to nongeminate recombination. In contrast for RRa-P3HT/Si, geminate recombination of bound carriers is observed as the dominant loss mechanism. Site-selective excitation by variation of pump wavelength uncovers an energy transfer from P3HT coils to aggregates with a 1/e transfer time of 3 ps and reveals a factor of 2 more efficient polaron formation using aggregated RR-P3HT compared to disordered RRa-P3HT. Therefore, we find that polymer structural order rather than excess energy is the key criterion for free charge generation in hybrid P3HT/Si solar cells.
Organic solar cells (OSCs) have achieved much attention and meanwhile reach efficiencies above 10%. One problem yet to be solved is the lack of long term stability. Crosslinking is presented as a ...tool to increase the stability of OSCs. A number of materials used for the crosslinking of bulk heterojunction cells are presented. These include the crosslinking of low bandgap polymers used as donors in bulk heterojunction cells, as well as the crosslinking of fullerene acceptors and crosslinking between donor and acceptor. External crosslinkers often based on multifunctional azides are also discussed. In the second part, some work either leading to OSCs with high efficiencies or giving insight into the chemistry and physics of crosslinking are highlighted. The diffusion of low molar mass fullerenes in a crosslinked matrix of a conjugated polymer and the influence of crosslinking on the carrier mobility is discussed. Finally, the use of crosslinking to make stable interlayers and the solution processing of multilayer OSCs are discussed in addition to presentation of a novel approach to stabilize nanoimprinted patterns for OSCs by crosslinking.
Three promising applications of crosslinking in organic solar cells are reviewed. Most importantly, crosslinking is used to stabilize the blend morphology in bulk heterojunction solar cells. In addition, stable interlayers can be formed and crosslinking enables solution processing of multilayer devices. A third possibility is the stabilization of nanoimprinted patterns in the active layers.
The conserved eight-subunit COP9 signalosome (CSN) is required for multicellular fungal development. The CSN deneddylase cooperates with the Cand1 exchange factor to control replacements of E3 ...ubiquitin cullin RING ligase receptors, providing specificity to eukaryotic protein degradation.
Aspergillus nidulans
CSN assembles through a heptameric pre-CSN, which is activated by integration of the catalytic CsnE deneddylase. Combined genetic and biochemical approaches provided the assembly choreography within a eukaryotic cell for native fungal CSN. Interactomes of functional GFP-Csn subunit fusions in pre-CSN deficient fungal strains were compared by affinity purifications and mass spectrometry. Two distinct heterotrimeric CSN subcomplexes were identified as pre-CSN assembly intermediates. CsnA-C-H and CsnD-F-G form independently of CsnB, which connects the heterotrimers to a heptamer and enables subsequent integration of CsnE to form the enzymatically active CSN complex. Surveillance mechanisms control accurate Csn subunit amounts and correct cellular localization for sequential assembly since deprivation of Csn subunits changes the abundance and location of remaining Csn subunits.
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