Compounds displaying delayed fluorescence (DF), from severe concentration quenching, have limited applications as nondoped organic light-emitting diodes and material sciences. As a nondoped fluorescent emitter, aggregation-induced emission (AIE) materials show high emission efficiency in their aggregated states. Reported herein is an AIE-active, DF compound in which the molecular interaction is modulated, thereby promoting triplet harvesting in the solid state with a high photoluminescence quantum yield of 93.3%, which is the highest quantum yield, to the best of our knowledge, for long-lifetime emitters. Simultaneously, the compound with asymmetric molecular structure exhibited strong mechanoluminescence (ML) without pretreatment in the solid state, thus exploiting a design and synthetic strategy to integrate the features of DF, AIE, and ML into one compound.

As a promising candidate for low‐cost and environmentally friendly thin‐film photovoltaics, the emerging kesterite‐based Cu2ZnSn(S,Se)4 (CZTSSe) solar cells have experienced rapid advances over the past decade. However, the record efficiency of CZTSSe solar cells (12.6%) is still significantly lower than those of its predecessors Cu(In,Ga)Se2 (CIGS) and CdTe thin‐film solar cells. This record has remained for several years. The main obstacle for this stagnation is unanimously attributed to the large open‐circuit voltage (V OC) deficit. In addition to cation disordering and the associated band tailing, unpassivated interface defects and undesirable energy band alignment are two other culprits that account for the large V OC deficit in kesterite solar cells. To capture the great potential of kesterite solar cells as prospective earth‐abundant photovoltaic technology, current research focuses on cation substitution for CZTSSe‐based materials. The aim here is to examine recent efforts to overcome the V OC limit of kesterite solar cells by cation substitution and to further illuminate several emerging prospective strategies, including: i) suppressing the cation disordering by distant isoelectronic cation substitution, ii) optimizing the junction band alignment and constructing a graded bandgap in absorber, and iii) engineering the interface defects and enhancing the junction band bending.

A fluorescent compound, 9,10-bis(2-(10-hexyl-10H-phenothiazin-3-yl)vinyl) anthracene, has been synthesized and studied. The results show that the compound possesses piezofluorochromic properties as well as aggregation-induced emission enhancement effect. The spectroscopic properties and morphological structures are reversibly exhibited upon pressing (or grinding) or annealing (or fuming). The piezofluorochromic nature is generated through phase transformation under the stimulus of external pressure. The reason for the phase transformation caused by external pressure is ascribed to the twisted conformation of the molecule which leads to poor solid molecular packing and weak interactions in the interfaces of lamellar layers confirmed by its single-crystal X-ray diffraction analysis.

Despite the tremendous commercial success of radio frequency quadrupole ion traps for bottom-up proteomics studies, there is growing evidence that peptides decorated with labile post-translational modifications are less amenable to low-energy, resonate excitation MS/MS analysis. Moreover, multiplexed stable isotope reagents designed for MS/MSbased quantification of peptides rely on accurate and robust detection of low-mass fragments for all precursors. Collectively these observations suggest that beam-type or tandem in-space MS/MS measurements, such as that available on traditional triple quadrupole mass spectrometers, may provide beneficial figures of merit for quantitative proteomics analyses. The recent introduction of a multipole collision cell adjacent to an Orbitrap mass analyzer provides for higher energy collisionally activated dissociation (HCD) with efficient capture of fragment ions over a wide mass range. Here we describe optimization of various instrument and post-acquisition parameters that collectively provide for quantification of iTRAQ-labeled phosphorylated peptides isolated from complex cell lysates. Peptides spanning a concentration dynamic range of 100:1 are readily quantified. Our results indicate that appropriate parameterization of collision energy as a function of precursor m/z and z provides for optimal performance in terms of peptide identification and relative quantification by iTRAQ. Using this approach, we readily identify activated signaling pathways downstream of oncogenic mutants of Flt-3 kinase in a model system of human myeloid leukemia. [4][5][6], extended mass range capability [7], use of helium buffer gas [3], and automated control of trapped ion populations [8], all combined to catapult trap-based instruments to the forefront of proteomics research. Concomitant advances in CPU and embedded systems provided for rapid and automated control of instrument parameters and yielded heretofore unattainable throughput for peptide sequence analysis via LC-MS/MS. Today, several years past the emergence of proteomics as a field of active research [9], it is clear that "typical" tryptic peptides are very amenable to sequence analysis via low-energy MS/MS. More recently, the introduction of hybrid geometries [10 -12] and other instrument configurations [13,14], along with protocols for enrichment of post-translationally modified peptides [15,16], have dramatically increased the experimental dynamic range of proteomics analyses. Collectively, these results have revealed that peptides decorated with labile modifications often are not well behaved under low-energy MS/MS conditions. For example, facile loss of phosphoric acid from the side chains of serine-and threoninephosphorylated peptides often limits the available sequence-specific information contained in associated MS/MS spectra [17,18]. Interestingly, recent reports [19,20] suggest that higher energy, or "triple quadrupole like," MS/MS can provide improved sequence analysis, particularly for phosphorylated peptides. In the work repo...

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