Conquer the fine structure splitting of excitons in self-assembled InAs/GaAs quantum dots via combined stresses

Eliminating the fine structure splitting (FSS) of excitons in self-assembled quantum dots (QDs) is essential to the generation of high quality entangled photon pairs. It has been shown that the FSS has a lower bound under uniaxial stress. In this letter, we show that the FSS of excitons in a general self-assembled InGaAs/GaAs QD can be fully suppressed via combined stresses along the [110] and [010] directions. The result is confirmed by atomic empirical pseudopotential calculations. For all the QDs we studied, the FSS can be tuned to be vanishingly small ($<$ 0.1 $\mu$eV), which is sufficient small for high quality entangled photon emission.Comment: 4 pages, 3 figure, 1 tabl

Bis[1,3-bis­(diphenyl­phosphinoylimino)isoindolinato-κ3 O,N,O′]calcium(II)

In the title compound, [Ca(C32H24N3O2P2)2], the 1,3-bis­(diphenyl­phosphinoylimino)isoindoline ligand adopts a tridentate coordination mode. The compound exhibits a distorted octa­hedral geometry. The Ca atom lies on a twofold rotation axis

Ammonium diphenyl­phosphinate monohydrate

In the title salt, NH4 +·C12H10O2P−·H2O, the ion pair and water mol­ecule inter­act through hydrogen bonds to form a layer structure

Dual phosphorylation of Sin1 at T86 and T398 negatively regulates mTORC2 complex integrity and activity

Mammalian target of rapamycin (mTOR) plays essential roles in cell proliferation, survival and metabolism by forming at least two functional distinct multi-protein complexes, mTORC1 and mTORC2. External growth signals can be received and interpreted by mTORC2 and further transduced to mTORC1. On the other hand, mTORC1 can sense inner-cellular physiological cues such as amino acids and energy states and can indirectly suppress mTORC2 activity in part through phosphorylation of its upstream adaptors, IRS-1 or Grb10, under insulin or IGF-1 stimulation conditions. To date, upstream signaling pathways governing mTORC1 activation have been studied extensively, while the mechanisms modulating mTORC2 activity remain largely elusive. We recently reported that Sin1, an essential mTORC2 subunit, was phosphorylated by either Akt or S6K in a cellular context-dependent manner. More importantly, phosphorylation of Sin1 at T86 and T398 led to a dissociation of Sin1 from the functional mTORC2 holo-enzyme, resulting in reduced Akt activity and sensitizing cells to various apoptotic challenges. Notably, an ovarian cancer patient-derived Sin1-R81T mutation abolished Sin1-T86 phosphorylation by disrupting the canonical S6K-phoshorylation motif, thereby bypassing Sin1-phosphorylation-mediated suppression of mTORC2 and leading to sustained Akt signaling to promote tumorigenesis. Our work therefore provided physiological and pathological evidence to reveal the biological significance of Sin1 phosphorylation-mediated suppression of the mTOR/Akt oncogenic signaling, and further suggested that misregulation of this process might contribute to Akt hyper-activation that is frequently observed in human cancers

Network Structure and Employee Creativity in a Heterogeneous Team

This paper investigates the relationships between individual creativity, social network position, and knowledge sharing in a heterogeneous team with personnel from four different companies to complete a software outsourcing project. Our research model is based on a theoretical construction attained from the analysis of previous frameworks proposed in the literature. Based on the survey data of the team members, we construct the advice social network, extract employee network centrality, and obtain employee behavioural variables. We find that a positive and strong relationship between knowledge sharing and creativity. The relationship between network centrality and creativity is also positive, but the relationship is moderated by knowledge sharing. Based on the findings, we propose measures and strategies for the hosting company to effectively coordinate the heterogeneous team