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Directional Mn dopant migration (outward/inward) was achieved by inserting a CdZnS “atomic trap” with a small size mismatch with dopants in core/multi-shell QDs. A larger initial substitutional site allows for active trapping and dopant migration. 

Here, we study the homogenization behavior and microstructure of seven Ni-Al-Ti alloys with quaternary additions of γ forming elements 4Cr, 4Co, 4Ru, 4Mo, 4Hf, 4 W and 2Re. To design a homogenization treatment, the as-cast microstructure is analyzed revealing the diffusion distances x between dendrite cores and interdendritic regions. The temperatures for homogenization are determined using differential scanning calorimetry (DSC) and Thermo-Calc simulations, to be between 1150 and 1275 °C. The time to achieve homogenization is modelled based on the residual segregation index δ utilizing diffusion distance, homogenization temperature and diffusion data. Electron probe micro analyzer (EPMA) measurements show that our predictions match for the 4Cr, 4Co, 4Ru, 4 W and 2Re alloys while the 4Hf alloy shows insufficient homogenization. Transmission electron microscopy (TEM) reveals a two-phase γ/γ’ microstructure after 750 °C / 24 h, whereby the 4Co and 4Ru alloys form hierarchical microstructures. We observe γ plates in the 4Co alloy and γ spheres in the 4Ru alloy. Ru in the 4Ru alloy is involved in stabilizing the morphology of γ spheres. We provide a straightforward method for the design of homogenization treatments of Ni-based superalloys and demonstrate an alloy design pathway for tailoring the phase stability of hierarchical microstructures. 

Abstract Online innovation competitions are ecosystems where institutions source numerous solutions from knowledge workers through a platform intermediary. By considering how an individual competitor’s performance varies based on their social positioning in a competition ecosystem’s collaboration network, we illustrate the value of social networks for individual outcomes in online competitions. The study reports results from Kaggle, a popular online competition platform for data science, where a sample of 350,956 users participated in 2,789 competitions over 4 years. We investigate how the number of collaborations, membership in the largest connected component in the network, and diversity of collaboration experiences impact the points and medals earned and how quickly competitors earn their first medal. Results show that positioning has a positive relationship with performance in competitive ecosystems. Relevant to the future of work, the study considers how knowledge workers in future workplaces should manage their online collaborations. 

Using sunlight to produce hydrogen gas via photocatalytic water splitting is highly desirable for green energy harvesting and sustainability. In this work, Mn 2+ doped 1-dimensional (1D) CdS nanorods (NRs) with Pt tips ( i.e. , 1D Mn:CdS-Pt NRs) were synthesized for photocatalytic water splitting to generate hydrogen gas. The incorporation of Mn 2+ dopants inside the 1D CdS NRs with a significantly longer lifetime (∼ms) than that of host excitons (∼ns) facilitates charge separation; the electron transfer to metal Pt tips leads to enhanced photocatalytic activity in water splitting redox reactions. The as-synthesized Mn 2+ doped CdS NR-based photocatalyst generated an order of magnitude greater yield of hydrogen gas compared to the undoped CdS NR-based photocatalyst. The enhanced charge transport from the long lifetime excited state of Mn 2+ dopants in light harvesting semiconductor nanomaterials presents a new opportunity to increase the overall photocatalytic performance. 

The high bond dissociation energy of C–C σ-bonds presents a challenge to chemical conversions in organic synthesis, polymer degradation, and biomass conversion that require chemoselective C–C bond cleavage at room temperature. Dye-sensitized photoelectrochemical cells (DSPECs) incorporating molecular organic dyes could offer a means of using renewable solar energy to drive these types of energetically demanding chemoselective C–C bond cleavage reactions. This study reports the solar light-driven activation of a bicyclic aminoxyl mediator to achieve C–C bond cleavage in the aryl-ether linkage of a lignin model compound (LMC) at room temperature using a donor–π-conjugated bridge–acceptor (D–π–A) organic dye-based DSPEC system. Mesoporous TiO 2 photoanode surfaces modified with 5-[4-(diphenylamino)phenyl]thiophene-2-cyanoacrylic acid (DPTC) D–π–A organic dye were investigated along with a bicyclic aminoxyl radical mediator (9-azabicyclo[3,3,1]nonan-3-one-9-oxyl, KABNO) in solution with and without the presence of LMC. Photophysical studies of DPTC with KABNO showed intermolecular energy/electron transfer under 1 sun illumination (100 mW cm −2 ). Under illumination, the D–π–A type DPTC sensitized TiO 2 photoanodes facilitate the generation of the reactive oxoammonium species KABNO+ as a strong oxidizing agent, which is required to drive the oxidative C–C bond cleavage of LMC. The photoelectrochemical oxidative reaction in a complete DSPEC with KABNO afforded C–C bond cleavage products 2-(2-methoxyphenoxy)acrylaldehyde (94%) and 2,6-dimethoxy-1,4-benzoquinone (66%). This process provides a first report utilizing a D–π–A type organic dye in combination with a bicyclic nitroxyl radical mediator for heterogeneous photoelectrolytic oxidative cleavage of C–C σ-bonds, modeled on those found in lignin, at room temperature.