Trapping-influenced photoluminescence intensity decay in semiconductor nanoplatelets

We present a diffusion-based simulation model for explanation of long time power-law decay of photoluminescence (PL) emission intensity in semiconductor nanoplatelets. In our model the shape of emission curves is an outcome of interplay of recombination, diffusion and trapping of excitons. At short times the excitons diffuse freely following the normal diffusion behaviour. The emission decay is purely exponential and is defined by recombination. At long times the transition into the subdiffusive motion happens and the emission occurs due to the release of excitons from surface traps. A power-law tail for intensity is a consequence of the release. The crossover from onelimit to another is controlled by diffusion properties. The approach reproduces the properties of experimental curves measured for different nanoplatelet systems.

Mitigation of Platinum Depletion in Platinum Diffused Single Phase Bond Coat on CMSX-4 Superalloy

Pt-diffused bond coat with a mixture of γ/γ’ phase has just been developed in the recent decades as a cheaper alternative to the Pt-enriched β-phase Aluminide bond coat that contains a higher content of Al. However, concerns are raised on the inevitable depletion of Pt near the coating interface that may endanger the component after long-term service. In this study, modified Pt-diffused bond coats with a single phase (γ or γ’) were made by applying selective etching on CMSX-4 single crystal superalloys prior to the electroplating of Pt. The single-phase bond coats show distinctive diffusion behaviour in comparison with the conventional γ/γ’ bond coat. Surprisingly, Pt remains more stable in the γ’-phase bond coat with significantly less depletion after diffusion, which implies a potential in saving a considerable amount of Pt. On the other hand, however, the depletion of Pt is more severe in the γ-phase bond coat. The mechanism that governs the diffusion behavior of Pt in the γ and γ’-phase was also discussed that mainly concerns with thermodynamic and kinetic factors.

Model of local hydrogen permeability in stainless steel with two coexisting structures

The dynamics of hydrogen in metals with mixed grain structure is not well understood at a microscopic scale. One of the biggest issues facing the hydrogen economy is “hydrogen embrittlement” of metal induced by hydrogen entering and diffusing into the material. Hydrogen diffusion in metallic materials is difficult to grasp owing to the non-uniform compositions and structures of metal. Here a time-resolved “operando hydrogen microscope” was used to interpret local diffusion behaviour of hydrogen in the microstructure of a stainless steel with austenite and martensite structures. The martensite/austenite ratios differed in each local region of the sample. The path of hydrogen permeation was inferred from the time evolution of hydrogen permeation in several regions. We proposed a model of hydrogen diffusion in a dual-structure material and verified the validity of the model by simulations that took into account the transfer of hydrogen at the interfaces.

Investigations on the Diffusion of Platinum between CMSX-4 Superalloy and Platinum-Enriched Bond Coat

The depletion of Pt in Pt-enriched bond coats due to inter-diffusion with superalloys has been a critical concern for the long-term oxidation resistance of thermal barrier coatings. This study investigated the diffusion behaviour of Pt between CMSX-4 superalloys and two commercial Pt-enriched bond coats comprising intermetallic γ′/γ-phase or β-phase, with the aim to understand the mechanism that leads to the depletion of Pt at high temperatures. The results demonstrated that the diffusion of Pt in superalloy disrupts its phase equilibrium, causes a significant lattice parameter misfit between the γ-phase and γ′-phase, and results in the formation of large γ′-grains with irregular shapes and random orientations. In addition, by using the Thermo-Calc software, Pt was found to have negative chemical interactions with both Al and Ta that stabilise Pt by decreasing its chemical activity. The depletion of Al due to the growth of Al2O3 scale during oxidation increases the activity of Pt and therefore accelerates the inwards depletion of Pt towards superalloys.