This review highlights doping effects on the intrinsic catalytic activities and oxygen evolution reaction mechanisms of state-of-the-art catalysts, including oxides, non-oxides and carbon-based catalysts, from experimental to theoretical studies.

High‐quality joints between titanium alloys and stainless steels have found applications for nuclear, petrochemical, cryogenic, and aerospace industries due to their relatively low cost, lightweight, high corrosion resistance, and appreciable mechanical properties. This article reviews diffusion bonding between titanium alloys and stainless steels with or without interlayers. For diffusion bonding of a titanium alloy and a stainless steel without an interlayer, the optimized temperature is in the range of 800–950°C for a period of 60–120 min. Sound joint can be obtained, but brittle FeTi and Fe‐Cr‐Ti phases are formed at the interface. The development process of a joint mainly includes three steps: matching surface closure, growth of brittle intermetallic compounds, and formation of the Kirkendall voids. Growth kinetics of interfacial phases needs further clarification in terms of growth velocity of the reacting layer, moving speed of the phase interface, and the order for a new phase appears. The influence of Cu, Ni (or nickel alloy), and Ag interlayers on the microstructures and mechanical properties of the joints is systematically summarized. The content of FeTi and Fe‐Cr‐Ti phases at the interface can be declined significantly by the addition of an interlayer. Application of multi‐interlayer well prevents the formation of intermetallic phases by forming solid solution at the interface, and parameters can be predicted by using a parabolic diffusion law. The selection of multi‐interlayer was done based on two principles: no formation of brittle intermetallic phases and transitional physical properties between titanium alloy and stainless steel.

Scintillator materials convert high-energy radiation into photons in the ultraviolet to visible light region for radiation detection. In this review, advances in X-ray emission dynamics of inorganic scintillators are presented, including inorganic halides (alkali-metal halides, alkaline-earth halides, rare-earth halides, oxy-halides, rare-earth oxyorthosilicates, halide perovskites), oxides (binary oxides, complex oxides, post-transition metal oxides), sulfides, rare-earth doped scintillators, and organic-inorganic hybrid scintillators. The origin of scintillation is strongly correlated to the host material and dopants. Current models are presented describing the scintillation decay lifetime of inorganic materials, with the emphasis on the short-lived scintillation decay component. The whole charge generation and the de-excitation process are analyzed in general, and an essential role of the decay kinetics is the de-excitation process. We highlighted three decay mechanisms in cross luminescence emission, exitonic emission, and dopant-activated emission, respectively. Factors regulating the origin of different luminescence centers controlling the decay process are discussed.