The Edge Effects Boosting Hydrogen Evolution Performance of Platinum/Transition Bimetallic Phosphide Hybrid Electrocatalysts

Platinum (Pt) is regarded as a promising electrocatalyst for hydrogen evolution reaction (HER). However, its application in an alkaline medium is limited by the activation energy of water dissociation, diffusion of H⁺, and desorption of H*. Moreover, the formation of effective structures with a low Pt usage amount is still a challenge. Herein, guided by the simulation discovery that the edge effect can boost local electric field (LEF) of the electrocatalysts for faster proton diffusion, platinum nanocrystals on the edge of transition metal phosphide nanosheets are fabricated. The unique heterostructure with ultralow Pt amount delivered an outstanding HER performance in an alkaline medium with a small overpotential of 44.5 mV and excellent stability for 80 h at the current density of −10 mA cm⁻². The mass activity of as-prepared electrocatalyst is 2.77 A mg⁻¹_Pt, which is 15 times higher than that of commercial Pt/C electrocatalysts (0.18 A mg⁻¹_Pt). The density function theory calculation revealed the efficient water dissociation, fast adsorption, and desorption of protons with hybrid structure. The study provides an innovative strategy to design unique nanostructures for boosting HER performances via achieving both synergistic effects from hybrid components and enhanced LEF from the structural edge effect.     

Electron Transfer-Induced Metal Spin-Crossover at NiCo2S4/ReS2 2D–2D Interfaces for Promoting pH-universal Hydrogen Evolution Reaction

The development of an efficient pH-universal hydrogen evolution reaction (HER) electrocatalyst is essential for practical hydrogen production. Here, an efficient and stable pH-universal HER electrocatalyst composed of the strongly coupled 2D NiCo₂S₄ and 2D ReS₂ nanosheets (NiCo₂S₄/ReS₂) is demonstrated. The NiCo₂S₄/ReS₂ 2D–2D nanocomposite is directly grown on the surface of the carbon cloth substrate, which exhibits excellent HER performance with overpotentials of 85 and 126 mV at a current density of 10 mA cm⁻² and Tafel slopes of 78.3 and 67.8 mV dec⁻¹ under both alkaline and acidic conditions, respectively. Theoretical and experimental characterizations reveal that the chemical coupling between NiCo₂S₄ and ReS₂ layers induces electron transfer from Ni and Co to interfacial Re-neighbored S atoms, enabling beneficial H atom adsorption and desorption for both acidic and alkaline HER. Simultaneously, an electron transfer-induced spin-crossover generates high-spin interfacial Ni and Co atoms that promote water dissociation kinetics at the NiCo₂S₄/ReS₂ interface, which is the origin of the superior alkaline HER activity. NiCo₂S₄/ReS₂ also shows decent catalytic activity and long-term durability for oxygen evolution reaction, and finally bifunctionality for overall water splitting. This study suggests a rational strategy to enhance water dissociation kinetics by inducing spin-crossover via electron transfer.     

Self‐Powered,Room‐Temperature Electronic Nose Based on Triboelectrification and Heterogeneous Catalytic Reaction

Herein, a self‐powered electronic nose strategy with highly selective gas detection is described. The electronic nose is a two‐dimensional microarray based on the triboelectrification between ZnO nanowires and the dielectric layers, and the heterogeneous catalytic reaction occurring on the nanowires and on the NiO nanoparticles. These electronic noses show the ability to distinguish between four volatile organic compound (VOC) gases (methanol, ethanol, acetone, and toluene) with a detection limit of 0.1% at room temperature using no external power source.     

Nucleoside Triphosphates as Promoters to Enhance Nanoceria Enzyme‐like Activity and for Single‐Nucleotide Polymorphism Typing

Nucleoside triphosphates (NTPs) can improve the oxidase‐like activity of nanoceria and the enhancement is correlated with the type of NTP. This effect is demonstrated to be as a result of the coupling of the oxidative reaction with the NTP hydrolysis reactions, as the nanoceria has both oxidase‐like and phosphatase‐like activities. The differences reflect the different dephosphorylation catalytic activities of nanoceria to the NTP used. Furthermore, based on the NTP‐promoted oxidase‐like activity of nanoceria and the differences among the different types of NTPs, series effective and high‐throughput colorimetric assays for single‐nucleotide polymorphism (SNP) typing are developed.     

Bifunctional Edge-Rich Nitrogen Doped Porous Carbon for Activating Oxygen and Sulfur

Oxygen reduction reaction (ORR) and sulfur reduction reaction (SRR) play key roles in advanced batteries. However, they both suffer from sluggish reaction kinetics. Here, an interesting nitrogen doped porous carbon material that can simultaneously activate oxygen and sulfur is reported. The carbon precursor is a nitrogen containing covalent organic framework (COF), constituting periodically stacked 2D sheets. The COF structure is well preserved upon pyrolysis, resulting in the formation of edge-rich porous carbon with structure resembling stacked holey graphene. The nitrogen containing groups in the COF are decomposed into graphitic and pyridinic nitrogen during pyrolysis. These edge sites and uniform nitrogen doping endow the carbon product with high intrinsic catalytic activities toward ORR and SRR. The COF derived carbon delivers outstanding performances when assembling as cathodes in the Li-S and Li-O₂ batteries. Simultaneous activation of oxygen and sulfur also enables a new battery chemistry. A proof-of-concept Li-S/O₂ hybrid battery is assembled, delivering a large specific capacity of 2,013 mAh g⁻¹. This study may inspire novel battery designs based on oxygen and sulfur chemistry.     

Electrochemical polishing of monocrystalline silicon with specific crystallographic planes

In this study, an electrolytic polishing experimental system was developed to obtain a uniform, flat-surfaced monocrystalline silicon with specific crystallographic planes. Several key factors reflecting specific electrolytic polishing on monocrystalline silicon with specific crystallographic planes were summarized. These factors, including electrolyte, conduction mode, Schottky barrier, semiconductor body resistance, and unidirectional conductivity, were analyzed comprehensively through energy spectrum analysis, theoretical modeling, and potential simulation. The effects of electrolytic polishing process were obtained, and corresponding solutions were proposed. Finally, the electrolytic polishing experiment for monocrystalline silicon with specific crystallographic planes was conducted. A uniform, flat-surfaced monocrystalline silicon with no metamorphic layer was then obtained. The flatness error of the center area was less than 0.201 µm. Furthermore, the crystallographic planes of monocrystalline silicon wafers showed no change.     

Phase reactions at semiconductor metallization interfaces

During, or following, the fabrication of a microelectronic device, it is possible for the material phases at critical interfaces to react with one another, and so alter the elec-trical performance. This is particularly important for metallization contacts to semi-conductors and for multilevel interconnects. The present article shows that application of phase diagram principles can successfully predict the mutual stability or chemical reactivity in such circumstances. Since most relevant phase diagrams are not available, it is shown how they may be calculated from known thermochemical data, or deduced from observations on thin-film reactions. The article is illustrated by the behavior of titanium silicide with a diffusion barrier layer (TiN) and the surrounding dielectric SiO₂. In addition the Al-Si-O-N and W-N-Ga-As systems are described, and metastable amor-phous phase formation at the Ti-Si interface is discussed.     

Study of wetting reaction between eutectic AuSn and Au foil

Wetting reactions between eutectic AuSn solder and Au foil have been studied. During the reflow process, Au foil dissolution occurred at the interface of AuSn/Au, which increases with temperature and time. The activation energy for Au dissolution in molten AuSn solder is determined to be 41.7 kJ/mol. Au₅Sn is the dominant interfacial compound phase formed at the interface. The activation energy for the growth of interfacial Au₅Sn phase layer is obtained to be 54.3 kJ/mol over the temperature range 360–440°C. The best wettability of molten AuSn solder balls on Au foils occurred at 390°C (wetting angle is about 25°). Above 390°C, the higher solder oxidation rate retarded the wetting of the molten AuSn solder.     

A Possible Reaction Pathway to Fabricate a Half‐Metallic Wire on a Silicon Surface

Based on first‐principles electronic structure calculations and molecular dynamics simulations, a possible reaction pathway for fabricating half‐metallic Mo‐borine sandwich molecular wires on a hydrogen‐passivated Si(001) surface is presented. The molecular wire is chemically bonded to the silicon surface and is stable up to room temperature. Interestingly, the essential properties of the molecular wire are not significantly affected by the Si substrate. Furthermore, their electronic and magnetic properties are tunable by an external electric field, which allows the molecular wire to function as a molecular switch or a basic component for information storage devices, leading to applications in future molecular electronic and spintronic devices.