Correlating the Microstructure and Current Density of the Li/Garnet Interface.

Solid-state lithium batteries hold great promise for next-generation energy storage systems. However, the formation of lithium filaments within the solid electrolyte remains a critical challenge. In this study, we investigate the crucial role of morphology in determining the resistance of garnet-type electrolytes to lithium filaments. By proposing a new test method, namely, cyclic linear sweep voltammetry, we can effectively evaluate the electrolyte resistance against lithium filaments. Our findings reveal a strong correlation between the microscopic morphology of the solid electrolyte and its resistance to lithium filaments. Samples with reduced pores and multiple grain boundaries demonstrate remarkable performance, achieving a critical current density of up to 3.2 mA cm-2 and excellent long-term cycling stability. Kelvin probe force microscopy and finite element method simulation results shed light on the impact of grain boundaries and electrolyte pores on lithium-ion transport and filament propagation. To inhibit lithium penetration, minimizing pores and achieving a uniform morphology with small grains and plenty of grain boundaries are essential.

A Visual Color Response Test Paper for the Detection of Hydrogen Sulfide Gas in the Air.

Hydrogen sulfide (H2S) is widely found in oil and natural gas wells and industrial wastewater tanks. Owing to its high toxicity, the monitoring and detection of H2S in the air is essential. However, recent techniques for the quantitative detection of H2S gas suffer from limitations such as high cost, complicated operation, and insufficient sensitivity, preventing their practical application in industry. Thus, we have developed a portable test paper for real-time and inexpensive monitoring of H2S gas by color changes. The test paper had a significantly low H2S detection limit of 200 ppb, which is considered safe for humans. Moreover, the color of the test paper did not change noticeably when exposed to CO2, N2, O2, and air environments, indicating that the test paper is selective for H2S gas and can be stored for a long time. In addition, we fitted a color difference linear model between the color difference values (ΔE) and the concentrations of H2S gas. The establishment of the linear model substantiates that the test paper can provide accurate intensity information when detecting H2S gas leakage.

Numerical and Experimental Investigations of Cold-Sprayed Basalt Fiber-Reinforced Metal Matrix Composite Coating.

The aluminum-basalt fiber composite coating was prepared for the first time with basalt fiber as the spraying material by cold-spraying technology. Hybrid deposition behavior was studied by numerical simulation based on Fluent and ABAQUS. The microstructure of the composite coating was observed on the as-sprayed, cross-sectional, and fracture surfaces by SEM, focusing on the deposited morphology of the reinforcing phase basalt fibers in the coating, the distribution of basalt fibers, and the interaction between basalt fibers and metallic aluminum. The results show that there are four main morphologies of the basalt fiber-reinforced phase, i.e., transverse cracking, brittle fracture, deformation, and bending in the coating. At the same time, there are two modes of contact between aluminum and basalt fibers. Firstly, the thermally softened aluminum envelops the basalt fibers, forming a seamless connection. Secondly, the aluminum that has not undergone the softening effect creates a closed space, with the basalt fibers securely trapped within it. Moreover, the Rockwell hardness test and the friction-wear test were conducted on Al-basalt fiber composite coating, and the results showed that the composite coating has high wear resistance and high hardness.

A pH-Controlled Solid Inhibitor Based on PAM Hydrogel for Steel Corrosion Protection in Wide Range pH NaCl Medium.

To provide carbon steel a long-term corrosion protection effect in NaCl solutions with different pH values, based on poly-acrylamide (PAM) and oleate imidazoline (OIM), a solid corrosion inhibitor with the properties of pH-controlled release was synthesized. SEM, FTIR and TGA results indicated that the OIM inhibitors were successfully loaded into PAM hydrogel with a high OIM encapsulation content (39.64 wt.%). The OIM release behavior from the hydrogel structure has two stages, quick release and sustained release. The pH of solutions could affect the initial release kinetics of OIM inhibitors and the diffusion path in the hydrogel structure. Weight loss measurement of L80 steel in different pH solutions with OIM@PAM proved the inhibitor responsive release mechanism and anticorrosion performance. The inhibition efficiency of OIM@PAM can maintain over 80% after long-term immersion in a harsh corrosive environment (pH 3), which is much higher than the inhibition efficiency of OIM@PAM in a moderate corrosive solution.

The Effect of the Modification of Mica by High-Temperature Mechanochemistry on the Anticorrosion Performance of Epoxy Coatings.

Epoxy resin was directly grafted onto the surface of mica powder by high-temperature mechanical ball milling. This method was used to achieve a chemical reaction between the epoxy resin and mica that cannot be carried out under conventional circumstances. The results show that an epoxy resin layer with a thickness of approximately 10 nm formed on the surface of the mica. This modified mica filler exhibited a significant change in its hydrophilic properties. The dispersion of mica and its compatibility with organic coatings also significantly improved. In addition, the modified mica filler was added to the epoxy coating. The improvement of the coating's compactness and toughness is the reason for its anti-corrosion performance enhancement.

Li/Garnet Interface Optimization: An Overview.

Solid-state lithium batteries can improve the safety and energy density of the present liquid-electrolyte-based lithium-ion batteries. To achieve this goal, both solid electrolyte and lithium anode technology are the keys. Lithium garnet is a promising electrolyte to enable the next generation solid-state lithium batteries due to its high ionic conductivity, good chemical, and electrochemical stability, and easiness to scale up. It is relatively stable against Li metal but the poor contact area and the presence of resistive impurity or decomposition layers at the interface interfere with fast charge transfer, thereby, spiking the interfacial resistance, overpotential, local current density, and the propensity for dendrite growth. In this Review, we first summarize the recent understanding of the interfacial problems at the Li/garnet interface from both computational and experimental viewpoints while seizing the opportunity to shed light on the chemical/electrochemical stability of garnet against Li metal anode. Also, we highlight various interface optimization strategies that have been demonstrated to be effective in improving the interface performance. We conclude this Review with a few suggestions as guides for future work.