Electronic Skin for Health Monitoring Systems: Properties, Functions, and Applications.

Electronic skin (e-skin), a skin-like wearable electronic device, holds great promise in the fields of telemedicine and personalized healthcare because of its good flexibility, biocompatibility, skin conformability, and sensing performance. E-skin can monitor various health indicators of the human body in real time and over the long term, including physical indicators (exercise, respiration, blood pressure, etc.) and chemical indicators (saliva, sweat, urine, etc.). In recent years, the development of various materials, analysis, and manufacturing technologies has promoted significant development of e-skin, laying the foundation for the application of next-generation wearable medical technologies and devices. Herein, the properties required for e-skin health monitoring devices to achieve long-term and precise monitoring and summarize several detectable indicators in the health monitoring field are discussed. Subsequently, the applications of integrated e-skin health monitoring systems are reviewed. Finally, current challenges and future development directions in this field are discussed. This review is expected to generate great interest and inspiration for the development and improvement of e-skin and health monitoring systems.

Interface Optimizing Core-Shell PZT@Carbon/Polyurethane Composites with Enhanced Passive Piezoelectric Vibration Damping Performance.

Presently, piezoelectric materials are gradually playing a significant role within composites to improve the damping and vibrational attenuation capacities of host composites. Previous studies paid attention to isolating the mechanical damping contribution and piezoelectric contribution of polymer-based piezoelectric composites (PPCs). However, reports detailing the piezoelectric damping of such materials have not paid sufficient attention to the technologies and methods to improve the piezoelectric damping of PPCs. In this study, we propose novel damping polyurethane (PU)-based piezoelectric composites with carbon-coated piezoelectric fillers (PZT@C/PU) with improved piezoelectric damping ability. The mechanical damping and piezoelectric damping of composites were theoretically decoupled, and we elaborate on the mechanism enhancing piezoelectric damping through the carbon coating strategy by comparing with the composites with nonpiezoelectric fillers. The as-fabricated core-shell structure having an optimized interface exhibits the proposed PZT@C/PU composite pads with relatively prominent damping ability (loss factor tan δmax = 1.0, tan δRT = 0.3), ductility (400.63%), and sound isolating behavior (transmission loss TL > 23 dB). Moreover, the vibration test results of as-fabricated sandwich structural PZT@C/PU composite damping devices exhibit outstanding vibration attenuating behavior (damping ratio ζ = 0.198). The study herein validates that the carbon shell coated on piezoelectric fillers would effectively increase damping performance of PU-based piezoelectric composites by the enhancement of piezoelectric performance caused by carbon coating piezoelectric fillers, which indicates that this material has potential for future applications in the field of vibration and noise reduction, thereby driving forward and expanding the fundamental understanding in the area of PPCs damping and vibration attenuation.

One-Step Cooperative Growth of High Reaction Kinetics Composite Homogeneous Core-Shell Heterostructure.

Reaction kinetics can be improved by the enhanced electrical contact between different components growing symbiotically. But so far, due to the necessity for material synthesis conditions match, the component structures of cooperative growth are similar, and the materials are of the same type. The collaborative growth of high-reaction kinetics composite homogeneous core-shell heterostructure between various materials is innovatively proposed with different structures in one step. The NiCo-LDH and PPy successfully symbiotically grow on activated carbon fiber fabric in one step. The open channel structure of the NiCo-LDH nanosheets is preserved while PPy effectively wrapped around the NiCo-LDH. The well-defined nanostructure with abundant active sites and convenient ion diffusion paths is favorable for electrolyte entry into the entire nanoarrays. In addition, owing to the enhanced electronic interaction between different components through XPS analysis, the NiCo-LDH@PPy electrode shows outstanding reaction kinetics and structural stability. The as-synthesized NiCo-LDH@PPy exhibited excellent super-capacitive storage capabilities, robust capacitive activity, and good rate survival. Furthermore, an asymmetric supercapacitor (ASC) device made of NiCo-LDH@PPy and activated carbon (AC) is able to maintain a long cycle life while achieving high power and energy densities.

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.

Stretchable, Strong, Recyclable Helicide Elastomer Based on Dynamic Covalent Interactions.

Current methods for making and disposing synthetic polymers have been widely pursued and are largely unsustainable. As a part of the solution, the reversible nature of dynamic covalent bonds emerges as an extraordinarily diverse and valuable feature in the development of exotic molecules and extended structures. With these bonds, it should be possible to construct recyclable and mechanically interlocked molecular structures using relatively simple precursors with preorganized geometries. A new helicide-based elastomer network is developed here with self-healing, recycling, and degradation features using a similar concept. The best self-healing performance (100%) was noted over 10-20 min, with various H2O, HCl, and NaOH solutions that delivered mechanical properties in the 1-1.4 MPa range. For hydrolytic degradation, the parameters are defined based on the type of binding, the pH of the solutions, and the copolymer network, which endowed a degradation time of approximately 4-11 h for each prepared sample. However, due to the reversible nature of the dynamic bonds, the material showed good recyclable mechanical properties compared to the pristine samples after five consecutive cycles, which meet the requirements of recyclable materials and recyclable packaging.

Platelet-Rich Plasma Composite Organohydrogel with Water-Locking and Anti-Freezing to Accelerate Wound Healing.

Hydrogels have gained impressive attention in biological medicine due to their excellent biosafety, softness, and varied functional components. However, conventional hydrogels have inherent defects, such as low tensile strength, weak water-locking, and poor anti-freezing. In tissue engineering, once the hydrogel loses water or freezes, it will harden the interaction interfaces and destroy the nascent granulation tissue. Herein, based on the design concept of "hard frame-soft penetration", a composite adhesive organohydrogel is fabricated by introducing bacterial cellulose and platelet-rich plasma (PRP) into a poly-N-(tris[hydroxymethyl]methyl)acrylamide (THMA)/N-acryloyl aspartic acid (AASP) hybrid gel network infiltrated with glycerol/water binary solvent. The resultant organohydrogels exhibit excellent antifreeze properties at low temperatures (-80 °C) and demonstrate stable long-term water retention (91%) in the open environment within 12 days and can adhere firmly to the tissues by the action of "hydrogen bond clusters". Additionally, the introduction of bacterial cellulose matrix endows the organohydrogel with high tensile strength similar to that of skin. In vivo, the PRP-loaded organohydrogel can release a variety of growth factors to accelerate the wound healing process through collagen deposition and angiogenesis. Altogether, this strategy will extend the life of the hydrogel in some harsh medical environments.

Revealing the influence of conversion-type Co3O4 dimensionality on cyclic and rate performance for lithium storage.

Cobalt tetraoxide (Co3O4) is regarded as a promising anode material for Li-ion batteries owing to its high theoretical capacity (890 mAh g-1), simple preparation, and controllable morphology. Nanoengineering has been proven to be an effective method for producing high-performance electrode materials. However, systematic research on the influence of material dimensionality on battery performance is lacking. Herein, we prepared Co3O4 with various dimensionalities (one-dimensional (1D) Co3O4 nanorod (NR), two-dimensional (2D) Co3O4 nanosheet (NS), three-dimensional (3D) Co3O4 nanocluster (NC), and 3D Co3O4 nanoflower (NF)) using a simple solvothermal heat treatment method, and their morphologies were controlled by varying the precipitator type and solvent composition. The 1D Co3O4 NR and 3D samples (3D Co3O4 NC and 3D Co3O4 NF) exhibited poor cyclic and rate performances, respectively, while the 2D Co3O4 NS exhibited the best electrochemical performance. The mechanism analysis revealed that the cyclic stability and rate performance of the Co3O4 nanostructures are closely related to their intrinsic stability and interfacial contact performance, respectively, and the 2D thin-sheet structure can achieve an optimal balance between the two, resulting in the best performance. This work presents a comprehensive study on the effect of dimensionality on the electrochemical performance of Co3O4 anodes, providing a new concept for the nanostructure design of conversion-type materials.

Nanoarchitectonics of RGO-Wrapped CNF/GO Aerogels with Controlled Pore Structures by PVA-Assisted Freeze-Casting Approach for Efficient Sound and Microwave Absorption.

Acoustic absorption materials play an important role in eliminating the negative effects of noise. Herein, a polyvinyl alcohol (PVA)-assisted freeze-casting was developed for controllably fabricating reduced graphene oxide wrapped carbon nanofiber (RGO@CNF)/graphene oxide composite aerogel. During the freeze-casting, PVA was used as an icing inhibitor to control the size of ice crystals. While the concentration of PVA increased from 0 to 15 mg ⋅ ml-1 , the average pore size of the aerogel was reduced from 154 to 45 µm. Due to the modulation of the pore size and composition, the propagation path and friction loss for sound were optimized, especially at low frequency. For instance, the normalized sound absorption coefficient of RGO@CNF/GO-10 achieves 0.79 (250-6300 Hz). The sample also exhibits a desirable microwave absorbing property whose maximum reflection loss is -47.3 dB (9.44 GHz, d=3.0 mm). Prospectively, this synthetic strategy can be extended to develop other forms of elastic aerogel with a controlled pore size.

High Multi-Environmental Mechanical Stability and Adhesive Transparent Ionic Conductive Hydrogels Used as Smart Wearable Devices.

Ionic conductive hydrogels used as flexible wearable sensor devices have attracted considerable attention because of their easy preparation, biocompatibility, and macro/micro mechanosensitive properties. However, developing an integrated conductive hydrogel that combines high mechanical stability, strong adhesion, and excellent mechanosensitive properties to meet practical requirements remains a great challenge owing to the incompatibility of properties. Herein, we prepare a multifunctional ionic conductive hydrogel by introducing high-modulus bacterial cellulose (BC) to form the skeleton of double networks, which exhibit great mechanical properties in both tensile (83.4 kPa, 1235.9% strain) and compressive (207.2 kPa, 79.9% strain) stress-strain tests. Besides, the fabricated hydrogels containing high-concentration Ca2+ show excellent anti-freezing (high ionic conductivities of 1.92 and 0.36 S/m at room temperature and -35 ∘C, respectively) properties. Furthermore, the sensing mechanism based on the conductive units and applied voltage are investigated to the benefit of the practical applications of prepared hydrogels. Therefore, the designed and fabricated hydrogels provide a novel strategy and can serve as candidates in the fields of sensors, ionic skins, and soft robots.

Mechanoactive Nanocomposite Hydrogel to Accelerate Wound Repair in Movable Parts.

Dynamic full-thickness skin wound healing remains an intricate problem due to the humid environment and frequent exercise. Recently, multifunctional hydrogels have a great promise in wound repair. However, traditional hydrogels only keep the wound moist, protect the wound from bacterial infection, and cannot actively drive dynamic wound closure. Inspired by embryo wound active closure, we constructed a double-sided thermoresponsive mechanoactive (DTM) hydrogel that combines good flexibility, self-healing, wet-tissue adhesion, and antibacterial functions. The strong adhesion of the hydrogel to biological tissues is attributed to "multiple hydrogen bonding clusters" without any chemical reaction. The contraction force triggered by temperature is quickly transmitted to dynamic wound edges to resist external mechanical forces and drive wound closure, which can effectively avoid damage to surrounding healthy tissue and reduce the risk of scarring, infection, and inflammation caused by sutures, staples, or clips. Strikingly, in vivo, this hydrogel bandage actively enhanced wound repair in a full-thickness skin defect model by promoting collagen deposition, facilitating angiogenesis, and accelerating wound re-epithelialization. This mechanoactive biological method will provide a facile strategy for joint wound management and demonstrates strong potential in tissue remodeling.

Photoinduced Dual Shape Programmability of Covalent Adaptable Networks with Remarkable Mechanical Properties.

As classic shape memory polymers featuring shape reconfiguration of temporary state, covalent adaptable networks containing reversible bonds can enable permanent-state reconfigurability through topological rearrangement via dynamic bond exchange. Yet, such an attractive dual shape programmability is limited by the actuation mode of direct heat transfer and poor mechanical properties, restricting its control precision and functionality. Herein, we presented a method to create nanocomposites with photomodulated dual shape programmability and remarkable mechanical properties leading the fields of covalent adaptable networks. MXene, whose photothermal efficiency was revealed to be regulated by the etching method and delamination, was introduced into polyurethane networks. Upon adjusting the light intensity, the dual shape programmability of both permanent and temporary states could be accomplished, which exhibited potential in information recognition, photowriting paper, etc. Furthermore, owing to the dynamic transcarbamoylation at elevated temperatures, such a phototriggered dual shape programmability could be maintained after the self-healing and reprocessing.

Design and synthesis of cellulose nanofiber-derived CoO/Co/C two-dimensional nanosheet toward enhanced and stable lithium storage.

Nano-sized two-dimensional carbonaceous materials have been widely used as the matrix for alloying-type and conversion-type anode materials for Li-ion batteries (LIBs) to improve structural stability and rate performance. However, relevant synthesis usually requires rigorous conditions and chronic reaction processes. Herein, we have designed a simple solvothermal reaction and heat treatment to prepare a novel CoO/Co/C two-dimensional nanosheet (CoO/Co/C 2DNS) by adopting cellulose nanofibers (CNFs) as the precursor. The unique characteristics of CNFs facilitate the uniform distribution of active materials on the surface and the construction of two-dimensional nanostructure via self-assembly. It is worth noting that CoO/Co/C 2DNS exhibits a striking synergistic effect since the porous 2D carbon framework offers additional pseudo-capacitance and enhances the electronic conductivity, while the ultrafine active materials encapsulated inside shorten the Li-ions diffusion pathways and relieve the volume change. Benefit from the unique structure, the composite anode delivered outstanding rate performance (∼500 mAh g-1 at 10 A g-1) and superior long-range cycling performance up to 800 cycles even at 2 A g-1. This work provides a new strategy for the synthesis of nano-sized 2D composite, offering a promising route to construct high performance conversion-type anodes for next-generation LIBs.

High-energy-density shape memory materials with ultrahigh strain for reconfigurable artificial muscles.

Programmable and reconfigurable artificial muscles are highly promising and desirable for applications in various fields, including soft robotics, flexible devices, and biomedical devices. However, the combination of considerable strain and high energy density remains a dilemma to overcome. As stimulus-responsive polymers, shape memory polymers (SMPs) with enhanced mechanical properties and programmability have the potential to solve this problem. However, the purest shape memory polymer lacks reconfigurability, and it is challenging to achieve precise control due to its intrinsic thermal stimulation. Herein, we report a novel reconfigurable multi-block shape memory polymer and its composite with a granular micro-phase separated structure. The polymer demonstrated outstanding artificial muscle performance through the energy storing and releasing method, whose energy density and strain reached 717.8 kJ m-3 and 947%, respectively (17.9 and 23.7 times higher than that of mammalian skeletal muscles). Moreover, by incorporating Fe3O4 nanoparticle (Fe3O4 NP) photothermal transducers, the composite could achieve contraction, reversible muscle-like bending and complex programmable and reconfigurable deformation under near-infrared laser irradiation, including deformation into a specific letter shape, precise origami and bending with loads. Therefore, the prepared materials have excellent prospects as artificial muscles and high-power actuators for broad applications.

Ferromagnetic Ti3CNCl2-decorated RGO aerogel: From 3D interconnecting conductive network construction to ultra-broadband microwave absorber with thermal insulation property.

It remains urgent challenges to adopt suitable strategies to consume unwanted microwave pollution emitted by high-tech electronic devices satisfactorily. Confronted with narrow effective absorption bandwidth (EAB) and high filler loading bottlenecks of MXene-Based microwave absorber, herein, we employ Lewis molten salt etching approach to both exfoliate Ti3AlCN powders into Ti3CNCl2 suspension and intercalate ferromagnetic composition into interlamination simultaneously. By utilizing the crosslinking effect of dopamine, the Ti3CNCl2 are anchored on the surfaces of graphene oxide (GO) nanosheets, constructing interconnecting microstructure. Both the 3D conductive network and the modification of MXene manifest crucial impacts on enhancing microwave absorption performance of the resulting ultra-lightweight reduced GO (RGO)-based aerogel. The minimum intensity of reflection loss achieves -62.62 dB with the absorber mass loading of 0.7 wt%. Remarkably, more than 90% of the incident microwave is qualified to be absorbed over the whole Ku band. The EAB is broadened while tailoring the thickness to 3 mm, ranging from 10.2 to 18 GHz. Besides, the aerogel presents valuable thermal insulation properties. Our methodology of synthesizing MXene/RGO aerogel not only provides promising insights into microstructural construction but also endows the possibility for integrating thermal insulation property towards next-generation high-performance microwave absorption devices.

Heat Treatment-Induced Microstructure and Property Evolution of Mg/Al Intermetallic Compound Coatings Prepared by Al Electrodeposition on Mg Alloy from Molten Salt Electrolytes.

A method of forming an Mg/Al intermetallic compound coating enriched with Mg17Al12 and Mg2Al3 was developed by heat treatment of electrodeposition Al coatings on Mg alloy at 350 °C. The composition of the Mg/Al intermetallic compounds could be tuned by changing the thickness of the Zn immersion layer. The morphology and composition of the Mg/Al intermetallic compound coatings were characterized using scanning electron microscopy (SEM), X-ray diffraction (XRD), and electron backscattered diffraction (EBSD). Nanomechanical properties were investigated via nano-hardness (nHV) and the elastic modulus (EIT), and the corrosion behavior was studied through hydrogen evolution and potentiodynamic (PD) polarization. The compact and uniform Al coating was electrodeposited on the Zn-immersed AZ91D substrate. After heat treatment, Mg2Al3 and Mg17Al12 phases formed, and as the thickness of the Zn layer increased from 0.2 to 1.8 µm, the ratio of Mg2Al3 and Mg17Al12 varied from 1:1 to 4:1. The nano-hardness increased to 2.4 ± 0.5 GPa and further improved to 3.5 ± 0.1 GPa. The Mg/Al intermetallic compound coating exhibited excellent corrosion resistance and had a prominent effect on the protection of the Mg alloy matrix. The control over the ratio of intermetallic compounds by varying the thickness of the Zn immersion layer can be an effective approach to achieve the optimal comprehensive performance. As the Zn immersion time was 4 min, the obtained intermetallic compounds had relatively excellent comprehensive properties.

Multifunctional conductive hydrogels and their applications as smart wearable devices.

Recently, hydrogel-based conductive materials and their applications as smart wearable devices have been paid tremendous attention due to their high stretchability, flexibility, and excellent biocompatibility. Compared with single functional conductive hydrogels, multifunctional conductive hydrogels are more advantageous to match various demands for practical applications. This review focuses on multifunctional conductive hydrogels applied for smart wearable devices. Representative strategies for conduction of hydrogels are discussed firstly: (1) electronic conduction based on the conductive fillers and (2) ionic conduction based on charged ions. Then, the common and intensive research on multiple functionalities of conductive hydrogels, such as mechanical properties, conductive and sensory properties, anti-freezing and moisturizing properties, and adhesion and self-healing properties is presented. The applications of multifunctional conductive hydrogels such as in human motion sensors, sensory skins, and personal healthcare diagnosis are provided in the third part. Finally, we offer our perspective on open challenges and future areas of interest for multifunctional conductive hydrogels used as smart wearable devices.

Tailoring conductive network nanostructures of ZIF-derived cobalt-decorated N-doped graphene/carbon nanotubes for microwave absorption applications.

Confronted with microwave pollution issues, there is an urgent need for microwave absorption materials that possess optimal combinations of dielectric loss and magnetic loss properties. While a variety of studies focus on the components, the construction of nanostructure is rarely studied, which is of equivalent significance to microwave absorber design. In this work, Co-ZIF-67 was adopted as self-template to grow N-doped graphene/carbon nanotube interlinked conductive networks in-situ under a one-step carbonization process with tailored microwave absorption properties. Diverse microwave absorption performance could be achieved by directly adjusting the proportions among ingredients and the calcination temperature, obtaining a maximum value of reflection loss of -65.45 dB at 17.5 GHz with a sample thickness of just 1.5 mm. The effective absorption bandwidth could be tailored from 3.75 to 18 GHz among different thickness as required. The nanostructures had an apparent impact on the corresponding microwave absorption performance, in which the N-doped carbon-based conductive networks, ferromagnetic cobalt atoms, and interfaces among heterostructure strengthened the dipolar polarization and conductivity loss, magnetic loss, and interfacial polarization, respectively. This synthesis strategy offers a promising pathway for integrating nanostructures and functions, catering to requirements for designing and optimizing prospective microwave absorbers.

Multiple-Stimuli-Responsive and Cellulose Conductive Ionic Hydrogel for Smart Wearable Devices and Thermal Actuators.

Stimulus-responsive hydrogels, such as conductive hydrogels and thermoresponsive hydrogels, have been explored extensively and are considered promising candidates for smart materials such as wearable devices and artificial muscles. However, most of the existing studies on stimulus-responsive hydrogels have mainly focused on their single stimulus-responsive property and have not explored multistimulus-responsive or multifunction properties. Although some works involved multifunctionality, the prepared hydrogels were incompatible. In this work, a multistimulus-responsive and multifunctional hydrogel system (carboxymethyl cellulose/poly acrylic-acrylamide) with good elasticity, superior flexibility, and stable conductivity was prepared. The prepared hydrogel not only showed excellent human motion detection and physiological signal response but also possessed the ability to respond to environmental temperature changes. By integrating a conductive hydrogel with a thermoresponsive poly(N-isopropylacrylamide) (PNIPAM) hydrogel to form a bilayer hydrogel, the prepared bilayer also functioned as two kinds of actuators owing to the different degrees of swelling and shrinking under different thermal stimuli. Furthermore, the different thermochromic properties of each layer in the bilayer hydrogel endowed the hydrogel with a thermoresponsive "smart" feature, the ability to display and conceal information. Therefore, the prepared hydrogel system has excellent prospects as a smart material in different applications, such as ionic skin, smart info-window, and soft robotics.

Electrodeposition of Aluminum Coatings from AlCl3-NaCl-KCl Molten Salts with TMACl and NaI Additives.

The Al coatings achieved via electrodeposition on a Cu electrode from AlCl3-NaCl-KCl (80-10-10 wt.%) molten salts electrolyte with Tetramethylammonium Chloride (TMACl) and Sodium Iodide (NaI) additives is reported. The effect of the two additives on electrodeposition were investigated by cyclic voltammetry (CV), chronopotentiometry (CP), scanning electron microscopy (SEM) and X-ray diffraction (XRD). Results reveal that compact and smooth Al coatings are obtained at 150 °C by the electrodeposition process from the electrolyte with 1% TMACl and 10% NaI. The Al coatings exhibit great corrosion resistance close to that of pure Al plate, with a corrosion current of 3.625 µA. The average particle size is approximately 2 ± 1 µm and the average thickness of the Al layer is approximately 7 ± 2 µm. The nucleation/growth process exhibits irrelevance with TMACl or NaI during the electrodeposition of Al. TMACl cannot affect and improve the electrodeposition effectively. However, the addition of TMACl and NaI can intensify the cathodic polarization, producing an inhibition of Al deposition, and contribute to form uniform Al deposits. This can increase the conductivity and facilitate in refining the size of Al particles, contributing to forming a continuous, dense and uniform layer of Al coating, which can be used as effective additives in molten salts electrolyte.

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.