Development of high energy density solid-state batteries with Li metal anodes has been limited by uncontrollable growth of Li dendrites in liquid and solid electrolytes (SEs). This, in part, may be caused by a dearth of information about mechanical properties of Li, especially at the nano- and microlength scales and microstructures relevant to Li batteries. We investigate Li electrodeposited in a commercial LiCoO2/LiPON/Cu solid-state thin-film cell, grown in situ in a scanning electron microscope equipped with nanomechanical capabilities. Experiments demonstrate that Li was preferentially deposited at the LiPON/Cu interface along the valleys that mimic the domain boundaries of underlying LiCoO2 (cathode). Cryogenic electron microscopy analysis of electrodeposited Li revealed a single-crystalline microstructure, and in situ nanocompression experiments on nano-pillars with 360–759 nm diameters revealed their average Young's modulus to be 6.76 ± 2.88 GPa with an average yield stress of 16.0 ± 6.82 MPa, ~24x higher than what has been reported for bulk polycrystalline Li. We discuss mechanical deformation mechanisms, stiffness, and strength of nano-sized electrodeposited Li in the framework of its microstructure and dislocation-governed nanoscale plasticity of crystals, and place it in the parameter space of existing knowledge on small-scale Li mechanics. The enhanced strength of Li at small scales may explain why it can penetrate and fracture through much stiffer and harder SEs than theoretically predicted.

Lithium-ion batteries have enabled the widespread use of portable electronic devices and are propelling the growing electric vehicle market, but new battery technologies with improved performance are necessary for emerging applications such as electric aircraft. The solid-state battery is one such technology that could exhibit enhanced safety and higher energy density compared to conventional lithium-ion batteries. The use of a pure lithium metal anode within solid-state batteries is key for higher energy density (Figure 1a), and it is thought that using solid-state electrolytes instead of conventional liquids could increase the chemical and structural stability of lithium metal.1 Despite continued progress in the development of new inorganic solid-state electrolyte materials; however, a persistent problem has emerged: lithium metal tends to grow as filaments during charging instead of as a flat film, and these filaments can penetrate and fracture the stiff solid-state electrolyte to short circuit the cell (Figure 1b).2–4 To prevent this chemo-mechanical degradation process and enable filament-free charging, it is critical to understand the mechanical properties of lithium metal, which have been elusive because of the highly reactive nature of lithium.

Hydrogen is a promising alternative fuel for efficient energy production and storage, with water splitting considered one of the cleanest, environmentally friendly, and sustainable approaches to generate hydrogen. Electrochemically catalyzed water splitting plays an important role in energy conversion for the development of hydrogen-based energy sources. Porphyrin and macrocycle derivatives are versatile and can electrochemically catalyze water splitting efficiently. Because of the significance of molecule activation of electrochemical water splitting, this article covers recent progress in hydrogen evolution and oxygen evolution reactions catalyzed by porphyrin and macrocycle derivatives.

Functionally graded nanocomposite materials (FGNMs) have been known since the 1980s, although nanocomposite materials date back to the space race era of the 1960s. FGNMs are defined as materials in which the chemical and structural composition changes over their entire volume. Today, due to our current understanding, technology, and control over the nanostructure of materials, we can tune these properties at the nanoscale. Although FGNM applications have mostly focused on protective coatings, they have performed well in catalysis and hydrogen production applications. In this article, FGNMs are presented in a new light beyond their well-established applicability as protective coatings. This article focuses on the synergistic potential among mechanical/tribological properties and competitive catalytic performance, with special emphasis on energy and remediation applications. Also, ways by which the rational design and tailoring of catalytic properties can be achieved by means of FGNMs are described.

Sustainable and green energy sources are in high demand to meet the current human energy needs and environmental requirements. Hydrogen energy, with the highest energy density and zero carbon emission, is considered a potential solution. Hydrogen is primarily produced by splitting water. Rationally designed electrocatalysts are required to promote the cathodic hydrogen evolution reaction (HER) and the anodic oxygen evolution reaction (OER). Organic polymer matrices provide new opportunities for electrocatalytic water splitting due to their special physical and chemical characteristics and thermal stability. This article explains the role of organic polymers in electrocatalytic water decomposition from three aspects: ion-conductive polymers, conjugated conductive polymers, and carbon materials derived from organic polymers. We hope that this article will provide more rational ideas and promote the design of organic polymers for water-splitting electrocatalysis, and furnish more technical insights for the future of water electrolysis.

The electrochemical reaction that involves the splitting of water into hydrogen and oxygen gas is the superior technique for sustainable energy conversion and storage without the environmentally damaging effects of fossil fuels. To date, a large number of electrocatalysts have been used for electrochemical water splitting (EWS). Nowadays, the quest for a universal pH stable bifunctional electrocatalyst that can efficiently enhance the hydrogen and oxygen evolution reactions (HERs and OERs) is gaining significant interest in the research community. This approach avoids the divergence in the pH of the electrolyte for OER and HER activity and effectively reduces the difficulty and system cost in practical EWS. This article highlights engineering strategies and challenges in designing prospective universal pH-stable electrocatalysts with feasible OER and HER pathways for full water splitting over a wide pH range.

Hydrogen production from water electrolysis with renewable energy input has been the focus of tremendous attention, as hydrogen is widely advocated as a clean energy carrier. In order to realize large-scale hydrogen generation from water splitting, it is essential to develop competent and robust electrocatalysts that will substantially decrease the overpotential requirement and improve energy efficiency. Recent advances in electrocatalyst design reveal that interfacial engineering is an effective approach in tuning the adsorption–desorption abilities of key catalytic intermediates on active sites, accelerating electron transfer, and stabilizing the active sites for long-term operation. Consequently, a large number of hybrid electrocatalysts consisting of metal/compound interfaces have been demonstrated to exhibit superior performance for electrocatalytic hydrogen evolution from water. This article highlights examples of these hybrid electrocatalysts, including noble metal and non-noble metal candidates interfaced with a variety of compounds. Specific emphasis is placed on the synthetic methods, reaction mechanisms, and electrocatalytic activities, which are envisioned to inspire the design and development of further improved electrocatalysts for hydrogen evolution from water splitting on an industrial scale.

This is the third and final part of a series in MRS Bulletin on achieving a path to a green card in the United States as it relates to scientific researchers. Following articles will focus on more specific aspects of the immigration process and go into more depth using practical examples.