New Insights on the Origin of Chemical Instabilities Between Poly(carbonate)-based Polymer and Li-containing Inorganic Materials.

Composite electrolytes, owing to their ability to combine both polymeric and ceramic properties are promising candidates for Solid-State-Batteries (SSBs). In this paper, we assess the effect of ceramic fillers (Li1+x Alx Ti2-x P3 O12 , Li6.55 Ga0.15 La3 Zr2 O12 and Al2 O3 ) in a poly(ethylene oxide carbonate)-LiTFSI matrix. First, the role of the filler chemistry on thermal and electrochemical properties is evaluated: reduced polymer crystallinity leads to an increased ionic conductivity at low temperatures; and the ionic conductivity at low temperatures (<30 °C) is improved for LLZO filler particles. This behaviour is commonly attributed to new conduction pathways generated within the fillers. However, we also demonstrate that a polymer degradation is induced by the filler chemistry by modifying the polymer chemistry in poly(ethylene glycol), initiated by LiOH that can be found on the LLZO surface. The electrolyte containing LATP or Al2 O3 does not induce any degradation. Hence, special attention must be paid to surface impurities, as degradation may occur.

Atomistic Insight into Ion Transport and Conductivity in Ga/Al-Substituted Li7La3Zr2O12 Solid Electrolytes.

Garnet-structured Li7La3Zr2O12 is a promising solid electrolyte for next-generation solid-state Li batteries. However, sufficiently fast Li-ion mobility required for battery applications only emerges at high temperatures, upon a phase transition to cubic structure. A well-known strategy to stabilize the cubic phase at room temperature relies on aliovalent substitution; in particular, the substitution of Li+ by Al3+ and Ga3+ ions. Yet, despite having the same formal charge, Ga3+ substitution yields higher conductivities (10-3 S/cm) than Al3+ (10-4 S/cm). The reason of such difference in ionic conductivity remains a mystery. Here, we use molecular dynamic simulations and advanced sampling techniques to precisely unveil the atomistic origin of this phenomenon. Our results show that Li+ vacancies generated by Al3+ and Ga3+ substitution remain adjacent to Ga3+ and Al3+ ions, without contributing to the promotion of Li+ mobility. However, while Ga3+ ions tend to allow limited Li+ diffusion within their immediate surroundings, the less repulsive interactions associated with Al3+ ions lead to a complete blockage of neighboring Li+ diffusion paths. This effect is magnified at lower temperatures and explains the higher conductivities observed for Ga-substituted systems. Overall, this study provides a valuable insight into the fundamental ion transport mechanism in the bulk of Ga/Al-substituted Li7La3Zr2O12 and paves the way for rationalizing aliovalent substitution design strategies for enhancing ionic transport in these materials.

Investigating the Dendritic Growth during Full Cell Cycling of Garnet Electrolyte in Direct Contact with Li Metal.

All-solid-state batteries including a garnet ceramic as electrolyte are potential candidates to replace the currently used Li-ion technology, as they offer safer operation and higher energy storage performances. However, the development of ceramic electrolyte batteries faces several challenges at the electrode/electrolyte interfaces, which need to withstand high current densities to enable competing C-rates. In this work, we investigate the limits of the anode/electrolyte interface in a full cell that includes a Li-metal anode, LiFePO4 cathode, and garnet ceramic electrolyte. The addition of a liquid interfacial layer between the cathode and the ceramic electrolyte is found to be a prerequisite to achieve low interfacial resistance and to enable full use of the active material contained in the porous electrode. Reproducible and constant discharge capacities are extracted from the cathode active material during the first 20 cycles, revealing high efficiency of the garnet as electrolyte and the interfaces, but prolonged cycling leads to abrupt cell failure. By using a combination of structural and chemical characterization techniques, such as SEM and solid-state NMR, as well as electrochemical and impedance spectroscopy, it is demonstrated that a sudden impedance drop occurs in the cell due to the formation of metallic Li and its propagation within the ceramic electrolyte. This degradation process is originated at the interface between the Li-metal anode and the ceramic electrolyte layer and leads to electromechanical failure and cell short-circuit. Improvement of the performances is observed when cycling the full cell at 55 °C, as the Li-metal softening favors the interfacial contact. Various degradation mechanisms are proposed to explain this behavior.

Linear topology in amorphous metal oxide electrochromic networks obtained via low-temperature solution processing.

Amorphous transition metal oxides are recognized as leading candidates for electrochromic window coatings that can dynamically modulate solar irradiation and improve building energy efficiency. However, their thin films are normally prepared by energy-intensive sputtering techniques or high-temperature solution methods, which increase manufacturing cost and complexity. Here, we report on a room-temperature solution process to fabricate electrochromic films of niobium oxide glass (NbOx) and 'nanocrystal-in-glass' composites (that is, tin-doped indium oxide (ITO) nanocrystals embedded in NbOx glass) via acid-catalysed condensation of polyniobate clusters. A combination of X-ray scattering and spectroscopic characterization with complementary simulations reveals that this strategy leads to a unique one-dimensional chain-like NbOx structure, which significantly enhances the electrochromic performance, compared to a typical three-dimensional NbOx network obtained from conventional high-temperature thermal processing. In addition, we show how self-assembled ITO-in-NbOx composite films can be successfully integrated into high-performance flexible electrochromic devices.

Nanostructured electrochromic smart windows: traditional materials and NIR-selective plasmonic nanocrystals.

Electrochromic devices, which dynamically change colour under applied potential, are widely studied for use in energy-efficient smart windows. To improve the viability of smart windows, many researchers are utilizing nanomaterials, which can provide electrochromic devices with improved colouration efficiencies, faster switching times, longer cycle lives, and potentially reduced costs. In an effort to demonstrate a new type of electrochromic device that goes beyond the capabilities of commonly used electrochromic materials, researchers have turned to plasmonic transparent conductive oxide (TCO) nanocrystals. Electrochemical injection of electrons into plasmonic TCO nanocrystal films induces a shift in the plasmon frequency and gives rise to the new functionality of selective optical modulation in the near-infrared region of the solar spectrum. These nanocrystals can be used as building blocks to enable creation of advanced electrochromic devices containing mesoporous electrodes or nanocrystal-in-glass composites. Such devices have been important in advancing the field towards achieving the ideal smart window with independent control over visible and NIR transmittance.

Defect Chemistry and Plasmon Physics of Colloidal Metal Oxide Nanocrystals.

Plasmonic nanocrystals of highly doped metal oxides have seen rapid development in the past decade and represent a class of materials with unique optoelectronic properties. In this Perspective, we discuss doping mechanisms in metal oxides and the accompanying physics of free carrier scattering, both of which have implications in determining the properties of localized surface plasmon resonances (LSPRs) in these nanocrystals. The balance between activation and compensation of dopants limits the free carrier concentration of the most common metal oxides, placing a ceiling on the LSPR frequency. Furthermore, because of ionized impurity scattering of the oscillating plasma by dopant ions, scattering must be treated in a fundamentally different way in semiconductor metal oxide materials when compared with conventional metals. Though these effects are well-understood in bulk metal oxides, further study is needed to understand their manifestation in nanocrystals and corresponding impact on plasmonic properties, and to develop materials that surpass current limitations in free carrier concentration.

Constructing functional mesostructured materials from colloidal nanocrystal building blocks.

Through synthesizing colloidal nanocrystals (NCs) in the organic phase, chemists gain fine control over their composition, size, and shape. Strategies for arranging them into ordered superlattices have followed closely behind synthetic advances. Nonetheless, the same hydrophobic ligands that help their assembly also severely limit interactions between adjacent nanocrystals. As a result, examples of nanocrystal-based materials whose functionality derives from their mesoscale structure have lagged well behind advances in synthesis and assembly. In this Account, we describe how recent insights into NC surface chemistry have fueled dramatic progress in functional mesostructures. In these constructs, intimate contact between NCs as well as with heterogeneous components is key in determining macroscopic behavior. The simplest mesoscale assemblies we consider are networks of NCs constructed by in situ replacement of their bulky, insulating surface ligands with small molecules. Transistors are a test bed for understanding conductivity, setting the stage for new functionality. For instance, we demonstrated that by electrochemically charging and discharging networks of plasmonic metal oxide NCs, the transmittance of near infrared light can be strongly and reversibly modulated. When we assemble NCs with heterogeneous components, there is an even greater potential for generating complex functionality. Nanocomposites can exhibit favorable characteristics of their component materials, yet the interaction between components can also have a strong influence. Realizing such opportunities requires an intimate linking of embedded NCs to the surrounding matrix phase. We accomplish this link by coordinating inorganic anionic clusters directly to NC surfaces. By exploiting this connection, we found enhanced ionic conductivity in Ag2S-in-GeS2 nanocrystal-in-glass electrodes. In another example, we also found enhanced optical contrast when linking electrochromic niobium oxide to embedded tin-doped indium oxide (ITO) NCs. These dramatic effects emerge from reconstruction of the inorganic glass immediately adjacent to the NC interface. When co-assembling NCs with block copolymers, direct coordination of the polymer to NC surfaces again opens new opportunities for functional mesoscale constructs. We strip NCs of their native ligands and design block copolymers containing a NC tethering domain that bonds strongly, yet dynamically, to the resulting open coordination sites. This strategy enables their co-assembly at high volume fractions of NCs and leads to well-ordered mesoporous NC networks. We find these architectures to be exceptionally stable under chemical transformations driven by cation insertion, removal, and exchange. These developments offer a modular toolbox for arranging NCs deliberately with respect to heterogeneous elements and open space. We have control over metrics that define such architectures from the atomic scale (bonding and crystal structure) through the mesoscale (crystallite shapes and sizes and pore dimensions). By tuning these parameters and better understanding the interactions between components, we look forward to boundless opportunities to employ mesoscale structure, in tandem with composition, to develop functional materials.

Tunable near-infrared and visible-light transmittance in nanocrystal-in-glass composites.

Amorphous metal oxides are useful in optical, electronic and electrochemical devices. The bonding arrangement within these glasses largely determines their properties, yet it remains a challenge to manipulate their structures in a controlled manner. Recently, we developed synthetic protocols for incorporating nanocrystals that are covalently bonded into amorphous materials. This 'nanocrystal-in-glass' approach not only combines two functional components in one material, but also the covalent link enables us to manipulate the glass structure to change its properties. Here we illustrate the power of this approach by introducing tin-doped indium oxide nanocrystals into niobium oxide glass (NbOx), and realize a new amorphous structure as a consequence of linking it to the nanocrystals. The resulting material demonstrates a previously unrealized optical switching behaviour that will enable the dynamic control of solar radiation transmittance through windows. These transparent films can block near-infrared and visible light selectively and independently by varying the applied electrochemical voltage over a range of 2.5 volts. We also show that the reconstructed NbOx glass has superior properties-its optical contrast is enhanced fivefold and it has excellent electrochemical stability, with 96 per cent of charge capacity retained after 2,000 cycles.

Tunable infrared absorption and visible transparency of colloidal aluminum-doped zinc oxide nanocrystals.

Plasmonic nanocrystals have been attracting a lot of attention both for fundamental studies and different applications, from sensing to imaging and optoelectronic devices. Transparent conductive oxides represent an interesting class of plasmonic materials in addition to metals and vacancy-doped semiconductor quantum dots. Herein, we report a rational synthetic strategy of high-quality colloidal aluminum-doped zinc oxide nanocrystals. The presence of substitutional aluminum in the zinc oxide lattice accompanied by the generation of free electrons is proved for the first time by tunable surface plasmon absorption in the infrared region both in solution and in thin films.

Dynamically modulating the surface plasmon resonance of doped semiconductor nanocrystals.

Localized surface plasmon absorption features arise at high doping levels in semiconductor nanocrystals, appearing in the near-infrared range. Here we show that the surface plasmons of tin-doped indium oxide nanocrystal films can be dynamically and reversibly tuned by postsynthetic electrochemical modulation of the electron concentration. Without ion intercalation and the associated material degradation, we induce a > 1200 nm shift in the plasmon wavelength and a factor of nearly three change in the carrier density.