Matrix transformation of lunar regolith and its use as a feedstock for additive manufacturing.

Building a sustainable human habitat on the Moon requires advances in excavation, paving, and additive manufacturing to construct landing pads, surface transportation arteries, resilient shelters, and scientific outposts. Construction of infrastructure elements on the lunar surface necessitates exploration of the interfacial reactivity of locally sourced regolith and the adaptation of Earth-based construction techniques. Various crosslinking frameworks and sintering methods have been proposed as a means of consolidating lunar regolith into load-bearing structures but each have challenges related to incomplete understanding of reaction chemistry, excessive thermal budgets, and lack of universal applicability to different mineral components of regolith. We describe here a versatile experimental and computational study of the consolidation of a regolith simulant through formation of siloxane networks enmeshing mineral particles by surface dissolution-precipitation and polycondensation reactions. Furthermore, by tailoring the rheological properties of the formulation an additive manufacturing feedstock can be developed for the construction of lunar infrastructure.

Tunnel-Structured ζ-V2O5 as a Redox-Active Insertion Host for Hybrid Capacitive Deionization.

Much of the earth's water has a salt content that is too high for human consumption or agricultural use. Enhanced oil recovery operations generate massive volumes of produced water waste with a high mineral content that can substantially exacerbate water distress. Current deionization techniques such as reverse osmosis function by removing the water (majority phase) from the salt (minority phase) and are thus exceedingly energy-intensive. Furthermore, these methods are limited in their ability to selectively extract high-value ions from produced water waste and brine streams. Hybrid capacitive deionization holds promise for enabling both desalination and resource recovery. In this work, we demonstrate the construction of a hybrid capacitive deionization cell that makes use of tunnel-structured ζ-V2O5 as a redox-active positive electrode material. By augmenting surface adsorption with Faradaic insertion processes, a 50% improvement in the ion removal capacity for K and Li ions is obtained as compared to a capacitive high-surface-area carbon electrode. The extracted ions are accommodated in surface sites and interstitial sites within the one-dimensional tunnel framework of ζ-V2O5. The kinetics of ion removal depend on the free energy of hydration, which governs the ease of desolvation at the electrode/electrolyte interface. The overall ion removal capacity additionally depends on the solid-state diffusion coefficient. ζ-V2O5 positive electrodes show substantial selectivity for Li+ removal from mixed flow streams and enrichment of the Li-ion concentration from produced water waste derived from the Permian Basin.

Thermochromic Fenestration Elements Based on the Dispersion of Functionalized VO2 Nanocrystals within a Polyvinyl Butyral Laminate.

The energy required to heat, cool, and illuminate buildings continues to increase with growing urbanization, engendering a substantial global carbon footprint for the built environment. Passive modulation of the solar heat gain of buildings through the design of spectrally selective thermochromic fenestration elements holds promise for substantially alleviating energy consumed for climate control and lighting. The binary vanadium(IV) oxide VO2 manifests a robust metal-insulator transition that brings about a pronounced modulation of its near-infrared transmittance in response to thermal activation. As such, VO2 nanocrystals are potentially useful as the active elements of transparent thermochromic films and coatings. Practical applications in retrofitting existing buildings requires the design of workflows to embed thermochromic fillers within industrially viable resins. Here, we describe the dispersion of VO2 nanocrystals within a polyvinyl butyral laminate commonly used in the laminated glass industry as a result of its high optical clarity, toughness, ductility, and strong adhesion to glass. To form high-optical-clarity nanocomposite films, VO2 nanocrystals are encased in a silica shell and functionalized with 3-methacryloxypropyltrimethoxysilane, enabling excellent dispersion of the nanocrystals in PVB through the formation of siloxane linkages and miscibility of the methacrylate group with the random copolymer. Encapsulation, functionalization, and dispersion of the core-shell VO2@SiO2 nanocrystals mitigates both Mie scattering and light scattering from refractive index discontinuities. The nanocomposite laminates exhibit a 22.3% modulation of NIR transmittance with the functionalizing moiety engendering a 77% increase of visible light transmittance as compared to unfunctionalized core-shell particles. The functionalization scheme and workflow demonstrated, here, illustrates a viable approach for integrating thermochromic functionality within laminated glass used for retrofitting buildings.

Syntheses, Structures, and Characterization of Nickel(II) Stibines: Steric and Electronic Rationale for Metal Deposition.

Reactions of the homoleptic and heteroleptic antimony ligands Sb iPr3, Sb iPr2Ph, SbMe2Ph, and SbMePh2 with NiI2 generate rare NiII stibine complexes in either square planar or trigonal bipyramidal (TBP) geometries, depending on the steric size of the ligands. Tolman electronic parameters were calculated (DFT) for each antimony ligand to provide a tabulated resource for the relative strengths of simple antimony ligands. The electronic absorbance spectra of the square planar complexes exhibit characteristic bands [λmax ≈ 560 nm (17 900 cm-1), ε ≈ 4330 M-1 cm-1] at lower energies compared to the reported phosphine complexes, indicating the weak donor strength of the stibine ligands and resultant low-energy ligand field d→ d transitions. The square planar complex Ni(I)2(Sb iPr3)2 reacts with CO to form the TBP complex Ni(I)2(Sb iPr3)2(CO). Lastly, the complexes were investigated for nickel metal deposition on Si|Cu(100 nm) substrates. The complexes with the strongest donating ligand, Sb iPr3, deposited the purest layer of NiCu alloy according to the balanced reaction Ni(I)2(SbIII iPr3)2 → Ni0 + SbV( iPr3)I2; the iodinated SbV byproduct was unambiguously detected in the supernatant by 1H NMR and mass spectrometry. Complexes with weaker ligands (poor I2 acceptors/scavengers) resulted undesired deposition of iodine and CuI on the surface. This work thus serves as a guide for the design and synthesis of 3 d metal complexes with neutral, heavy main-group donors that are useful for metal deposition applications.