Sodium-ion batteries (SIBs) are a more sustainable alternative to lithium-ion batteries (LIBs) considering the abundance, global distribution, and low cost of sodium. However, their economic impact remains small compared to LIBs, owing in part to the lag in materials development where significant improvements in energy density and safety remain to be realized. Deep eutectic solvents (DESs) show promise as alternatives to conventional electrolytes in SIBs because of their nonflammable nature. However, their practical application has thus far been hindered by their limited electrochemical stability window. In particular, DESs based on N-methylacetamide have thus far been reported not to be stable with sodium metal. In contrast, this work reports a superconcentration strategy where sodium-ion conducting DESs, based on the dissolution of NaFSI in N-methylacetamide, are simultaneously stable with sodium metal and Prussian blue as state-of-the-art positive electrode material. At 60 degrees C, the nonflammable DES outperforms a conventional liquid electrolyte in terms of rate performance and capacity retention. Therefore, these novel DES compositions pave the way for the use of DESs in practical applications with an improved safety and sustainability.

This work introduces a polymeric backbone eutectogel (P-ETG) hybrid solid-state electrolyte with an N-isopropylacrylamide (NIPAM) backbone for high-energy lithium-ion batteries (LIBs). The NIPAM-based P-ETG is (electro)chemically compatible with commercially relevant positive electrode materials such as the nickel-rich layered oxide LiNi0.6Mn0.2Co0.2O2 (NMC622). The chemical compatibility was demonstrated through (physico)chemical characterization methods. The nonexistence (within detection limits) of interfacial reactions between the electrolyte and the positive electrode, the unchanged bulk crystallographic composition, and the absence of transition metal ions leaching from the positive electrode in contact with the electrolyte were demonstrated by Fourier transform infrared spectroscopy, powder X-ray diffraction, and elemental analysis, respectively. Moreover, the NIPAM-based P-ETG demonstrates a wide electrochemical stability window (1.5-5.0 V vs Li+/Li) and a reasonably high ionic conductivity at room temperature (0.82 mS cm-1). The electrochemical compatibility of a high-potential NMC622-containing positive electrode and the P-ETG is further demonstrated in Li|P-ETG|NMC622 cells, which deliver a discharge capacity of 134, 110, and 97 mAh g-1 at C/5, C/2, and 1C, respectively, after 90 cycles. The Coulombic efficiency is >95% at C/5, C/2, and 1C. Hence, gaining scientific insights into the compatibility of the electrolytes with positive electrode materials that are relevant to the commercial market, like NMC622, is important because this requires going beyond the electrolyte design itself, which is essential to their practical applications.

Solid electrolytes are regarded as good alternatives for liquid carbonate-based electrolytes, as they show much better safety. In polymeric eutectogel (P-ETG) hybrid solid-state electrolytes, a deep eutectic solvent (DES) is enclosed within a polymer host. They are promising for application in high-energy-density lithium-ion batteries (LIBs) due to their relatively high ionic conductivity at room temperature, compatibility with high-potential positive electrode materials, and improved safety compared to conventional electrolytes. After all, they are less prone to leakage and are potentially nonflammable. Further, they can be obtained through a facile synthesis method, i.e., by ultraviolet (UV) curing. In this work, we study in great detail how the DES-polymer interaction depends on the relative amounts and on the nature of the polymer. The ionic conductivity of the P-ETGs depends on the monomer and cross-linker, reaching values from 0.400 up to 1.011 mS cm(-1) at 25 degrees C. The choice of cross-linker has a significant effect on the ionic conductivity as amides result in less mobile chains compared to esters due to increased rotational barriers. Furthermore, we also study the compatibility with the electrodes, their performance in Li | NMC622 cells, and the correlation with the chemical structure of the polymer. Therefore, the P-ETG electrolyte is an interesting electrolyte for solid-state batteries due to their low cost, flexibility, and compatibility with NMC622 positive electrode materials.

Quasi-spherical undoped ZnO and Al-doped ZnO nanoparticles with different aluminum content, ranging from 0.5 to 5 at% of Al with respect to Zn, were synthesized. These nanoparticles were evaluated as photocatalysts in the photodegradation of the Rhodamine B (RhB) dye aqueous solution under UV-visible light irradiation. The undoped ZnO nanopowder annealed at 400 °C resulted in the highest degradation efficiency of ca. 81% after 4 h under green light irradiation (525 nm), in the presence of 5 mg of catalyst. The samples were characterized using ICP-OES, PXRD, TEM, FT-IR, 27Al-MAS NMR, UV-Vis and steady-state PL. The effect of Al-doping on the phase structure, shape and particle size was also investigated. Additional information arose from the annealed nanomaterials under dynamic N2 at different temperatures (400 and 550 °C). The position of aluminum in the ZnO lattice was identified by means of 27Al-MAS NMR. FT-IR gave further information about the type of tetrahedral sites occupied by aluminum. Photoluminescence showed that the insertion of dopant increases the oxygen vacancies reducing the peroxide-like species responsible for photocatalysis. The annealing temperature helps increase the number of red-emitting centers up to 400 °C, while at 550 °C, the photocatalytic performance drops due to the aggregation tendency.

This study reports the low temperature and low pressure conversion (up to 160 °C, p = 3.5 bar) of CO2 and H2 to CO using plasmonic Au/TiO2 nanocatalysts and mildly concentrated artificial sunlight as the sole energy source (up to 13.9 kW·m−2 = 13.9 suns). To distinguish between photothermal and non-thermal contributors, we investigated the impact of the Au nanoparticle size and light intensity on the activity and selectivity of the catalyst. A comparative study between P25 TiO2-supported Au nanocatalysts of a size of 6 nm and 16 nm displayed a 15 times higher activity for the smaller particles, which can only partially be attributed to the higher Au surface area. Other factors that may play a role are e.g., the electronic contact between Au and TiO2 and the ratio between plasmonic absorption and scattering. Both catalysts displayed ≥84% selectivity for CO (side product is CH4). Furthermore, we demonstrated that the catalytic activity of Au/TiO2 increases exponentially with increasing light intensity, which indicated the presence of a photothermal contributor. In dark, however, both Au/TiO2 catalysts solely produced CH4 at the same catalyst bed temperature (160 °C). We propose that the difference in selectivity is caused by the promotion of CO desorption through charge transfer of plasmon generated charges (as a non-thermal contributor).

The preparation of Ru nanoparticles supported on γ-Al2O3 followed by chemical reduction using RuCl3 as a precursor is demonstrated, and their properties are compared to Ru nanoparticles supported on γ-Al2O3 prepared by impregnation of γ-Al2O3 with Ru3(CO)12 and subsequent thermal decomposition. The Ru nanoparticles resulting from chemical reduction of RuCl3 are slightly larger (1.2 vs. 0.8 nm). In addition, Ru nanoparticles were deposited on Stöber SiO2 using both deposition techniques. These particles were larger than the ones deposited on γ-Al2O3 (2.5 and 3.4 nm for chemical reduction and thermal decomposition, respectively). Taking into account the size differences between the Ru nanoparticles, all catalysts display similar activity (0.14–0.63 mol·gRu−1·h−1) and selectivity (≥99%) in the sunlight-powered Sabatier reaction. Ergo, the use of toxic and volatile Ru3(CO)12 can be avoided, since catalysts prepared by chemical reduction of RuCl3 display similar catalytic performance.

LiNi0.5Mn1.5O4-delta (LNMO) is a potential candidate for high voltage Co-free cathodes in lithium-ion batteries. In this study, pre-calcination temperature, time, and oven type are showcased as important parameters influencing the particle size and morphology of the LNMO powder synthesized from the aqueous citric acidacetates-NH3 based method. These parameters determine the amount of organic residues in the precursor powder. A superior initial discharge capacity and capacity retention are obtained by an optimum combination of the particle size and morphology for the Li vertical bar LNMO coin cells. Pre-calcination in a forced convection oven at 200 degrees C for 40 h results in a voluminous and foam-like LNMO precursor powder morphology with the lowest amount of organic residue, leading to a similar to 1-4 mu m powder with well-defined facets. Applying 24 h pre-calcination at 170 degrees C in a natural convection oven results in large LNMO aggregates of similar to 70 mu m. Ballmilling of the crystalline LNMO powder is effective to reduce the agglomeration and particle size but deteriorates the electrochemical performance. An initial discharge capacity of 121 mA h g(-1) at 0.2 C and a capacity retention of 90% after 400 cycles at 2 C are obtained from the samples prepared by 40 h pre-calcination at 200 degrees C in a forced-convection oven. (C) 2021 Elsevier B.V. All rights reserved.