New Environmental-Thermal Barrier Coatings for Ultrahigh Temperature Alloys

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High-throughput, combinatorial synthesis of multimetallic nanoclusters

Multimetallic nanoclusters (MMNCs) offer unique and tailorable surface chemistries that hold great potential for numerous catalytic applications. The efficient exploration of this vast chemical space necessitates an accelerated discovery pipeline that supersedes traditional “trial-and-error” experimentation while guaranteeing uniform microstructures despite compositional complexity. Herein, we report the high-throughput synthesis of an extensive series of ultrafine and homogeneous alloy MMNCs, achieved by 1) a flexible compositional design by formulation in the precursor solution phase and 2) the ultrafast synthesis of alloy MMNCs using thermal shock heating (i.e., ∼1,650 K, ∼500 ms). This approach is remarkably facile and easily accessible compared to conventional vapor-phase deposition, and the particle size and structural uniformity enable comparative studies across compositionally different MMNCs. Rapid electrochemical screening is demonstrated by using a scanning droplet cell, enabling us to discover two promising electrocatalysts, which we subsequently validated using a rotating disk setup. This demonstrated high-throughput material discovery pipeline presents a paradigm for facile and accelerated exploration of MMNCs for a broad range of applications

Rapid liquid phase–assisted ultrahigh-temperature sintering of high-entropy ceramic composites

High-entropy ceramics and their composites display high mechanical strength and attractive high-temperature stabilities. However, properties like strong covalent bond character and low self-diffusion coefficients make them difficult to get sintered, limiting their mass popularity. Here, we present a rapid liquid phase-assisted ultrahigh-temperature sintering strategy and use high-entropy metal diboride/boron carbide composite as a proof of concept. We use a carbon-based heater to fast-heat the composite to around 3000 K, and a small fraction of eutectic liquid was formed at the interface between high-entropy metal diborides and boron carbide. A crystalline dodecaboride intergranular phase was generated upon cooling to ameliorate the adhesion between the components. The as-sintered composite presents a high hardness of 36.4 GPa at a load of 0.49 N and 24.4 GPa at a load of 9.8 N. This liquid phase-assisted rapid ultrahigh-temperature strategy can be widely applicable for other ultrahigh-temperature ceramics as well

Synthesizing Carbon‐Supported, High‐Loading, Ultra‐Small Pt3Ni Nanoparticles via Tuning the Surface Electrostatic Effect

Carbon‐supported nanoparticles (NPs) are widely used as catalysts in fuel cells and electrolyzers. While it is well known that NPs with smaller size and higher loading often lead to better catalytic activity, they remain challenging to synthesize due to the weak control over the surface properties of the support. Herein, a facile approach to synthesize carbon‐supported, high‐loading, and ultra‐small Pt3Ni NPs via applying thermal shock on strongly interacted carbon support with metal salt is reported. Specifically, sodium citrate is introduced into the precursor solution and substrate mixture, which induces strong electrostatic effect between metal salts and carbon particles that markedly improves precursor anchoring and dispersion, thereby achieving high particle loading as well as small size and distribution. As a proof‐of‐concept, the synthesis of Pt3Ni NPs supported on carbon black with particle size of 1.56 ± 0.36 nm at 30 wt% loading and 1.66 ± 0.56 nm at 40 wt% loading is reported, where the sizes are among the smallest while the loadings are among the highest in the literature. This approach can be readily extended to many compositions and substrates, with tunable particle size and loading, thereby substantially expanding the synthesis space for NP catalysts in various electrochemical applications

Morphophysiological Responses of Two Cool-Season Turfgrasses with Different Shade Tolerances

Understanding the differences in cool-season turfgrass responses to shade is critical for future turfgrass management and breeding for improved shade tolerance. The purpose of this study was to evaluate the shade-tolerance mechanisms of two cool-season turfgrass species in terms of turf performance, growth, and physiological characteristics. Two turfgrass species, namely, ’SupraNova’ (Poa. supina Schrad.) and ‘Lark’ (Lolium perenne L.), were subjected to 0 (CK, unshaded), 35% (LS), 70% (MS), and 92% (HS) shade, respectively. Compared with ‘Lark’, ‘SupraNova’ showed better turf quality (TQ) and turf color intensity (TCI) under shade. The total length and surface area of the roots of ‘Lark’ gradually decreased as the shade increased, while those of ‘SupraNova’ increased and then decreased with increasing shade. The chlorophyll fluorescence photochemical quenching coefficient (qP), electron transport rate (ETR), and maximum quantum yield of primary photosystem II (PSII) photochemistry (Fv/Fm) decreased significantly under HS; however, these decreases were more significant in ‘Lark’ than in ‘SupraNova’. The leaf reflectance of the two turfgrasses under shade was lower than that under CK, but the leaf reflectance of ‘Lark’ was higher than that of ‘SupraNova’ in the visible light band. The normalized difference vegetation index (NDVI) of the two grasses first decreased and then increased. The NDVI of ‘Lark’ under shade was slightly higher than that under CK. ‘SupraNova’ showed strong tolerance on the basis of malondialdehyde (MDA), hydrogen peroxide (H2O2), superoxide anion (O2·−), and ascorbic acid (AsA) contents and superoxide dismutase (SOD), peroxidase (POD), and catalase (CAT) activity. The MDA, H2O2, O2·−, and AsA contents and SOD, POD, and CAT activity (which represent indicators) changed the most under MS. Taken together, the results indicated that the adaptability of ‘SupraNova’ to shade was better than that of ‘Lark’

Morphophysiological Responses of Two Cool-Season Turfgrasses with Different Shade Tolerances

Understanding the differences in cool-season turfgrass responses to shade is critical for future turfgrass management and breeding for improved shade tolerance. The purpose of this study was to evaluate the shade-tolerance mechanisms of two cool-season turfgrass species in terms of turf performance, growth, and physiological characteristics. Two turfgrass species, namely, ’SupraNova’ (Poa. supina Schrad.) and ‘Lark’ (Lolium perenne L.), were subjected to 0 (CK, unshaded), 35% (LS), 70% (MS), and 92% (HS) shade, respectively. Compared with ‘Lark’, ‘SupraNova’ showed better turf quality (TQ) and turf color intensity (TCI) under shade. The total length and surface area of the roots of ‘Lark’ gradually decreased as the shade increased, while those of ‘SupraNova’ increased and then decreased with increasing shade. The chlorophyll fluorescence photochemical quenching coefficient (qP), electron transport rate (ETR), and maximum quantum yield of primary photosystem II (PSII) photochemistry (Fv/Fm) decreased significantly under HS; however, these decreases were more significant in ‘Lark’ than in ‘SupraNova’. The leaf reflectance of the two turfgrasses under shade was lower than that under CK, but the leaf reflectance of ‘Lark’ was higher than that of ‘SupraNova’ in the visible light band. The normalized difference vegetation index (NDVI) of the two grasses first decreased and then increased. The NDVI of ‘Lark’ under shade was slightly higher than that under CK. ‘SupraNova’ showed strong tolerance on the basis of malondialdehyde (MDA), hydrogen peroxide (H2O2), superoxide anion (O2·−), and ascorbic acid (AsA) contents and superoxide dismutase (SOD), peroxidase (POD), and catalase (CAT) activity. The MDA, H2O2, O2·−, and AsA contents and SOD, POD, and CAT activity (which represent indicators) changed the most under MS. Taken together, the results indicated that the adaptability of ‘SupraNova’ to shade was better than that of ‘Lark’

Synthesis of 18-Membered Open-Cage Fullerenes through Controlled Stepwise Fullerene Skeleton Bond Cleavage Processes and Substituent-Mediated Tuning of the Redox Potential of Open-Cage Fullerenes

Oxidation of the fullerenediol C₆₀(OH)₂(O)­(OAc)­(OO<i>t</i>Bu)₃ with PhI­(OAc)₂ yields the open-cage fullerene derivative C₆₀(O)₂(O)­(OAc)­(OO<i>t</i>Bu)₃ <b>2</b> with an 11-membered orifice. Compound <b>2</b> reacts with aniline to form a new open-cage derivative with a 14-membered orifice, which yields an 18-membered open-cage fullerene derivative upon addition of another molecule of aniline. Two different types of aniline derivatives with either electron-donating or electron-withdrawing substituents can be added sequentially, affording an unsymmetrical moiety in the open-cage structure. Reduction potentials of the 18-membered open-cage fullerene derivatives can be fine-tuned by changing the substituents on the aniline. The results provide new insights about the mechanism of open-cage reactions of fullerene-mixed peroxide

Garnet Solid Electrolyte Protected Li-Metal Batteries

Garnet-type solid state electrolyte (SSE) is a promising candidate for high performance lithium (Li)-metal batteries due to its good stability and high ionic conductivity. One of the main challenges for garnet solid state batteries is the poor solid–solid contact between the garnet and electrodes, which results in high interfacial resistance, large polarizations, and low efficiencies in batteries. To address this challenge, in this work gel electrolyte is used as an interlayer between solid electrolyte and solid electrodes to improve their contact and reduce their interfacial resistance. The gel electrolyte has a soft structure, high ionic conductivity, and good wettability. Through construction of the garnet/gel interlayer/electrode structure, the interfacial resistance of the garnet significantly decreased from 6.5 × 10⁴ to 248 Ω cm² for the cathode and from 1.4 × 10³ to 214 Ω cm² for the Li-metal anode, successfully demonstrating a full cell with high capacity (140 mAh/g for LiFePO₄ cathode) over 70 stable cycles in room temperature. This work provides a binary electrolyte consisting of gel electrolyte and solid electrolyte to address the interfacial challenge of solid electrolyte and electrodes and the demonstrated hybrid battery presents a promising future for battery development with high energy and good safety