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Filamentous fungus biomass is a protein-rich food, which can serve as an alternative to animal, plant, and legume protein sources. Neurospora crassa is a filamentous fungus that typically grows in tropical and sub-tropical regions. Traditionally, N. crassa has served as a model eukaryotic organism due to its ease of growth and propagation and suitability for genetic manipulation. However, filamentous fungi, such as Neurospora, have also been consumed or used to produce fermented foods for centuries and have been developed into protein-rich biomass ingredients to be used in conventional foods and meat substitutes. A panel of toxicological tests including genotoxic, acute, and subchronic studies were conducted on dried N. crassa biomass to support its safe use in food. The dried N. crassa biomass was found to be not genotoxic in a bacterial reverse mutation (Ames) assay, an in vitro chromosomal aberration test, and an in vivo micronucleus test. In the acute and subchronic toxicity studies, rats were orally gavaged with N. crassa biomass at concentrations of 0, 1,000, 2,500, and 5,000 mg/kg body weight/day for 14 and 90 days, respectively. At the conclusion of the studies, there were no test article-related toxicity results observed in clinical observations, body weight, food consumption, ophthalmology, hematology, clinical chemistry, coagulation, thyroid hormone, urinalysis, and macroscopic and microscopic findings. The no-observed-adverse-effect level for the dried N. crassa biomass ingredient was determined to be 5,000 mg/kg body weight/day, the highest dose tested.

Filamentous fungus biomass is a protein-rich food, which can serve as an alternative to animal, plant, and legume protein sources.

All-solid-state sodium batteries (ASSSBs) with nonflammable electrolytes and ubiquitous sodium resource are a promising solution to the safety and cost concerns for lithium-ion batteries. However, the intrinsic mismatch between low anodic decomposition potential of superionic sulfide electrolytes and high operating potentials of sodium-ion cathodes leads to a volatile cathode-electrolyte interface and undesirable cell performance. Here we report a high-capacity organic cathode, Na4 C6 O6 , that is chemically and electrochemically compatible with sulfide electrolytes. A bulk-type ASSSB shows high specific capacity (184 mAh g-1 ) and one of the highest specific energies (395 Wh kg-1 ) among intercalation compound-based ASSSBs. The capacity retentions of 76 % after 100 cycles at 0.1 C and 70 % after 400 cycles at 0.2 C represent the record stability for ASSSBs. Additionally, Na4 C6 O6 functions as a capable anode material, enabling a symmetric all-organic ASSSB with Na4 C6 O6 as both cathode and anode materials.

Pseudocapacitive materials offer an opportunity to bridge the energy storage gap between supercapacitor and battery technologies. Herein is chronicled the first report of pseudocapacitance in a system devoid of liquid electrolytes, using the cathode material LiTiS2. It is demonstrated that due to extreme crystallite reduction to less than 3 nm, additional charge storage is derived by reducing surface Ti3+ to Ti2+ at higher voltages and more reversibly than traditionally shown. Due to facile diffusion pathways in 3-fold coordinated lithium along the TiS2 surfaces, disordered LiTiS2 can be used as a singular cathode without conductive additives. The result is a system exhibiting nearly 300 mA h g−1 at a rate of C/2 for 1000 cycles. Whereas active materials in liquid cells typically have size limitations before irreversibilities appear, the high pseudocapacitance demonstrated in this report indicates that active materials used in the solid-state could benefit from size reduction. Hopefully, a new avenue of research stems from this work to investigate mixed conductor nano-domains for solid-state battery/capacitor hybrids. The prospect of a solid-state pseudocapacitor unlocks a series of new applications that offer long shelf life, high temperature capabilities, and enhanced safety.

Biomass can serve as a sustainable template for the synthesis of carbon materials but is limited by the intrinsic properties of the precursor organism. In this study we demonstrate that the properties of a fungal biotemplate can be tuned during cultivation, establishing a new electrode manufacturing process and ultimately improving the electrochemical performance of the biomass-derived electrode. More specifically, the carbon/nitrogen ratio of Neurospora crassa mycelia mats was shifted by 5-fold while generating cobalt nanoparticles into the hyphal structure originating from macroconidia spores. This shift was achieved through nitrate limitation and equal molar concentrations of Mg2+ and Co2+ in the growth media. The resulting mycelia mat was converted via a high-temperature pyrolysis process (800 °C) to produce a freestanding cobalt and nitrogen codoped electrode material with no postmodification. Ultimately, nitrogen doping resulted in one of the highest recorded specific reversible capacity for a frees...

Thin solid membranes are formed by a new strategy, whereby an in situ derived self-healing polymer matrix that penetrates the void space of an inorganic solid is created. The concept is applied as a separator in an all-solid-state battery with an FeS2 -based cathode and achieves tremendous performance for over 200 cycles. Processing in dry conditions represents a paradigm shift for incorporating high active-material mass loadings into mixed-matrix membranes.

© 2015 The Electrochemical Society.This paper details a new binder for mesoporous Si (mp-Si) via the in-situ polymerization and stabilization of polyacrylonitrile (PAN). Using this method mp-Si@PAN electrodes for Li-ion battery anodes have been fabricated. Though the mp-Si@PAN electrodes delivered a reversible specific capacity in excess of 800 mAh g-1 (electrode), the first cycle coulombic efficiency of these electrodes was still less than 50% without a pre-lithiation treatment. The results of an all-solid-state battery experiment confirmed that low first cycle reversibility should be attributed primarily to mechanical pulverization of the internal porous structure of mp-Si particles.

Pure tin (Sn) metal nano-powder is investigated as a high capacity negative electrode for rechargeable all-solid-state Li-ion batteries. Sn is used to form a fully dense network intertwining with solid electrolyte negating necessary conductive additive. Galvanostatic cycling of the Sn composite electrode delivers a reversible capacity 800 mAh g −1 of Sn with a constant coulombic efficiency over 99.2%.Wereportontheeffectofpressureandrateuponthedelithiationmechanics,drawingcorrelationsbetweenSnvolumeincrease factors and stress accumulation over the course of Sn-Li phase transformations. Due to the fabricated electrode microstructure, we are able to operate the cell at ambient pressure conditions ‐ the next step toward commercialization of the solid-state battery. We believe that this initial work provides new opportunities to study the electrochemical expansion of Sn with the inclusion of rigid electrolyte particles. © The Author(s) 2015. Published by ECS. This is an open access article distributed under the terms of the Creative Commons Attribution 4.0 License (CC BY, http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse of the work in any

In order to address the poor energy density of bulk all-solid-state lithium-ion batteries a new composite electrode preparation method is proposed. This study demonstrates the concurrent synthesis of the FeS2 active material and a glass electrolyte which is similar to the (100-x)P2S5:xLi2S system of glass electrolytes. This is accomplished through the successive mechanochemical and thermal treatments of Fe2P, S, and Li 2S. The composite electrode’s ionic conductivity of 5.46 × 10−5 Sc m −1 at 60◦C and specific energy of 1.2 Wh g −1 versus a lithium metal anode suggest that this method may provide a more intimate solid-solid interfacial contact between active material and glass electrolyte. The results of this study provide a completely new perspective on the preparation of all-solid-state composite electrodes.

A new concept of pairing an active material and a mixed conductor is explored as a solid-state battery electrode. By imbedding nano-FeS2 domains into an amorphous LiTiS2 matrix, a hybrid power-energy system is achieved while additionally improving upon many common solid electrode design flaws. High-resolution transmission electron microscopy is used to probe the active material/mixed conductor interface over the course of cycling. Arguably the most beneficial development is enhancement of charge transfer, manifesting in a significantly increased exchange current as captured in a Tafel analysis. By developing a solution to active material isolation and creating a more homogenous electrode design, cycling at a high rate of C/2 for 500 cycles is obtained. Additionally, the electrode can recover full capacity simply by reducing system rate. Capacity recovery implicates a lack of active material isolation, a common problem in solid-state batteries.