Search for: All records

Synopsis Interdisciplinary collaborations are essential for addressing complex global challenges, yet forming and sustaining such teams is often hindered by institutional barriers, differences in discipline-specific languages, and cultural divides. Existing tools and platforms frequently fail to foster the deep, ongoing engagement necessary for successful interdisciplinary work. This paper proposes a novel web-based platform designed to stimulate and support interdisciplinary collaborations by integrating social media elements, such as user-friendly communication tools, algorithms for identifying and connecting individuals with complementary and unique skills, and smart suggestions for potential collaborators. The platform would facilitate building and maintaining the engagement of target users, and provide guardrails to engender community trust, with a goal to also tackle issues related to power dynamics, cultural differences, institutional structures, and varying levels of prestige or funding. By addressing these challenges, the proposed platform would enable and accelerate productive interdisciplinary research and collaborative ideation, and ultimately stimulate more innovative and effective solutions to complex scientific and societal problems. 

Abstract Advancing grid‐scale energy storage technologies is crucial for realizing a fully renewable energy landscape, with non‐aqueous redox flow batteries (NRFBs) presenting a promising solution. One of the current challenges in NRFBs stems from the low energy density of redox active materials, primarily due to their limited solubility in non‐aqueous solvents. Herein, this study explores the solubility of vanadium(IV/V) bis‐hydroxyiminodiacetate (VBH) crystals in acetonitrile, aiming to use them as anionic catholytes in NRFBs. We focused on enhancing VBH solubility by modifying the structure of the alkylammonium cation. Employing periodic density functional theory and a solvation model, we calculated the dissolution free energy ), which includes sublimation ( ) and solvation ( ) energies. Our results indicate that neither elongating straight‐chain alkyl groups beyond a tetrabutylammonium baseline nor introducing bulky substituents at the nitrogen center significantly enhances solubility. However, the introduction of carbon spacers combined with terminal bulky substituents markedly improves solubility by favorably altering both and . These findings underline the nuanced impact of cation structure on solubility and suggest a viable approach to optimize VBH‐based anionic catholytes. This advancement promises to enhance NRFB efficiency and sustainability, marking a significant step forward in energy storage technology.