11 research outputs found

    Decoupling, quantifying, and restoring aging-induced Zn-anode losses in rechargeable aqueous zinc batteries

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    The search for batteries beyond Li-ion that offer better performance, reliability, safety, and/or affordability has led researchers to explore a diverse array of candidates. The advantages of Zn-ion batteries reside in zinc’s relatively low reactivity, raising the prospect of a rechargeable battery with a simple aqueous electrolyte and a cheaper, safer option to the organic electrolytes that must be paired with reactive lithium. However, water still reacts with the zinc in corrosion reactions. These consume zinc, lowering the battery’s capacity, and generate gas that accumulates in the sealed cell. We diagnose the contribution of corrosion to performance decay in zinc batteries and reveal the critical role of gas accumulation in deactivating large sections of electrode, which cripples cell performance. Fortunately, electrodes can be reactivated by removal of the gas, demonstrating the importance of designing future cells that either prevent gas formation or facilitate its safe release

    Well-Defined Selenium-Containing Aliphatic Polycarbonates via Lipase-Catalyzed Ring-Opening Polymerization of Selenic Macrocyclic Carbonate Monomer

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    The synthesis of well-defined, biodegradable selenium-containing polymers remains a formidable challenge in polymer chemistry. Herein, a selenic cyclic carbonate dimer monomer (M<sub>Se</sub>) was developed to generate well-defined, biodegradable aliphatic polycarbonates with selenide functionality on the backbone. The monomer was synthesized via the intermolecular cyclization of di­(1-hydroxyethylene) selenide and diphenyl carbonate with lipase CA as catalysts in a mass of anhydrous toluene with very dilute monomer concentration. Then living ring-opening polymerization (ROP) was executed by solution method using the same lipase CA as catalysts. Similarly, the copolymerizations with commercial trimethylene carbonate (TMC) generated random copolymers demonstrated by <sup>13</sup>C NMR, regulating the density of selenium functional groups. The resulting polymers exhibited a living polymerization characteristic, as evidenced by polymerization kinetics, predictable molecular weights, narrow molecular-weight distribution, and controlled copolymer compositions. Using hydrophilic macroinitiators (PEG), amphiphilic di/triblock copolymers could be obtained, suggesting their potential as controlled drug delivery system (DDS) and hydrogel scaffolds for tissue engineering
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