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These examples highlight structural optimization as a pivotal strategy for enhancing the stability, efficacy, and translational potential of PRLM-based therapies [295]

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In the resultant 1 M KFSI-DME/PFPN/FEMC (3 vol %) electrolyte, the cyclotriphosphazene group of PFPN is revealed to not only mitigate the flammability of DME but also diminish the K + -DME interaction through steric hindrance