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The creates a large molecular dipole (~5 D per molecule). The hydrogen‑bonded NH₃⁺ network provides a cooperative proton‑transfer pathway , analogous to the mechanism in KH₂PO₄ , but with a significantly lower activation barrier due to the Zr‑O‑NH₃⁺ coordination that stabilizes the transition state. This dual contribution—electronic dipole and dynamic proton lattice—explains the high Curie temperature and low coercive field .

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