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(Keynote) Architectural Re-Design of Zinc Anodes Physically Thwarts Dendrite Formation—with Zinc Batteries Now Rechargeable, What’s Next?

Thursday, 7 March 2019: 16:00
Samuel H. Scripps Auditorium (Scripps Seaside Forum)
D. R. Rolison, J. F. Parker (U.S. Naval Research Laboratory), J. S. Ko (U S. Naval Research Laboratory, Former NRL/NRC Postdoctoral Associate), B. J. Hopkins (U.S. Naval Research Laboratory, NRL/National Research Council Postdoctoral Associate), C. N. Chervin, A. B. Geltmacher, and J. W. Long (U.S. Naval Research Laboratory)
We recently demonstrated that redesigning dendrite-prone zinc anodes as 3D monolithic Zn architectures solves the limited rechargeability of alkaline batteries. Three structural features of these emulsion–derived “sponges” physically ensure dendrite suppression: (i) long-range electronic conductivity within the electrode volume throughout charge–discharge; (ii) more uniform current distribution; and (iii) confined internal void volume that controls Zn/Zn2+ precipitation/dissolution dynamics and product redistribution.

With Li-ion competitive cyclability to deep depths-of-discharge (theoretical DODZn), primary utilization to >90% DODZn (with >90% recovery), and tens of thousands of cycles at low-DODZn creates new performance curves for the entire family of alkaline Zn batteries (Ni–Zn, Ag–Zn, MnO₂–Zn, Zn–air) plus neutral pH zinc-ion batteries. Our second-generation emulsion protocol increases volumetric density of the sponge, which improves the energy density of the cell, and adds mechanical ruggedness to the anode. Development paths for this safer energy-storage breakthrough will be discussed.