Influence of Potassium Metal‐Support Interactions on Dendrite Growth

Author:

Liu Pengcheng1,Yen Dean2,Vishnugopi Bairav S.3,Kankanallu Varun R.2,Gürsoy Doğa4,Ge Mingyuan5,Watt John6,Mukherjee Partha P.3,Chen‐Wiegart Yu‐chen Karen25,Mitlin David1ORCID

Affiliation:

1. Materials Science and Engineering Program & Texas Materials Institute (TMI) The University of Texas at Austin Austin TX 78712-1591 USA

2. Department of Materials Science and Chemical Engineering Stony Brook University Stony Brook NY 11794 USA

3. School of Mechanical Engineering Purdue University West Lafayette IN 47907 USA

4. Advanced Photon Source Argonne National Laboratory Lemont IL 60439 USA

5. National Synchrotron Light Source II (NSLS-II) Brookhaven National Laboratory Upton NY 11973-5000 USA

6. Center for Integrated Nanotechnologies Los Alamos National Laboratory Los Alamos NM 87545 USA

Abstract

AbstractCombined synchrotron X‐ray nanotomography imaging, cryogenic electron microscopy (cryo‐EM) and modeling elucidate how potassium (K) metal‐support energetics influence electrodeposit microstructure. Three model supports are employed: O‐functionalized carbon cloth (potassiophilic, fully‐wetted), non‐functionalized cloth and Cu foil (potassiophobic, nonwetted). Nanotomography and focused ion beam (cryo‐FIB) cross‐sections yield complementary three‐dimensional (3D) maps of cycled electrodeposits. Electrodeposit on potassiophobic support is a triphasic sponge, with fibrous dendrites covered by solid electrolyte interphase (SEI) and interspersed with nanopores (sub‐10 nm to 100 nm scale). Lage cracks and voids are also a key feature. On potassiophilic support, the deposit is dense and pore‐free, with uniform surface and SEI morphology. Mesoscale modeling captures the critical role of substrate‐metal interaction on K metal film nucleation and growth, as well as the associated stress state.

Funder

U.S. Department of Energy

National Science Foundation

Publisher

Wiley

Subject

General Medicine

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