Bottom-preferred stripping mechanism towards quantified inactive metallic Zn0-dominant zinc loss in rechargeable zinc metal battery

Electrically isolated metallic Zn (Zn 0 ) and electrochemically side reaction (ECSR), causes irreversible anode capacity loss and limited cycle life in zinc metal battery. However, the quantitative distinguishment between inactive metallic Zn 0 and ECSR, their formation mechanism and correlation with anode cycling reversibility have never been disclosed, limiting further anode modification design. Here, we develop an acid-assisted continuous titration-collection-gas chromatography technique (AAC-TCGC) that accurately quantify the amount of inactive Zn 0 and ECSR in anode, and discover that inactive Zn 0 accounts for the majority of Zn loss, rather than the commonly-assumed electrochemically side reaction-derived ECSR-dominant Zn anode capacity loss. Detailed component of SEI (Solid Electrolyte Interface Layer) compound is also characterized, illustrating a solvent-derived zinc oxide/hydroxide-dominant SEI that facilitates vertical/inclined thin-plate Zn deposition, but salt-derived ZnF 2 -dominant SEI that favors horizontal platelet-shaped Zn(002) deposition. Simulation results reveal a new electric resistance-derived, bottom-preferred Zn stripping mechanism that leads to abundant inactive Zn 0 formation in vertical thin-plate Zn deposition structure, but few inactive Zn 0 in dumpy platelet-shaped Zn structure. Our study provides new theories and strategies on the distinguishment, formation mechanism and structure-performance relationship of inactive Zn, important for building more efficient Zn metal battery.