Identifying Heteroatomic and Defective Sites in Carbon with Dual-Ion Adsorption Capability for High Energy and Power Zinc Ion Capacitor

Aqueous zinc-based batteries (AZBs) attract tremendous attention due to the abundant and rechargeable zinc anode. Nonetheless, the requirement of high energy and power densities raises great challenge for the cathode development. Herein we construct an aqueous zinc ion capacitor possessing an unrivaled combination of high energy and power characteristics by employing a unique dual-ion adsorption mechanism in the cathode side. Through a templating/activating co-assisted carbonization procedure, a routine protein-rich biomass transforms into defect-rich carbon with immense surface area of 3657.5 m(2) g(-1) and electrochemically active heteroatom content of 8.0 at%. Comprehensive characterization and DFT calculations reveal that the obtained carbon cathode exhibits capacitive charge adsorptions toward both the cations and anions, which regularly occur at the specific sites of heteroatom moieties and lattice defects upon different depths of discharge/charge. The dual-ion adsorption mechanism endows the assembled cells with maximum capacity of 257 mAh g(-1) and retention of 72 mAh g(-1) at ultrahigh current density of 100 A g(-1) (400 C), corresponding to the outstanding energy and power of 168 Wh kg(-1) and 61,700 W kg(-1). Furthermore, practical battery configurations of solid-state pouch and cable-type cells display excellent reliability in electrochemistry as flexible and knittable power sources.

Automated summary

Aqueous zinc ion capacitors with a unique dual-ion adsorption mechanism in the cathode side exhibit outstanding energy and power characteristics. The carbon cathode with immense surface area and electrochemically active heteroatom content shows superior capacitive charge adsorptions. The dual-ion adsorption mechanism enables the assembled cells to achieve exceptional energy and power performance at ultrahigh current density.