Apr 24, 2024
5:00pm - 7:00pm
Flex Hall C, Level 2, Summit
Jose Florez Gomez1,Nischal Oli1,Songyang Chang2,Shen Qiu2,Swati Katiyar2,Ram Katiyar1,Gerardo Morell1,Xianyong Wu2
University of Puerto Rico at Rico-Rio1,University of Puerto Rico at Río Piedras2
Jose Florez Gomez1,Nischal Oli1,Songyang Chang2,Shen Qiu2,Swati Katiyar2,Ram Katiyar1,Gerardo Morell1,Xianyong Wu2
University of Puerto Rico at Rico-Rio1,University of Puerto Rico at Río Piedras2
The Voltaic battery (zinc-copper battery) is the very first battery built by humanity, which plays a critical role in battery development history. However, the inevitable copper ion dissolution-crossover issue leads to its primary battery nature. The ion-exchange membranes and alkaline electrolytes represent two leading approaches to mitigate this issue; however, they incur the disadvantages of complicated battery design, high cost, and zinc anode corrosion. Herein, we build a rechargeable zinc-copper Voltaic battery from simple and cost-effective electrode/electrolyte materials, where the cathode is a nano-sized copper, and the electrolyte is a near-neutral zinc sulfate solution. Interestingly, the copper electrode experiences a synergistic cation-anion insertion reaction, where copper transforms to zinc-copper alloy (Zn<sub>x</sub>Cu) during discharge and converts to copper (I) oxide (Cu<sub>2</sub>O) during charge. Therefore, multivalent Zn<sup>2+</sup> cations and multivalent O<sup>2-</sup> anions participate in the redox reaction, giving a high capacity of ~370 mAh g<sup>-1</sup>. Moreover, the structural similarity between Zn<sub>x</sub>Cu, Cu, and Cu<sub>2</sub>O endows high reaction reversibility, leading to impressive cycling of ~500 cycles. Such a concerted cation-anion insertion is rarely reported in the battery field, which offers a mechanism-based approach for developing high-capacity and long-cycling multivalent-ion batteries.