ABSTRACT
Quasi-solid-state rechargeable zinc-air batteries (ZABs) are suitable for the generation of portable clean energy due to their high energy and power density, safety, and cost-effectiveness. Compared to the typical alkaline aqueous electrolyte in a ZAB, polymer or gel-based electrolytes can suppress the dissolution of zinc, preventing the precipitation of undesirable irreversible zinc compounds. Their low electronic conductivity minimizes zinc dendrite formation. However, gel electrolytes suffer from capacity fade due to the loss of the volatile solvent, failing to deliver high-energy and high-power ZABs. Consequently, developing polymers with high hydroxide ion conductivity and chemical durability is paramount. We report cationic C-C bonded robust polymers with stoichiometrically controlled mobile hydroxide ions as solid-state hydroxide ion transporters. To boot, we increased the viologen-hydroxide-ion concentration through "by-design" monomers. The polymers constructed with these designer monomers exhibit a commensurate increase in their ionic conductivity. The polymer prepared with 4 OH- ion-containing monomer was superior to the one with 3 OH-. The conductivity increases from 7.30 × 10-4 S cm-1 (30 °C) to 2.96 × 10-3 S cm-1 (30 °C) at 95% RH for IISERP-POF12_OH (2_OH) and IISERP-POF13_OH (3_OH), respectively. A rechargeable ZAB (RZAB) constructed using 3_OH@PVA (polyvinyl alcohol) as the electrolyte membrane and Pt/C + RuO2 catalyst delivers a power density of 158 mW cm-2. In comparison, RZABs with a PVA interlayer provided only 72 mW cm-2. Notably, the device suffered an initial charge-discharge voltage gap of merely 0.55 V at 10 mA cm-2, which increased by only 2 mV after 50 hours of running. The battery operated at 10 mA cm-2 and worked steadily for 67 hours. We accomplished a flexible and rechargeable zinc-air battery (F-RZAB) exhibiting a maximum power density of 79 mW cm-2. This demonstration of a cationic viologen-bakelite polymer-based flexible secondary ZAB with versatile stochiometric hydroxide-ion tunability marks an important achievement in hydroxide-ion conducting solid-state electrolyte development.
ABSTRACT
Improving the electronic conductivity and the structural robustness of covalent organic frameworks (COFs) is paramount. Here, we covalently cross-link a 2D COF with polypyrrole (Ppy) chains to form a quasi-3D COF. The 3D COF shows well-defined reflections in the SAED patterns distinctly indexed to its modeled crystal structure. This knitting of 2D COF layers with conjugated polypyrrole units improves electronic conductivity from 10-9 to 10-2 S m-1. This conductivity boost is affirmed by the presence of density of states near the Fermi level in the 3D COF, and this elevates the COF's valence band maximum by 0.52 eV with respect to the parent 2D pyrrole-functionalized COF, which agrees well with the opto-electro band gaps. The extent of HOMO elevation suggests the predominant existence of a polaron state (radical cation), giving rise to a strong EPR signal, most likely sourced from the cross-linking polypyrrole chains. A supercapacitor devised with COF20-Ppy records a high areal capacitance of 377.6 mF cm-2, higher than that of the COF loaded with noncovalently linked polypyrrole chains. Thus, the polypyrrole acts as a "conjugation bridge" across the layers, lowering the band gap and providing polarons and additional conduction pathways. This marks a far-reaching approach to converting many 2D COFs into highly ordered and conducting 3D ones.
