Spontaneous Molecule Aggregation for Nearly Single-Ion Conducting Sol Electrolyte to Advance Aqueous Zinc Metal Batteries: The Case of Tetraphenylporphyrin.

Angew Chem Int Ed Engl

Key Laboratory of Colloid and Interface Chemistry, Ministry of Education, School of Chemistry and Chemical Engineering, Shandong University, Jinan, 250100, P. R. China.

Published: May 2024

Zn metal as a promising anode of aqueous batteries faces severe challenges from dendrite growth and side reactions. Here, tetraphenylporphyrin tetrasulfonic acid (TPPS) is explored as an electrolyte additive for advanced Zn anodes. It is interesting to note that TPPS spontaneously assembles into unique aggregates. As they adsorb on the Zn anode, the aggregates enhance the resistance to electrolyte percolation and dendrite growth compared to single molecules. Meanwhile, TPPS facilitates anion association in the solvation sheath of Zn, and boosts the transference number of Zn up to 0.95. Therefore, anion-related side reactions and anion-induced electrode overpotentials are reduced accordingly. In this context, the electrolyte containing TPPS exhibits excellent electrochemical performance. Even under a high loading of MnO (25 mg cm), a limited Zn supply (N/P ratio=1.7), and a lean electrolyte (15 μL mAh), the full cells still represent a higher cumulative capacity compared to the reported data. The advantages of this electrolyte are also adapted to other cathode materials. The pouch cells of Zn||NaVO ⋅ 1.5HO realize a capacity of ~0.35 Ah at 0.4 C under harsh conditions.

Download full-text PDF

Source
http://dx.doi.org/10.1002/anie.202401441DOI Listing

Publication Analysis

Top Keywords

dendrite growth
8
side reactions
8
electrolyte
6
spontaneous molecule
4
molecule aggregation
4
aggregation single-ion
4
single-ion conducting
4
conducting sol
4
sol electrolyte
4
electrolyte advance
4

Similar Publications

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!