Aqueous rechargeable zinc ion batteries are promising in electric grid storage due to their low cost and intrinsic safety. However, the practical implementation is hindered by the poor reversibility of the zinc anode, primarily caused by the chaotic Zn deposition present as dendrite and side reactions.

The researchers found that metal organic framework (MOF) nanosheets featuring migration capability under an electric field due to their one-dimensional (1D) channel structure and preferential Zn2+ adsorption, as well as unique reductive chemistry due to the weak coordination between ligands and zinc ions, enabling them to serve as dynamic Zn2+ ion carriers.

The dynamic MOF nanosheets could continually optimize zinc anode during cycling. Specifically, the zinc electrode was gradually reconstructed towards a horizontally aligned lamellae-like morphology and enhanced (002) texture, showing a relative texture coefficient of a 96.9 (maximum value of 100). This optimization on the morphology and texture could be attributed to the horizontal alignment of Zn2+ ions by the constraints of the MOF nanosheets.

Additionally, the presence of MOF ligands contributed to the elimination of undesirable Zn4SO4(OH)6·4H2O byproducts. These byproducts were spontaneously converted into useful MOF nanosheets through unique properties of ligands. Consequently, Zn||Zn symmetric cells and Zn||(NH4)2V10O25·8H2O full cells employing MOF nanosheets in electrolytes exhibited outstanding cycling performance at both low and high rates.

"The versatility of the 'ion carrier' holds promise for potential expansion into achieving highly reversible cycling in other rechargeable metal cells, owing to its broad applicability to various ligands, substrates and electrolytes," said Prof. YANG.

This work was supported by the National Natural Science Foundation of China and the Youth Innovation Fund of DICP

The article links：http://xlink.rsc.org/?DOI=D3EE01747H