Tunnel Structured α-MnO 2 with Different Tunnel Cations (H + , K + , Ag + ) as Cathode Materials in Rechargeable Lithium Batteries: The Role of Tunnel Cation on Electrochemistry
α-MnO 2 type manganese dioxide is an interesting prospective cathode material for reversible lithium insertion owing to its cation accessible tunnels (0.46nm x 0.46nm), high voltage, and low cost. The tunneled structure is synthetically formed by the assistance of cations acting as structure directing agents where the cations may remain in the tunnel. The electrochemistry of this family of materials is strongly dependent on the morphological and physicochemical (i.e. surface area, crystallite size, and average manganese oxidation state) properties as well as tunnel occupancy. For this work, we prepared a set of materials Mn 8 O 16 ·0.81H 2 O, K 0.81 Mn 8 O 16 ·0.78H 2 O and Ag 1.33 Mn 8 O 16 ·0.95H 2 O with similar nanorod morphology, crystallite size, surface area, and tunnel water content. This set of samples allowed us to investigate the role of tunnel cations in the electrochemistry of α-MnO 2 type manganese dioxide in a lithium based environment while minimizing the effects of the other parameters. The electrochemistry was evaluated using cyclic voltammetry, galvanostatic cycling, rate capability, and galvanostatic intermittent titration type testing. Mn 8 O 16 ·0.81H 2 O showed higher loaded voltages, improved capacity retention, and higher specific energy relative to K 0.81 Mn 8 O 16 ·0.78H 2 O and Ag 1.33 Mn 8 O 16 ·0.95H 2 O. After 100 cycles, Mn 8 O 16 ·0.81H 2 O delivered ~200% more capacity than Ag 1.33 Mn 8 O 16 ·0.95H 2 O (64 vs. 129 mAh/g) and ~35% more capacity than K 0.81 Mn 8 O 16 ·0.78H 2 O (85 vs. 129 mAh/g). Mn 8 O 16 ·0.81H 2 O also showed higher effective lithium diffusion coefficients (DLi+) and higher rate capability compared to K 0.81 Mn 8 O 16 ·0.78H 2 O and Ag 1.33 Mn 8 O 16 ·0.95H 2 O suggesting faster Li+ ion diffusion in the absence of large metal tunnel cations.