Sodium Metal Anode with Na/Na3Bi Penetration for Dendrite-Free and High-Rate Sodium-Ion Battery
1. Introduction
Here, we introduced “sodiophilic” Na3Bi penetration into Na anodes to build abundant phase-boundary ion-transport channels. Ion diffusion along the phase boundaries is supposed to enable several orders of magnitude faster than lattice diffusion. Thus, Na ions quickly extract/insert along the boundaries between Na and Na3Bi phase during stripping and plating processes, thus maintaining the even ion-flux distribution as shown in Fig. 1(a). Moreover, the sodiophilic bismuthide enables uniform and dense Na deposition during cycling, thus aiding high volumetric capacity. The Na3Bi-penetrated Na hybrid anode delivers a high current density of 5?mA?cm?2 along with a capacity of 5?mA?h?cm?2 for over 300?h and ultralong cycle life (over 2800?h) at 2?mA?cm?2 under 2?mA?h?cm?2. The Na3V2(PO4)3 (NVP)/(Na/Na3Bi) full cell exhibits superior electrochemical performance than those with the bare Na foil anodes.
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3. Conclusions
In this work, bulk Na–metal anodes with sodiophilic Na3Bi penetration, which holds even nucleation and uniform and dense Na deposition, could deliver a high rate, a long cycle life, and a high volumetric capacity. As a result, abundant Na/Na3Bi phase boundaries, which proved to enable Na+ diffusion several orders of magnitude faster than lattice diffusion, ensure sufficient and rapid Na+ migration taking place upon plating and stripping. During initial deposition, the exposed “sodiophilic” Na3Bi framework induces uniform local ion distribution, thereby delivering homogenous inner-space Na+ plating and suppressing volume fluctuations. In subsequent stripping and plating processes, Na+ rapidly exits and enters along the boundaries of Na and Na3Bi phase, maintaining the stability of the anode/electrolyte interface. Furthermore, the obtained anode delivers superior cycling and rate performances coupled with the NVP cathodes.