Anode-free lithium metal batteries are the most promising candidate to outperform lithium metal batteries due to higher energy density and reduced safety hazards with the absence of metallic lithium anode during initial cell fabrication. In general, researchers report capacity retention, reversible capacity, or rate capability of the cells to study the electrochemical performance of anode-free lithium metal batteries. However, evaluating the behavior of batteries from limited aspects may easily overlook other information hidden deep inside the meretricious results or even lead to misguided data interpretation. In this work, we present an integrated protocol combining different types of cell configuration to determine various sources of irreversible coulombic efficiency in anode-free lithium metal cells. The decrypted information from the protocol provides an insightful understanding of the behaviors of LMBs and AFLMBs, which promotes their development for practical applications.

Zinc metal is considered a promising anode material for aqueous zinc ion batteries. However, it suffers from dendrite growth, corrosion, and low coulombic efficiency (CE) during plating/stripping. Herein, a concentrated hybrid (4 m Zn(CF 3 SO 3 ) 2 + 2 m LiClO 4 ) aqueous electrolyte (CHAE) to overcome the challenges facing the Zn anode is reported. The developed electrolyte achieves dendrite-free Zn plating/stripping and obtains an excellent CE of ≈100%, surpassing the previously reported values. The combination of synchrotron-based in operando transmission X-ray microscopy, X-ray diffraction, and ex situ X-ray photoelectron spectroscopy analyses indicate that the denser, anion-derived passivation layer formed using the CHAE facilitates homogeneous current distribution and better prevents freshly deposited Zn from directly contacting the electrolyte than the looser, solvent-derived layers formed from a dilute hybrid aqueous electrolyte (DHAE). The beneficial effects of the CHAE on the compact, dense, and stable salt-anion-derived passivation layer can be attributed to its unique solvation structure, which suppresses the water-related side reactions and widens the electrochemical potential window. In the hybrid Zn||LiFePO 4 configuration, the CHAE-based cell delivered a stable performance of CE >99% and capacity retention >90% after 285 cycles. In contrast, the DHAE-based cell exhibits capacity retention of <65% after 170 cycles.

Because of the high specific capacity and low redox potential, lithium metal constitutes a promising material and might be an option for high energy density next-generation battery technologies, though application of lithium metal batteries (LMBs) is currently limited by poor long-term performance and severe safety issues when liquid electrolytes are used. These challenges arise from formation of “dead” lithium or inhomogeneous lithium deposits as well as ineffective solid electrolyte interphase (SEI) layers on lithium metal electrodes. Notably, lithium consumed by SEI formation and fractions of “dead” lithium was derived from in situ 7Li nuclear magnetic resonance (NMR) of pouch-type cells, while 19F 1D magnetic resonance imaging (MRI) profiling along with operando optical microscopy analysis revealed the nature of lithium deposits, considering the impact of electrode kinetics on the occurrence of dendritic lithium microstructures, governed by processes of electrodeposition and electrodissolution. Various electrolyte formulations were compared in view of different cell configurations, including Li||Li symmetric cells as well Li||Cu cells, Cu||NMC cells, and finally NMC||Li full cell systems, establishing the origin and likely contributions to irreversible capacity losses while systematically evaluating different active materials (including electrolyte formulations, cathode material, and lithium metal anodes). Indeed, a mixture of film-forming additivesfluoroethylene carbonate (FEC) and lithium difluorophosphate (LiPO2F2)was demonstrated to afford both “better” interfacial/interphasial properties and more homogeneous lithium deposition, thus exhibiting promising electrochemical performance.

Dendrite growth and low Coulombic efficiency impede the practical application of Li-metal batteries. As such, monitoring Li deposition and stripping in real-time is crucial to understanding the fundamental lithium growth kinetics. This work presents an operando optical microscopic technique that enables precise current density control and quantification of Li layer properties (i.e., thickness and porosity) to study Li growth in various electrolytes. We discover the robustness and porosity of the remaining capping layer after the Li stripping process as the critical features governing the subsequent dendrite propagation behavior, resulting in distinct capping and stacking phenomena that affect Li growth upon cycling. While dendrite propagation quickly occurs through the fracture of the fragile Li capping layer, uniform Li plating/stripping can be facilitated by the compact and robust capping layer even at high current densities. This technique can be extended to evaluate dendrite suppression treatments in various metal batteries, providing in-depth information on metal growth mechanisms.

Lithium metal batteries (LMBs) have been revisited and gained great attention due to significantly mitigated formation of Li dendrite in the past decade. Recently, anode-free lithium metal batteries (AFLMBs) are proposed and have been studied intensively to potentially outperform LMBs due to higher energy density and reduced safety hazards since the absence of Li metal during the fabrication process of the cell. In general, researchers compare capacity retention, reversible capacity, or rate capability of the cells to study the electrochemical performance of batteries. However, evaluating the behavior of batteries from limited aspects would easily overlook other information hidden deep inside the meretricious results or even lead to misguided data interpretation. In this work, an integrated protocol combining different types of cell configuration is proposed and validated for the first time to unravel the concealed messages in LMBs and AFLMBs. Irreversible coulombic efficiency (irr-CE) from various contributions including reductive electrolyte decomposition, dead Li formation, 1st intrinsic irreversible capacity of a cathode, and the subsequent irreversible reactions at cathode containing oxidative electrolyte decomposition and cathode degradation upon cycling are successfully determined separately by the integrated protocol for the first time. The decrypted information obtained from the proposed protocol provides an insightful understanding of behaviors of LMBs and AFLMBs, which promotes their development for practical applications.