We are the first to examine the role of graphene host structure/chemistry in plating-stripping in lithium metal anodes employed for lithium metal batteries (LMBs). Structural and chemical defects are bad since highly defective graphene promotes unstable solid electrolyte interphase (SEI) growth. This consumes the FEC additive in the carbonate electrolyte and is correlated with rapid decay in CE and formation of filament-like Li dendrites. A unique flow-aided sonication exfoliation method is employed to synthesize "defect-free" graphene (df-G), allowing for a direct performance comparison with conventional reduced graphene oxide (r-GO). At cycle 1, the r-GO is better electrochemically wetted by Li than df-G, indicating that initially it is more lithiophilic. With cycling, the nucleation overpotential with r-GO becomes higher than with df-G, indicating less facile plating reactions. The df-G yields state-of-the-art electrochemical performance, with the post cycled metal surface being relatively-smooth and dendrite-free. Conversely, r-GO templates have CE rapidly degrade from the onset, with extensive dendrites after cycling. Severe SEI growth and associated FEC depletion with r-This article is protected by copyright. All rights reserved. 2GO are further confirmed by electrochemical impedance analysis (EIS) and surface science methods (XPS). We provide a new design rule for Li metal templates: An ideal host must be non-catalytic towards SEI formation per se.

Sodium metal battery (SMB, NMB) anodes can become dendritic due to an electrochemically unstable native Na-based solid electrolyte interphase (SEI). Herein Li-ion activated tin sulfide graphene nanocomposite membrane (A-SnS-G) is...

To date, lithium-ion batteries (LIBs) as one of the most promising means of energy storage have witnessed progressive upgrades of cell energy density and cost reduction, enabling, for example, longer EVs travel ranges (>300 km/charge) and deeper penetration of renewables into grid electricity. Despite the fast growing market of LIBs [3] and the worldwide conspicuous rise in LIBs production, the practical specific energy density of prevailing LIBs adopting graphite anode is approaching its theoretical limit, that is, ≈250 Wh kg −1 when paired with high-energy ceramic cathode such as nickel cobalt manganese oxides. Nevertheless, to meet the everpresent relentless demand from end-users such as portable electronics and EVs, the battery ought to be upgraded to provide 400-500 Wh kg −1 , 700-800 Wh L −1 with lower cost (<9.5 US cents/Wh, expected in 2030), and fast charge capabilities (>2C, i.e., fully charged within 1/2 h). [4] To achieve these goals, the core strategy for developing next-generation LIBs is to exploit higher-capacity battery materials that are cheap and abundant.Silicon (Si) is recognized to be one of the most appealing choices of anode materials due to its inherent low-cost, natural abundance, and the ultrahigh theoretical capacity of 3590 mAh g −1 (based on Li 15 Si 4 ) at low potential (<0.4 V vs Li/ Li + ). [5] Pioneering battery manufacturers like CATL and Tesla have Due to its uniquely high specific capacity and natural abundance, silicon (Si) anode for lithium-ion batteries (LIBs) has reaped intensive research from both academic and industrial sectors. This review discusses the ongoing efforts in tailoring Si particle surfaces to minimize the cycle-induced changes to the integral structure of particles or electrodes. As an upgrade or alternative to conventional coatings (e.g., carbons), the emerging organic moieties on Si offer new avenues toward tuning the interactions with various battery components that are key to electrochemical performances. The recent progress on understanding Si surfaces is reviewed with an emphasis on newly emerged diagnostic tools, which increasingly points to the critical role of organic components in stabilizing Si. The detailed analysis on the chemistry-structure-performance relationships in Si surface are discussed and the successful cases demonstrating the functions of the organic layers are provided, that is, via tailored interactions toward electrolyte or binder or conductive agents, are recapped. Various synthetic strategies for designing the surface organic layers are discussed and compared, highlighting the versatility and tunability of surface organic chemistry. The holistic considerations and promising research directions are summarized, shedding light on in-depth understanding and engineering Si surface chemistry toward practical LIBs application.