RESUMEN
The cycling lifespan of Li-metal batteries is compromised by the unstable solid electrolyte interphase (SEI) and the continuous Li dendrites, restricting their practical implementations. Given these challenges, establishing an artificial SEI holds promise. Herein, a trinitarian gradient interphase is innovatively designed through composite coatings of magnesium fluoride (MgF2), N-hexadecyltrimethylammonium chloride (CTAC), and polyvinylidene fluoride-hexafluoropropylene copolymer (PVDF-HFP) on Li-metal anode (LMA). Specifically, the MgF2/CTAC/PVDF-HFP SEI spontaneously forms a lithium fluoride (LiF)-rich PVDF-HFP-based SEI, along with lithium-magnesium (Li-Mg) alloy substrate as lithiophilic electronic conductor and positively charged CTAC during plating. Noticeably, the Li-Mg alloy homogenizes the distribution of electric field and reduce the internal resistance, while the electronically insulated LiF/PVDF-HFP composite SEI offers fast ion-conducting and mechanical flexibility, accommodating the volumetric expansion and ensuring stable Li-ion flux. Additionally, CTAC at the dendritic tip is pivotal for mitigating dendrites through its electrostatic shield mechanism. Innovatively, this trinitarian synergistic mechanism, which facilitates colossal granular Li deposits, constructs a dendrite-free LMA, leading to stable cycling performances in practical Li||LFP, popular Li||NCM811, and promising Li||S full cells. This work demonstrates the design of multifunctional composite SEI for comprehensive Li protection, thereby inspiring further advancements in artificial SEI engineering for alkali-metal batteries.
RESUMEN
In a conventional (Stroop) priming paradigm, it was well documented that objective prime-target incongruency delays response time (RT) to target compared to prime-target congruent condition. Recent evidence suggests that incongruency between the target and subjectively reported prime identity also delays RT over and above the classic congruency effect. When the prime is rendered invisible, the former effect is fundamentally a bottom-up (BU) stimulus-driven congruency effect and the latter a top-down (TD) guess-driven congruency effect. An influential theory of consciousness, global neuronal workspace theory, postulates that the long-lasting simultaneous and reciprocal interaction between TD decision network and BU input network is preserved during conscious processing and disabled during unconscious processing. Current study is focused on testing this theoretical postulation using two behavioral experiments. Our results showed that indeed TD-congruency and BU-congruency produced additive RT effects on prime-invisible trials, which implies that TD and BU prime representations are activated in independent neuronal populations. Meanwhile, an underadditive interaction effect was observed as prime visibility rose, which is a signature that TD and BU prime representations recruited overlapping neuronal populations during conscious perception. In addition, we suggest that current behavioral paradigm might be a financially friendly alternative to detect the presence of representational overlap in the brain between a wide range of mental representations, such as expectation, prediction, conscious/unconscious perception, and conscious/unconscious working memory. (PsycInfo Database Record (c) 2024 APA, all rights reserved).
Asunto(s)
Encéfalo , Estado de Conciencia , Humanos , Estado de Conciencia/fisiología , Tiempo de Reacción , Concienciación/fisiologíaRESUMEN
Silicon (Si) is considered a high-capacity anode material with potential for next-generation lithium-ion batteries. However, the commercial application of Si anode is seriously hindered by huge volume variation (>300%) and limited Li+ diffusion ability. Herein, lithium metasilicate (LS), a novel inorganic binder, was innovatively developed to accommodate these challenges. Favorable compatibility is observed between the LS binder and Si nanoparticles (SiNPs) due to the existence of Si element within the LS skeleton. The interaction of the LS binder and SiNPs leads to a strong adhesion effect, enhancing the cycling stability of Si anode. The Si electrode with the LS binder presented an average discharge capacity of 2123 mAh/g at 0.84 A/g after 100 cycles. Furthermore, the presence of the Li+ transport channel within the LS binder enhances Li+ diffusion ability within Si anode. As a result, the average discharge capacity reaches 663 mAh/g at 8.4 A/g. This work thus explored new inorganic binder design approaches for Si anode, contributing to the advancement of high-performance Si anode.