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The development of high-energy lithium metal batteries (LMBs) is essential for advances in next-generation energy storage and electric vehicle technologies. Nevertheless, the practical applications of LMBs are constrained by current electrolyte designs that inherently rely on dominant solvation structures, preventing transformative progress in performance optimization. Here, we address this limitation through a delocalized electrolyte design that fosters a more disordered solvation microenvironment, thereby mitigating dynamic barriers and stabilizing interphases. The resulting delocalized electrolyte delivers notable energy densities of 604.2 Wh kg in a 5.5-Ah LiNiCoMnO (Ni90)||Li pouch cell with a lean electrolyte design (1.0 g Ah) and 618.2 Wh kg in a 5.2-Ah Ni90||Li pouch cell with an ultralean electrolyte design (0.9 g Ah), maintaining significant cycle stability over 100 and 90 cycles, respectively. In addition, the 70-104 V NCM811||Li battery pack (3,904 Wh) exhibits a high energy density of 480.9 Wh kg and stable cycling over 25 cycles. These results demonstrate the need to circumvent inherent reliance on dominant solvation structures in electrolyte design to achieve the high-energy Battery600 and scalable Pack480 targets.
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http://dx.doi.org/10.1038/s41586-025-09382-4 | DOI Listing |
J Am Chem Soc
September 2025
Confucius Energy Storage Lab, School of Energy and Environment & Z Energy Storage Center, Southeast University, Nanjing 211189, China.
Developing efficient and durable catalysts for the oxygen evolution reaction (OER) in acidic media is essential for advancing proton exchange membrane water electrolysis (PEMWE). However, catalyst instability caused by lattice oxygen (O) depletion and metal dissolution remains a critical barrier. Here, we propose an oxophilic-site-mediated dynamic oxygen replenishment mechanism (DORM), in which O actively participates in O-O bond formation and is continuously refilled by water-derived species.
View Article and Find Full Text PDFNeuropsychiatr Dis Treat
August 2025
Geriatric Medicine Department II, Qingdao Mental Health Center, Qingdao, Shandong, People's Republic of China.
Purpose: Previous studies have shown that serum uric acid (UA) levels are significantly higher in patients with bipolar disorder (BD) than in patients with depressive disorder (DD), schizophrenia, and healthy controls. Currently, studies generally report that there is a complex bidirectional interaction between mood disorders (MD) and hyperuricemia (HUA). We investigated the prevalence and related factors of hyperuricemia in Chinese patients with mood disorders to find out potential mechanisms and build a predictive model.
View Article and Find Full Text PDFACS Nano
September 2025
Key Laboratory of Applied Surface and Colloid Chemistry (Ministry of Education), School of Chemistry and Chemical Engineering, Shaanxi Normal University, Xi'an 710119, P. R. China.
Transition metal chalcogenides (TMCs) have garnered significant attention as high-capacity anode materials, yet the unconventional role of the Cu collector meditating atomic-level substitution of metal-site cations by Cu ions during electrochemical cycling remains mechanistically unclear. To address this, herein, Cu-doped MoSe@C ultrathin nanosheets were synthesized via the solvothermal process and carbonization strategies. A systematic investigation was conducted to elucidate the underlying driving forces for Cu substitution at Mo sites and the crucial regulatory effects of solid electrolyte interphase (SEI) formation.
View Article and Find Full Text PDFMater Horiz
September 2025
New Cornerstone Science Laboratory, State Key Laboratory for Physical Chemistry of Solid Surfaces, Collaborative Innovation Center of Chemistry for Energy Materials, and College of Chemistry and Chemical Engineering, Xiamen University, Xiamen, 361005, China.
Dispersing iridium onto high-specific-surface-area supports is a widely adopted strategy to maximize iridium utilization in anode catalysts of proton exchange membrane water electrolysis (PEMWE). However, here we demonstrate that the overall cell performance, including initial efficiency and long-term stability, does not benefit from the typical high specific surface area of catalyst supports. The conventional understanding that high iridium utilization on high-specific-surface-area supports increases activity holds only in aqueous electrolytes, while under the typical working conditions of PEMWE, the mass transport within the anode catalyst layers plays a more significant role in the overall performance.
View Article and Find Full Text PDFMater Horiz
September 2025
Faculty of Science, School of Chemistry and Physics, Queensland University of Technology (QUT), Brisbane, QLD 4000, Australia.
Organic electrochemical transistors (OECTs) continue to be the subject of much detailed and systematic study, being suitable for a diverse range of applications including bioelectronics, sensors, and neuromorphic computing. OECTs conventionally use a liquid electrolyte, and this architecture is well suited for sensing or bio-interfacing applications where biofluids or liquid samples can be used directly as the electrolyte. A more recent trend is solid-state OECTs, where a solid or semi-solid electrolyte such as an ion gel, hydrogel or polyelectrolyte replaces the liquid component for an all-solid-state device.
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