Short process for Li2CO3 synthesis and spent LiCoO2 remediation via Glycine-LiOH slurry electrolysis DOI
Ling Hu, Jiancheng Shu,

Yunhui Han

и другие.

Separation and Purification Technology, Год журнала: 2024, Номер 357, С. 129986 - 129986

Опубликована: Окт. 5, 2024

Язык: Английский

Electrochemical reactivity of PZT materials in Li-ion and Na-ion batteries DOI Creative Commons
M. Taha Demirkan, Mehbare Doğrusöz

Discover Electrochemistry., Год журнала: 2025, Номер 2(1)

Опубликована: Март 31, 2025

Язык: Английский

Процитировано

1

Electrochemical Self‐Assembly of Boron‐Based Cathode‐Electrolyte Interphase to Stabilize 4.65 V LiCoO2 DOI

Hengyu Ren,

Xiaohu Wang, Wangyang Ding

и другие.

Advanced Functional Materials, Год журнала: 2025, Номер unknown

Опубликована: Апрель 26, 2025

Abstract The cathode‐electrolyte interphase (CEI) is vital for the stability of LiCoO 2 (LCO) beyond 4.55 V (vs Li/Li + ). Herein, full coverage boron‐based CEI achieved on LCO surface via utilizing self‐wetting synthesis boric acid (i.e., B‐LCO), accompanying with subsequent electrochemical self‐assembly process upon cycles. Initially, B‐LCO coated borate deposits (size 10–20 nm), then it melts and fully covers sintering, leading to artificial CEI, which directly reduces side reactions induced by highly oxidative Co 4+ /O n− (0 < n 2). Significantly, during cycling, in situ interfacial between species LiF promote formation crystalline LiB 6 O 9 F components, showing mechanically robust Li conductive characteristics. Due synergism structurally tough rocksalt (RS) phase, not only more reversible phase transition uniform (de)lithiation are achieved, but also particle cracks deterioration issues effectively inhibited. As a result, B‐LCO||Li cells show excellent cycle stability, high retention 84.0% 500 cycles 3–4.65 V.

Язык: Английский

Процитировано

1

Reversible Configurations of 3‐Coordinate and 4‐Coordinate Boron Stabilize Ultrahigh‐Ni Cathodes with Superior Cycling Stability for Practical Li‐Ion Batteries DOI
Haifeng Yu, Cheng Jin, Huawei Zhu

и другие.

Advanced Materials, Год журнала: 2024, Номер unknown

Опубликована: Окт. 30, 2024

Abstract Ultrahigh‐Ni layered oxide cathodes are the leading candidate for next‐generation high‐energy Li‐ion batteries owing to their cost‐effectiveness and ultrahigh capacity. However, increased Ni content causes larger volume variations worse lattice oxygen stability during cycling, resulting in capacity attenuation kinetics hysteresis. Herein, a Li 2 SiO 3 ‐coated Li(Ni 0.95 Co 0.04 Mn 0.01 ) 0.99 B O ultrahigh‐Ni cathode that well‐addresses all above issues, which is also first time realize real doping of ions demonstrated. The as‐obtained delivers reversible up 237.4 mAh g −1 (924 Wh kg superior retention 84.2% after 500 cycles at 1C pouch‐type full‐cells. Advanced characterizations calculations verify boron‐doping existed terms 3‐coordinate 4‐coordinate configurations high electrochemical reversibility de‐/lithiation, greatly stabilizes anions impedes Ni‐ion migration layer. Furthermore, B‐doping engineers primary particle microstructure better relaxing strain accelerating diffusion. This work advances energy density materials into domain 900 , concept will inspire more intensive study on cathodes.

Язык: Английский

Процитировано

9

In Situ Interphasial Engineering Enabling High‐Rate and Long‐Cycling Li Metal Batteries DOI Creative Commons
Chenrui Li, Chengwei Yang,

Tianrun Huang

и другие.

Advanced Functional Materials, Год журнала: 2024, Номер unknown

Опубликована: Июнь 10, 2024

Abstract The practical implementation of Li metal anode has long been hindered by the significant challenges notorious dendritic growth and severe interphase instability during repeated cycling. Herein, a highly lithiophilic NiSe‐modified host rationally constructed to stabilize facile mechanical rolling strategy. in situ configurated high‐flux 2 Se‐enriched layer can facilitate fast interfacial charge transfer, high plating/stripping reversibility homogeneous nucleation/growth. Consequently, achieved modified demonstrates ultrahigh rate capability (10 mA cm −2 ) ultralong‐term cycling stability (6600 cycles) with dendrite‐free deposition. Li|LiFePO 4 (LFP) cell exhibits an extraordinarily lifespan over 500 cycles ultra‐low decay only ≈0.0092% per cycle at 1 C. Furthermore, 4.5 V high‐voltage Li|LiCoO pouch areal capacity (≈1.9 mAh still reveals impressively prolonged cyclability 200 even under harsh test condition low negative‐to‐positive‐capacity (N/P) ratio ≈3.4 lean electrolyte ≈5.5 µL −1 . This work provides scalable strategy toward stable for reliable usage.

Язык: Английский

Процитировано

7

Compositional Gradient Design of Ni-Rich Co-Poor Cathodes Enhanced Cyclability and Safety in High-Voltage Li-Ion Batteries DOI

Wenshuai Guo,

Haifeng Yu, Min Wang

и другие.

ACS Nano, Год журнала: 2025, Номер unknown

Опубликована: Фев. 20, 2025

Developing cost-effective high-voltage Ni-rich cathodes has reached a consensus to replace conventional ultrahigh Ni counterparts for high-energy Li-ion batteries, but more rigorous requirements are put forward their mechanical and chemical stability. Herein, we report the design synthesis of full concentration gradient LiNi0.75Mn0.20Co0.05O2 cathode with Mn-rich Ni-poor surface, which been realized by in situ forming PO43- distribution retard transition-metal ions' interdiffusion during high-temperature lithiation process. This mitigates stress at source high morphological integrity refrains lattice oxygen loss under 4.5 V operation. After Li0.1B0.967PO4 is coated, surface parasitic reactions further ameliorated stable interface chemistry. The resultant deliver reversible capacity as 212.6 mAh g-1 2.7-4.5 an energy density >800 Wh kg-1cathode, almost equivalent state-of-the-art Ni-content 90% 2.7-4.3 V. In commercial-grade cells, superior cycle life 80.5% retention achieved 1C within after 1700 cycles, exhibiting promising opportunities compositional cathodes.

Язык: Английский

Процитировано

1

High Rate Performance of Single‐Crystalline NCM Upcycled from Spent Lithium‐Ion Batteries Via Direct Recovery and Modification DOI Open Access

Kaipei Wang,

Hao Zhang,

Wentao Dou

и другие.

Advanced Functional Materials, Год журнала: 2024, Номер unknown

Опубликована: Дек. 17, 2024

Abstract The global expansion of spent lithium‐ion batteries (LIBs) presents both an urgent environmental issue and a significant economic opportunity, driving the development diverse recycling processes worldwide. Direct regeneration is promising method for recovering materials from LIBs. However, most existing direct methods focus solely on cathodes without addressing further improvements in their performance. Herein, reported to upcycle single‐crystalline lithium nickel manganese cobalt oxides (NCM) polycrystalline NCM based facile phosphoric acid etching approach. Moreover, Li 3 PO 4 coating 3− polyanion doping are simultaneously achieved surface single‐crystal during upcycling process. enlarged lattice spacing fast ionic conductor layer enhance + diffusion mitigate phase transformations delithiation/lithiation. Benefiting synergistic effect single crystal structure modification, upcycled LiNi 0.65 Co 0.2 Mn 0.15 O 2 demonstrates excellent electrochemical performances, including large reversible capacity (≈186 mAh g −1 at 0.1C), high‐rate capability (≈142 10C), cycling stability (≈99% retention 100 cycles). This approach provides novel effective pathway transform LIBs into value‐added cathode materials, achieving win–win situation protection resource conservation.

Язык: Английский

Процитировано

4

Enhanced Graphitization of CO2-Derived Carbon Anodes via Joule Heating Reformation for High-Performance Lithium-Ion Batteries DOI
Minghao Liu, Hao Shi, Lei Guo

и другие.

Carbon, Год журнала: 2024, Номер unknown, С. 119781 - 119781

Опубликована: Окт. 1, 2024

Язык: Английский

Процитировано

3

Unraveling Inherent Degradation Mechanism of Electrolyte at High-Voltage and the d2sp3 Hybridization Strategy for Non-Flammable 4.8 V LiCoO2 Battery DOI

Zhaoyu Sun,

Yuxuan Liu, Jiahe Chen

и другие.

Опубликована: Янв. 1, 2025

The potential risk of transition metal (TM) ion dissolution is a prevalent issue in nearly all layered oxide cathodes. While the detrimental effects this are widely discussed context cathode material design, implications for electrolyte design receive comparatively less attention. In fact, severe decomposition frequently occurs after TM ions. This phenomenon typically attributed to catalytic However, there lack research that clearly explains destabilization electrolyte. study delves into different interface behaviors between Co3+ and Li+. Near anode surface, significant proportion solvent molecules PF6- ions escape from Li+ solvation sheath, with only small portion contributing formation electrode/electrolyte interface. Subsequently, free reduced, interpolated or deposited anode. contrast, exhibit stronger binding ability than ions, leading challenges desolvation. sheaths demonstrate reduction instability, trapped must be reduced. order mitigate hazard dissolution, fluorinated cathode/electrolyte was applied inhibit Isobutyronitrile (IBN) used capture harmful electrolyte, resulting d2sp3 hybrid orbitals when IBN combines Co3+. stable chelated complex effectively eliminated associated sheaths. developed through hybridization strategy addresses dissolved Co, even 0.1M Co intentionally added LCO batteries utilizing an impressive increase capacity retention, rising 56.6% 84.5% 300 cycles at 4.7 V. Additionally, retention battery 73.3% 200 4.8

Язык: Английский

Процитировано

0

Enhanced electrochemical properties of hard carbon anode derived from phenolic resin modified via an oxygen-induced plasma surface treatment for lithium-ion batteries DOI
Wen-Dung Hsu,

Shivnath Babu,

Chien-Te Hsieh

и другие.

Surfaces and Interfaces, Год журнала: 2025, Номер unknown, С. 106282 - 106282

Опубликована: Март 1, 2025

Язык: Английский

Процитировано

0

Research progress on cathode materials for lithium-ion batteries DOI

Bao Yuanyuan,

Xiaoying Guo, Wei Li

и другие.

Journal of Solid State Electrochemistry, Год журнала: 2025, Номер unknown

Опубликована: Апрель 1, 2025

Язык: Английский

Процитировано

0