A novel electrochemical sensor with NiSx@MoS2 composite for efficient NO2- sensing.

Excess nitrites are potentially threatening to human health, so it is urgent to develop accurate and sensitive methods. The development of sensors can provide early warning of possible hazards and alert people to protect public health. This work presents an NiSx@MoS2-composite with excellent electrochemical activity, representing a key finding for highly sensitive NO2- detection and sensor development. With the assistance of NiSx@MoS2, this electrochemical sensor has excellent quantitative detection performance. It has a wide detection range (0.0001-0.0020 mg/mL) and a low detection limit (1.863*10-5 mg/mL) for NO2-. This electrochemical sensor maintains excellent specificity among numerous interferences, and it completes the accurate detection of different real food samples. Pleasingly, the electrochemical sensor has satisfactory repeatability stability, and potential for practical applications. It would demonstrate tremendous potential in scientific dietary guidance, food safety detection and other fields.

In situ growth of iron incorporated Ni3S2 nanosheet on nickel foam in mediating electron transfer to peroxymonosulfate for pollutant abatement.

Catalytic oxidation of organic pollutants is a well-known and effective technique for pollutant abatement. Unfortunately, this method is significantly hindered in practical applications by the low efficiency and difficult recovery of the catalysts in a powdery form. Herein, a three-dimensional (3D) framework of Fe-incorporated Ni3S2 nanosheets in-situ grown on Ni foam (Fe-Ni3S2@NF) was fabricated by a facile two-step hydrothermal process and applied to trigger peroxymonosulfate (PMS) oxidation of organic compounds in water. A homogeneous growth environment enabled the uniform and scalable growth of Fe-Ni3S2 nanosheets on the Ni foam. Fe-Ni3S2@NF possessed outstanding activity and durability in activating PMS, as it effectively facilitated electron transfer from organic pollutants to PMS. Fe-Ni3S2@NF initially supplied electrons to PMS, causing the catalyst to undergo oxidation, and subsequently accepted electrons from organic compounds, returning to its initial state. The introduction of Fe into the Ni3S2 lattice enhanced electrical conductivity, promoting mediated electron transfer between PMS and organic compounds. The 3D conductive Ni foam provided an ideal platform for the nucleation and growth of Fe-Ni3S2, accelerating pollutant abatement due to its porous structure and high conductivity. Furthermore, its monolithic nature simplified the catalyst recycling process. A continuous flow packed-bed reactor by encapsulating Fe-Ni3S2@NF catalyst achieved complete pollutant abatement with continuous operation for 240 h, highlighting its immense potential for practical environmental remediation. This study presents a facile synthesis method for creating a novel type of monolithic catalyst with high activity and durability for decontamination through Fenton-like processes.

Co-doped cryptomelane-type manganese oxide in situ grown on a nickel foam substrate for high humidity ozone decomposition.

Monolithic catalysts with excellent O3 catalytic decomposition performance were prepared by in situ loading of Co-doped KMn8O16 on the surface of nickel foam. The triple-layer structure with Co-doped KMn8O16/Ni6MnO8/Ni foam was grown spontaneously on the surface of nickel foam by tuning the molar ratio of KMnO4 to Co(NO3)2·6H2O precursors. Importantly, the formed Ni6MnO8 structure between KMn8O16 and nickel foam during in situ synthesis process effectively protected nickel foam from further etching, which significantly enhanced the reaction stability of catalyst. The optimum amount of Co doping in KMn8O16 was available when the molar ratio of Mn to Co species in the precursor solution was 2:1. And the Mn2Co1 catalyst had abundant oxygen vacancies and excellent hydrophobicity, thus creating outstanding O3 decomposition activity. The O3 conversion under dry conditions and relative humidity of 65%, 90% over a period of 5 hr was 100%, 94% and 80% with the space velocity of 28,000 hr-1, respectively. The in situ constructed Co-doped KMn8O16/Ni foam catalyst showed the advantages of low price and gradual applicability of the preparation process, which provided an opportunity for the design of monolithic catalyst for O3 catalytic decomposition.

Health risk assessment of bread wheat grown under cadmium and nickel stress and impact of silicic acid application on its growth, physiology, and metal uptake.

Heavy metal stress poses a significant threat to the productivity of agricultural systems and human health. Silicon (Si) is widely reported to be very effective against the different heavy metal stresses in crops. According to reports, it can help plants that are under cadmium (Cd) and nickel (Ni) stress. The presented work investigated how silicon interacted in Cd- and Ni-stressed wheat and mitigated metal toxicity. A pot experiment was carried out in which wheat crop was irrigated with Cd- and Ni-contaminated water. Application of Cd and Ni-contaminated water to wheat significantly reduced the root and shoot growth parameters and physiological and biochemical factors while increasing the antioxidant enzymatic activity and bioaccumulation of Cd and Ni metal in shoot and root as compared to the control. Application of Si led to an improvement in physiological parameters, i.e., greenness of leaves, i.e., SPAD values (17% and 26%), membrane stability (26% and 25%), and growth parameters i.e., root surface area (42% and 23%), root length (81% and 79%), root dry weight (456% and 190%), root volume (64% and 32%), shoot length (41% and 35%), shoot dry weight of shoot (111% and 117%), and overall grain weight (62% and 72%) under Cd and Ni stress, respectively. It increased the activity of antioxidant activity (max. up to 20%) whereas decreased the metal bioaccumulation of Cd and Ni in the roots and shoot (max. up to 62%) of wheat. It was concluded that the application of Si potentially increases antioxidant activity and metal chelation resulting in decreased oxidative damage and reducing the effect of Cd and Ni stress on wheat which improves growth and physiological parameters as well as inhibits Cd and Ni inclusion in food chain under Cd and Ni toxicity reducing health risks associated with these metals.

Lignocellulosic materials extraction from waste baby diaper to prepare light-responsive metal oxide/carbon composite for efficient organic dye pollutant removal.

The bimetal oxide comprising nickel incorporated ß-Bi2O3 on graphitic carbon in the form of bismuth nickel oxide (BNO@C) was prepared by waste lignocellulosic materials collected from cheap and readily available baby diapers. The prepared BNO@C was used to photocatalytically degrade methylene blue under UV-light irradiation. Prior to the photocatalytic performance analysis, the formation of BNO@C was confirmed by various morphological and structural analysis including SEM, TEM, XRD, and XPS analyses. As a result, the two-dimensional nanosheet morphology and tetragonal primitive lattice-structure with 2+ and 3+ oxidation stated Ni and Bi in BNO@C structural formulation were confirmed. In photocatalysis experimentation examined with BNO@C, the maximum methylene blue removal percentage of 96.7 % was achieved within 16 min. The influence of Ni2+ in BNO@C was identified by performing the photocatalytic performance of bare NiO@C and Bi2O3@C, yielding maximum dye removal of 32.8 % and 64.5 %, respectively. The efficacy of Ni in BNO@C toward increasing catalytic efficiency was identified using DFT analysis, revealing the acting of Ni as active sites for improved light absorption tendency. These findings show a novel strategy to prepare a low-cost BNO@C catalyst with efficient photocatalytic activity, opening a new path for a cost-efficient wastewater treatment approach.

Intraperitoneal hepatorenal toxicity of zinc oxide and nickel oxide nanoparticles in rats: a systematic review.

Zinc oxide (ZnO) and nickel oxide (NiO) nanoparticles (NPs) are widely used in various industries due to their distinctive physico-chemical and biological properties. However, concerns have been raised about their potential toxicity in humans. While many studies have reviewed their effects on visceral organs upon ingestion, inhalation, or skin contact, limited reviews are available regarding their adverse consequences on the liver and kidneys resulting from intraperitoneal administration in rats. Hence, this systematic review is the first to uniquely address this issue. A systematic search was performed on PubMed and Google scholar to identify articles that explored the toxic effects of ZnO-NPs and NiO-NPs in rats following intraperitoneal injection. The quality of the articles was assessed using SYCLE's risk of bias tool, leading to the selection of 16 articles; 14 for ZnO-NPs, 1 for NiO-NPs and 1 for both NPs. This review revealed that ZnO-NPs induces an acute toxicity in liver and kidney that is dose dependent. The impairments were marked by changes in organs functional markers, lipid and glucose levels and antioxidant deficiencies and lipid peroxidation. NiO-NPs also showed considerable toxicity, despite the limited studies. Further, variability of physico-chemical properties among studies complicated the toxicity assessment. To conclude, this study provides a novel contribution by summarizing the literature findings that suggest potential adverse intraperitoneal hepatorenal toxic outcomes associated with ZnO-NPs and NiO-NPs. Future research should focus on long-term effects and standardizing protocols to ensure the safe use of ZnO-NPs and NiO-NPs in industrial and clinical practices.

Stereoselective Vinylic C-H Addition via Metallaphotoredox Migration.

Geometrically defined allylic alcohols with SE, SZ, RE and RZ stereoisomers serve as valuable intermediates in synthetic chemistry, attributed to the stereoselective transformations enabled by the alkenyl and hydroxyl functionalities. When an ideal scenario presents itself with four distinct stereoisomers as potential products, the simultaneous control vicinal stereochemistry in a single step would offer a direct pathway to any desired stereoisomer. Here, we unveil a metallaphotoredox migration strategy to access stereodefined allylic alcohols through vinylic C-H activation with aldehydes. This method harnesses a chiral nickel catalyst in concert with a photocatalyst to enable a 1,4-Ni migration by using readily accessible 2-vinyl iodoarenes as starting materials. The efficacy of this methodology is highlighted by the precise construction of all stereoisomers of allylic alcohols bearing analogous substituents and the efficient synthesis of key intermediates en route to Myristinin family. Experimental and computational studies have shed light on pivotal aspects including the synergy of metal catalysis and photocatalysis, the driving forces behind the migration, and the determination of absolute configuration in the C-H addition process.

Revealing Gliding-Induced Structural Distortion in High-Nickel Layered Oxide Cathodes for Lithium-Ion Batteries.

After charging to a high state-of-charge (SoC), layered oxide cathodes exhibit high capacities but suffer from gliding-induced structural distortions caused by deep Li depletion within alkali metal (AM) layers, especially for high-nickel candidates. In this study, we identify the essential structure of the detrimental H3 phase formed at high SoC to be an intergrowth structure characterized by random sequences of the O3 and O1 slabs, where the O3 slabs represent Li-rich layers and the O1 slabs denote Li-depleted (or empty) layers that glide from the O3 slabs. Moreover, we adopt two doping strategies targeting different doping sites to eliminate the formation of Li-vacant O1 slabs. First, we introduce direct transition metal (TM) pillars between TMO2 slabs achieved through dopants (e.g., Nb) positioned within AM layers, significantly improving the cycling stability. Second, we introduce indirect Li pillars achieved through dopants located at TM layers to adjust the Li-O bond strength. While this strategy can regulate the uniformity of Li at the slab level, it results in an uneven Li distribution at the particle scale, ultimately failing to enhance the electrochemical performance. Our established research strategy facilitates the realization of diverse pillars between TMO2 slabs through doping, thereby offering guidance for stabilizing high-capacity layered oxide cathodes at high SoC.

Enantioselective Construction of Oxindoles Bearing a Quaternary Carbon via Ni-Al Bimetal-Catalyzed Formyl C-H Alkylation.

Enantioselective transition metal-catalyzed C-H alkylation emerges as one of the most atom- and step-economical routes to chiral quaternary carbons, while big challenges still remain with acyl C-H alkylations. Herein, we use a Ni-Al bimetallic catalyst to facilitate a highly regioselective and highly enantioselective C-H alkylation of formamides with alkenes, constructing various oxindoles bearing a chiral quaternary carbon in up to 94% yield and up to 95% ee.

Biology-Based Synthesis of Nickel Single Atoms on the Surface of Geobacter sulfurreducens as an Efficient Electrocatalyst for Alkaline Water Electrolysis.

Single-atom metal catalysts are promising electrocatalysts for water electrolysis. Nickel-based electrocatalysts have shown attractive application prospects for water electrolysis. However, synthesizing stable Ni single atoms using chemical and physical approaches remains a practical challenge. Here, a facile and precise method for synthesizing stable nickel single atoms on the surface of Geobacter sulfurreducens using a microbial-mediated extracellular electron transfer (EET) process is demonstrated. It is shown that G. sulfurreducens can effectively anchor nickel single atoms on their surface. X-ray absorption near-edge structure and Fourier-transformed extended X-ray absorption fine structure spectroscopy confirm that the nickel single atom is coordinated to nitrogen in the cytochromes. The as-synthesized nickel single atoms on G. sulfurreducens exhibit excellent bifunctional catalytic properties for alkaline water electrolysis with low overpotential (η) to achieve current density (10 mA cm-2) for both hydrogen evolution reactions (η = 80 mV) and oxygen evolution reaction (η = 330 mV) with minimal catalyst loading of 0.0015 mg Ni cm-2. The nickel single-atom catalyst shows long-term stability at a constant electrode potential. This synthesis method based on the EET capability of electroactive bacteria provides a simple and scalable approach for producing low-cost and highly efficient nonnoble transition metal single-atom catalysts for practical applications.

Facile Combination of Bismuth Vanadate with Nickel Tellurium Oxide for Efficient Photoelectrochemical Catalysis of Water Oxidation Reactions.

Bismuth vanadate (BVO) having suitable band edges is one of the effective photocatalysts for water oxidation, which is the rate-determining step in the water splitting process. Incorporating cocatalysts can reduce activation energy, create hole sinks, and improve photocatalytic ability of BVO. In this work, the visible light active nickel tellurium oxide (NTO) is used as the cocatalyst on the BVO photoanode to improve photocatalytic properties. Different NTO amounts are deposited on the BVO to balance optical and electrical contributions. Higher visible light absorbance and effective charge cascades are developed in the NTO and BVO composite (NTO/BVO). The highest photocurrent density of 6.05 mA/cm2 at 1.23 V versus reversible hydrogen electrode (VRHE) and the largest applied bias photon-to-current efficiency (ABPE) of 2.13% are achieved for NTO/BVO, while BVO shows a photocurrent density of 4.19 mA/cm2 at 1.23 VRHE and ABPE of 1.54%. Excellent long-term stability under light illumination is obtained for NTO/BVO with photocurrent retention of 91.31% after 10,000 s. The photoelectrochemical catalytic mechanism of NTO/BVO is also proposed based on measured band structures and possible interactions between NTO and BVO. This work has depicted a novel cocatalytic BVO system with a new photocharging material and successfully achieves high photocurrent densities for catalyzing water oxidation.

Effects of Coprecipitation Conditions on the Electrochemical Properties of Cobalt-Free LiNi0.9Mn0.1-xAlxO2 Cathodes.

Commercializing high-nickel, cobalt-free cathodes, such as LiNi0.9Mn0.1-xAlxO2 (NMA-90), hinges on effectively incorporating Al3+ during the hydroxide coprecipitation reaction. However, Al3+ coprecipitation is nontrivial as Al3+ possesses unique precipitation properties compared to Ni2+ and Mn2+, which impact the final precursor morphology and consequently the cathode properties. In this study, the nuance of Al3+ coprecipitation and its influence on the cycling stability of NMA with increasing Al3+ content is elucidated. While low reaction pH and ammonia concentration are suitable for producing Al-free LiNi0.9Mn0.1O2 (NM-90) effectively, the same coprecipitation environment leads to porous precursor morphology and poor cycle life in Al-containing LiNi0.9Mn0.08Al0.02O2 (NMA-900802) and LiNi0.9Mn0.05Al0.05O2 (NMA-900505). By systematically increasing the reaction pH and ammonia concentration for the Al-containing compositions, the precursor morphology becomes denser and the cathode cycling stability is greatly improved. It is hypothesized that the improvement in cycling stability stems from the reduction in Al(OH)3 nucleation, which promotes hydroxide particle growth with optimal Al3+ incorporation into the cathode lattice.

Size-dependent Curie temperature of Ni nanoparticles from spin-lattice dynamics simulations.

The magnetic properties of Ni nanoparticles (NPs) with diameter D are investigated using spin-lattice dynamics (SLD) simulations. Using exchange interactions fitted to ab-initio results we obtain a Curie temperature, T c , similar, but lower, than experiments. In order to reproduce quantitatively the bulk Curie temperature and the experimental results, the exchange energy has to be increased by 25% compared to the ab-initio value. During the simulated time, Ni NPs remain ferromagnetic down to the smallest sizes investigated here, containing around 500 atoms. The average magnetic moment of the NPs is slightly smaller than that determined experimentally. By considering a core-shell model for NPs, in which the shell atoms are assigned a larger magnetic moment, this discrepancy can be removed. T c is lower for a moving lattice than for a frozen lattice, as expected, but this difference decreases with NP size because smaller NPs include higher surface disorder which dominates the transition. For NPs, T c decreases with the NP diameter D by at most 10% at D = 2  nm, in agreement with several experiments, and unlike some modeling or theoretical scaling results which predict a considerably larger decrease. The decrease of T c is well described by finite-size scaling models, with a critical exponent that depends on the SLD settings for a frozen or moving lattice, and also depends on the procedure for determining T c . Extrapolating the inverse of the magnetization as function of temperature near T c gives a lower T c than the maximum of the susceptibility.

Dinuclear Cyclometalated Pincer Nickel(II) Complexes with Metal-Metal-to-Ligand Charge Transfer Excited States and Near-Infrared Emission.

Facile non-radiative decay of low-lying metal-centered (MC) d-d excited states has been well documented to pose a significant obstacle to the development of phosphorescent NiII complexes due to substantial structural distortions between the d-d excited state and the ground state. Herein, we prepared a series of dinuclear Ni2II,II complexes by using strong σ-donors, carbene-phenyl-carbene (CNHC^Cphenyl^CNHC) pincer ligands, and prepared their dinuclear Pt2II,II and Pd2II,II analogues. Dinuclear Ni2II,II complexes bridged by formamidinate/α-carbolinato ligand exhibit short Ni-Ni distances of 2.947-3.054 Å and singlet metal-metal-to-ligand charge transfer (1MMLCT) transitions at 500-550 nm. Their 1MMLCT absorption energies are red-shifted relative to the Pt2II,II and Pd2II,II analogues at ~450 nm and ≤420 nm respectively. One-electron oxidation of these Ni2II,II complexes produces valence-trapped dinuclear Ni2II,III species, which are characterized by EPR spectroscopy. Upon photoexcitation, these Ni2II,II complexes display phosphorescence (τ=2.6-8.6 µs) in the NIR (800-1400nm) spectral region in 2-MeTHF and in solid state at 77 K, which is insensitive to π-conjugation of the coordinated [CNHC^Cphenyl^CNHC] ligand. Combined with DFT calculations, the NIR emission is assigned to originate from the 3dd excited state. Studies have found that the dinuclear Ni2II,II complex can sensitize the formation of singlet oxygen and catalyze the oxidation of cyclo-dienes under light irradiation.

Sulfate salt assistant fabrication of Fe-doped Ni2P modified with SO42-/carbon as highly efficient oxygen evolution reaction electrocatalyst.

The incorporation of oxyanion groups offers a greater potential for enhancing the activity of oxygen evolution reaction (OER) electrocatalysts compared to traditional metal cations doping, owing to their unique configurations and high electronegativity. However, the incorporation of oxyanion groups that differ from those derived from the oxidation of anions in transition metal monoxides poses significant challenges, thereby limiting further applications of oxyanion group modification approach. Herein, we present a novel sulfate salt assistant approach to fabricate Fe-doped Ni2P modified with SO42-/carbon (Fe-Ni2P-S/C) nanofibers as highly efficient OER electrocatalyst. The optimized Fe-Ni2P-S/C nanofibers display superb OER activity, requiring low overpotentials of 266, 323, and 357 mV at 100, 500, and 1000 mA cm-2, respectively. Theoretical calculations reveal that the co-adsorption of PO43- and SO42- on the surface of reconstructed electrocatalyst can reduce the energy barrier of rate-determining step, thereby resulting in enhanced OER activity. The present study emphasizes the crucial role played by anion groups in OER activity as well as proposes a novel approach for incorporating anion groups into electrocatalysts.

Colloidal Bimetallic RuNi Particles and their Behaviour in Catalytic Quinoline Hydrogenation.

Colloidal metal nanoparticles exhibit interesting catalytic properties for the hydrogenation of (hetero)arenes. Catalysts based on precious metals, such as Ru and Rh, proceed efficiently under mild reaction conditions. In contrast, heterogeneous catalysts based on earth-abundant metals can selectively hydrogenate (hetero)arenes but require harsher reaction conditions. Bimetallic catalysts that combine precious and earth-abundant metals are interesting materials to mitigate the drawbacks of each component. To this end, RuNi nanoparticles bearing a phosphine ligand were prepared through the decomposition of [Ru(η4-C8H12)(η6-C8H10)] and [Ni(η4-C8H12)2] by H2 at 85°C. Wide angle X-ray scattering confirmed a bimetallic segregated structure, with Ni predominantly on the surface. Spectroscopic analyses revealed that the phosphine ligand coordinated to the surface of both metals, suggesting, as well, a partial Ni shell covering the Ru core. The RuNi-based nanomaterials were used as catalysts in the hydrogenation of quinoline to assess the impact of the metallic composition and of the stabilizing agent on their catalytic performance.

Co-based metal-organic frameworks for enhanced nickel adsorption and its impact on nitrifying microbial activity.

The release of nickel "Ni(II)" into aquatic environments is of great concern because of environmental and health issues. Metal-organic frameworks (MOFs) are one of the most promising technologies for removing heavy metals from water. In this work, an octahedral Co-based MOF (Co-MOF) was synthesized with a high Ni(II) removal capacity (qmax of 1534.09 ± 45.49 mg g-1) in aqueous media. For the first time, the effect of Co-MOF alone and in co-exposure with Ni(II) on nitrifying microbial consortium was assessed using dynamic microrespirometry. A single concentration of Co-MOF had no significant effects on nitrifying microbial consortium, while the concentration of Ni(II) exerted non-competitive inhibition on the nitrifying microbial consortium with an IC50 of 1.67 ± 0.03 mg L-1. In addition, the theoretical speciation analysis showed a decrease of 40% of IC50 when the free Ni(II) concentration was considered. Co-exposure of Co-MOF and Ni(II) during the nitrifying process allowed us to conclude that Co-MOF is an effective adsorbent for Ni(II) and can be used to mitigate the inhibitory effects of nickel on nitrifying microbial consortia, which is crucial for maintaining the good operation of wastewater treatment and balance of nitrogen cycle.

Nickel release from 316L stainless steel following a Ni-free electroplating cycle.

Electroplating can induce nickel release even from 316L stainless steel, typically considered safe. In this work, the influence of different electroplating processes and surface treatments on nickel release was evaluated. The nickel release was tested according to the EN 1811 standard. The impact of surface roughness on nickel release was assessed by comparing polished and unpolished samples. Results indicate that internal stresses can worsen nickel release, while increasing the thickness of the precious metal layer is beneficial. To corroborate our hypothesis, it was verified that coatings obtained through physical vapor deposition (PVD), without removing the passivation layer of the steel, did not release nickel. For these reasons, we identified the main cause of nickel release as the combined effect of the removal of the passivation layer of stainless steel and the microporosity of the electroplating process.

The Mediating Role of Abnormal ZEB1 Methylation in the Association between Nickel Exposure and Non-Syndromic Orofacial Cleft.

Our previous study found a positive relationship between fetal nickel exposure and the risk of OFCs. The teratogenic mechanism of nickel is not clear. In this study, we aim to examine the mediating effect of DNA methylation on the association of nickel(Ni) exposure with NSOFC in fetuses. 10 cases and 10 controls was used for screening target gene by Illumina Infinium Methylation EPIC(850k) BeadChip. 36 cases and 78 controls was conducted to determine DNA methylation level of selected gene in umbilical cord blood by Mass spectrometry assay. Mediation analysis was used to evaluate the potential mediating effect of selected gene methylation on the relation between concentrations of Ni and the risk for NSOFC. In the discovery stage, ZEB1 gene was identified to be hypermethylated in both nickel exposure and NSOFC group for validation. In the verification stage, the overall average methylation level of ZEB1 was significant higher in NSOFC cases(median=8.70, interquartile range(IQR): 5.75-11.53) as compared to controls (median=5.35, IQR: 4.30-7.78). The risk for NSOFC was increased by 1.43-fold with hypermethylation of ZEB1. Significant correlation was observed between concentrations of Ni in umbilical cord and methylation level of ZEB1. The hypermethylation of ZEB1 had a mediating effect by 20.47% of total effect of Ni on NSOFC risk. Hypermethylation of ZEB1 is associated with the risk for NSOFC and may partially explain the association between Ni exposure and NSOFC risk. Our findings provide new insights into the epigenetic mechanisms underlying NSOFC and suggesting potential targets for future therapeutic interventions.

A Comprehensive Review of Functional Gel Polymer Electrolytes and Applications in Lithium-Ion Battery.

The rapid expansion of flexible and wearable electronics has necessitated a focus on ensuring their safety and operational reliability. Gel polymer electrolytes (GPEs) have become preferred alternatives to traditional liquid electrolytes, offering enhanced safety features and adaptability to the design requirements of flexible lithium-ion batteries. This review provides a comprehensive and critical overview of recent advancements in GPE technology, highlighting significant improvements in its physicochemical properties, which contribute to superior long-term cycling stability and high-rate capacity compared with traditional organic liquid electrolytes. Special attention is given to the development of smart GPEs endowed with advanced functionalities such as self-protection, thermotolerance, and self-healing properties, which further enhance battery safety and reliability. This review also critically examines the application of GPEs in high-energy cathode materials, including lithium nickel cobalt manganese (NCM), lithium nickel cobalt aluminum (NCA), and thermally stable lithium iron phosphate (LiFePO4). Despite the advancements, several challenges in GPE development remain unresolved, such as improving ionic conductivity at low temperatures and ensuring mechanical integrity and interfacial compatibility. This review concludes by outlining future research directions and the remaining technical hurdles, providing valuable insights to guide ongoing and future efforts in the field of GPEs for lithium-ion batteries, with a particular emphasis on applications in high-energy and thermally stable cathodes.