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JOURNAL OF SOLID STATE ELECTROCHEMISTRY · 2023 ·Vol. 27 ·期 5 ·1165-1175 · IF 2.5

A high-performance binder-free freestanding film anode constructed by Si/NC nanoparticles anchoring in 3D porous N-doped graphene-CNTs networks for Li-ion batteries

Liu Shuling,Zhang Wei,An Yiming,Li Ying,Wang Jie,Wang Chao

The Si-based flexible electrodes attracted increasing research interests owing to the growing demand for high-performance flexible energy storage devices. Herein, a facile and smart self-assembly strategy is adopted to address huge volume expansion and particle aggregation issues of Si-based anodes, and a high-performance freestanding film anode (NC@Si/CNTs/N-rGO) is synthesized. The 3D-crosslinked porous graphene-CNTs networks offer abundant electric conductive pathways, high active sites, large internal space to accommodate the expansion of Si NPs, and facilitate Li + diffusion and insertion/extraction kinetics. The synergistic effect between the well-dispersed Si/NC nanoparticles and 3D porous networks significantly enhances electrochemical performance of Si NPs. The as-prepared NC@Si/CNTs/N-rGO electrode exhibits a high reversible specific capacity of 1089 mAh·g −1 at a charge–discharge current density of 1 A·g −1 after 500 cycles. Even at 2 A·g −1 , the electrode still exhibits an excellent reversible specific capacity of 606 mAh·g −1 after 300 cycles. These indicate that the NC@Si/CNTs/N-rGO is a promising candidate for high-performance flexible anode material in lithium-ion batteries.

研究领域: 材料科学 · 电化学 · 纳米科技 · 能源存储 · 先进电池技术
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ELECTROCHIMICA ACTA · 2019 · IF 5.383

V2(PO4)O encapsulated into crumpled nitrogen-doped graphene as a high-performance anode material for sodium-ion batteries

Bin Xiao,Wen-hai Zhang,Peng-bo Wang,Lin-bo Tang,Chang-sheng An,Zhen-jiang He,Hui Tong,Jun-chao Zheng,Bo Wang

Phosphate-based polyanion-structured materials have attracted considerable attention as anode materials in lithium-/sodium-ion batteries due to their stable crystal structure, affordability, and environmental friendliness. V 2 (PO 4 )O was encapsulated into crumpled nitrogen-doped graphene (VPO@N-G) through a facile spray-drying method in which VPO particles were completely encapsulated by N-doped graphene. For the first time, VPO@N-G was explored as an anode material for sodium-ion batteries. The Na + storage behavior of VPO@N-G was systematically investigated at the voltage range of 0.01–3.0 V (versus Na/Na + ). Results indicated that the VPO@N-G anode can deliver a highly reversible discharge capacity of 539 mAh g −1  at 0.05 A g −1 and achieve a highly reversible discharge capacity of 235.9 mAh g −1 even at a high current density of 10 A g −1 . Thus, VPO@N-G can be applied as a high-rate anode material for sodium-ion batteries.

研究领域: 材料科学 · 电化学 · 能源存储 · 纳米复合材料 · 无机功能材料
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ChemSusChem · 2019 ·Vol. 12 ·期 4 ·858-865 · IF 7.804

Pyridinic Nitrogen-Doped Graphene Nanoshells Boost the Catalytic Efficiency of Palladium Nanoparticles for the N-Allylation Reaction

Xinxin Li,Qingshan Zhao,Xiang Feng,Lei Pan,Zhuangzhuang Wu,Xiaocui Wu,Tianwen Ma,Jialiang Liu,Yuanyuan Pan,Yan Song,Mingbo Wu

Graphical Nitrogen-doped graphene nanoshells supporting palladium nanoparticles (Pd/N-GNS) have been developed as a superior catalyst for the N -allylation reaction. Experimental results and DFT calculations reveal strong metal–support interactions between the pyridinic N and palladium species, which significantly boost the catalytic efficiency and stability of the catalyst. In this study, nitrogen-doped graphene nanoshells (N-GNS) were developed to support palladium nanoparticles (Pd/N-GNS) as an efficient and recyclable catalyst for the N -allylation reaction. N-GNS was synthesized through a facile hard-template method by using petroleum asphalt, followed by nitrogen doping by thermal annealing with urea, the contents and species of which could be altered by the calcination temperature. Palladium nanoparticles (Pd NPs) with an average diameter of 3.3 nm were homogeneously deposited onto the N-GNS support through a mild solvent-growth approach. The Pd/N-GNS exhibited a superior activity towards the N -allylation reaction, 6-fold higher than that of the pristine graphene nanoshells supporting the palladium catalyst. The Pd/N-GNS could be recycled several times without activity deterioration and metal leaching. The catalytic activity showed a linear correlation relationship with the pyridinic N content. Experimental and theoretical studies reveal strong metal–support interactions between the pyridinic N and palladium species, which can downsize the Pd NPs, modulate the electronic properties, and promote the adsorption of reactant, thereby significantly boosting the catalytic efficiency and stability for the N -allylation process. The present work could help unravel the roles of nitrogen-doped carbon supports and provides a feasible strategy to rationally design superior palladium catalysts for chemical transformations.

研究领域: 材料科学 · 催化化学
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Small · 2023 ·Vol. 20 ·期 17 ·2308632 · IF 13.3

Stable Aluminum Metal Anode Enabled by Dual-Functional Molybdenum Nanoparticles

Shunlong Ju,Qing Qiao,Tian Xu,Zhongchen Zhao,Tengfei Zhang,Guanglin Xia,Xuebin Yu

Constructing robust anode with strong aluminophilicity and rapid desolvation kinetics is essential for achieving high utilization, long-term durability, and superior rate performance in Al metal-based energy storage, yet remains largely unexplored. Herein, molybdenum nanoparticles embedded onto nitrogen-doped graphene (Mo@NG) are designed and prepared as Al host to regulate the deposition behavior and achieve homogeneous Al plating/stripping. The monodispersed Mo nanoparticles reduce the desolvation energy barrier and promote the deposition kinetics of Al. Additionally, Mo nanoparticles act as aluminophilic nucleation sites to minimize the Al nucleation overpotential, further guiding uniform and dense Al deposition. As a result, the dual-functional Mo@NG endows Al anodes with low voltage hysteresis, reversible Al plating/stripping with high coulombic efficiency, and excellent high-rate capability under 5 mA cm −2 . Moreover, the as-designed Al metal full batteries deliver a high capacity retention of 92.8% after 3000 cycles at 1 A g −1 . This work provides an effective solution to optimize the electrochemical properties of Al metal anode from the perspective of desolvation and deposition reactions, towards the development of high-safety and long-cycling aluminum-ion batteries.

研究领域: 材料科学 · 电化学 · 能源存储 · 纳米技术 · 金属负极 · 电池化学 · 界面工程
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Nano Energy · 2019 · IF 15.548

Elevated polysulfide regulation by an ultralight all-CVD-built ReS2@N-Doped graphene heterostructure interlayer for lithium–sulfur batteries

Nan Wei,Jingsheng Cai,Ruochen Wang,Menglei Wang,Wei Lv,Haina Ci,Jingyu Sun,Zhongfan Liu

Lithium–sulfur battery is amongst the most promising next-generation energy storage technology owing to their high theoretical capacity and energy density . Nevertheless, the notorious shuttle effect of lithium polysulfides (LiPSs) seriously impedes its practical applications. Here, we report an all-CVD approach to realize the direct growth of ReS 2 @N-doped graphene (NG) heterostructure , which serves as an ultralight high-performance interlayer for elevated LiPS regulation via easy transfer onto the commercial separator. In contrast to the traditional interlayers constructed via vacuum filtration of nanostructured materials that inevitably increase the thickness and weight of the separator, our all-CVD-enabled ReS 2 @NG film possesses an area of 15 mm × 100 mm, a thickness of ~0.5 μm and a negligible areal weight of 80–90 μg cm −2 . Benefiting from the two-dimensional (2D) vertically-erected nanostructure , adsorptive ReS 2 -conductive NG interface, and favorable electrical conductivity , thus-derived ReS 2 @NG interlayer readily enhances reaction kinetics for LiPS conversion and boosts the reutilization of trapped LiPS whilst guaranteeing smooth transportation of lithium ions . Accordingly, an initial discharge capacity of 854 mAh g −1 with an average capacity decay of 0.064% per cycle after 800 cycles can be harvested at 2.0 C. Even at a high sulfur loading of 6.4 mg cm −2 , an initial areal capacity of 6.1 mAh cm −2 can be gained, which still retains 5.8 mAh cm −2 after 40 cycles at 0.1 C. This work is anticipated to shed light upon the construction of CVD-enabled versatile 2D heterostructures for enriching the interlayer design with multifunctionality and cost-effectiveness.

研究领域: 材料科学 · 电化学 · 能源存储 · 纳米材料 · 界面工程 · 电池技术
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ENVIRONMENTAL SCIENCE AND POLLUTION RESEARCH · 2024 ·Vol. 31 ·期 32 ·44759-44769 · IF 0

Fabrication of versatile Fe3O4/GO/Au composite nanomaterial as SERS-active substrate for detection of pesticide residue

Wu Rui,Song Xi,Tian Guanghui

Highly active Fe 3 O 4 /GO/Au composite nanomaterial was fabricated as a substrate of surface-enhanced Raman spectroscopy (SERS) and applied for pesticide residue detection. The three-layer multifunctional Fe 3 O 4 /GO/Au nanoparticles (NPs) were designed by facile method, with high hotspots, and were characterized by various techniques, including ultraviolet spectrophotometry (UV), X-ray diffraction (XRD), infrared absorption spectrometer (IR), and transmission electron microscopy (TEM). The performance of Fe 3 O 4 /GO/Au was evaluated by Raman spectroscopy with R6G as a probe molecule to verify its enhancement effect. It exhibited a strong Raman signal with 10 −6  M of R6G. Furthermore, the presence of Fe 3 O 4 /GO/Au nanohybrid enabled the SERS-based method to detect mancozeb and showed an excellent linear relationship in the range of 0.25–25 ppm, with a low limit of detection (0.077 ppm), satisfactory EF, stability, and repeatability. In addition, the mechanism of SERS enhancement with electromagnetic mechanism (EM) and chemical mechanism (CM) was discussed in detail. Therefore, the proposed SERS approach holds promise as an auxiliary technique for screening contaminated agricultural products, environmental sample, and food in the future.

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Journal of Energy Storage · 2025 · IF 9.8

Research on thermal energy storage of graphene-based phase change energy storage materials based on cross-dimensional collaborative modification of MXene and copper nanowires

Liwei Yang,Xinshuai Yan,Jianguo Duan,Xiaoxiao Huang,Qing Ma

As an intermittent energy source, the efficient utilization of solar energy relies on stable and efficient energy conversion and storage technologies. Phase change materials (PCM) have become ideal candidate materials for solar thermal storage due to their high energy storage density and reversible cycling characteristics. However, traditional organic solid-liquid phase transition materials are prone to leakage during the phase transition process and have a relatively low photothermal conversion efficiency, which limits their practical application. To address the above issues, this study designed a novel composite phase change material (CPCM). By collaboratively loading nanomaterials of different dimensions, such as copper nanowires (CuNWs) and MXene, into a graphene porous framework and encapsulating paraffin (PW), the reduced graphene oxide (rGO)/ CuNWs/MXene/PW (rGCuMPW) composite material was successfully constructed. Among them, the high light absorption capacity of MXene, combined with the excellent thermal conductivity of CuNWs, significantly improved the photothermal conversion efficiency (92.11 %) and thermal energy storage density (ΔH = 165.77 J·g −1 ) of the material. In addition, this material still maintains a stable phase transition enthalpy value after 100 cycles, demonstrating excellent cycle stability and reusability. The CuNWs-MXene synergistic modification strategy proposed in this study not only effectively reduces the leakage rate of organic PCM, but also significantly improves the performance of photothermal conversion and thermal energy storage, providing a new type of high-performance CPCM for the efficient utilization of solar energy.

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Materials Science and Engineering B-Advanced Functional Solid-State Materials · 2025 · IF 4.6

In situ growth of Ni/Cu-BTC nanocatalysts on rGO surfaces: electrochemical sensors for glucose detection

Jiangnan Chen,Zhouchao Wang,Lin Xu,Huifang Wang,Xianghua Gao,Baolong Niu,Wenfeng Li

In the realm of glucose detection, nickel-based and copper-based nanocomposites have garnered significant attention due to their exceptional catalytic performance and high sensitivity. This study realized linear detection across dual concentration ranges in alkaline media by in situ growing Ni/Cu-BTC spherical nanocatalysts on reduced graphene oxide (rGO). From 350 μM to 2.95 mM, with a low detection limit (LOD L ) of 21.7 μM (S/N = 3) and a sensitivity (S L ) of 40 nA mM −1  cm −2 ; from 2.95 mM to 9.45 mM, the high-concentration detection limit (LOD H ) is 1.1 mM (S/N = 3), with an improved sensitivity (S H ) of 165.7 nA mM −1  cm −2 . The response time (t) is under 2 s. Additionally, the sensor demonstrated robust interference resistance, excellent stability (%RSD = 3.57 %), repeatability (%RSD = 2.27 %), and reproducibility (%RSD = 2.34 %). In real-world sample testing, this sensor measured glucose concentrations in plasma from healthy individuals both on an empty stomach and half an hour after eating, with a relative standard deviation range of 0.94 %–2.33 %. These results suggest that the rGO-Ni/Cu-BTC composite is a promising enzyme-free electrochemical sensing material for glucose detection

CAS / MDL: 7782-42-5
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WATER AIR AND SOIL POLLUTION · 2025 ·Vol. 237 ·期 1 ·8 · IF 3

Adsorption of Methylene Blue using Poly(N-vinylpyrrolidone)-Graphene Oxide Composite: Kinetics, Equilibrium, Thermodynamics, and Mechanisms

Li Xiaoya,Zheng Ru,Duan Guangyu,Cao Zhanfang,Han Kai,Zhong Hong,Ma Xin,Wang Shuai

A poly( N -vinylpyrrolidone)-graphene oxide (NVP-GO) composite with high adsorption capacity for methylene blue (MB) was synthesized and comprehensively characterized using SEM, XRD, FT-IR, TG, elemental analysis, nitrogen physical adsorption, and XPS. The adsorption of MB onto NVP-GO was examined in relation to several variables, including contact time, adsorption temperature, initial concentration of MB, and pH. Adsorption kinetics, isotherms, and thermodynamics were thoroughly investigated. The adsorption kinetics followed the pseudo-second-order model, and the Langmuir isotherm model indicated a monolayer adsorption pattern of MB onto NVP-GO, with the maximum adsorption capacities ranging from 116.6 to 161.3 mg·g −1 at temperatures between 25 and 45 °C. Thermodynamic assessments and activation energy calculations demonstrated that the adsorption process was spontaneous, endothermic, and ​controlled by chemical activation. XPS analysis highlighted the significance of electrostatic interactions, n–π interactions, π–π stacking, and hydrogen bonding in mediating the adsorption mechanisms between NVP-GO and MB. Notably, NVP-GO maintained stable adsorption efficiency over three consecutive adsorption–desorption cycles, highlighting its potential as a promising adsorbent for wastewater treatment. Graphical

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Journal of Energy Storage · 2025 · IF 9.8

Integrated GaAs-based betavoltaic batteries and graphite lithium-metal battery system for high-efficiency beta radiation energy conversion and storage

Haoran Gu,Hongyi Tian,Xinxu Yuan,Jingbin Lu,Haolin Li,Ke Zhang,Hanxiao Yan,Shuaiwen Yi

To address the low power output issue of Betavoltaic Batteries in practical applications, this paper proposes a novel isotope beta radiation energy conversion and storage system integrating a GaAs-based Betavoltaic Batteries with a low self-discharge lithium metal battery utilizing flake graphite. This system enables simultaneous collection, conversion, and storage of beta radiation energy. In experiments, we fabricated a lithium metal battery employing flake graphite as the cathode, lithium metal as the anode, and LiFSI in DME electrolyte supplemented with 4-n-pentyl-4′-cyanobiphenyl(5CB) additive. This battery was then connected to the GaAs-based Betavoltaic Batteries. Experimental results demonstrate successful energy harvesting from the Betavoltaic Batteries alone, which effecttively powered an LCD display.

CAS / MDL: 7782-42-5 872-50-4
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DESALINATION · 2026 · IF 9.9

Form-stable cellulose nanofiber/alginate double-layer aerogel prepared by freeze-assisted structuring and ambient-pressure final drying for solar desalination

Yuwen Yang,Zhi Wu,Kelang Wang,Jingyi Wang,Yunrong Liao,Zhiming Zhang,Renjie Chen,Fei Pan,Wenjun Meng

High-value utilization of agricultural waste • Green and low-cost fabrication • Synergistic double-layer design • Efficient solar desalination performance • Practical applicability Sorghum distillers' grains (SDG) are abundant by-product of sorghum liquor production but are often underutilized. In this study, we report a form-stable, carbohydrate-based double-layer aerogel (DLA) fabricated via directional freezing followed by ambient-pressure drying, which avoids energy-intensive supercritical freeze-drying routes. Cellulose nanofibers (CNF) extracted from SDG via TEMPO-mediated oxidation were combined with sodium alginate to form a Ca 2+ -crosslinked skeleton, and an rGO/g-C 3 N 4 photothermal layer was integrated on top to construct the DLA evaporator. By tuning the rGO/g-C 3 N 4 ratio, A 3 (0.6/0.4, w /w) exhibited markedly enhanced dimensional stability during cycling, showing only 3.2% projected-area shrinkage after 10 days, compared with severe shrinkage in the control samples. Meanwhile, A 3 maintained efficient solar evaporation with an evaporation rate of 1.43 kg·m −2 ·h −1 and a photothermal conversion efficiency of 93.14% under simulated irradiation. Outdoor tests further confirmed robust freshwater production across seasons (maximum 2.74 kg·m −2 ·h −1 ), and the collected condensate satisfied WHO ion-concentration guidelines. This work demonstrates an ambient-pressure-drying-enabled, form-stable CNF aerogel platform for scalable solar desalination and SDG valorization.

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Journal of Energy Storage · 2026 · IF 10.7

Performance study of flexible, flame-retardant, and sustainable energy storage composite phase change materials based on phosphorylated cellulose skeleton

Xinyu He,Min Du,Wanqing Wu,Dedi Zhou,Yihang Zhao,Haokun Shi,Qinggong Zheng

In recent years, with the development of electric vehicles and electric vessels, the issues of battery thermal safety have garnered significant attention. Composite phase-change materials (CPCMs) hold great potential as passive cooling systems in battery thermal management systems (BTMS), but their high flammability remains an unresolved challenge. This study successfully developed a flexible composite phase-change material, CPCM/P-CSF@rGO, by encapsulating a eutectic phase-change material composed of mannitol and galactitol in a three-dimensional hydrogen-bonded network, self-polymerised by phosphated corn straw cellulose (P-CSF) and reduced graphene oxide (rGO). The study demonstrates that the strong hydrogen bonding network formed between the phosphate groups introduced by phosphoric acid modification and rGO constructs highly efficient thermal conduction pathways, achieving a thermal conductivity of 1.039 W/(m•K) and significantly accelerating thermal response rates. Simultaneously, the incorporation of the P-CSF@rGO framework endows the material with excellent flexibility and shape stability. Due to the in-situ flame-retardant modification of the framework, the phase-change material maintains a high latent heat of phase-change (194.7 J/g) and achieves superior flame retardancy through gas-phase and condensation-phase mechanisms. It exhibits a limiting oxygen index of up to 30.64% and rapidly extinguishes itself when exposed to open flame in atmospheric conditions. Thus, the flexible composite phase-change material (CPCM/P-CSF@rGO) supported by a phosphorylated cellulose framework emerges as a promising candidate for ensuring safety and high performance in thermal management applications.

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