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Journal of Energy Storage · 2024 · IF 8.9

In-situ differential electrochemical mass spectrometry study on the effects of negative/positive ratios on gas evolution in lithium-ion full batteries

Yongqi Wang,Rongwei Huang,Jiyue Hou,Ao Li,Wenchang Han,Wengxiang Ai,Chunman Yang,Qian Wang,Yiyong Zhang,Xue Li

s Gas generation in Li-ion batteries has a negative impact on their electrochemical performance and safety characteristics, the accumulation of flammable gases may result in explosion and combustion. In this work, we investigated the electrochemical performance and gas behavior of LiFePO 4 // Li 4 Ti 5 O 12 lithium-ion full batteries with varying negative/positive(N/P) ratios. Firstly, studied their initial capacity, initial efficiency, multiplicity, and cycling performance. Additionally, we employed in situ differential electrochemical mass spectrometry (DEMS) to analyze the gas precipitation behavior of the full cell during charging and discharging at varying N/P ratios. Electrochemistry data indicate that excessively high or low N/P ratios impact the capacity performance, cycle stability, and gas behavior of the materials. DEMS monitoring revealed that as the N/P ratio increases, so do the production rates of H 2 , CO 2 , and CO. However, the production rate of C 2 H 4 increases as the N/P ratio decreases. The continuous accumulation of gases can adversely affect battery performance. The optimal N/P ratio for achieving maximum performance with minimal gas production is found to be 0.95. This suggests that the N/P design is crucial in optimizing the electrochemical performance of the complete battery, particularly its safety performance.

CAS / MDL: 872-50-4
研究领域: 材料科学 · 电化学
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MATERIALS CHEMISTRY AND PHYSICS · 2018 · IF 2.21

Synthesis and characterization of pyrene modified polyethylenimine as a novel fluorescent self-reporter for gene condensation

Yi Wang,Yuan Zhong,Li Luo,Xiuhua Li,Tieying Yin,Junli Huang,Xiaojuan Zhang,Wei Wu,Guixue Wang

The appropriate composite ratio of cationic polymer and gene is fundamental but paramount determinant for efficient gene condensation . In this study, we proposed to construct a novel strategy to comprehensively understand gene condensation situation by using the pyrene (Py) modified polyethylenimine as fluorescent self-reporter, owing to the unique monomer and excimer fluorescence of Py groups highly depending on their intermolecular interval. Constant with the traditional measurements for polymer-gene complex including gel retardation analysis, DLS, ζ-potential, and TEM , the typical curve of fluorescence intensity ratio at I 380 / I 490 was verified to easily have an insight into the gene condensing process, and further recommend the appropriate range of N/P ratio (the ratios of moles of the amine groups of cationic polymers to those of the phosphate ones of DNA) for enhancing gene delivery. Thus, the facilely fabricated fluorescigenic cationic polymer based on an unique excimer-monomer switch could be used as an novel fluorescent self-reporter for comprehensively discerning the gene condensation, which may provide a feasible way to improving the optimal gene encapsulation for efficient and safe gene delivery.

研究领域: 生物技术 · 基因治疗 · 材料科学
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ACS Applied Energy Materials · 2022 · IF 6.959

Dual-Layered 3D Composite Skeleton Enables Spatially Ordered Lithium Plating/Stripping for Lithium Metal Batteries with Ultra-Low N/P Ratios

Zichun Xiao,Ya-Nan Zhou,Xiaowei Wang,Jiawu Cui,Mingyu Yang,Chengyong Shu,Duzhao Han,Jiangqi Zhou,Chengxin Peng,Wei Tang,Yuping Wu

Lithium metal is considered as the ultimate anode for next-generation high energy-density batteries. However, its practical application is still severely hindered by Li dendrite growth as well as infinite volume variation along plating and stripping. Herein, we report a dual-layered, spatially ordered composite skeleton for bottom-up lithium growth by uniformly incorporating Li6.06La3Zr2Al0.2O12 (LLZO) in the upper layer and ZnO in the bottom layer, respectively, in the matrix of carbon fibers (CFs). The well-dispersed ZnO nanoparticles on CFs in the bottom layer function as lithiophilic nucleation sites to homogenize Li nucleation, while LLZO nanoparticles on CFs in the upper layer facilitate Li ion diffusion and distribution for stable lithium growth owing to the high ion conductivity of LLZO. Benefiting from this synergetic effect, the CFs@LLZO//CFs@ZnO composite skeleton can effectively induce Li plating/stripping in a controllable spatially ordered manner, suppressing the volume variation and inhibiting the formation of dendritic lithium. As a result, the symmetric cell using Li|CFs@LLZO//CFs@ZnO||CFs@LLZO//CFs@ZnO|Li presents good cycling stability over 2500 h with a small overpotential of 12 mV at 1 mA cm–2. Notably, under a harsh negative-to-positive N/P ratio of 1, the Li|CFs@LLZO//CFs@ZnO||NCM811 full cell delivers a lifespan of 100 cycles with a capacity fading of only 0.175% per cycle and an average CE of 99.3%.

研究领域: 材料科学 · 电化学 · 能源存储 · 电池技术
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Food Bioscience · 2024 · IF 4.8

Preparation of Fe3O4 magnetic nanomaterials for the enrichment of phosvitin phosphopeptides

Shuze Ren,Songming Li,Mahmoud Abou-Elsoud,Rui Cui,Xing Fu,Xi Huang

Phosvitin phosphopeptides (PPP) have a high ability to chelate mineral ions and promote calcium absorption. In this study, The Fe 3 O 4 nanospheres were first synthesized by hydrothermal method, then the three magnetic nanoparticles (Fe 3 O 4 @PDA@PMAA@PAMAM, Fe 3 O 4 @PDA@Ce 4+ , and Fe 3 O 4 @PDA@TiO 2 ) were obtained by layer modification on their surfaces, respectively. The magnetic nanoparticles were characterized by TEM, XRD, VSM, and Zeta potential. TEM analysis revealed that the nanoparticles were spherical and regular in shape. XRD diffraction analysis showed that the modified nanoparticles have a complete crystal structure. Meanwhile, PAMAM, Ce 4+ , TiO 2 , and other groups have been successfully modified on the nanoparticles. VSM hysteresis regression line results revealed that the magnetic nanoparticles are superparamagnetic. The three kinds of magnetic nanoparticles still maintained excellent enrichment performance after five times of repeated use. Fe 3 O 4 @PDA@TiO 2 has the best enrichment performance (167 mg g −1 ). The N/P ratio of the enriched PPP decreased from 1.36 to 0.98, which also showed that it had excellent PPP enrichment performance. Therefore, the modified magnetic nanoparticles could be an optimal PPP enrichment and purification material.

研究领域: 材料科学 · 纳米技术 · 生物化学
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Science Bulletin · 2025 · IF 21.1

Anion-mediated electrolyte engineering unlocks high-energy-density and long-cycling sulfur-based batteries at ultra-low N/P ratio

Huangwei Zhang,Yuluo Chen,Xiaoyu Ge,Kai Huang,Jiulin Wang,Jia-Qi Huang,Zhen Li,Yunhui Huang

High energy density and long cycle life are considered to be incompatible in battery design. Lithium metal batteries often have high energy density but poor cycle stability, while graphite (Gr)-based batteries usually have long cycle life but are limited in energy density. Therefore, mixing lithium with Gr as the anode is expected to balance high energy density and long cycle life. Reducing the negative/positive areal capacity (N/P) ratio to less than 1 is the simplest means to achieve a hybrid anode. The battery with sulfurized poly(acrylonitrile) (SPAN) as the cathode and an ultra-low N/P ratio (N/P=0.6) is expected to leverage the significant advantage of its cathode’s energy density far exceeding that of traditional cathodes, while maintaining stable cycling performance. This makes it a highly promising battery system. Through the design of anion-mediated electrolyte engineering, the capacity retention rate of the SPAN||Gr pouch cell at N/P=0.6 after 300 cycles was 92%, and its energy density was increased by 24% compared with that at N/P=1.1, achieving a balance between energy density and cycling stability. This strategy establishes N/P engineering coupled with electrolyte design as a scalable paradigm for next-generation energy-dense batteries.

CAS / MDL: 7704-34-9
研究领域: 储能 · 电化学 · 电池技术 · 材料科学 · 化学工程
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ORGANIC & BIOMOLECULAR CHEMISTRY · 2011 ·Vol. 9 ·期 22 ·7799-7806 · IF 3.451

The influence of cyclodextrin modification on cellular uptake and transfection efficiency of polyplexes

Wenyu Li,Lina Chen,Zhixiong Huang,Xiaofei Wu,Yuanfeng Zhang,Qiaoling Hu,Youxiang Wang

Cyclodextrin-modified polycations have been studied widely due to their low cytotoxicity, low immunogenicity and the ability to form inclusion complexes. However, the influence of CD modification on cellular uptake and transfection efficiency of polyplexes is still unclear. In this research, cyclodextrin-modified polyethylenimines (PEI-CD) with different CD-grafting levels were synthesized, which were named PEI-CD15 and PEI-CD41, respectively, according to the CD number per PEI chain. CD modification showed great influence on the DNA condensation ability of the polycation. PEI-CD15 could protect DNA completely above N/P ratio of 2. The particle sizes of these polyplexes were about 120 nm. However, PEI-CD41 could not protect DNA below N/P of 6, and PEI-CD41/DNA polyplexes were larger than 1 μm, even at N/P ratio of 10. Therefore, this research was mainly focused on PEI-CD15. It was interesting that the PEI-CD15/DNA polyplexes at N/P ratio of 8 and 10 displayed excellent stability in physiological salt conditions, probably due to the hydration shell of CDs. The influence of CD modification on the cellular uptake and transfection efficiency of polyplexes depended on the type of the cells. Uptake inhibition experiments indicated that PEI/DNA polyplexes were internalized by HEK293T cells by both clathrin-mediated endocytosis and caveolae-mediated endocytosis. The route of caveolae-mediated endocytosis was significantly promoted after CD modification. So the cell uptake and transfection efficiency of PEI-CD15/DNA polyplexes were significantly improved for HEK293T cells. However, the uptake and transfection efficiency of PEI-CD15/DNA polyplexes in HepG2 cells was similar to that of PEI/DNA polyplexes, probably due to the lack of endogenous caveolins.

CAS / MDL: 7585-39-9 98-59-9
研究领域: 生物医学工程 · 分子生物学 · 基因治疗 · 药物递送系统
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ADVANCED MATERIALS · 2020 ·Vol. 33 ·期 1 ·2002325 · IF 27.398

All-Solid-State Batteries with a Limited Lithium Metal Anode at Room Temperature using a Garnet-Based Electrolyte

Shaojie Chen,Jingxuan Zhang,Lu Nie,Xiangchen Hu,Yuanqi Huang,Yi Yu,Wei Liu

Metallic lithium (Li), considered as the ultimate anode, is expected to promise high-energy rechargeable batteries. However, owing to the continuous Li consumption during the repeated Li plating/stripping cycling, excess amount of the Li metal anode is commonly utilized in lithium-metal batteries (LMBs), leading to reduced energy density and increased cost. Here, an all-solid-state lithium-metal battery (ASSLMB) based on a garnet-oxide solid electrolyte with an ultralow negative/positive electrode capacity ratio (N/P ratio) is reported. Compared with the counterpart using a liquid electrolyte at the same low N/P ratios, ASSLMBs show longer cycling life, which is attributed to the higher Coulombic efficiency maintained during cycling. The effect of the species of the interface layer on the cycling performance of ASSLMBs with low N/P ratio is also studied. Importantly, it is demonstrated that the ASSLMB using a limited Li metal anode paired with a LiFePO 4 cathode (5.9 N/P ratio) delivers a stable long-term cycling performance at room temperature. Furthermore, it is revealed that enhanced specific energies for ASSLMBs with low N/P ratios can be further achieved by the use of a high-voltage or high mass-loading cathode. This study sheds light on the practical high-energy all-solid-state batteries under the constrained condition of a limited Li metal anode.

CAS / MDL: 1310-66-3 1314-23-4
研究领域: 材料科学 · 电化学 · 能量存储 · 电池技术
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BIOMACROMOLECULES · 2019 · IF 5.667

Reactive Oxygen Species (ROS)-Degradable Polymeric Nanoplatform for Hypoxia-Targeted Gene Delivery: Unpacking DNA and Reducing Toxicity

Yuxin Zhang,Jie Zhou,Shengnan Ma,Yiyan He,Jun Yang,Zhongwei Gu

Smart polymers as ideal gene carriers have drawn increasing attentions due to the effective DNA release once triggered by intrinsic stimuli, as well as reduced cytotoxicity. Herein, a stimulus-responsive, positively charged and water-soluble polymer (OEI-TKx) was facilely engineered by cross-linking low molecular weight oligoethylenimine (OEI) via thioketal (TK) linkages that would cleave selectively in reactive oxygen species (ROS)-rich environments induced by hypoxia. Agarose gel electrophoresis assay demonstrated that the threshold N/P ratios for complete retardation of negatively charged DNA migration were above 5 for OEI-TKx. The reduction in DNA-condensing capability and the changes in particle size, size distribution and particle morphology all illustrated that OEI-TKx possessed excellent ROS responsiveness. OEI-TKx/DNA polyplexes showed lower toxicity and higher gene transfection efficiency compared with PEI/DNA polyplexes. The optimum formulation, OEI-TKx/DNA polyplexes (N/P = 40), showed a little better performance than PEI/DNA polyplexes in cellular uptake profile. Furthermore, OEI-TKx/DNA polyplexes could escape from endosomes to the cytosol as efficiently as PEI/DNA polyplexes. Confocal images confirmed that OEI-TKx/DNA polyplexes could more effectively release DNA than PEI/DNA polyplexes, mainly owing to the valid cleavage of thioketal linkages induced by characteristic rich-ROS in Hela cells. These results suggested that OEI-TKx could represent an on-demand stimulus-responsive gene delivery platform.

CAS / MDL: 107-96-0
研究领域: 生物医学工程 · 药学 · 纳米技术 · 分子生物学 · 癌症治疗
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