JOURNAL OF ALLOYS AND COMPOUNDS
·
2021
·
IF 5.316
Cheng Cheng,Xiaoxian Zang,Wenxiu Hou,Changcong Li,Qing Huang,Xiangang Hu,Chencheng Sun,Yu Zhang,Jun Yang,Fuyuan Ma
The NASICON (Sodium super ion conductor)-type of Na 3 V 2 (PO 4 ) (NVP) has a great potential for energy storage application due to its high voltage plateau, three-dimensional (3D) ionic diffusion channel, perfect thermal stability, and high structural robustness. Here, Na 3 V 2 (PO 4 )-based composites with 3D porous carbon skeleton structure were synthesized via hydrothermal methods . After a series of hydrolysis and polymerization processes, transparent colloid mainly containing (NH 4 ) 4 Na 2 V 10 O 28 phase was formed. The 3D porous hydrogel with the (NH 4 ) 4 Na 2 [V 10 O 28 ]·10H 2 O phase was produced by adjusting the reaction time. The product has a lamellar structure , and its ion is suitable to grow the nanosheets , and the present PO 4 3- groups may be distributed in the (NH 4 ) 4 Na 2 [V 10 O 28 ]·10H 2 O phase of the interlayer structure, leading to the enhanced electronic conductivity . The 3D porous Na 3 V 2 (PO 4 )/C (NVP/C) with the size of 100–200 nm particles can be used as cathode for sodium ion batteries . The NVP/C delivers a specific capacity of 62.1 mAh g −1 at 10 C. The excellent stability of NVP/C can be obtained with 98% capacity retention after 140 cycles at 1 C. After 2000 cycles (5 C), the capacity is still 80.4 mAh g −1 , with the capacity retention of about 86%. Our encouraging results may boost further studies of SIBs device by smart engineering of the electrode materials.
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高影响因子
CERAMICS INTERNATIONAL
·
2017
·Vol. 43
·期 12
·9327-9333
·
IF 2.986
Nan Zhou,Shengxiong Huang,Tao Hong,Wei Luo,Yun Tian,Xiangyang Lu,Zhi Zhou
In this paper, LiTi 2 (PO 4 ) 3 @carbon composite as anode for aqueous lithium ion battery has been successfully synthesized by in-situ carbon coating method using oxalic acid and glucose as double carbon sources. XRD results confirm the rhombohedral NASICON-type LiTi 2 (PO 4 ) 3 structure of the as-prepared composite. The LiTi 2 (PO 4 ) 3 @carbon composite using double carbon sources (LTP-OG-10) disperses well, and the coated carbon layer has the appropriate thickness of 3–7 nm, which result in proper balance of the good electrical conductivity and the fast kinetics of diffusion of lithium ions . LTP-OG-10 exhibits better electrochemical performance compared with those using oxalic acid (LTP-O) or glucose (LTP-G) single carbon source. LTP-OG-10 anode delivers the discharge capacity of 112.5 mA h g −1 , 96.8 mA h g −1 , and 54.2 mA h g −1 at 0.2 C, 5 C and 20 C, respectively, much larger than that of LTP-O and LTP-G. Moreover, LTP-OG-10 demonstrated excellent cycling performance, with the capacity retention of 71.1% after 400 cycles at 0.2 C, 22.9% higher than that of LTP-G. The good electrochemical properties of LTP-OG-10 is mainly ascribed to the increase of defects, high-quality and appropriate thickness of carbon layer. Our study reveals that preparing LiTi 2 (PO 4 ) 3 @carbon composite using double carbon sources is an efficient approach to enhance its electrochemical properties.
研究领域:
材料科学
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电化学
·
能源存储
·
无机非金属材料
·
功能材料
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高影响因子
ACS Applied Materials & Interfaces
·
2020
·
IF 8.758
Yu Zhou,Xiji Shao,Kwok-ho Lam,You Zheng,Lingzhi Zhao,Kedong Wang,Jinzhu Zhao,Fuming Chen,Xianhua Hou
Symmetric sodium-ion batteries possess promising features such as low cost, easy manufacturing process, and facile recycling post-process, which are suitable for the application of large-scale stationary energy storage. Herein, we proposed a symmetric sodium-ion battery based on dual-electron reactions of a NASICON-structured Na3MnTi(PO4)3 material. The Na3MnTi(PO4)3 electrode can deliver a stable capacity of up to 160 mAh g–1 with a Coulombic efficiency of 97% at 0.1 C by utilizing the redox reactions of Ti3+/4+, Mn2+/3+, and Mn3+/4+. This is the first time to investigate the symmetric sodium-ion full cell using Na3MnTi(PO4)3 as both cathode and anode in the organic electrolyte, demonstrating excellent reversibility and cycling performance with voltage plateaus of about 1.4 and 1.9 V. The full cell exhibits a reversible capacity of 75 mAh g–1 at 0.1 C and an energy density of 52 Wh kg–1. In addition, both ex situ X-ray diffraction (XRD) analysis and first-principles calculations are employed to investigate the sodiation mechanism and structural evolution. The current research provides a feasible strategy for the symmetric sodium-ion batteries to achieve high energy density.
研究领域:
储能
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电化学
·
材料科学
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电池技术
·
钠离子电池
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高影响因子
ACS Sustainable Chemistry & Engineering
·
2023
·
IF 8.4
Tianyu Zhu,Cuiping Yu,Yucheng Wu,Yan Wang
The capacity of Li4Ti5O12 (LTO) at high rates is limited due to the polarization caused by its modest Li-ion (Li+) diffusion coefficient and low electrical conductivity. Coating with ionic conductors is an available method to ameliorate charge transport. Li1+xAlxTi2–x(PO4)3 ion conductors with thermal, chemical, and electrochemical stabilities have been proven to be modification materials for electrodes. Herein, the Li1.4Al0.4Ti1.6(PO4)3 (LATP) precursor dispersion with optimized preparation is applied to the surface modification of LTO by a dynamic mix-drying method. A proper amount of LATP ultrafine particle coating could develop the ion transport rate in the electrode and restrain side reactions. The 2 wt % LATP–LTO anode exhibits an optimized capacity of 168.2 mA h g–1 at 0.1 A g–1 and retains 96.7% of its capacity after 5000 cycles at 5.0 A g–1, while the P-LTO anode retains 86.3% of the capacity. Improved Li+ transport and interface stability in the electrodes lead to the boosted rate and cycling stability. The LATP-modified LTO composites provide a possibility for the further application of related materials in the energy storage field.
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高影响因子
JOURNAL OF ALLOYS AND COMPOUNDS
·
2023
·
IF 6.2
Jingrui Kang,Xu Guo,Rui Gu,Yi Tang,Honglei Hao,Yu Lan,Li Jin,Xiaoyong Wei
Li 1.3 Al 0.3 Ti 1.7 (PO 4 ) 3 (LATP) is a promising candidate as the solid electrolyte in energy storage devices. For practical considerations, the most common ways to ameliorate the low density and high ionic resistance of LATP are usually to use glass additives. In this work, the boron-based (B 2 O 3 , B 2 O 3 -SiO 2 -PbO (BSP), and B 2 O 3 -SiO 2 -K 2 O-Al 2 O 3 (BSKA)) glass are added into LATP by solid method. As the results, the main diffraction peaks of all prepared samples maintain the NASICON-type with the R-3c space group. Meanwhile, the symmetric stretching vibrations of O-P-O bands is redshifted with the addition of boron-based glass, which plays a positive role in bulk conductivity. Additionally, the introduction of boron-based glass additives is effective to increase the grain sizes of the LATP samples. The relative density of the sample is obtained from 93.37% to 95.42%. Furthermore, the total conductivities of 1.33 × 10 −4 , 1.37 × 10 −4 , 1.97 × 10 −4 S cm −1 are obtained in ceramic samples after B 2 O 3 , BSP and BSKA glass additives adding, respectively. The activation energy shows a reduction of 5.26% to 0.36 eV after BSP and BSKA glass adding. Satisfactorily, B 2 O 3 , BSP and BSKA glass have a certain influence on the conductivity, and bear a more favorable argument for the regulation of the morphology and density in the future.
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高影响因子
ACS Applied Materials & Interfaces
·
2021
·
IF 9.229
Jiapin Liu,Yun Huang,Zhixing Zhao,Wenhao Ren,Zhuangzhi Li,Chao Zou,Ling Zhao,Zhaomin Tang,Xing Li,Mingshan Wang,Yuanhua Lin,Haijun Cao
The sodium super ion conductor (NASICON) structure materials are essential for sodium-ion batteries (SIBs) due to their robust crystal structure, excellent ionic conductivity, and flexibility to regulate element and valence. However, the poor electronic conductivity and inferior energy density caused by the nature of these materials have always been obstacles to commercialization. Herein, using yeast as a template to derive NASICON structure Na3MnTi(PO4)3 (NMTP) materials (noted as Yeast@NMTP/C) is presented. The Yeast@NMTP/C material retains the microsphere morphology of the yeast template and not only controls the particle size (around 2 μm) to shorten the Na+ diffusion pathways but also improves the electronic conductivity to optimize the electrochemical kinetics. The Yeast@NMTP/C cathode delivers reversible multielectron redox reactions including Ti4+/3+, Mn3+/2+, and Mn4+/3+ and exhibits a high capacity of 108.5 mAh g–1 with a 79.2% capacity retention after 1000 cycles at a 2C rate. The sodium storage mechanism of Yeast@NMTP/C reveals that the addition of Ti4+/3+ redox plays a key role in improving the Na+ diffusion kinetics, and both solid-solution and two-phase reactions take place during the desodiation and sodiation process. Additionally, the high-rate and long-span cycle performance of Yeast@NMTP/C at 10C is ascribed to contribute to pseudocapacitance.
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PubMed
高影响因子
CERAMICS INTERNATIONAL
·
2023
·
IF 5.2
Xingrui Pu,Xing Cheng,Qiaohong Yan,Yueming Lin,Rentai Yan,Ruize Yang,Xiaohong Zhu
The need to develop safe solid-state lithium batteries has stimulated intense research efforts for Li + solid electrolytes. However, the low conductivity limits the development of NASICON LiZr 2 (PO 4 ) 3 (LZP) electrolyte. Here, the doping effects of Ta on the structure, surface morphologies and electrochemical properties of Li 1- x Zr 2- x Ta x (PO 4 ) 3 (LZTP, x = 0, 0.01, 0.02, 0.04, 0.06 and 0.08) solid electrolyte were analyzed. LZTP was prepared using a simple solid-state reaction route, followed by sintering at 1200 °C for 12 h. A proper content of Ta 5+ substitution for Zr 4+ is beneficial to stabilize the high conductive rhombohedral (α) phase of LZP at room temperature. Doping Ta 5+ is conducive to unblocking of Li + at the M1 site and facilitates the occupation of Li + at the M2 site, thereby expanding the pathway for Li + conduction. Rietveld refinement data demonstrated that the Zr–O and P–O bond lengths ( d Zr-O and d P-O ) increased with a decrease in Zr–O–P bond angles ( θ Zr-O-P ) as x rose. The distortions in the ZrO 6 octahedron may weaken the coulomb attraction in Li + -O 2- , resulting in a lower activation energy ( E a ) and a higher Li + conductivity. The highest room-temperature conductivity (6.06 × 10 −5 S cm −1 ) was obtained at x = 0.06, which reached 1.5 × 10 −4 S cm −1 at 50 °C. The E a was found to decrease from 0.388 eV ( x = 0) to 0.306 eV ( x = 0.06). In addition, Ta doping resulted in improved connectivity and reduced pore formation, which also contributed to the decrease in resistance. The Raman spectrum demonstrated that some phonon modes of bending vibration in PO 4 were degenerate and external modes became too weak to be observed or even disappeared as Ta content increased. This change in the modes also had an impact on the Li + conductivity. Overall, the LZTP-0.06 appears to be a promising candidate for the solid electrolyte.
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高影响因子
JOURNAL OF COLLOID AND INTERFACE SCIENCE
·
2021
·
IF 8.128
Minhui Zheng,Zhoulu Wang,Qiang Ru,Haikuo Fu,Jun Zhang,Zikang Pan,Jiaqi Wang,Qizhen Xie,Xing Zhao
NASICON type KTi 2 (PO 4 ) 3 decorated by NTCDA-derived carbon layer (KTP/NC) was prepared as anode material to obtain sustainable lithium/sodium ion storage (LIBs/SIBs). Due to its prominent capacitance, good electronic conductivity and ability to constrain volume, the KTP/NC composite realizes highly electrochemical kinetics both in LIBs and SIBs . For LIBs, the KTP/NC composite delivers a superior reversible capacity of 598.1 mAh g −1 after 200 cycles at 0.5C, impressive cyclability with 225.5 mAh g −1 after 3000 cycles at an ultrahigh current density of 26.1 C and conspicuous rate performance of 160.6 mAh g −1 even at 52.2 C. In addition, the composite has a wide operation-temperature window with favorable capacities of 147.1–372.9 mAh g −1 from −10 °C to 50 °C. As for SIBs, the KTP/NC composite maintains a stable discharge capacity of 112.5 mAh g −1 after 700 cycles at a current density of 2.6 C and conspicuous rate performance of 86.7 mAh g −1 at 5.2 C. The KTP/NC anode exhibits discharge capacities of 29.9–112.6 mAh g −1 from −10 °C to 40 °C. The results demonstrate that the KTP/NC composite would be a promising electrode material for LIBs and SIBs.
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高影响因子
CHEMICAL COMMUNICATIONS
·
2017
·Vol. 53
·期 11
·1805-1808
·
IF 6.319
Jin Han,Guan-Nan Li,Feng Liu,Minqiang Wang,Yan Zhang,Linyu Hu,Chunlong Dai,Maowen Xu
Novel K3V2(PO4)3 and three-dimensional conductive network K3V2(PO4)3/C nanocomposites are successfully fabricated and further evaluated as cathode materials for potassium-ion batteries for the first time. The K3V2(PO4)3/C nanocomposite exhibits a high-potential platform of 3.6–3.9 V and a good capacity retention of at least 100 cycles. This work may provide new insight into developing cathode materials for potassium-ion batteries.
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PubMed
高影响因子
ACS Applied Materials & Interfaces
·
2024
·
IF 8.3
Caixia Li,Shuping Pu,Jiapin Liu,Yun Huang,Jiepeng Chen,Xinyan Xiang,Lei Fu,Chao Zou,Xing Li,Mingshan Wang,Yuanhua Lin,Haijun Cao
Sodium (Na) super ion conductor (NASICON) structure Na3MnTi(PO4)3 (NMTP) is considered a promising cathode for sodium-ion batteries due to its reversible three-electron reaction. However, the inferior electronic conductivity and sluggish reaction kinetics limit its practical applications. Herein, we successfully constructed a three-dimensional cross-linked porous architecture NMTP material (AsN@NMTP/C) by a natural microbe of Aspergillus niger (AsN), and the structure of different NMTP cathodes was optimized by adjusting different transition metal Mn/Ti ratios. Both approaches effectively altered the three-dimensional NMTP structure, not only improving electronic conductivity and controlling Na+ diffusion pathways but also enhancing the electrochemical kinetics of the material. The resultant AsN@NMTP/C-650, sintered at 650 °C, exhibits better electrochemical performance with higher reversible three-electron reactions corresponding to the voltage platforms of Ti4+/3+, Mn3+/2+, and Mn4+/3+ around 2.1, 3.6, and 4.1 V (vs Na+/Na), respectively. The capacity retention rate is up to 89.3% after 1000 cycles at a 2C rate. Moreover, a series of results confirms that the Na3.4Mn1.2Ti0.8(PO4)3 cathode has the most excellent electrochemical performance when the Mn/Ti ratio is 1.2/0.8, with a high capacity of 96.59 mAh g–1 and 97.1% capacity retention after 500 cycles.
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PubMed
高影响因子
ACS Applied Materials & Interfaces
·
2017
·
IF 7.504
Lei Chen,Yanming Zhao,Shenghong Liu,Long Zhao
Although the NASICON-type of Na3V2(PO4)3 is regarded as a potential cathode candidate for advanced sodium-ion batteries (SIBs), it has an undesirable rate performance and low cyclability, which are a result of its poor electronic conductivity. Here, we utilized conductive polyaniline (PANI) grown in situ to obtain the hard carbon-coated porous Na3V2(PO4)3@C composite (NVP@C@HC) with a typically simple and effective sol–gel process. Based on the restriction of double carbon layers, the NVP size decreases distinctly, which can curtail the sodium-ion diffusion distance and enhance the electronic conductivity. As expected, the product displays good discharge capacity (111.6 mA h g–1 at 1 C), outstanding rate capacity (60.4 mA h g–1 at 50 C), and remarkable cycling stability (63.3 mA h g–1 with a retention of 83.3% at 40 C over 3000 cycles). Also, it performs a long-term cycling capacity of 58.5 mA h g–1 exceeding 15 000 cycles at 20 C (with a capacity loss of 0.24% per cycle).
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PubMed
高影响因子
CARBON
·
2025
·
IF 11.6
Jin Chen,Pei Liu,Kai Xu,Zhilei Hao,Guohui Tang,Changtian Zhu,Zixuan Ding,Shuai Yin,Zhiqiang Li,Zhen Ding,Yi Wang,Zhanpeng Liu,Siwen Yu,Xing Xin,Fenghua Liu
Na 3 V 2 (PO 4 ) 3 (NVP) material has evolved as a significant candidate for electrode materials in the development of sodium-ion batteries. However, the low conductivity of NVP material leads to low cycling performance, limiting their application in high-efficiency battery materials. To address this issue, this work proposes a novel strategy for materials design through constructing 3D network carbon-coatings on the surface of NVP materials. The carbon-coatings are achieved via a combination of sol-gel technique and heat treatment using pyrolytic carbon (C), carbon nanotubes (CNTs) and graphene (GN). In comparison to NVP@C, the electrochemical properties of NVP@C/GN, NVP@C/CNTs, and NVP@C/GN/CNTs have shown improvements. Among these, NVP@C/GN/CNTs exhibit the most outstanding electrochemical performance in the half-cell test. Specifically, this material demonstrates exceptional cycling stability, with a capacity of 92 mAh g −1 that can be maintained even after 800 cycles at a high-rate performance of 10C, with an attenuation of 10.6 %. The enhanced electrochemical performance is attributed to the specific ternary carbon-coating conductive structure, which significantly shortens the diffusion paths of Na + ions and electrons within NVP, resulting in improved Na + ion and electron transport kinetics. This study provides a new design paradigm for improving the conductivity of cathode material for sodium-ion batteries.
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高影响因子
危险品化学品经营许可证（带存储）