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Journal of Materials Chemistry A · 2014 ·Vol. 2 ·期 32 ·12835-12848 · IF 0

Polyhedral LiNi0.5Mn1.5O4 with excellent electrochemical properties for lithium-ion batteries

Zhanjun Chen,Ruirui Zhao,Peng Du,Hang Hu,Tao Wang,Licai Zhu,Hongyu Chen

Alternative micro-sized LiNi0.5Mn1.5O4 spinels with octahedral structure (showing only one type of {111} crystal face) or chamfered polyhedral structure with extra other faces have been synthesized via a controllable method. A possible growth model, complexing–pyrolyzing-oriented, is also proposed for the formation of chamfered polyhedral LiNi0.5Mn1.5O4 spinel based on the experimental results in this paper. The chamfered polyhedral LiNi0.5Mn1.5O4 can provide a large capacity of 103 mA h g−1 even at a discharge rate as high as 50 C, which is far superior to that of the octahedral structure. Besides, the capacity retentions of the chamfered polyhedral composites are found to be 90.82% at 25 °C after 500 cycles and 90.00% at 55 °C after 200 cycles, which are also better than those of the octahedral composites. These results represent the first experimental evidence for lattice-plane anisotropy in LiNi0.5Mn1.5O4 crystals. Moreover, the pseudo-sphere structure is beneficial for obtaining high volumetric energy density and excellent processability in practical applications. In short, we have revealed for the first time that, through chamfering an octahedron to a pseudo-sphere-like polyhedron rather than doping or coating, a micro-sized LiNi0.5Mn1.5O4 spinel with good compatibility between energy/power density and cycle life can be synthesized successfully without sacrificing other properties.

研究领域: 材料科学 · 电化学 · 能源存储 · 无机固体化学 · 纳米结构材料
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JOURNAL OF PETROLEUM SCIENCE AND ENGINEERING · 2022 · IF 5.168

Comprehensive evaluation of self-healing polyampholyte gel particles for the severe leakoff control of drilling fluids

Lili Yang,Chunlin Xie,Tian Ao,Kaixiao Cui,Guancheng Jiang,Baojun Bai,Yongwei Zhang,Jun Yang,Xingxing Wang,Weiguo Tian

Lost circulation has been a serious problem to be solved in many drilling practices during oil, gas and geothermal well drillings. Many materials have been developed and evaluated for the purpose. However, their performance to plug severe leakoff is very limited. Herein, an injectable self-healing hydrogel based on polyampholyte with sulfonated and quaternary ammonium functionalities (P(MPTC- co -NaSS)) was developed and comprehensively evaluated to prevent the severe loss of fluids to formation. By incorporating cation-π (π is for aromatic residues) interaction, the hydrogel shown self-healing property and robustness in severe environment (temperature, salt) by comparison with other hydrogels merely consisting of cation-anion and H-bonding interactions. Aromatic residues enhanced thermal stability above 310 °C. The plugging measurement shown that an addition of 2 wt% dried gel particles can plug high-permeability formation and endure a high pressure of 6 MPa, produce much lower circulation loss and result in a dramatically increased loss volume reduction rate (63.5%) compared with a commercial polymer gel product and an inert material (9.4%) after a self-healing process. Markedly, P(MPTC- co -NaSS) can be used in a wide range of formation temperature (as high as 150 °C) and salt concentrations (NaCl, CaCl 2 , as high as 15 wt %). In addition to suitable particle size and mechanically robustness, it was also attributed to the soft, swelling, deformable, toughness and self-healable features of P(MPTC- co -NaSS) gel particles as well as the strong adhesion to negatively charged formations in water, even under high thermal and saline condition. These characteristics also contributed to a long-term plugging performance, beneficial to avoid repeated lost circulation in drilling operation. Besides, this self-healing polyampholyte gel particles dispersed well in saline fluid and maintained stable rheological properties after hot rolling, which was favorable to drilling fluid circulation. This study shown the application potential of self-healing materials as plugging material candidate in petroleum drilling industry.

研究领域: 石油工程 · 钻井技术 · 功能高分子材料 · 流体损失控制 · 油田化学
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Energy Technology · 2018 ·Vol. 6 ·期 11 ·2139-2145 · IF 3.175

Suppressing the Voltage Decay and Enhancing the Electrochemical Performance of Li1.2Mn0.54Co0.13Ni0.13O2 by Multifunctional Nb2O5 Coating

Wei Pan,Wenjie Peng,Guochun Yan,Huajun Guo,Zhixing Wang,Xinhai Li,Weihua Gui,Jiexi Wang,Ning Chen

This study focuses on suppressing the voltage decay and improving the electrochemical performance of Li-rich and manganese-based (LRM) material by Nb 2 O 5 coating, which is realized by an effective soft-chemical route using a mixture of ethanol and water as co-solvent. After Nb 2 O 5 coating, the resulted material demonstrates superior electrochemical performance as cathode material for LIBs. Particularly, it shows an excellent capacity retention of 98 % after 200 cycles at 1 C (1 C=250 mA g −1 ). Voltage decay within cycling is also obviously suppressed by Nb 2 O 5 coating. Moreover, it exhibits superior rate capacities, delivering 189 and 152 mAh g −1 at high current densities of 2 and 5 C, respectively. The improved electrochemical performance of Nb 2 O 5 coated sample can be attributed to that Nb 2 O 5 can suppress the phase transformation and voltage decay by acting as not only a fast ion conductor to accelerate the lithium ion diffusion at the cathode/electrolyte interface, but also an inert protective layer to reduce the direct contact between the cathode and electrolyte.

研究领域: 材料科学 · 电化学 · 能源存储 · 无机非金属材料 · 固态离子学
✓ 已验证 DOI 高影响因子
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RSC Advances · 2016 ·Vol. 6 ·期 62 ·57009-57012 · IF 3.289

Solvent-free synthesis of crystalline mesoporous γ-Fe2O3 as an anode material in lithium-ion batteries

Di Wu,Jing Ye,Lie Chen,Yongzheng Wang,Kai Fang,Mingjiang Xie,Luming Peng,Xuefeng Guo,Weiping Ding

Crystalline mesoporous γ-Fe2O3 with a high surface area was prepared by a novel solvent-free route. This material exhibits a high reversible capacity with superior cycle performance and an exceptional high-rate capability as an anode material for Li-ion batteries.

研究领域: 材料科学 · 电化学 · 纳米材料 · 能源存储 · 固体化学 · 电池技术
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MATERIALS LETTERS · 2014 · IF 2.269

Preparation and thermal characterization of capric–myristic–palmitic acid/expanded graphite composite as phase change material for energy storage

Yaguang Yuan,Yanping Yuan,Nan Zhang,Yanxia Du,Xiaoling Cao

Capric–myristic–palmitic acid ternary eutectic mixture (CA–MA–PA) was prepared as phase change material (PCM). A novel composite PCM of CA–MA–PA/expanded graphite (EG) with an optimum mass ratio (CA–MA–PA:EG=13:1) was prepared by uniformly absorbing CA–MA–PA into the porous network structure of the EG. The melting and freezing temperatures of CA–MA–PA/EG composite PCM were measured by differential scanning calorimeter as 18.61   °C and 16.58   °C, respectively, while the melting and freezing latent heats were 128.2   J/g and 124.5   J/g, respectively. The thermal conductivity of the CA–MA–PA/EG composite PCM was measured as 3.67   W/m   K and thus the thermal storage and release rates were significantly increased. The thermal cycling test results showed that CA–MA–PA/EG composite PCM has a good thermal reliability. All the above results show that the CA–MA–PA/EG composite PCM is a potential solution for latent heat storage system.

研究领域: 材料科学 · 能源化学 · 热物理 · 功能材料 · 储能技术
✓ 已验证 DOI 高影响因子
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JOURNAL OF ALLOYS AND COMPOUNDS · 2022 · IF 6.371

B, F Co-doping flexible carbon nanofibers as a fast and stable anode for potassium-ion hybrid capacitor

Zuocheng Luo,Qingfeng Zhang,Wei Xie,Tong Yuan,Qisheng Zang,Ning Wang,Hanxiao Fan,Shuhong Xie,Xiaoping Ouyang

Potassium ion hybrid capacitors (PIHCs) have attracted widespread attention as combining the advantages of potassium ion batteries (PIBs) with supercapacitors . However, the sluggish kinetics caused by the large radius of K + hinder the practical application of PIHCs. Herein, we synthesized a boron and fluorine co-doping interlaced network porous carbon nanofibers (BF-PCNFs), which was used as the freestanding anode of PIHCs the freestanding anode of PIHCs to alleviate large volume expansion and increase conductivity. Benefiting from the B, F co-doping and porous interlace nanostructure of BF-PCNFs, the anode shows 185 mA h g −1 under a load of 12.6 mg cm −2 , a reversible capacity of 176 mA h g −1 at 1000 mA g −1 after 6000 cycles, and the capacity retention from 100 mA g −1 to 5000 mA g −1 is 62%. Furthermore, the PIHCs based on BF-PCNFs as anode and activated carbon as cathode exhibit an energy density of 87 Wh kg −1 and a power density of 393 W kg −1 . The capacity retention is as high as 78% over 4000 cycles. Considering the exceptional rate performance, long cyclability and high-mass-loading, our work may supply a new strategy for designing novel energy storage devices with outstanding performance.

研究领域: 材料科学 · 电化学 · 能源存储 · 纳米科技 · 功能材料
✓ 已验证 DOI 高影响因子
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Journal of Energy Chemistry · 2023 · IF 13.1

Manipulating Na occupation and constructing protective film of P2-Na0.67Ni0.33Mn0.67O2 as long-term cycle stability cathode for sodium-ion batteries

Yiran Sun,Pengfei Zhou,Siyu Liu,Zhongjun Zhao,Yihao Pan,Xiangyan Shen,Xiaozhong Wu,Jinping Zhao,Junying Weng,Jin Zhou

P2-Na 0.67 Ni 0.33 Mn 0.67 O 2 (NNMO) is promising cathode material for sodium-ion batteries (SIBs) due to its high specific capacity and fast Na + diffusion rate. Nonetheless, the irreversible P2-O2 phase transformation, Na + /vacancy ordering, and transition metal (TM) dissolution seriously damage its cycling stability and restrict its commercialization process. Herein, Na occupation manipulation and interface stabilization are proposed to strengthen the phase structure of NNMO by synergistic Zn/Ti co-doping and introducing lithium difluorophosp (LiPO 2 F 2 ) film-forming electrolyte additive . The Zn/Ti co-doping regulates the occupancy ratio of Na e /Na f at Na sites and disorganizes the Na + /vacancy ordering, resulting in a faster Na + diffusion kinetics and reversible P2-Z phase transition for P2-Na 0.67 Ni 0.28 Zn 0.05 Mn 0.62 Ti 0.05 O 2 (NNZMTO). Meanwhile, the LiPO 2 F 2 additive can form homogeneous and ultrathin cathode-electrolyte interphase (CEI) on NNZMTO surface, which can stabilize the NNZMTO-electrolyte interface to prevent TM dissolution, surface structure transformation, and micro-crack generation. Combination studies of in situ and ex situ characterizations and theoretical calculations were used to elucidate the storage mechanism of NNZMTO with LiPO 2 F 2 additive. As a result, the NNZMTO displays outstanding capacity retention of 94.44% after 500 cycles at 1C with 0.3 wt% LiPO 2 F 2 , excellent rate performance of 92.5 mA h g −1 at 8C with 0.1 wt% LiPO 2 F 2 , and remarkable full cell capability. This work highlights the important role of manipulating Na occupation and constructing protective film in the design of layered materials, which provides a promising direction for developing high-performance cathodes for SIBs.

研究领域: 材料科学 · 电化学 · 能源存储 · 无机化学 · 固态化学 · 电池技术
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Small · 2023 ·Vol. 19 ·期 40 ·2303227 · IF 13.3

Sodium-Ion Substituted Water Molecule in Layered Vanadyl Phosphate Enhancing Electrochemical Kinetics and Stability of Zinc Ion Storage

YuanZhe Wu,Quan Zong,Chaofeng Liu,Yanling Zhuang,Daiwen Tao,Jiangying Wang,Jingji Zhang,Qilong Zhang,Guozhong Cao

Vanadyl phosphate (VOPO 4 ·2H 2 O) has been regarded as one of the most promising cathode materials for aqueous Zn-ion batteries due to its distinct layered structure. However, VOPO 4 ·2H 2 O has not yet demonstrated the exceptional Zn ion storage performance owing to the structural deterioration during repeated charging/discharging process and poor intrinsic conductivity. In this work, 2D sodium vanadyl phosphate (NaVOPO 4 ·0.83H 2 O, denoted as NaVOP) is designed as a cathode material for Zn-ion batteries, in which sodium ions are preinserted into the interlayer, replacing part of water. Benefiting from the in situ surface oxidization, improved electronic conductivity, and increased hydrophobicity, the NaVOP electrode exhibits a high discharge capacity of 187 mAh g −1 at 0.1 A g −1 after activation, excellent rate capability and enhanced cycling performance with 85% capacity retention after 1500 cycles at 1 A g −1 . The energy storage mechanism of the NaVOP nanoflakes based on the rapid Zn 2+ and H + intercalation pseudocapacitance are investigated via multiple ex situ characterizations.

研究领域: 材料科学 · 电化学 · 能源存储 · 无机化学 · 纳米材料
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JOURNAL OF APPLIED ELECTROCHEMISTRY · 2023 ·Vol. 53 ·期 12 ·2411-2419 · IF 2.9

Electrochemical deposition of GaTe thin films for photoelectrochemical applications

Mai Manfang,Liao Bin,Liao Yijun,Lin Donghai,Ma Xinzhou

GaTe thin films are electrochemically deposited on indium tin oxide for photoelectrochemical applications. The electrochemical deposition behavior of GaTe thin films in acidic solution of HTeO 2 + with Ga 3+ is studied with cyclic voltammetry combining with operando transmittance spectroscopy. Underpotential deposition of Ga on Te starts at potential of − 0.35 V. The presence of Ga 3+ in the solution can strongly suppressed the formation of H 2 Te. XPS analysis reveals that Ga-rich GaTe is deposited over a wide potential range. The photoelectrochemical performance of the thin films as photocathodes is strongly dependent on the deposition potential. The GaTe films deposited at − 1.0 V produced the highest photocurrent of about − 0.03 mA cm −2 . Meanwhile the film deposited at − 0.35 V shows improved performance during photoelectrochemical measurement, which can be ascribed to the increased GaTe content during photoelectrochemical measurements, as confirmed by XPS analysis. Graphical

研究领域: 材料科学 · 电化学 · 半导体物理 · 光电功能材料 · 能源材料 · 表面科学 · 薄膜技术
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ELECTROCHIMICA ACTA · 2017 · IF 4.798

Chemical integration of reduced graphene oxide sheets encapsulated ZnCo2O4 quantum dots achieving excellent capacity storage for lithium-ion batteries

Chang Chen,Kwok-ho Lam,Bao-jun Liu,Xian-hua Hou,Yu-ping Wu

Chemically integrated hybrid quantum dots ZnCo 2 O 4 /reduced graphene oxide (QDs ZCO/rGO) sheets nanocomposites are synthesized through polyol processes. rGO sheets grow and interweave to form basic skeletons. Ultrafine ZCO particles with a size of around 3.66   nm grow and embed on both sides of the rGO sheets, and the rGO sheets restrain the reunion of ZCO nanoparticles . The existence of rGO sheets and ZCO nanoparticles can engender the mutual synergistic effects so that hybrid QDs ZCO/rGO electrodes exhibit the excellent electrochemical properties . Owing to this special nanoparticles-on-sheets structure, the hybrid QDs ZCO/rGO electrodes exhibit an excellent initial discharge capacity for rechargeable lithium-ion batteries (1325.9   mAh   g −1 at the current density of 200   mA   g −1 ), high rate stability (532.3/566.1   mAh   g −1 at 4000   mA   g −1 ) and outstanding electrochemical cyclic stability (657.6/668.2   mAh   g −1 at 2000   mA   g −1 after 2000 cycles with a capacity retention of 68.6%). For full-cells, high initial reversible discharging capacity (646   mAh   g −1 at 200   mA   g −1 ) and good cyclic stability (514   mAh   g −1 at 200   mA   g −1 after 100 cycles) are obtained. The superior performance of the as-prepared electrodes is ascribed to the advantage of nano-sized particles. With the successful synthesis of hybrid QDs ZCO/rGO nanocomposites, the facile synthetic route and unique growth of nanostructuring method can be extended to high electrochemical performance electrodes for commercial lithium-ion batteries.

研究领域: 材料科学 · 电化学 · 纳米科技 · 能源存储 · 功能材料 · 先进电池技术
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JOURNAL OF ALLOYS AND COMPOUNDS · 2022 · IF 6.371

Using tetramethylammonium hydroxide electrolyte to inhibit corrosion of Mg-based amorphous alloy anodes: A route for promotion energy density of Ni-MH battery

Jianling Huang,ChengWei Liao,Hui Wang,YuJun Zhao,Liuzhang Ouyang,Jiangwen Liu,Min Zhu

Mg-based alloy anodes suffer from severe corrosion in conventional electrolytes (KOH solution) and this substantially obstructs the cycle life, which is a great challenge for using them in the Ni-MH battery. Herein, a high concentration tetramethylammonium hydroxide (TMAH) aqueous electrolyte with a special hydrate structure is explored and enables excellent cycle stability and high capacity for Mg-based alloy anodes. In this electrolyte, the Mg 0.4 Ti 0.1 Ni 0.5 alloy anode delivers a maximum discharge capacity of 466 mAh g −1 , and maintains 210 mAh g −1 after 100 cycles owing to the reduced corrosion rate , which are much better than that in 6 M KOH electrolyte, being 425 mAh g −1 and 69 mAh g −1 , respectively. Furthermore, by in-situ forming Cu coating on the Mg 0.4 Ti 0.1 Ni 0.5 electrode surface during charging process with the adding 0.01 M of Cu(OH) 2 in TMAH electrolyte, the corrosion of the electrode is further suppressed and the reversible capacity can reach 313 mAh g −1 after 100 cycles. The high conducting Cu coating can also increase the rate capability of the electrode by promoting the charge transfer. Thus, using TMAH electrolytes provides a new approach to promote the electrochemical performances of Ni-MH batteries with Mg-based alloy anodes.

研究领域: 材料科学 · 电化学 · 能源存储 · 金属腐蚀与防护 · 功能材料 · 电池技术
✓ 已验证 DOI 高影响因子
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INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES · 2022 · IF 8.025

Converting soy protein isolate into biomass-based polymer electrolyte by grafting modification for high-performance supercapacitors

Jian Wang,Zhiyu Xun,Chenyang Zhao,Yang Liu,Jiyou Gu,Pengfei Huo

Soy protein isolate (SPI) is one of the most abundant plant proteins in nature. Enormous studies have been carried out on SPI-based materials, however, the application for energy storage devices is still limited due to its fiddly film forming process and lack of electrochemical performance. Herein, we presented a SPI-based polymer electrolyte by grafting modification with the hydrophilic functional monomer acrylamide (AM). The optimized gel polymer electrolyte (GPE) exhibited an excellent ionic conductivity up to 5.10 mS cm −1 , which was greatly higher than gel polymer electrolyte based on original pure SPI (1.84 mS cm −1 ). More significantly, supercapacitors constructed by grafting-modified SPI delivered a specific capacitance of 141.74 F g −1 at 1.0 A g −1 and exhibited high capacitance retention of 95% after 8000 charge−discharge cycles. Beyond that, redox-active polymer electrolyte based on grafting-modified SPI combining with KI enormously improved the energy density of supercapacitor up to 27.52 Wh kg −1 at a current density of 0.5 A g −1 . This work provided a novel and facile strategy to obtain a high-performance SPI-based polymer electrolyte and laid an experimental foundation for the high-value application of SPI in the field of energy storage devices.

研究领域: 材料科学 · 高分子化学 · 能源存储 · 生物基材料 · 电化学
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