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Green Chemical Engineering · 2024 ·Vol. 7 ·期 1 ·51-60 · IF 9.1

High-performance single crystal Ni-rich cathode with regulated lattice and interface constructed by separated lithiation and crystallization calcination

Siqi Chen,Xin Zhou,Shuo Wang,Ping Zhang,Wenbin Wu,Xiaohong Liu,Guilin Feng,Bin Zhang,Wangyan Xing,Meihua Zuo,Ping Zhang,Wei Xiang

Incorporating high valence dopants, such as W 6+ and Mo 6+ has been verified to be effective for tuning the microstructure and grain boundary of polycrystal Ni-rich cathode. However, the hindered consolidation of primary particles induced by dopants during lithiation calcination limits the utilization of those dopants to crystalize single-crystal Ni-rich cathodes with stabilized lattice and surface. Herein, high performance single crystal LiNi 0.84 Co 0.11 Mn 0.05 O 2 cathode with Al 3+ and W 6+ regulated lattice and boundary phase was construed based on commercial process with two-step calcination process containing separated lithiation and crystallization. The introduction of appropriate amount of Al 3+ in the first lithiation calcination of 6 h endows the bulk of crystalline with enhanced lattice stability, while the incorporation of W 6+ with stoichiometrical LiOH in the secondary crystallization calcination of 6 h renders uniformly distributed surface layer without hampering the growth of single-crystal. With the Al 3+ doped bulk lattice, W 6+ doped subsurface region and hetero-epitaxially grown Li 2 WO 4 , the cathode infused by two-step calcination exhibits high discharge capacity, rate performance, and cycling stability. Specifically, the modified LiNi 0.84 Co 0.11 Mn 0.05 O 2 exhibits exceptional capacity retention, maintaining 88.98% of its initial capacity after 200 cycles at a rate of 1 C within a voltage window of 2.7–4.3 V at a temperature of 25 °C in half-cell. This performance is markedly superior to the capacity retention of 72.96% observed for pristine cathode. Even when subjected to a stringent test after 200 cycles at the same rate, the modified cathode sustains an impressive capacity retention of 82.41% at an elevated cut-off voltage of 4.5 V and a temperature of 30 °C.

研究领域: 材料科学 · 电化学 · 能源存储 · 无机化学 · 固体化学
✓ 已验证 DOI 高影响因子
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CERAMICS INTERNATIONAL · 2019 ·Vol. 45 ·期 10 ·13150-13157 · IF 3.45

Enhanced CH4 sensing properties of Pd modified ZnO nanosheets

Yan Wang,Xiaoning Meng,Mengxia Yao,Guang Sun,Zhanying Zhang

In this paper, pristine ZnO and Pd modified ZnO nanosheets have been successfully prepared via a facile hydrothermal route and the subsequent calcination process. The composition, morphology and nanostructure of the as-obtained materials were characterized by X-ray diffraction (XRD), field-emission scanning electron microscopy (FESEM) and transmission electron microscopy (TEM). The methane (CH 4 ) sensing properties of Pd/ZnO were compared with those of pure ZnO , and the materials showed the noticeable sensing capability when the loading amount of Pd was 1 at%. Moreover, the optimal working temperature of ZnO was reduced from 240 °C to 200 °C after loading Pd. The synthesized 1% Pd/ZnO nanocomposites not only showed the maximum response value 19.20 toward 5000 ppm CH 4 at 200 °C, but also exhibited the excellent selectivity and good repeatability. The improvement of CH 4 sensing performance by Pd nanoparticles could be attributed to the synergy effect with the spill-over effect and the nano-Schottky barriers.

研究领域: 材料科学 · 纳米科技 · 传感器技术 · 表面化学 · 半导体材料
✓ 已验证 DOI 高影响因子
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COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS · 2018 · IF 2.829

Alginate-based colloid particles from direct chemical self-assembly using as particulate emulsifiers

Rongli Zhang,Jingjing Lv,Cuige Zhang,Renchun Yang,Xingchen Sun,Bo Song,Ching-Ping Wong

A new kind of dopamine modified alginate colloid particles (DA-ALG CPs) was prepared via the direct chemical self-assembly triggered by the amidation reaction between dopamine and alginate in aqueous solution. The structure and morphology of the DA-ALG CPs were characterized by infrared spectroscopy , Zeta PALS and scanning electron microscope . The prepared DA-ALG CPs were then used as particulate emulsifier to prepare Pickering emulsions . The properties of the emulsion were characterized by optical microscope . The results revealed that the prepared DA-ALG CPs exhibited good emulsifying property at a wide pH value range, which will endow the potential application of the Pickering emulsions stabilized by DA-ALG CPs in food and biological medicine fields.

研究领域: 高分子材料学 · 胶体与界面化学 · 食品科学 · 生物医学工程 · 药物递送 · 纳米医学
✓ 已验证 DOI 高影响因子
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JOURNAL OF POWER SOURCES · 2019 · IF 7.467

Metallically conductive TiB2 as a multi-functional separator modifier for improved lithium sulfur batteries

Liming Jin,Jie Ni,Chao Shen,Fenglai Peng,Qiang Wu,Donghao Ye,Junsheng Zheng,Gaoran Li,Cunman Zhang,Zhoupeng Li,Jim P. Zheng

A metallically conductive TiB 2 is developed to construct multifunctional separator toward improved lithium-sulfur (Li–S) battery performance. Coupled with two-dimensional graphene, the obtained TiB 2 @G separator fulfills a synergistic combination of strong physical and chemical sulfur immobilization as well as a high-efficiency sulfur reutilization, thus establishing a robust barrier against the polysulfide shuttling and enabling a fast and durable sulfur electrochemistry . As a result, cells based on TiB 2 @G separator exhibit a high sulfur utilization with 1350 mA h g −1 capacity at 0.05C, superb rate capability up to 5.0C, and excellent cyclability with a high capacity retention over 85% after 300 cycles at 0.5C. Moreover, significantly mitigated self-discharge and considerably high areal capacity of 5.8 mA h cm −2 can be also achieved, indicating the great promise of this separator design for the development of high-performance Li–S batteries.

研究领域: 电化学 · 能源材料 · 纳米材料科学 · 储能技术 · 电池化学
✓ 已验证 DOI 高影响因子
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ELECTROCHIMICA ACTA · 2021 · IF 6.901

A facile and scalable Fe-Cr decorating strategy to boost the lithium storage of SiOx anode

Xiaozhong Zhou,Zhaoyi Qi,Yuyuan Jiang,Pengfei Yan,Juanxia Ding,Haiyan Wang,Hongkai Lu,Dongxu Liu,Kaifa Dong,Yougen Tang,Dongfei Sun,Ziqiang Lei

SiO x is regarded as a promising anode material for the next-generation lithium-ion batteries with high energy density. However, the reduplicative volume changes during cycling cause the pulverizations of Si, leading to decreased utilization of active Si component and poor cycling performance. Herein, a facile and scalable Fe-Cr decorating strategy is reported to boost the lithium storage of SiO x anode. Our comprehensive characterizations indicate that there are strong interactions between Fe-Cr and SiO x during a facile ball milling process. After cycling, Fe-Cr nanoparticles are dispersed in the in-situ formed lithium silicates and Li 2 O matrix, which can maintain superior conductivity of lithium ion and electron for the active components through point-to-point connections. This unique structure boosts the electrochemical de-alloying process of the low-valent Li x Si (0 ≤  x  ≤ 2), and increases effective utilization of the active Si component during cycling, resulting in improvement of reversible capacity and cycling stability. This bm SiO x -FeCr electrode can deliver high reversible specific capacity (1370 m Ah g −1 at 200 mA g −1 ), good rate capability (653.8 m Ah g −1 at 2000 mA g −1 ), and superior cycling stability. This work provides a promising route for improving the utilization of active Si component and the structural stability of SiO x -based anodes.

研究领域: 材料科学 · 电化学 · 纳米材料 · 能源存储 · 电池技术 · 固态物理
✓ 已验证 DOI 高影响因子
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CERAMICS INTERNATIONAL · 2016 ·Vol. 42 ·期 6 ·7767-7773 · IF 2.758

Effect of surface modification and medium on the rheological properties of silica nanoparticle suspensions

Shuangbing Li,Jixiao Wang,Song Zhao,Wei Cai,Zhi Wang,Shichang Wang

The unmodified and 3-(trimethoxysilyl) propyl methacrylate (TPM) modified silica nanoparticles were synthesized via the modified Stöber method. The structure and chemical composition of silica nanoparticles were determined by scanning electron microscope (SEM), X-ray diffraction (XRD) characterization, Fourier Transform Infrared Spectroscopy (FTIR) and X-ray photoelectron spectroscopy (XPS). The results demonstrate that silica nanoparticles with the diameter of 90   nm and amorphous state are successfully modified by TPM. The rheological test results demonstrated that surface modification of nanoparticles and medium exerted great influence on the rheological properties of silica particle suspension. Under high shear rate of about 250   s −1 , the viscosity of suspension comprising unmodified silica nanoparticles and deionized water , TPM-modified silica nanoparticles and deionized water, TPM-modified silica nanoparticles and polyethylene glycol , is about 0.4   Pa.s, 0.1   Pa.s and 30   Pa.s, respectively. The results are significant for preparing homogenous and stable silica nanoparticle suspension, and meaningful for ceramic processing .

研究领域: 材料科学 · 纳米技术 · 陶瓷加工 · 胶体化学 · 高分子材料
✓ 已验证 DOI 高影响因子
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APPLIED SURFACE SCIENCE · 2024 · IF 6.3

Multi-element doped hexagonal sheet Ni/Mn-based layered oxide with ZrO2 surface modification for sodium ion batteries cathode with high capacity and good cycle/air stability

Yaoliang Huang,Yunru Zhang,Guizhi Yuan,Dingshan Ruan,Xinlong Zhang,Weijian Liu,Zhongshuai Zhang,Xiaoyuan Yu

Ni/Mn-based layered oxides have been widely studied for sodium ion battery cathode because of high capacity and simple preparation. However, its application has been restricted owing to unstable structure and poor cycling performance. Herein, the multi-element doped hexagonal sheet Ni/Mn-based layered oxide with ZrO 2 surface modification O3-NaNi 0.3 Mn 0.5-x Fe 0.1 Cu 0.1 Zr x O 2 @ZrO 2 (NFMCZ-x) cathode materials have been successfully synthesize by high temperature calcination method accompanied by ball milling activation. XRD refinement results show Zr 4+ substitution of Mn 3+ can increase interlayer distance of sodium layer. Benefiting from the synergetic effect of multi-element doping and ZrO 2 surface modification, the optimized NFMCZ-0.03 sample exhibits a higher discharge capacity of 178 mAh/g at 0.1C and good capacity retention (77 % after 50 cycles at 2C). Furthermore, NFMCZ-0.03 has an excellent air stability with a capacity retention rate of 86 % during 50 cycles at 1C after being exposed in the air for 20 days. The ex-situ XRD results of NMFC at different charge/discharge voltages show Zr 4+ doping can suppress O3 + P3′'–O3′-O3 + P3′' phase transition during charge/discharge process. These results confirm that synergistic effect of multi-doping combined with surface modification can improve electrochemical performance of layered oxides cathodes, which provides a research idea for development of Ni/Mn-based layered oxides cathodes for sodium-ion batteries.

研究领域: 材料科学 · 电化学 · 能源存储 · 无机化学 · 固态化学
✓ 已验证 DOI 高影响因子
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MATERIALS CHEMISTRY AND PHYSICS · 2019 · IF 2.781

Achieving superior electrochemical performances on LiNi0.8Co0.15Al0.05O2 cathode materials by cadmium oxide modification

Yunjiao Li,Shilei Wang,Yongxiang Chen,Tongxing Lei,Shiyi Deng,Jie Zhu,Jinping Zhang,Jia Guo

Cadmium oxides (CdO), an important semiconductor material , have many superior properties when used as a cathode material for nickel-cadmium batteries. Here, the coating and the doped co-modified LiNi 0.8 Co 0.15 Al 0.05 O 2 cathode are constructed by a continuous wet chemical process and a high-temperature sintering process, wherein the Cd 2+ are uniformly doped in a gradient form and the CdO protective layer is distributed on the outer surface of secondary particles. The Cd-modified NCA material has more stable interfacial and crystal lattice structure, thereby inhibiting harmful phase transitions and side-reactions. Accordingly, the modified sample has excellent electrochemical performance and maintaining a complete spherical morphology during long cycling compared to the pristine sample. In addition, as a pillar ion, cadmium increases the plate spacing and lithium-ion diffusion kinetics. The electrochemical results show that the capacity retention of the modified sample Cd-2000 reached 96.5% and 90.6% after 100 cycles and 200 cycles respectively at 1 C. At the high current rate of 8 C, the initial capacity and retention (100 cycles, 3.0–4.3 V) reach 166.2 mAh g −1 and 95.2%, respectively. Besides, the results of electrochemical impedance spectroscopy (EIS) reveal that CdO modification could decrease the resistance of the cell polarization and impedance increment upon cycling.

研究领域: 材料科学 · 电化学 · 能源存储 · 无机化学 · 半导体材料
✓ 已验证 DOI 高影响因子
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RSC Advances · 2018 ·Vol. 8 ·期 15 ·8026-8038 · IF 2.936

Rapid removal of Pb2+ from aqueous solution by phosphate-modified baker's yeast

Shuli Liu,Zhengyang Duan,Changhua He,Xiaojun Xu,Tianguo Li,Yuhuan Li,Xuan Li,Yao Wang,Longqian Xu

Phosphate-modified baker's yeast (PMBY) was prepared, and used as a novel bio-sorbent for the adsorption of Pb2+ from aqueous solution. The influencing factors, absorption isotherms, kinetics, and mechanism were investigated. The scanning electron microscopy (SEM), Fourier-transform infrared spectroscopy (FTIR) characterization and elemental analysis of PMBY showed that phosphate groups were successfully grafted onto the surface of yeast. The kinetic studies suggested that the adsorption process followed a pseudo-second-order chemisorption. The adsorption process of Pb2+ using PMBY was spontaneous and endothermic. Furthermore, the adsorption of Pb2+ on PMBY can rapidly achieve adsorption equilibrium (in just 3 min), and the maximum adsorption capacity of Pb2+ on PMBY was found to be 92 mg g−1 at 30 °C, which was about 3 times that of the pristine baker's yeast. The suggested mechanism for Pb2+ adsorption on PMBY was based upon ion-exchange, electrostatic interaction and chelation between the phosphate groups and Pb2+. However, compared with the pristine baker's yeast, the higher capacity and rapid adsorption of PMBY for Pb2+ was mainly due to the chelation and electrostatic interactions between the phosphate groups and Pb2+. In addition, the regeneration experiments indicated that the PMBY was easily recovered through desorption in 0.01 M HCl, and that PMBY still exhibited 90.77% of the original adsorption capacity for Pb2+ after five regeneration cycles. These results showed the excellent regeneration capability of PMBY for Pb2+ adsorption. PMBY has shown significant potential for the removal of heavy metals from aqueous solution due to its rapid adsorption, high-capacity and facile preparation.

研究领域: 环境科学 · 生物化学 · 环境污染治理 · 重金属吸附 · 材料科学
✓ 已验证 DOI 高影响因子
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International Journal of Electrochemical Science · 2023 ·Vol. 7 ·期 6 ·5172-5184 · IF 1.5

Reduction of Graphene Oxide Via Ascorbic Acid and Its Application for Simultaneous Detection of Dopamine And Ascorbic Acid

Xu Zhu,Qin Liu,Xiaohua Zhu,Chunlan Li,Maotian Xu,Yong Liang

A new approach to synthesize graphene was applied by reduction of graphene oxide using ascorbic acid. Chitosan/graphene modified electrode could be employed for simultaneous determination of dopamine and ascorbic acid. The modified electrode showed excellent electrocatalytic activity towards the oxidation of DA and AA. The calibration curves for DA and AA were obtained in the range of 0.3-1067.5μM and 0.6-1378.1μM, respectively. Detection limits were 0.1μM and 0.01μM for DA and AA, respectively. The present method was applied to the determination of AA and DA in human serum samples and the results were quite promising.

研究领域: 分析化学 · 电化学 · 生物传感器 · 纳米材料 · 临床检验 · 神经化学 · 药物分析
✓ 已验证 DOI 高影响因子
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SOLID STATE IONICS · 2019 · IF 2.886

Conformal, nanoscale γ-Al2O3 coating of garnet conductors for solid-state lithium batteries

Fan Deng,Yongmin Wu,Weiping Tang,Shufeng Song,Zhaoyin Wen,Masashi Kotobuki,Li Lu,Jianyao Yao,Ning Hu,Janina Molenda

The use of garnet-type conductors as electrolytes for safe lithium solid-state batteries is impeded by the lack of critical processing strategy to stabilize and densify the cubic lithium garnets. The synthesis and processing of dense cubic lithium garnets are typically depending on solid state reaction as a result of unintentional Al contamination from the alumina crucibles at temperatures up to 1230 °C. High Al concentration is also believed to induce the sluggish migration of lithium ions . Here, we demonstrate an ultrathin, conformal γ-Al 2 O 3 surface coating on garnet solids by a hybrid microemulsion solid-state method for accomplishing rational and controllable synthesis and processing of dense cubic garnets with low Al concentration. The γ-Al 2 O 3 coating demonstrates fast-ion conducting Al-doped Li 6.75 La 3 Zr 1.75 Ta 0.25 O 12 phase with low Al concentration (~0.17 mol per formula unit), low tetragonal-to-cubic phase transformation temperature of 500 °C, and total conductivity of ~4.4 × 10 − 4  S cm − 1 . Specifically, the desired microstructures of the sintered pellets with uniform grains are revealed. As a proof-of-concept, we demonstrate that the nanoscale γ-Al 2 O 3 modification garnet conductor Li 6.75 La 3 Zr 1.75 Ta 0.25 O 12 is available to suppress lithium dendrites in symmetric Li/γ-Al 2 O 3 coating Li 6.75 La 3 Zr 1.75 Ta 0.25 O 12 /Li cells during lithium plating/stripping at room temperature, with current densities of 0.026 to 0.5 mA cm − 2 . The Li/γ-Al 2 O 3 coating Li 6.75 La 3 Zr 1.75 Ta 0.25 O 12 /LiNi 0.5 Co 0.2 Mn 0.3 O 2 cell delivered a high initial discharge capacity of ~164.2 mAh g − 1 , more importantly, an outstanding cycling performance with a capacity retention of 90.16% after 30 cycles at 0.1C and room temperature. This new synthesis route and the utilization of nanoscale γ-Al 2 O 3 surface modification could open up new avenue to lithium garnet conductors with reliable synthesis for all-solid-state lithium batteries application.

研究领域: 材料科学 · 电化学 · 固态离子学 · 能源存储 · 纳米材料 · 电池技术
✓ 已验证 DOI 高影响因子
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Desalination and Water Treatment · 2024 · IF 1

Surface coating of a side-chain type polyelectrolyte for endowing perm-selectivity between specific anions to an anion-exchange membrane with a small loss of membrane conductivity

Yan-zhen Shen,Xun-liang Wang,Yu-xiang Jia,Meng Wang

The endowment of perm-selectivity for specific ions will further extend the applications of heterogeneous membrane. In this work, a side-chain type weak cationic polyelectrolyte, PVDF-g-PVP, was synthesized for surface hydrophobilization of heterogeneous anion-exchange membrane (AEM) in order to impart perm-selectivity between specific anions with different Gibbs hydration energy. After microstructure observation and chemical composition analyses by SEM, AFM, EA and FTIR, the perm-selectivity between specific anions, electrical resistance, transport number, limiting current density, surface homogeneity, as well as salt permeability of the modified AEMs were investigated. Series of electrodialysis experiments in SO 4 2– /Cl – system indicated that a significant perm-selectivity was indeed achieved by the attachment of PVDF-g-PVP coating. In particular, it was worth noting that only a small loss of membrane conductivity was observed after the functionalization. This should be closely related to the micro-phase separation morphology of the coating layer which was induced by the polarity difference between the main chains and side chains of PVDF-g-PVP. Besides, the chronopotentiometric analyses indicated surface homogeneity of the heterogeneous AEM was significantly enhanced and then effectively ameliorated concentration polarization behaviors at the membrane-solution interface. Meanwhile, the perm-selectivity for co-ions was also improved and suppressed back diffusion behaviors of salt driven by concentration gradient. In brief, the modifying scheme proposed in this work can effectively improve comprehensive transport properties of conventional heterogeneous AEM.

研究领域: 膜科学与技术 · 高分子材料化学 · 分离科学 · 电化学工程 · 功能材料
✓ 已验证 DOI 高影响因子
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