CHEMICAL ENGINEERING JOURNAL
·
2024
·
IF 13.3
Jingsheng Xu,Zhiyuan Wang,Runguo Zheng,Hongyu Sun,Yanguo Liu,Junhua You
Ni-rich cathodes especially with Ni content over 90 % are promising next-generation cathode materials for advanced high energy lithium − ion batteries. However, in comparison with Ni ≤ 80 % Ni-rich cathodes, these ultrahigh Ni-rich materials face more severe challenges in terms of harmful H2 − H3 phase transformations and structural degradation during cycling. Herein, we present a robust surface structure composted of defect-rich disordered structures and LiF/Li 2 SiO 3 coating for stabilizing the ultrahigh Ni-rich cathode LiNi 0.96 Co 0.03 Mn 0.01 O 2 (NCM96) by modification with (NH 4 ) 2 SiF 6 . The surface disordered structures including Li/TM mixing, spinel, and rock salt structure play a crucial role in inhibiting the irreversible H2-H3 phase transition and reducing lattice volume changes by lattice coherence effect. Moreover, the disordered surface in collaboration with the co-coating restrains the rapid growth of surface rock salt phase into the bulk, enhancing structural stability. The modified sample NSF-0.5 delivers a capacity of 238 mAh/g at 0.1C and maintains a capacity retention of 88.5 % at 0.5C after 100 cycles in half cell as well as 82.3 % at 1C after 300 cycles in full cell, significantly superior to the NCM96. The findings provide a simple and cost-effective surface modification strategy to enhance the structural stability and electrochemical performance of ultrahigh nickel cathodes for high-energy density LIBs.
研究领域:
材料科学
·
电化学
·
能源存储
·
锂离子电池
·
固态化学
·
表面工程
·
电池材料
✓ 已验证
DOI
高影响因子
Journal of Materials Chemistry A
·
2023
·Vol. 11
·期 36
·19536-19545
·
IF 11.9
Gege Wang,Feifan Zhang,Caiyu Ma,Jianhua Yang,Xiaowei Chi,Yu Liu
Aqueous zinc metal batteries (AZMBs) as one of the next-generation energy storage technologies have attracted both academic and industrial attention due to their high safety, low cost, and high specific energy, yet are facing interfacial challenges at the electrolyte/anode interface, e.g. uneven physical diffusion of Zn2+ flux, severe chemical corrosion, and disordered electrochemical deposition behavior of the zinc metal anode. To address these issues, herein, we propose a facile and effective electrolyte modulating strategy to construct a physico-chemo-electrochemically coupled stable interface between the aqueous electrolyte and zinc anode. The aqueous electrolyte modified using a tiny amount of water-soluble ionic liquid 1-ethyl-3-methylimidazolium tetrafluoroborate (EMIMBF4) can form a positively charged organic EMIM+ adsorption layer and a protective inorganic Zn2+-conducting layer through the in situ decomposition of BF4− on the zinc anode surface, thus effectively homogenizing the Zn2+ diffusion flux and decreasing the chemical corrosion rate. Moreover, EMIM+ provides an electrostatic shielding layer, leading to the preferential and ordered electrodeposition of Zn2+ along the Zn (002). Benefiting from this physico-chemo-electrochemically multifunctional interfacial layer, the Zn//Zn symmetric cells achieve a considerably extended lifespan of up to 1200 h at 5 mA cm−2 and 5 mA h cm−2, and more than 450 h even at an ultrahigh current density and large deposition capacity (10 mA cm−2 and 10 mA h cm−2). Zn//Cu asymmetric cells also exhibit excellent reversibility with a high coulombic efficiency of 99.75%. Furthermore, the physically, chemically, and electrochemically stabilized interface enables the AZMB with a quinone-based cathode to offer high specific capacity (256.9 mA h g−1) and a decent capacity retention rate (83.9% after 300 cycles).
研究领域:
电化学
·
能源材料
·
界面科学
·
储能技术
·
材料化学
✓ 已验证
DOI
高影响因子
JOURNAL OF FOOD PROTECTION
·
2018
·Vol. 81
·期 10
·1643-1650
·
IF 1.51
Huqing Yang,Xia Li,Guoquan Lu
Because of high water loss and rot observed in postharvest sweet potato ( Ipomoea batatas (L.) Lam.) roots, a carnauba wax (CW)–based nanoemulsion without or with glycerol monolaurate (CW-GML) was developed by a high-energy emulsification approach. The effects of the two coatings on decay, respiration rate, weight loss, surface color, total soluble sugar, and starch content as well as the sensory quality of sweet potato roots were investigated during storage at 20°C for 50 days. Compared with the control treatment (water) and CW coating alone, CW-GML coating exhibited higher emulsion stability and antifungal activity, and treatment resulted in a uniform and continuous coating on roots. The CW-GML and CW coatings both effectively reduced root weight loss and respiration rate and inhibited decay incidence compared with control roots during storage. The CW-GML coating showed markedly stronger inhibition of root rot than the CW coating. Both the CW-GML and CW coatings promoted an increase in root sweetness but did not negatively impact perceived flavor. The overall results demonstrate that the CW-GML coating holds great promise as an effective postharvest technology to preserve food quality and extend shelf life of sweet potato roots.
研究领域:
食品科学
·
采后生物学
·
农产品贮藏
·
食品保鲜技术
·
应用植物学
✓ 已验证
DOI
高影响因子
ELECTROCHIMICA ACTA
·
2020
·
IF 6.215
Yuexiu Du,Chongwu Liu,Yunzhao Liu,Qi Han,Xiaowei Chi,Yu Liu
Rechargeable metal batteries are desirable for next-generation high specific energy electrochemical energy storage systems . However, low coulombic efficiency and severe dendrite growth during the stripping/plating of metals (e.g. Li, Na, Zn and etc.) considerably hinder their practical applications. To address the above issues, in this work, a facile, versatile, and scalable approach by means of spray depositing carbon fiber micron film (CFMF) onto metals is developed. The porous, uniform, and highly conductive CFMF firmly attached to metal surface with a scaffold structure is found to effectively guide the uniform plating/stripping of both the Zn metal in aqueous electrolytes and the Li metal in organic electrolytes, thus enabling much higher efficiencies of Zn (98.4%) and Li (99.7%) for the 100th cycle on the CFMF-modified current collectors than those of bare current collectors. And the so far record high cycling stability for the symmetric cells using CFMF/Zn (2500 h) and CFMF/Li (1000 h) electrodes is achieved at 1 mA cm −2 and 4 mA cm −2 , respectively. Benefiting from the delicately designed CFMF-modified Zn or Li metal anodes , the full cells of Zn–MnO 2 and Li–LiMn 2 O 4 are rendered excellent rate capability and significantly extended cycle life.
研究领域:
材料科学
·
电化学
·
能源存储
·
纳米技术
·
电池技术
✓ 已验证
DOI
高影响因子
JOURNAL OF ALLOYS AND COMPOUNDS
·
2017
·
IF 3.133
Jianguang Jia,Chunmei Liu,Yuan Lin,Xiaowen Zhou
Charge recombination is an important factor that limits the cell efficiency of quantum dot sensitized solar cells (QDSSCs). Herein, we report a facile way to improve the cell performance of CdSe sensitized ZnO QDSSC by overcoating a thin layer of ZnSe on CdSe/ZnO film through a successive ionic layer adsorption and reaction (SILAR) procedure. Photovoltaic investigations indicate that ZnSe overcoating can increase photocurrent and photovoltage of the cell, resulting in significant enhancement of the cell efficiency, which is much better than the widely used traditional ZnS material. The superior role of ZnSe overcoating is ascribed to its large inhibition of charge recombination loss owing to its suitable band structure, efficient passivation of ZnO and CdSe QDs as well as its small lattice mismatch with CdSe that leads to the large decrease of surface/interface defects in CdSe/ZnO photoanode . This finding provides an alternative efficient way to enhance the cell performance of ZnO based QDSSC by suppressing the charge recombination.
研究领域:
材料科学
·
纳米科技
·
能源化学
·
半导体物理
·
光伏技术
✓ 已验证
DOI
高影响因子
Advanced Science
·
2024
·Vol. 11
·期 38
·2405276
·
IF 14.3
Huangzhe Dai,Chengqian Zhang,Hao Hu,Zhezai Hu,Haonan Sun,Kan Liu,Tiefeng Li,Jianzhong Fu,Peng Zhao,Huayong Yang
The rapid development of ocean exploration and underwater robot technology has put forward new requirements for underwater sensing methods, which can be used for hydrodynamic characteristics perception, underwater target tracking, and even underwater cluster communication. Here, inspired by the specialized undulated surface structure of the seal whisker and its ability to suppress vortex-induced vibration, a multidirectional hydrodynamic sensor based on biomimetic whisker array structure and magnetic 3D self-decoupling theory is introduced. The magnetic-based sensing method enables wireless connectivity between the magnetic functional structures and electronics, simplifying device design and endowing complete watertightness. The 3D self-decoupling capability enables the sensor, like a seal or other organisms, to perceive arbitrary whisker motions caused by the action of water flow without complex calibration and additional sensing units. The whisker sensor is capable of detecting a variety of hydrodynamic information, including the velocity (RMSE < 0.061 m s −1 ) and direction of the steady flow field, the frequency (error < 0.05 Hz) of the dynamic vortex wake, and the orientation (error < 7°) of the vortex wake source, demonstrating its extensive potential for underwater environmental perception and communication, especially in deep sea conditions.
研究领域:
生物医学工程
·
海洋生物学
·
传感器技术
·
流体力学
·
仿生学
·
水下机器人
·
环境感知
✓ 已验证
DOI
高影响因子
Small
·
2018
·Vol. 14
·期 31
·1801420
·
IF 9.598
Kuirong Deng,Jiaxiang Qin,Shuanjin Wang,Shan Ren,Dongmei Han,Min Xiao,Yuezhong Meng
A novel single-ion conducting polymer electrolyte (SIPE) membrane with high lithium-ion transference number, good mechanical strength, and excellent ionic conductivity is designed and synthesized by facile coupling of lithium bis(allylmalonato) borate (LiBAMB), pentaerythritol tetrakis (2-mercaptoacetate) (PETMP) and 3,6-dioxa-1,8-octanedithiol (DODT) in an electrospun poly(vinylidienefluoride) (PVDF) supporting membrane via a one-step photoinitiated in situ thiol–ene click reaction. The structure-optimized LiBAMB-PETMP-DODT (LPD)@PVDF SIPE shows an outstanding ionic conductivity of 1.32 × 10 −3 S cm −1 at 25 °C, together with a high lithium-ion transference number of 0.92 and wide electrochemical window up to 6.0 V. The SIPE exhibits high tensile strength of 7.2 MPa and elongation at break of 269%. Due to these superior performances, the SIPE can suppress lithium dendrite growth, which is confirmed by galvanostatic Li plating/stripping cycling test and analysis of morphology of Li metal electrode surface after cycling test. Li|LPD@PVDF|Li symmetric cell maintains an extremely stable and low overpotential without short circuiting over the 1050 h cycle. The Li|LPD@PVDF|LiFePO 4 cell shows excellent rate capacity and outstanding cycle performance compared to cells based on a conventional liquid electrolyte (LE) with Celgard separator. The facile approach of the SIPE provides an effective and promising electrolyte for safe, long-life, and high-rate lithium metal batteries.
研究领域:
材料科学
·
电化学
·
能源存储
·
高分子化学
·
电池技术
✓ 已验证
DOI
高影响因子
JOURNAL OF MATERIALS SCIENCE-MATERIALS IN ELECTRONICS
·
2024
·Vol. 35
·期 2
·140
·
IF 2.8
Ma Di,He Hao,Huang Xinglan,Wang Jingcheng,Hu Xuebu
The inhomogeneous plating/stripping of zinc and side reactions originating from the dissolution of the cathode material in water lead to the poor stability of zinc anode, which inevitably limits the practical application of zinc-based aqueous batteries. Therefore, a novel hydrogel electrolyte made of hydroxyethyl cellulose/polyacrylamide (HEC/PAM) with a 3D network-like structure is synthesized by radical polymerization and cross-linking reinforcement. Thanks to the porous crosslinked network and massive hydrophilic groups, the electrolyte has high ion conductivity of 3.17 × 10 –2 S cm −2 and decomposition voltage of 2.6431 V. The ion conductive hydrophilic groups facilitate the interfacial compatibility of the electrode with the electrolyte and stabilize zinc plating/stripping, which suppresses the formation of zinc dendrites. Meanwhile, the hydrogel electrolyte effectively alleviates the dissolution of the positive electrode and the occurrence of side reactions, and subsequently improves the stability of the electrode. As a result, the assembled Zn–Zn symmetric cell with HEC/PAM hydrogel electrolyte is stable without short circuit and rapid increase of overvoltage at 5 mA cm −2 . The polarization voltage of the assembled Zn–Cu half-cell is 59.2 mV and initial coulomb efficiency reaches 94.3%. The assembled Zn–V 2 O 5 ·nH 2 O/CNT full cell delivers an excellent cycling stability of 186.9 mAh g −1 at 0.5 A g −1 after 500 cycles with a high-capacity retention of 92.5% (only 52.1% in aqueous system). The new idea is provided for further development of functional hydrogel electrolytes in zinc-ion batteries.
研究领域:
电化学
·
能源材料
·
功能高分子
·
电池技术
·
界面化学
✓ 已验证
DOI
高影响因子
FUEL
·
2022
·
IF 8.035
Xue Zou,Mucong Zi,Tiantian Wu,Yuanxin Yao,Caifeng Yang,Daoyi Chen
Kinetic hydrate inhibitors (KHIs) have gradually gained more attention in the natural gas and oil transportation field due to their remarkable inhibition performance at low dosages. However, the inhibition performance of most commercial KHIs is poor under high subcooling conditions. In this work, a radical polymerization method was used to synthesize four new KHIs by introducing the 1-vinylimidazole (VI) or vinylacetate (VAc) monomer. These newly-synthesized copolymer KHIs were characterized by Fourier Transform Infrared, 1 H nuclear magnetic resonance, and gel permeation chromatography, respectively. The cloud point of HY-201 is remarkably as high as 92.3 °C and the four KHIs are all biodegradable. Under subcooling of 10 K and 15 K, the inhibitory performance of four new KHIs and three commercial KHIs on hydrate nucleation and growth are as follows: PVP < Luvicap EG < Inhibex 501 < HY-101 < HY-201 < HY-301 < HY-401. In addition, the hydrate volume fraction of the four new KHIs at the optimal concentration of 15 K subcooling for 12 h was 13.3 %, 1.7 %, 2.4 %, and 2.1 %, respectively, which did not exceed 1/3 of the tested commercial KHIs. Further, the novel mechanism hypothesis is proposed as follows: the surface charge of the hydrate nuclei is neutralized by KHIs, and the hydrate nuclei aggregates, hindering the gas from entering the hydrate. In addition, the strong entanglement and adsorption of KHIs molecules with better inhibition performance make the hydrate lose the space for growth and expansion. Overall results highlight the great application prospects of these new KHIs in natural gas transmission based on the remarkable inhibition performance under high subcooling conditions.
研究领域:
石油与天然气工程
·
化学工程
·
材料科学
·
环境友好材料
·
流体输送
✓ 已验证
DOI
高影响因子
POWDER TECHNOLOGY
·
2019
·
IF 3.413
Zhilin Xi,Shuhui Zhou,Longzhe Jin
In this work, a self-hardening foam-sol (SHF) is proposed to control the diffusion of static coal dust. The SHF was mainly synthesized by a foaming solution (composed of 1 g/L polyethylene oxide (PEO), 25 g/L sodium dodecyl sulfate (SDS), 100 g/L sodium silicate and 874 g/L water) and organic acid with a concentration range of 10 to 13 g/L. Based on fluorescence spectrophotometry , drop shape analysis, X-ray photoelectron spectroscopy and scanning electron microscopy, several conclusions could be found. The critical micelle concentration of SDS was 25 g/L, when most of the pyrene pendants were solubilized into the SDS micelles to form the hydrophobic mixed micelles, and excimer formation began to reach a maximum. The SHF had optimal wetting ability with the smallest contact angle of 17 o , due to PEO-bonded water and SDS forming hydrogen and a dual adsorption layer, which could enhance the wetting ability of the SHF on coal dust surfaces. The SHF had the best accepted loss of liquidity time (180–86 s) and self-hardening time (236–121 s) via the reaction of sodium silicate and organic acid. The pores and cracks among dust particles could be linked closely by SHF via the solid bridge force. The primary components were silica and sodium carbonate with crystal water and hydrophilic C O and C O or O–C–O functional groups. Based on the dust suppression experiment, the dust suppression efficiency was almost 100% at airflow speeds below 12 m/s. Obviously, the dust particles could be controlled via their surfaces being covered by a layer of SHF, since the SHF has strong hydrophilic properties and the solid bridge force. In addition, vehicle-mounted SHF preparation equipment was designed.
研究领域:
环境工程
·
矿业安全
·
胶体与界面化学
·
职业健康
·
颗粒物控制
✓ 已验证
DOI
高影响因子
CHEMICAL ENGINEERING JOURNAL
·
2022
·
IF 16.744
XinLong Zhang,HaiYan Zhang,Yuan Geng,ZhangQin Shi,Sheng Zhu,QunJie Xu,YuLin Min
Lithium–sulfur (Li–S) batteries are considered as very promising energy storage systems due to their higher theoretical performance and lower active material cost. However, the notorious shuttle effect and lithium dendrite growth have severely restricted the industrial production of Li–S batteries. In this study, we used polyethylene oxide (PEO) as the matrix and added multifunctional nanofillers (nano In 2 O 3 ) to effectively inhibit the shuttle effect caused by the dissolution of lithium polysulphides (LiPSs) in Li–S batteries. As a multifunctional filler, nano-In 2 O 3 not only improves the ionic conductivity of the PEO electrolyte, but also forms a Li–In alloy layer in situ at the polymer/anode interface, which can cause the rapid diffusion of lithium ions and prevent the side reactions between lithium metal anode and the electrolyte. Achieving the effect of stabilizing the lithium metal anode and suppressing the shuttle effect. Multiple problems in the system are solved by introducing a single component with multiple functions. The symmetrical lithium battery based on the PEO/LiTFSI/In 2 O 3 solid polymer electrolyte (PEO/LiTFSI/In 2 O 3 SPE) has higher cycle stability (over 1200 h) because it is more stable to the lithium metal anode. The Li–S full battery also exhibits excellent electrochemical performance. After 500 cycles at 1C, its capacity can be maintained at 570 mAh g −1 , the capacity decay rate is 0.038%. The coulombic efficiency (CE) during the cycle is also close 100%.
研究领域:
电化学
·
能源材料
·
固态离子学
·
电池技术
·
纳米复合材料
✓ 已验证
DOI
高影响因子
JOURNAL OF POWER SOURCES
·
2022
·
IF 9.794
Yuanyuan Li,Jun Cheng,Jianwei Li,Zhen Zeng,Yixuan Guo,Hongqiang Zhang,Hongbin Liu,Xiao Xu,Yiwei Rao,Deping Li,Lijie Ci
Sulfide solid state electrolytes capture much attention owing to their high conductivity and decent mechanical property. Nevertheless, the moisture instability and poor interfacial compatibility against lithium metal anode remain challenging and hinder the practical application. Herein, we report a novel indium (In) doping strategy based on the hard-soft-acid-base theory to tackle these issues. Optimized Li 7 P 2.9 S 10.9 In 0.1 electrolyte exhibits a high ionic conductivity of 4.1 × 10 −3 S cm −1 and achieves an enhanced interfacial compatibility. Importantly, as In partially replaces the phosphorus (P), the amount of released hydrogen sulfide can be significantly decreased and the air stability is improved. The all-solid-state battery assembled with the Li 7 P 2.9 S 10.9 In 0.1 electrolyte demonstrates a high discharge capacity and a good cycling stability under a high current density of 1.0 C. This work provides a practical and effective method to design sulfide-based solid-state electrolyte with high ionic conductivity and enhanced air stability for all-solid-state battery applications.
研究领域:
材料科学
·
电化学
·
能源存储
·
固态离子学
·
电池技术
✓ 已验证
DOI
高影响因子
危险品化学品经营许可证（带存储）