CERAMICS INTERNATIONAL
·
2024
·Vol. 50
·期 14
·24995-25004
·
IF 5.1
Zhiyi Li,Haili Sun,Wei Wei,Fengxia Liu,Xiaofei Xu,Zhijun Liu
The emerging market of high-power lithium-ion batteries (LIBs) highlights the importance of developing high-voltage cathodes. Lithium nickel phosphate (LiNiPO 4 ) with the highest theoretical discharge potential (∼5.1V) has attracted increasing attention due to its stable olivine structure. In this study, ultrathin carbon layer-coated LiNiPO 4 was synthesized using oleylamine-assisted solvothermal method under different solvothermal times, and the effect of solvothermal time (1h–18h) on LiNiPO 4 samples is fully investigated. X-ray diffraction (XRD) shows that high-purity LiNiPO 4 materials can be prepared after calcination of the solvothermal product under N 2 , but adding part of H 2 to the calcination atmosphere will lead to the generation of impurities in the target product. As the solvothermal time increases, the product will agglomerate and grow, the particle size will increase, and the morphology will change from nanoparticle to rodlike structure. After the high-temperature calcination step, the oleylamine is completely carbonized, and a conductive carbon layer is successfully coated on the LiNiPO 4 with the thickness of 2 nm. As the solvothermal time increases, the graphitization degree of oleylamine increases after carbonization. The existence of the carbon layer and the increase in the degree of graphitization are beneficial to improving the electrical conductivity and Li-ion diffusion rate of LiNiPO 4 . The initial discharge capacity of LNP@C-12h product prepared with 12 h solvothermal time is 35 mA h g −1 at 0.1 C. Rietveld analysis shows that the anti-site defect concentration of the LNP@C material is 1.07 %, and the proportion increases to 2.83 % after several cycles. This work provides a positive contribution to the synthesis and modification of high-voltage LiNiPO 4 materials and explains the electrochemical performance degradation of LiNiPO 4 from the perspective of increasing the concentration of anti-site defects.
研究领域:
材料科学
·
电化学
·
纳米科技
·
能源存储
·
锂离子电池
✓ 已验证
DOI
高影响因子
Energy & Environmental Materials
·
2023
·Vol. 7
·期 3
·e12641
·
IF 15
Huachao Yang,Yiheng Qi,Zifan Wang,Qinghu Pan,Chuanzhi Zhang,Jianhua Yan,Kefa Cen,Zheng Bo,Kostya (Ken) Ostrikov
Safe operation of electrochemical capacitors (supercapacitors) is hindered by the flammability of commercial organic electrolytes. Non-flammable Water-in-Salt (WIS) electrolytes are promising alternatives; however, they are plagued by the limited operation voltage window (typically ≤2.3 V) and inherent corrosion of current collectors. Herein, a novel deep eutectic solvent (DES)-based electrolyte which uses formamide (FMD) as hydrogen-bond donor and sodium nitrate (NaNO 3 ) as hydrogen-bond acceptor is demonstrated. The electrolyte exhibits the wide electrochemical stability window (3.14 V), high electrical conductivity (14.01 mS cm −1 ), good flame-retardance, anticorrosive property, and ultralow cost (7% of the commercial electrolyte and 2% of WIS). Raman spectroscopy and Density Functional Theory calculations reveal that the hydrogen bonds between the FMD molecules and NO 3 − ions are primarily responsible for the superior stability and conductivity. The developed NaNO 3 /FMD-based coin cell supercapacitor is among the best-performing state-of-art DES and WIS devices, evidenced by the high voltage window (2.6 V), outstanding energy and power densities (22.77 Wh kg −1 at 630 W kg −1 and 17.37 kW kg −1 at 12.55 Wh kg −1 ), ultralong cyclic stability (86% after 30 000 cycles), and negligible current collector corrosion. The NaNO 3 /FMD industry adoption potential is demonstrated by fabricating 100 F pouch cell supercapacitors using commercial aluminum current collectors.
研究领域:
电化学
·
材料科学
·
能源存储
·
应用化学
·
物理化学
✓ 已验证
DOI
高影响因子
Small
·
2019
·Vol. 15
·期 50
·1904854
·
IF 10.856
Junchao Zheng,Zhuo Yang,Alvin Dai,Linbo Tang,Hanxin Wei,Yunjiao Li,Zhenjiang He,Jun Lu
Although the high energy density and environmental benignancy of LiNi 0.8 Co 0.15 Al 0.05 O 2 (NCA) holds promise for use as cathode material in Li-ion batteries, present low rate capabilities, and fast capacity fade limit its broad commercial applications. Here, it is reported that surface modification of NCA cathode ( R-3m ) with 5 nm-thick nanopillar layers and Fm-3m structures significantly improves electrode structure, morphology, and electrochemical performance. The formation of nanopillar layers increases cycling and working voltage stability of NCA by shielding the host material from hydrofluoric acid and improves structural stability with the electrolyte. The modified NCA cathode exhibits an enhanced 89% capacity retention at a rate of 1 C over that of pristine NCA (75.2%) after 150 cycles and effectively suppresses working voltage fade (a drop of 0.025 V after 300 cycles) during repeated charge–discharge cycles. In addition, the diffusion barrier of Li ions in NCA crystals at 0.80 V is noticeably smaller than that of Li ions in pristine NCA (0.87 eV). These findings demonstrate that this unique surface structure design considerably enhances cycle and rate performance of NCA, which has potential applications in other Ni-rich layered cathode materials.
研究领域:
材料科学
·
电化学
·
能源存储
·
锂离子电池
·
纳米材料
✓ 已验证
DOI
高影响因子
JOURNAL OF POWER SOURCES
·
2021
·
IF 9.127
Shigen Bai,Yong Tang,Gong Chen,Yaopeng Wu,Yifu Liang,Shu Yang,Huilong Liu,Yingxi Xie
Supercapacitors (SCs) have garnered increasing attention as an alternative energy storage device but the relatively low potential window and energy density impede their application prospect. Herein, we propose a novel three-dimensional (3D) packaging method for the first time, utilizing high flexible phosphor-copper sheets (PCSs) sprayed with polytetrafluoroethylene (PTFE) and covered with polyimide (PI) films on their both sides as the serial medium followed by CO 2 laser irradiation to fabricate all-solid-state flexible high voltage supercapacitors (HVSCs). This method achieves double voltage output in the limited PI membrane compared with common 2D encapsulation. As a result, as-obtained HVSCs deliver not only an enhanced mechanical tensile strength up to 18.23 MPa but also the outstanding electrochemical performances, including ultrahigh working voltage window (10 V), high energy density (37.68 μWh/cm 2 ) and power density (3.38 mW/cm 2 ). Owing to the excellent flexibility, the HVSCs can be arbitrarily bent or twisted without obvious attenuation on capacitive property. After 10000 cycles, the capacitance retention of HVSCs still maintains to be 90.2%. This novel 3D packaging strategy may pave the way for developing high-performing SCs with wide operating voltage and high energy density for flexible displays, wearable equipment and integrated electrical devices.
研究领域:
材料科学
·
纳米技术
·
能源存储
·
柔性电子
·
电化学
·
高分子材料
·
先进制造
✓ 已验证
DOI
高影响因子
JOURNAL OF APPLIED POLYMER SCIENCE
·
2022
·Vol. 139
·期 23
·52314
·
IF 3.057
Xiangrong Chen,Zelin Hong,Chao Dai,Muhammad Awais,Fan-Bo Meng,Ashish Paramane,Hao Li
This paper investigates the influence of voltage stabilizer and nanofiller addition on the insulation performance of the cross-linked polyethylene (XLPE). The test samples of XLPE/stabilizer blends consisting of 1 wt% m-aminobenzoic acid, XLPE nanocomposites consisting of 0.5 wt% nano MgO and XLPE hybrid composite consisting of both voltage stabilizer and nanofillers were prepared. Various physicochemical and electrical properties were measured to analyze the performance of prepared samples. The obtained results show that the addition of nanofillers deteriorates the electrical insulation performance of the XLPE. On the other hand, the voltage stabilizer addition proves to be suitable for enhancing the electrical insulation performance of the XLPE. Meanwhile, the hybrid XLPE composites have shown medium behavior. The voltage stabilizer addition reduces, but the nanofillers increase the space charge density inside the XLPE compared to pure XLPE. It is also found that the dispersion of the voltage stabilizer in the material is uniform, whereas the nanofillers are aggregated. Furthermore, both additives slightly improve the thermal stability of the XLPE. The trap level theory based on quantum chemical calculation is proposed to explain the influence mechanism of the additives on the XLPE.
研究领域:
高分子材料科学
·
电气工程
·
绝缘材料
·
介电物理
·
材料化学
·
聚合物纳米复合材料
✓ 已验证
DOI
高影响因子
DYES AND PIGMENTS
·
2016
·
IF 4.055
Qing Bao,Hua Li,Yang Li,Jinghui He,Qingfeng Xu,Najun Li,Dongyun Chen,Lihua Wang,Jianmei Lu
In this paper, two acceptor-donor-acceptor (A-D-A) type organic small molecules, 4,4'-(5,5'-(benzo[c] [1,2,5]thiadiazole-4,7-diyl)bis(3-hexylthiophene-5,2-diyl))bis(N-(4-nitrophenyl)-N-phenylaniline) (NTPA 2 TBT) and 4,4'-(5,6-difluorobenzo[c] [1,2,5]thiadiazole-4,7-diyl)bis(N-(4-nitrophenyl)-N-phenylaniline) (NTPA 2 BTF 2 ), were synthesized and fabricated into resistive random access memory devices. Compared with our previously reported molecule NTPA 2 BT, NTPA 2 TBT has 3-hexylthiophene linkages bridging its donor and acceptor, while there are two additional fluorine atoms in the benzothiadiazole moiety for NTPA 2 BTF 2. Both the fabricated memory devices based on these two new molecules perform nonvolatile ternary memory characteristics with lower threshold voltages , higher reproducibility and better stability. The addition of 3-hexylthiophene bridges significantly promotes the planarity of the conjugation backbone and facilitates the molecular stacking, while the substitution hydrogen by fluorine improves the intermolecular interaction , and thus also induces an ordered molecular stacking. The insertion of 3-hexylthiophene bridges or fluorine atoms could be an effective strategy of tailoring organic molecules to improve data storage performance with lower power consumption.
研究领域:
材料科学
·
有机电子学
·
分子器件
·
非易失性存储器
·
高分子化学
✓ 已验证
DOI
高影响因子
Science China-Materials
·
2018
·Vol. 62
·期 4
·519-526
·
IF 4.318
Zhang Busheng,Lei Yan,Qi Ruijuan,Yu Haili,Yang Xiaogang,Cai Tuo,Zheng Zhi
Both bismuth and copper are non-toxic and earth-abundant elements suitable for lead-free halide perovskite-like photovoltaic devices. Here, we report a highly facile route for in-situ producing copper-bismuth-iodide (CuBiI 4 ) thin films directly on ITO substrate at room temperature, by utilizing a Bi-Cu alloy layer as precursor. X-ray diffraction and transmission electron microscopy (TEM) results verified the formation of well crystallized CuBiI 4 thin films with [222] orientation. The transient photovoltage (TPV) analysis revealed that the CuBiI 4 is an n-type semiconductor with a suitable band gap of ~1.81 eV, preferable to photoelectric conversion compared with CH 3 NH 3 PbI 3 . It is very interesting that the subsequent spin-coating process of the classical Spiro-MeOTAD organic solution with TBP and acetonitrile resulted in a dense and smooth CuBiI 4 :Spiro-MeOTAD bulk-heterojunction film. The preliminarily fabricated simple sandwich structures of ITO/CuBiI 4 :Spiro-MeOTAD/Au hybrid solar cell devices displayed efficient photovoltaic performance with the PCE up to 1.119% of the best sample. The room temperature direct metal surface elemental reaction (DMSER) method may provide a new insight for all-inorganic lead free perovskite-like A a B b X x compounds and high performance photovoltaic devices.
研究领域:
材料科学
·
光伏技术
·
无机化学
·
半导体物理
·
能源材料
✓ 已验证
DOI
高影响因子
Results in Physics
·
2020
·
IF 4.019
Zhengwei Xiong,Jiang Yang,Zhipeng Gao,Qiang Yang,Deli Shi
As a typical supercapacitor electrode material, the reported Mo-N compounds mostly own one part of outstanding electrochemical properties (specific capacitance (C sp ), voltage window and cycling stability), and the well integration with three aspects was rare. Here using a novel MoO 3 precursor with ultra-long nanobelts (NBs) and stable orthorhombic crystal structure, we prepared unique Mo 3 N 2 NBs, which inherited the morphology and structure of the precursor greatly. Compared with other Mo-N compounds, the Mo 3 N 2 NBs both possessed the high C sp (220.3 F/g at 0.4 A/g), great cycling stability (98.3% C sp retention after 1500 cycles) and wide voltage window (0.95 V) due to the improved morphology, stable structure and excellent conductivity.
研究领域:
材料科学
·
电化学
·
纳米科技
·
能源存储
·
功能材料
✓ 已验证
DOI
高影响因子
Energy Technology
·
2018
·Vol. 6
·期 11
·2139-2145
·
IF 3.175
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
Journal of Energy Chemistry
·
2023
·
IF 13.1
Xuexia Lan,Xingyu Xiong,Jie Cui,Renzong Hu
In the past two decades, a lot of high-capacity conversion-type metal oxides have been intensively studied as alternative anode materials for Li-ion batteries with higher energy density. Unfortunately, their large voltage hysteresis (0.8–1.2 V) within reversed conversion reactions results in huge round-trip inefficiencies and thus lower energy efficiency (50%–75%) in full cells than those with graphite anodes. This remains a long-term open question and has been the most serious drawback toward application of metal oxide anodes. Here we clarify the origins of voltage hysteresis in the typical SnO 2 anode and propose a universal strategy to minimize it. With the established in situ phosphating to generate metal phosphates during reversed conversion reactions in synergy with boosted reaction kinetics by the added P and Mo, the huge voltage hysteresis of 0.9 V in SnO 2 , SnO 2 -Mo, and 0.6 V in SnO 2 -P anodes is minimized to 0.3 V in a ternary SnO 2 -Mo-P (SOMP) composite, along with stable high capacity of 936 mA h g −1 after 800 cycles. The small voltage hysteresis can remain stable even the SOMP anode operated at high current rate of 10 A g −1 and wide-range temperatures from 60 to −30 °C, resulting in a high energy efficiency of 88.5% in full cells. This effective strategy to minimize voltage hysteresis has also been demonstrated in Fe 2 O 3 , Co 3 O 4 -basded conversion-type anodes. This work provides important guidance to advance the high-capacity metal oxide anodes from laboratory to industrialization.
研究领域:
电化学
·
材料科学
·
能源存储
·
纳米材料
·
固态化学
·
电池技术
✓ 已验证
DOI
高影响因子
ORGANIC ELECTRONICS
·
2019
·
IF 3.495
Xin Qi,Ganghong Liu,Duo Wang,Ning Zhu,Yuqing Zhang,Zehao Zhang,Cuncun Wu,Xiangdong Li,Wei Luo,Yingqiang Li,Haozhe Hu,Zhijian Chen,Lixin Xiao,Shufeng Wang,Bo Qu
Interfacial modification as a feasible strategy to improve the properties of perovskite solar cells (PSCs) has been widely studied in recent years. In this work, PbCl 2 modification at the interface of SnO 2 /CH 3 NH 3 PbI 3 was used for CH 3 NH 3 PbI 3 -based planar PSCs. The introduction of PbCl 2 between SnO 2 and CH 3 NH 3 PbI 3 layers boosted the crystallization of perovskite film, which promoted the photovoltaic properties of corresponding PSCs. The open circuit voltage ( V OC ) and fill factor (FF) of the PbCl 2 -modified devices (1 mg/mL) were 1.11 V and 0.79, respectively, which were both higher than those of the reference devices without PbCl 2 (1.04 V and 0.76). Moreover, a steady-state power output efficiency exceeding 19% was obtained for the PbCl 2 -modified devices (1 mg/mL), which implied that PbCl 2 modification was an effective and low cost strategy for efficient PSCs.
研究领域:
材料科学
·
光伏技术
·
纳米科技
·
表面与界面工程
·
能源材料
·
半导体器件
·
功能材料
✓ 已验证
DOI
高影响因子
ELECTROCHIMICA ACTA
·
2020
·
IF 6.215
Shi Wang,Qingyuan Li,Minglei Bai,Jixin He,Chongyang Liu,Zengxi Li,Xiangfeng Liu,Wen-yong Lai,Liaoyun Zhang
Lithium-ion batteries (LIBs) using solid-state electrolytes (SSEs) can improve safety and energy density comparable with the liquid electrolytes (LE)-based counterparts. Especially, employing garnet-type SSEs to prepare solid-state LIBs are promising to achieve high-energy cells. However, the unbending and brittle issues of the inorganic SSE films are not suitable to fabricate flexible and stretchable energy storage devices. Here, We find that introducing specific polymer (30 wt%) into Li 6.75 La 3 Zr 1.75 Ta 0.25 O 12 (LLZTO) can strongly increase the strength of the composite polymer-in-inorganic electrolyte (CIE) film. Both in-situ and ex-situ characterizations demonstrate that CIE delivers an excellent ability to suppress the growth of Li dendrites due to the close packing of LLZTO and effective filled grain boundaries and voids inside the CIE film by the polymer. The CIE inherits impressive electrochemical performance from LLZTO. As a result, the assembled LiFePO 4 (LFP)/CIE/Li cell delivers better cell performance than LFP/LE-separator/Li cell at ambient temperature (AT). The assembled high-voltage cathode (Li 1.2 Mn 0.6 Ni 0.2 O 2 , 4.8 V)/CIE/Li cell also displays an excellent cell performance at AT. The present study offers new insights into exploring of flexible polymer-in-ceramic electrolytes for high-voltage LIBs with improved safety and energy density .
研究领域:
材料科学
·
电化学
·
能源存储
·
固态电池
·
纳米复合材料
·
界面工程
✓ 已验证
DOI
高影响因子
危险品化学品经营许可证（带存储）