JOURNAL OF POWER SOURCES
·
2022
·
IF 9.794
Wei Feng,Huirong Liu,Mingliang Zhao,Jianling Li,Feiyu Kang
The poly(ethylene oxide) based composite solid electrolyte(PEO-CSE) is an effective solution for developing high-performance solid-state lithium battery . However, the poly(ethlene oxide)(PEO) based solid-state lithium battery using 4.0 V cathode suffers from severe interfacial instability problems. In this work, we add additive lithium difluorophosphate(LiPO 2 F 2 ) into the PEO-CSE to form a stable and low resistance interphase at the cathode/electrolyte interface during charge/discharge process. The electrochemical stability window of PEO-CSE increases to ∼5.0 V. Besides, the electrochemical performance of PEO based solid-state lithium battery with LiCoO 2 as cathode is excellent. The discharge capacity of LiCoO 2 /Li cell with LiPO 2 F 2 reaches 108.5 mAh g −1 at 1.0C. In contrast, the discharge capacity that without LiPO 2 F 2 is only 60.0 mAh g −1 . Meanwhile, the PEO-CSE with LiPO 2 F 2 cell delivers stable cycle performance at 4.2 V. The capacity retention maintains 88.5% compared with 16.1%(without LiPO 2 F 2 ) after 100 cycles. Furthermore, it's still maintains 83.3% after 150 cycles. In addition, the cathode/electrolyte interface is analyzed by transmission electron microscope(TEM) and X-ray photoelectron spectroscopy(XPS). Galvanostatic intermittent titration test(GITT) is used to analyze the dynamic diffusion performance. This strategy provides a simple and effective way to improve the high voltage stability of the cathode/electrolyte interface.
研究领域:
电化学
·
材料科学
·
能源存储
·
固态电池
·
界面工程
✓ 已验证
DOI
高影响因子
Small
·
2017
·Vol. 13
·期 25
·1700364
·
IF 8.643
Xuhai Liu,Dejian Yu,Fei Cao,Xiaoming Li,Jianping Ji,Jun Chen,Xiufeng Song,Haibo Zeng
All-inorganic photodetectors based on scattered CsPbBr 3 nanoplatelets with lateral dimension as large as 10 µm are fabricated, and the CsPbBr 3 nanoplatelets are solution processed governed by a newly developed ion-exchange soldering mechanism. Under illumination of a 442 nm laser, the photoresponsivity of photodetectors based on these scattered CsPbBr 3 nanoplatelets is as high as 34 A W −1 , which is the largest value reported from all-inorganic perovskite photodetectors with an external driven voltage as small as 1.5 V. Moreover, the rise and fall times are 0.6 and 0.9 ms, respectively, which are comparable to most of the state-of-the-art all-inorganic perovskite-based photodetectors. All the material synthesis and device characterization are conducted at room temperature in ambient air. This work demonstrates that the solution-processed large CsPbBr 3 nanoplatelets are attractive candidates to be applied in low-voltage, low-cost, ultra highly integrated optoelectronic devices.
研究领域:
材料科学
·
光电子学
·
纳米科技
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半导体器件
·
凝聚态物理
✓ 已验证
DOI
高影响因子
Physica Status Solidi-Rapid Research Letters
·
2020
·Vol. 14
·期 4
·1900723
·
IF 2.291
Yadan Deng,Jingzan Jiang,Jun Sun,Yufeng Hu,Qiuhong Cui,Zhenbo Deng,Zhidong Lou,Yanbing Hou,Feng Teng
Fabrication of nanowires in polymer films can dramatically enhance the mobility of thin-film transistors (TFTs). Unlike the popular method of forming nanowires after spin-coating films, here a water-bath method to fabricate the micrometer-long nanowires in the poly(3-hexylthiophene) (P3HT) solution is introduced, which is suitable for large-area printing electronic application. The resulting transistor exhibits significantly enhanced mobility and excellent device stability. However, the threshold voltage of the device is increased, compared with the amorphous film device. The underlying mechanism of the mesoscale crystalline induced threshold voltage increase has been rarely studied. The temperature-dependent characteristics imply that the activation energy of the device with nanowires is higher than that of the amorphous one, indicating nanowires can introduce deep traps. This suggests that the charge transport is mainly limited by the deep traps at the junctions between the nanowires considering the trap density inside the nanowires is significantly low. The deep traps introduced by the junctions can increase the threshold voltage as the device needs higher voltage to fill these traps in the channel before the device is turned on. This explains why the devices with nanowires have an increased threshold voltage while their mobilities are dramatically enhanced.
研究领域:
材料科学
·
凝聚态物理
·
有机电子学
·
薄膜晶体管
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半导体器件物理
✓ 已验证
DOI
高影响因子
POLYMERS FOR ADVANCED TECHNOLOGIES
·
2019
·Vol. 30
·期 11
·2781-2789
·
IF 2.162
Tingjun Zhong,Richard J. Mandle,John W. Goodby,Lanying Zhang,Cuihong Zhang
In this work, the thiol-ene click reaction is employed to fabricate polymer-dispersed liquid crystal (PDLC) films by photoinitiated polymerization. The PDLC films are prepared by systematic variation of key conditions: variety and content of -ene monomer, liquid crystal (LC) content, curing time, and curing light intensity. We find that both the morphologies and electro-optic properties of these films are adjustable. When increasing the length of alkyl main chain of -ene monomers, the driving voltages reduce, but in turn, the contrast ratio decreases. Increasing -ene monomer content raises the driving voltages as well as the response time, and the increase of LC content lowers the driving voltages but has a negative effect on the contrast ratio. The changes to the curing conditions (both curing time and UV light intensity) can be used to modify the driving voltages, response time, and contrast ratios of PDLC films. These comparative studies will elucidate new insights in commercial applications of intelligent PDLC films.
研究领域:
材料科学
·
高分子化学
·
软物质物理
·
光电功能材料
·
智能材料
✓ 已验证
DOI
高影响因子
Solar RRL
·
2019
·Vol. 3
·期 5
·1800346
·
IF 0
Jiang Cheng,Rong Hu,Kun Wang,Xiang Meng,Ying Li,Xin Yang,Xiaoqing Liao,Lu Li,Kok Boon Chong
Antimony chalcogenide is a promising absorber material for photovoltaic (PV) cells because of its tunable band gap, strong optical absorption, earth-abundant, and nontoxic constituents. Here, a novel hydrazine-free approach for fabricating antimony chalcogenide films prepared via spray pyrolysis deposition with further selenylation, as well as high performance solar cells are reported. The fabricated antimony chalcogenide solar cells exhibits remarkably high open-circuit voltage ( V OC ) comparing with that of Sb 2 Se 3 and Sb 2 S 3 devices. The distribution of Se during the selenylation process via refering to the Fick's second law is discussed. The results show that the selenized absorber has tremendously improved absorbance for visible light and a cascade-type energy level from surface to bulk, resulting in an ideal energy level matching for p-n junction. By introducing an efficient buffer layer, the detrimental short-circuit is avoided by reducing the cracks. Finally, 4.57% of the power conversion efficiency (PCE) of the solar cell is achieved. Furthermore, a module with a large-scale active area of 21 cm 2 is successfully fabricated, which shows a PCE of 3.19%, and a V OC of 3.42 V. The present work suggests that the antimony chalcogenide solar cells are promising for industrial application.
研究领域:
材料科学
·
光伏技术
·
半导体器件
·
能源材料
·
薄膜制备
·
表面工程
·
器件物理
✓ 已验证
DOI
DYES AND PIGMENTS
·
2021
·
IF 4.889
You Liu,Fang Liu,Jungan Wang,Hongyan Huang,Suhao Yan,Song Gao,Lin Wang,Wei Huang,Tianshi Qin
Wide-bandgap photovoltaics (WBPV) could not only provide electrical energy by photoelectronic conversion of the invisible part of the solar spectrum, but also usually had the unique advantage of high open circuit voltage ( V oc). In this work, we reported a novel HTM based on tetrakis (N-phenothiazine) Spirobifluorene (Spiro-PT), its HOMO energy level could be well matched with MAPbBr 3 perovskite HOMO energy level. This HTM could effectively suppress nonradiative recombination, which leads to an increase in the photovoltage of WBPV to more than 1.41 V. As a result, the n-i-p mesoscopic structured WBPV achieved a champion PCE of 7.36% as well as excellent operational stability exhibiting 91% of initial efficiency after 500 h continuous illumination without encapsulation. Based on the high V oc of the MAPbBr 3 /Spiro-PT device, the photovoltaic electrochromic device showed a response speed (the average coloring time was 40 s and the bleaching time was 272 s) and high average visible light transmittance contrast (about 37% in 450–780 nm), the corresponding electrochromic device with maximum dynamic contrast up to 46% at 600 nm between bleached and colored states. This WBPV-powered electrochromic system could provide a pathway towards stand-alone smart window technique for future energy-saving buildings.
研究领域:
材料科学
·
光伏技术
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纳米能源
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智能窗技术
·
器件物理
✓ 已验证
DOI
高影响因子
Sustainable Energy & Fuels
·
2020
·Vol. 4
·期 6
·2800-2807
·
IF 5.503
Haili Yu,Busheng Zhang,Ruijuan Qi,Nannan Qu,Chaoliang Zhao,Yan Lei,Xiaogang Yang,Zhi Zheng
Designing lead-free inorganic perovskite or perovskite-like structure materials and researching the corresponding photoinduced charge carrier dynamics are always promising due to both the environment and power conversion efficiency considerations. In this work, we intelligently employ a bilayer metal Bi/Cu thin film with different atomic ratios as the precursor to fabricate a CuBiI4 perovskite-like film in situ with a controlled Bi gradient at room temperature. This structure can significantly affect the photoinduced charge carrier dynamics of the resulting products. Next, a series of transient surface photovoltage (TSPV) measurements are carried out to investigate the photoinduced charge carrier dynamics of such CuBiI4 and CuBiI4:organic hybrid thin films. The results reveal that the gradually decreasing Bi content from ITO to CuBiI4 can facilitate the photoinduced charge carrier transportation. Finally, a champion PCE of 1.10% is obtained for an ITO/CuBiI4:polythieno[3,4-b]-thiophene-co-benzodithiophene (PTB7)/Au solar cell device. In particular, we find an exact negative correlation of the defined parameter L (the defined value for evaluating the photoinduced charge carrier dynamics in TSPV measurements) with the corresponding PCE of various devices for the first time, which may pave a new way for evaluating the potential photoelectric and photovoltaic performances of new materials without the assembly of solar cell devices.
研究领域:
材料科学
·
光伏技术
·
凝聚态物理
·
表面科学
·
能源化学
✓ 已验证
DOI
高影响因子
Small
·
2023
·Vol. 19
·期 39
·2302691
·
IF 13.3
Jing Yu,Guodong Zhou,Yueqing Li,Yuhao Wang,Dengjie Chen,Francesco Ciucci
Composite polymer-ceramic electrolytes have shown considerable potential for high-energy-density Li-metal batteries as they combine the benefits of both polymers and ceramics. However, low ionic conductivity and poor contact with electrodes limit their practical usage. In this study, a highly conductive and stable composite electrolyte with a high ceramic loading is developed for high-energy-density Li-metal batteries. The electrolyte, produced through in situ polymerization and composed of a polymer called poly-1,3-dioxolane in a poly(vinylidene fluoride)/ceramic matrix, exhibits excellent room-temperature ionic conductivity of 1.2 mS cm −1 and high stability with Li metal over 1500 h. When tested in a Li|electrolyte|LiFePO 4 battery, the electrolyte delivers excellent cycling performance and rate capability at room temperature, with a discharge capacity of 137 mAh g −1 over 500 cycles at 1 C. Furthermore, the electrolyte not only exhibits a high Li + transference number of 0.76 but also significantly lowers contact resistance (from 157.8 to 2.1 Ω) relative to electrodes. When used in a battery with a high-voltage LiNi 0.8 Mn 0.1 Co 0.1 O 2 cathode, a discharge capacity of 140 mAh g −1 is achieved. These results show the potential of composite polymer-ceramic electrolytes in room-temperature solid-state Li-metal batteries and provide a strategy for designing highly conductive polymer-in-ceramic electrolytes with electrode-compatible interfaces.
研究领域:
材料科学
·
电化学
·
能源存储
·
固态电池
·
高分子化学
·
无机非金属材料
✓ 已验证
DOI
高影响因子
JOURNAL OF POWER SOURCES
·
2024
·
IF 8.1
Zhengwu Wang,Yannan Zhang,Bao Zhang,Dong Yang,Kai Zhou,Yixue Huang,Fei Wang,Jianguo Duan,Xianshu Wang,Peng Dong,Yingjie Zhang
Spinel LiNi 0.5 Mn 1.5 O 4 (LNMO) has gained significant attention as a promising cathode material for lithium-ion batteries due to its high working voltage (>4.7 V) and energy density . However, challenges such as electrolyte decomposition-induced material interface erosion and transition metal dissolution under high operating voltage hinder its commercial use. In this study, a thin and uniform Sm 2 O 3 layer has been successfully deposited on the surface of LNMO using a wet chemical method . A comprehensive investigation of surface morphology , crystal structure, and electrochemical performance of the modified LNMO is conducted. The results demonstrate that the Sm 2 O 3 surface modification acts as a robust multifunctional protective layer, effectively shielding against hydrofluoric acid-induced chemical attack and enhancing the migration efficiency of lithium ions . Notably, the capacity retention rate of LNMO@Sm 2 O 3 (3 wt%) remains up to 88 % after 280 cycles, significantly surpassing the uncoated counterpart. The coated material exhibits a capacity of 114 mAh g −1 even under 10 C rate conditions. Moreover, the AC impedance values and manganese dissolution of the modified material in the organic electrolyte are considerably lower than those of the uncoated counterpart. Theoretical calculations strongly support the experimental findings, revealing higher Mn vacancy formation energy and density of states at the Fermi energy level for the Sm 2 O 3 -modified electrodes. This research contributes to the field of surface modification and paves the way for further enhancements in the electrochemical performance of other high-voltage manganese-based lithium-ion batteries (LIBs).
研究领域:
材料科学
·
电化学
·
能源存储
·
无机化学
·
纳米技术
·
表面工程
·
锂电池
✓ 已验证
DOI
高影响因子
Energy Technology
·
2019
·Vol. 7
·期 4
·1800981
·
IF 3.163
Bangwei Deng,Hao Wang,Xiang Li,Yan Ding,Daming Sun,Jun Ma,Mianzhong Chen,Tao Chen,Feng Gao,Meizhen Qu,Gongchang Peng
Tris(trimethylsilyl)phosphite (TMSPi) has been reported to be an excellent electrolyte additive. However, scarce reports exist on the effect of the charge cutoff potential on the cyclic stability using high-performance LiNi 0.6 Co 0.2 Mn 0.2 O 2 (NCM622)–mesocarbon microbead (MCMB) full cells. Herein, a high-loading and repeatable NCM622–MCMB coin-type full cell is successfully prepared, and the role of TMSPi on such a full cell at charge cutoff potentials of 4.25 and 4.45 V is studied. Theoretical calculations and detailed analyses reveal that it is oxidized in the first charging process due to its unsaturated P—O bonds, thus forming a stable P—O—F-rich cathode electrolyte interphase and preventing severe decomposition of the electrolyte over NCM622 during long-term cycling. In addition, the P—O and Si—O bonds of TMSPi both display HF-scavenging ability. Moreover, TMSPi may react directly with the LiPF 6 -based electrolyte to form some intermediate products that can be reduced on the MCMB electrode, thereby modifying the solid electrolyte interphase and improving the stability of MCMB during lithium intercalation.
研究领域:
电化学
·
材料科学
·
能源存储
·
锂离子电池
·
界面化学
·
电极材料
✓ 已验证
DOI
高影响因子
危险品化学品经营许可证（带存储）