首页 > 最新文献

2016 IEEE 16th International Conference on Nanotechnology (IEEE-NANO)最新文献

英文 中文
Development of drug delivery bioceramics cement for vital pulp therapy 生命髓治疗用生物陶瓷骨水泥的研制
Pub Date : 2016-08-01 DOI: 10.1109/NANO.2016.7751547
Wei-Chih Lin, P. Hung, Chun-Pin Lin
This paper demonstrates a dental pulp cell therapy method by using a mixture of a bioceramic materials, simvastatin and collagenase as a drug delivery bioceramic diluent. The drug releasing mechanism and speed are based on a natural diffusion of concentration differences and micro-pinhole sizes on the bioceramic cement, which is composed of the calcium phosphate cement (CPC) and calcium sulfate dihydrate (CSD) powders, respectively. The collagenase and simvastatin can release via the micro-pinhole channels from the cement to not only regenerate dental pulp stem cells but also stimulate the differentiation of pulp cells locally. Three different mixture ratios of CPC and CSD powders were characterized to study the relationship between pinhole sizes and releasing times and speeds. The mixture CPC/CSD ratio of 3:7, named CPC3CSD7, performs well release profile of the collagenase and simvastatin. The released simvastatin and collagenase are over 80 and 50 percentages, respectively. Furthermore, an in-vitro cell culture experiment was applied to identify the biocompatibility and cultured odontoblasts grown differentiated well on the cement surface.
本文介绍了一种利用生物陶瓷材料、辛伐他汀和胶原酶的混合物作为给药生物陶瓷稀释剂的牙髓细胞治疗方法。药物释放机制和速度是基于浓度差异和微针孔大小在生物陶瓷水泥上的自然扩散,生物陶瓷水泥分别由磷酸钙水泥(CPC)和硫酸钙二水合物(CSD)粉末组成。胶原酶和辛伐他汀可以通过微针孔通道从水泥中释放出来,不仅可以再生牙髓干细胞,还可以局部刺激牙髓细胞的分化。对三种不同配比的CPC和CSD粉末进行了表征,研究了针孔尺寸与释放时间和释放速度的关系。CPC/CSD比例为3:7的混合物,命名为CPC3CSD7,具有良好的胶原酶和辛伐他汀释放特性。辛伐他汀和胶原酶的释放量分别超过80%和50%。通过体外细胞培养实验,鉴定成牙髓细胞在水泥表面的生物相容性和分化程度。
{"title":"Development of drug delivery bioceramics cement for vital pulp therapy","authors":"Wei-Chih Lin, P. Hung, Chun-Pin Lin","doi":"10.1109/NANO.2016.7751547","DOIUrl":"https://doi.org/10.1109/NANO.2016.7751547","url":null,"abstract":"This paper demonstrates a dental pulp cell therapy method by using a mixture of a bioceramic materials, simvastatin and collagenase as a drug delivery bioceramic diluent. The drug releasing mechanism and speed are based on a natural diffusion of concentration differences and micro-pinhole sizes on the bioceramic cement, which is composed of the calcium phosphate cement (CPC) and calcium sulfate dihydrate (CSD) powders, respectively. The collagenase and simvastatin can release via the micro-pinhole channels from the cement to not only regenerate dental pulp stem cells but also stimulate the differentiation of pulp cells locally. Three different mixture ratios of CPC and CSD powders were characterized to study the relationship between pinhole sizes and releasing times and speeds. The mixture CPC/CSD ratio of 3:7, named CPC3CSD7, performs well release profile of the collagenase and simvastatin. The released simvastatin and collagenase are over 80 and 50 percentages, respectively. Furthermore, an in-vitro cell culture experiment was applied to identify the biocompatibility and cultured odontoblasts grown differentiated well on the cement surface.","PeriodicalId":6646,"journal":{"name":"2016 IEEE 16th International Conference on Nanotechnology (IEEE-NANO)","volume":"4 1","pages":"249-252"},"PeriodicalIF":0.0,"publicationDate":"2016-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"88595397","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 1
Electrical properties of chemically doped graphene with Aluminum ions 铝离子化学掺杂石墨烯的电学性质
Pub Date : 2016-08-01 DOI: 10.1109/NANO.2016.7751527
P. Jain, C. Zhang, Jiang'ao Huang, Kamal Ahmad, D. Xie, Zewen Liu
In this article, we report a Field Effect Transistor (FET) with Aluminum doped graphene channel. The graphene is doped by spin coating a chemical dopant solution which tailored the electrical properties of graphene, such as transfer characteristics and output characteristics. The Doping of graphene was successfully verified by X-Ray photoelectron spectra (XPS) measurements. The testing results showed that the Dirac point (the value of gate to source voltage at which minimum value of drain to source current is attained) in transfer characteristics of Graphene Field Effect Transistor (GFET) shifted from VGS = 6.42 V to VGS = 40 V after doping. The slope of the output characteristics of GFET for VGS = 0 V increased from 3.56 to 5.44.
本文报道了一种掺铝石墨烯沟道的场效应晶体管(FET)。石墨烯通过自旋镀膜的方式掺杂,这种化学掺杂溶液可以调整石墨烯的电学特性,如转移特性和输出特性。通过x射线光电子能谱(XPS)测量成功地验证了石墨烯的掺杂。测试结果表明,掺杂后石墨烯场效应晶体管(GFET)转移特性中的Dirac点(漏极到源极电流最小时的栅极到源电压值)从VGS = 6.42 V转变为VGS = 40 V。当VGS = 0 V时,GFET的输出特性斜率由3.56增加到5.44。
{"title":"Electrical properties of chemically doped graphene with Aluminum ions","authors":"P. Jain, C. Zhang, Jiang'ao Huang, Kamal Ahmad, D. Xie, Zewen Liu","doi":"10.1109/NANO.2016.7751527","DOIUrl":"https://doi.org/10.1109/NANO.2016.7751527","url":null,"abstract":"In this article, we report a Field Effect Transistor (FET) with Aluminum doped graphene channel. The graphene is doped by spin coating a chemical dopant solution which tailored the electrical properties of graphene, such as transfer characteristics and output characteristics. The Doping of graphene was successfully verified by X-Ray photoelectron spectra (XPS) measurements. The testing results showed that the Dirac point (the value of gate to source voltage at which minimum value of drain to source current is attained) in transfer characteristics of Graphene Field Effect Transistor (GFET) shifted from VGS = 6.42 V to VGS = 40 V after doping. The slope of the output characteristics of GFET for VGS = 0 V increased from 3.56 to 5.44.","PeriodicalId":6646,"journal":{"name":"2016 IEEE 16th International Conference on Nanotechnology (IEEE-NANO)","volume":"39 1","pages":"743-746"},"PeriodicalIF":0.0,"publicationDate":"2016-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"91214605","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Excitation of surface plasmon polaritons on titanium nitride thin films through energy transfer from dye molecules 通过染料分子的能量转移激发氮化钛薄膜表面等离子激元极化子
Pub Date : 2016-08-01 DOI: 10.1109/NANO.2016.7751441
S. Murai, Yohei Daido, R. Kamakura, K. Fujita, Katsuhisa Tanaka
We have fabricated titanium nitride (TiN) thin films on sapphire substrates by pulsed laser deposition (PLD) technique, and excited surface plasmon polaritons (SPPs) on TiN thin films by energy transfer from dye molecules. The system was fabricated by depositing a thin polymer layer containing rhodamine 6G (R6G) on a TiN thin film, separated by a thin spacer made of silica. The SPPs were excited by irradiating the dye layer with a blue laser. We successfully collected radiation from SPPs by converting them into far-field radiation using a prism coupling technique.
利用脉冲激光沉积(PLD)技术在蓝宝石衬底上制备了氮化钛(TiN)薄膜,并利用染料分子的能量转移在TiN薄膜上激发了表面等离子激元(SPPs)。该系统是通过将含有罗丹明6G (R6G)的薄聚合物层沉积在TiN薄膜上制成的,由二氧化硅制成的薄间隔层隔开。用蓝色激光照射染料层来激发SPPs。我们利用棱镜耦合技术将SPPs的辐射转化为远场辐射,成功地收集了SPPs的辐射。
{"title":"Excitation of surface plasmon polaritons on titanium nitride thin films through energy transfer from dye molecules","authors":"S. Murai, Yohei Daido, R. Kamakura, K. Fujita, Katsuhisa Tanaka","doi":"10.1109/NANO.2016.7751441","DOIUrl":"https://doi.org/10.1109/NANO.2016.7751441","url":null,"abstract":"We have fabricated titanium nitride (TiN) thin films on sapphire substrates by pulsed laser deposition (PLD) technique, and excited surface plasmon polaritons (SPPs) on TiN thin films by energy transfer from dye molecules. The system was fabricated by depositing a thin polymer layer containing rhodamine 6G (R6G) on a TiN thin film, separated by a thin spacer made of silica. The SPPs were excited by irradiating the dye layer with a blue laser. We successfully collected radiation from SPPs by converting them into far-field radiation using a prism coupling technique.","PeriodicalId":6646,"journal":{"name":"2016 IEEE 16th International Conference on Nanotechnology (IEEE-NANO)","volume":"14 1","pages":"59-62"},"PeriodicalIF":0.0,"publicationDate":"2016-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"91223920","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Single-Walled Carbon Nanotubes based sensors and amplifier circuit integrated on flexible substrates 基于单壁碳纳米管的柔性衬底传感器和放大电路
Pub Date : 2016-08-01 DOI: 10.1109/NANO.2016.7751495
Kang Zhang, Jianping Zou, Qing Zhang
Single-Walled Carbon Nanotubes (SWCNTs) have been shown to be a promising candidate for flexible electronics, especially logic circuits. However, very little study on SWCNT based analog circuit elements, such as amplifiers and comparators, on flexible substrates has been reported. For practical applications, fully functional flexible electronic devices must have an analog input circuitry to achieve appropriate functionalities. In this work, we demonstrate a resistive SWCNT gas sensor integrated with an amplifier circuit on flexible substrate to detect and amplify the sensing signals.
单壁碳纳米管(SWCNTs)已被证明是柔性电子,特别是逻辑电路的一个有前途的候选者。然而,基于swcnts的模拟电路元件,如放大器和比较器,在柔性衬底上的研究很少报道。在实际应用中,功能齐全的柔性电子器件必须具有模拟输入电路才能实现适当的功能。在这项工作中,我们展示了一种电阻式swcnts气体传感器,该传感器集成了柔性衬底上的放大电路,用于检测和放大传感信号。
{"title":"Single-Walled Carbon Nanotubes based sensors and amplifier circuit integrated on flexible substrates","authors":"Kang Zhang, Jianping Zou, Qing Zhang","doi":"10.1109/NANO.2016.7751495","DOIUrl":"https://doi.org/10.1109/NANO.2016.7751495","url":null,"abstract":"Single-Walled Carbon Nanotubes (SWCNTs) have been shown to be a promising candidate for flexible electronics, especially logic circuits. However, very little study on SWCNT based analog circuit elements, such as amplifiers and comparators, on flexible substrates has been reported. For practical applications, fully functional flexible electronic devices must have an analog input circuitry to achieve appropriate functionalities. In this work, we demonstrate a resistive SWCNT gas sensor integrated with an amplifier circuit on flexible substrate to detect and amplify the sensing signals.","PeriodicalId":6646,"journal":{"name":"2016 IEEE 16th International Conference on Nanotechnology (IEEE-NANO)","volume":"44 1","pages":"472-474"},"PeriodicalIF":0.0,"publicationDate":"2016-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"89898567","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Hydrogel-based electrical stimulation culture system to control the engineered cellular activities driven by nano biomolecules 基于水凝胶的电刺激培养系统,以控制纳米生物分子驱动的工程细胞活动
Pub Date : 2016-08-01 DOI: 10.1109/NANO.2016.7751448
K. Nagamine, Hirotaka Sato, Hiroyuki Kai, H. Kaji, M. Nishizawa
The hydrogel-based electrical stimulation culture device composed of portable cellular micropatterns and the flexible and stretchable PEDOT/PU electrode arrays were developed to afford in vitro cell-based bioassay system. Electrical regulation of muscle cellular contraction driven by intracellular nano-actuator composed of biomolecules was successfully demonstrated by using this system.
研制了一种由便携式细胞微模和柔性可拉伸PEDOT/PU电极阵列组成的水凝胶电刺激培养装置,用于体外细胞生物检测系统。利用该系统成功地演示了由生物分子组成的细胞内纳米致动器驱动的肌肉细胞收缩电调控。
{"title":"Hydrogel-based electrical stimulation culture system to control the engineered cellular activities driven by nano biomolecules","authors":"K. Nagamine, Hirotaka Sato, Hiroyuki Kai, H. Kaji, M. Nishizawa","doi":"10.1109/NANO.2016.7751448","DOIUrl":"https://doi.org/10.1109/NANO.2016.7751448","url":null,"abstract":"The hydrogel-based electrical stimulation culture device composed of portable cellular micropatterns and the flexible and stretchable PEDOT/PU electrode arrays were developed to afford in vitro cell-based bioassay system. Electrical regulation of muscle cellular contraction driven by intracellular nano-actuator composed of biomolecules was successfully demonstrated by using this system.","PeriodicalId":6646,"journal":{"name":"2016 IEEE 16th International Conference on Nanotechnology (IEEE-NANO)","volume":"11 1","pages":"232-233"},"PeriodicalIF":0.0,"publicationDate":"2016-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"90194750","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Photoluminescence emission from as-etched quantum nanodisks fabricated by bio-template and neutral beam etching process 生物模板和中性束刻蚀工艺制备的蚀刻量子纳米片的光致发光
Pub Date : 2016-08-01 DOI: 10.1109/NANO.2016.7751347
D. Ohori, K. Kondo, K. Sakai, A. Higo, C. Thomas, S. Samukawa, T. Ikari, A. Fukuyama
Quantum dot laser diodes are expected to replace conventional semiconductor laser diodes in new high-speed information and communication devices. We successfully fabricated disk-shaped quantum dots using a bio-template and neutral beam etching. Our original top-down process achieved defect-less and a high density of dots from etching process compared with conventional plasma processes. Therefore, we attempted to detect emission from the quantum energy levels in the quantum nanodisks (QNDs) for as-etched sample without post-fabrication process. We prepared 4-stacked GaAs/AlGaAs layer QNDs samples after etching (as-etched) and after regrowth. QNDs samples were investigated by photoluminescence (PL) measurements. Results showed some broad peaks appearing between the bandgaps of GaAs and AlGaAs. We compared our experimental results with energies theoretically estimated energies using a nextnano 3D simulator with QND different diameters. For both type of samples, we found that QND diameters increased from top to bottom. From PL measurement, we observed emission from QNDs for as-etched samples fabricated using our own original top-down process.
量子点激光二极管有望在新型高速信息通信器件中取代传统的半导体激光二极管。我们成功地利用生物模板和中性光束蚀刻技术制备了圆盘状量子点。与传统的等离子体工艺相比,我们独创的自顶向下工艺在蚀刻过程中实现了无缺陷和高密度的点。因此,我们试图在没有后处理的情况下检测蚀刻样品中量子纳米盘(QNDs)中量子能级的发射。我们在蚀刻(as-etched)和再生后制备了4层GaAs/AlGaAs层QNDs样品。采用光致发光(PL)方法对qnd样品进行了研究。结果表明,在GaAs和AlGaAs的带隙之间出现了宽峰。我们将实验结果与理论估计的能量进行了比较,并使用了不同直径量子点的nextnano 3D模拟器。对于这两种类型的样品,我们发现QND直径从上到下增加。从PL测量中,我们观察到使用我们自己的原始自上而下工艺制造的蚀刻样品的量子点发射。
{"title":"Photoluminescence emission from as-etched quantum nanodisks fabricated by bio-template and neutral beam etching process","authors":"D. Ohori, K. Kondo, K. Sakai, A. Higo, C. Thomas, S. Samukawa, T. Ikari, A. Fukuyama","doi":"10.1109/NANO.2016.7751347","DOIUrl":"https://doi.org/10.1109/NANO.2016.7751347","url":null,"abstract":"Quantum dot laser diodes are expected to replace conventional semiconductor laser diodes in new high-speed information and communication devices. We successfully fabricated disk-shaped quantum dots using a bio-template and neutral beam etching. Our original top-down process achieved defect-less and a high density of dots from etching process compared with conventional plasma processes. Therefore, we attempted to detect emission from the quantum energy levels in the quantum nanodisks (QNDs) for as-etched sample without post-fabrication process. We prepared 4-stacked GaAs/AlGaAs layer QNDs samples after etching (as-etched) and after regrowth. QNDs samples were investigated by photoluminescence (PL) measurements. Results showed some broad peaks appearing between the bandgaps of GaAs and AlGaAs. We compared our experimental results with energies theoretically estimated energies using a nextnano 3D simulator with QND different diameters. For both type of samples, we found that QND diameters increased from top to bottom. From PL measurement, we observed emission from QNDs for as-etched samples fabricated using our own original top-down process.","PeriodicalId":6646,"journal":{"name":"2016 IEEE 16th International Conference on Nanotechnology (IEEE-NANO)","volume":"22 1","pages":"321-322"},"PeriodicalIF":0.0,"publicationDate":"2016-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"73434701","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Dynamics of oxygen scattering on ionomer surface in catalyst layer of PEFC PEFC催化剂层中离子表面氧散射动力学
Pub Date : 2016-08-01 DOI: 10.1109/NANO.2016.7751557
M. Nakauchi, T. Mabuchi, I. Kinefuchi, H. Takeuchi, T. Tokumasu
Molecular dynamics simulations have been performed to clarify the scattering phenomena of oxygen molecules on ionomer thin films, which affect the transport resistance of oxygen in catalyst layers in polymer electrolyte fuel cells. We have evaluated the probability density functions of the translational energy and scattering angle of scattered molecules, and the residence time of oxygen molecules on the ionomer surface. It was found that the energy distributions of scattered oxygen molecules depend on the incident energy and differ from that of thermally equilibrated molecules. On the other hand, the angular distributions are independent of the incident energy, and well reproduced by the diffusive scattering model. These results indicate that oxygen molecules do not accommodate completely with ionomer surface during the collision. We also evaluated the trapping dynamics of oxygen molecules on the ionomer surface in the trajectory calculations. Increasing the normal component of the incident energy results in the longer residence time on the ionomer surface.
通过分子动力学模拟,阐明了聚合物电解质燃料电池中氧分子在离子薄膜上的散射现象,这影响了氧在催化剂层中的传输阻力。我们计算了分散分子的平动能和散射角的概率密度函数,以及氧分子在离聚体表面的停留时间。结果表明,分散氧分子的能量分布与入射能量有关,与热平衡氧分子的能量分布不同。另一方面,角分布与入射能量无关,并能很好地再现扩散散射模型。这些结果表明,在碰撞过程中,氧分子不能完全与离聚体表面相适应。我们还在轨迹计算中评估了氧分子在离聚体表面的捕获动力学。增加入射能量的法向分量会导致在离聚体表面停留时间的延长。
{"title":"Dynamics of oxygen scattering on ionomer surface in catalyst layer of PEFC","authors":"M. Nakauchi, T. Mabuchi, I. Kinefuchi, H. Takeuchi, T. Tokumasu","doi":"10.1109/NANO.2016.7751557","DOIUrl":"https://doi.org/10.1109/NANO.2016.7751557","url":null,"abstract":"Molecular dynamics simulations have been performed to clarify the scattering phenomena of oxygen molecules on ionomer thin films, which affect the transport resistance of oxygen in catalyst layers in polymer electrolyte fuel cells. We have evaluated the probability density functions of the translational energy and scattering angle of scattered molecules, and the residence time of oxygen molecules on the ionomer surface. It was found that the energy distributions of scattered oxygen molecules depend on the incident energy and differ from that of thermally equilibrated molecules. On the other hand, the angular distributions are independent of the incident energy, and well reproduced by the diffusive scattering model. These results indicate that oxygen molecules do not accommodate completely with ionomer surface during the collision. We also evaluated the trapping dynamics of oxygen molecules on the ionomer surface in the trajectory calculations. Increasing the normal component of the incident energy results in the longer residence time on the ionomer surface.","PeriodicalId":6646,"journal":{"name":"2016 IEEE 16th International Conference on Nanotechnology (IEEE-NANO)","volume":"12 1","pages":"218-221"},"PeriodicalIF":0.0,"publicationDate":"2016-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"78285411","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
In situ evaluation of mechanical and electrochemical degradation in silicon negative electrode for lithium-ion secondary batteries 锂离子二次电池硅负极力学和电化学降解的原位评价
Pub Date : 2016-08-01 DOI: 10.1109/NANO.2016.7751563
N. Yoshida, Tadashi Sakamoto, N. Kuwata, J. Kawamura, Kazuhisa Sato, T. Hashida
Silicon is a promising anode material for lithium-ion battery application due to its high specific capacity. Unfortunately, silicon undergoes a volume expansion of 300~400% full lithiation and suffers from severe capacity fade, which limit its successful application in commercial cells. In this study, we used in situ acoustic emission and laser microscope observation method for detecting the volume change in silicon negative electrodes. It was shown that the long-term performance of the silicon negative electrode was dictated by its spallation during the discharge steps, while only the first lithiation caused its delamination and spoliation in the charge step. This strongly indicates that the energy of emission, and hence the amount of damage, is related to capacity loss. This study demonstrate that AE is a powerful tool to survey the real-time mechanical damage and electrochemical degradation in the electrode.
硅具有很高的比容量,是一种很有前途的锂离子电池负极材料。不幸的是,硅经历了300~400%的完全锂化体积膨胀和严重的容量衰减,这限制了它在商业电池中的成功应用。在本研究中,我们采用原位声发射和激光显微镜观察的方法来检测硅负极的体积变化。结果表明,硅负极的长期性能取决于其在放电阶段的剥落,而在充电阶段只有第一次锂化导致其分层和剥落。这有力地表明,发射的能量,因此的损伤量,与容量损失有关。研究表明,声发射是实时监测电极力学损伤和电化学降解的有力工具。
{"title":"In situ evaluation of mechanical and electrochemical degradation in silicon negative electrode for lithium-ion secondary batteries","authors":"N. Yoshida, Tadashi Sakamoto, N. Kuwata, J. Kawamura, Kazuhisa Sato, T. Hashida","doi":"10.1109/NANO.2016.7751563","DOIUrl":"https://doi.org/10.1109/NANO.2016.7751563","url":null,"abstract":"Silicon is a promising anode material for lithium-ion battery application due to its high specific capacity. Unfortunately, silicon undergoes a volume expansion of 300~400% full lithiation and suffers from severe capacity fade, which limit its successful application in commercial cells. In this study, we used in situ acoustic emission and laser microscope observation method for detecting the volume change in silicon negative electrodes. It was shown that the long-term performance of the silicon negative electrode was dictated by its spallation during the discharge steps, while only the first lithiation caused its delamination and spoliation in the charge step. This strongly indicates that the energy of emission, and hence the amount of damage, is related to capacity loss. This study demonstrate that AE is a powerful tool to survey the real-time mechanical damage and electrochemical degradation in the electrode.","PeriodicalId":6646,"journal":{"name":"2016 IEEE 16th International Conference on Nanotechnology (IEEE-NANO)","volume":"496 1","pages":"974-977"},"PeriodicalIF":0.0,"publicationDate":"2016-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"75207064","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 2
Fabrication and evaluation of CVD diamond resonators CVD金刚石谐振器的制备与评价
Pub Date : 2016-08-01 DOI: 10.1109/NANO.2016.7751555
Y. Mochimaru, M. Toda, T. Ono
In this paper, thin film diamond resonators on Si wafer for high sensitivity force sensing have been developed. Patterned diamond structures have been formed on Ir/YSZ/Si substrate. The completed diamond resonator of cantilever shows a resonance frequency of 51.0 kHz with a quality factor of 14911. The both clamped resonator shows the force sensitivity of 3.36×10-13 N/Hz0.5 at 229.3 kHz with 23500 of Q factor. While the crystallites and surface roughness are required to be improved, the patterned diamond resonator can be used as a high sensitive physicochemical sensing tool.
本文研制了用于高灵敏度力传感的硅晶片薄膜金刚石谐振器。在Ir/YSZ/Si衬底上形成了图像化的金刚石结构。完成的悬臂式金刚石谐振器谐振频率为51.0 kHz,质量因数为14911。双箝位谐振器在229.3 kHz时的力灵敏度为3.36×10-13 N/Hz0.5, Q因子为23500。虽然晶体结构和表面粗糙度还有待改进,但图像化金刚石谐振器可以作为一种高灵敏度的物理化学传感工具。
{"title":"Fabrication and evaluation of CVD diamond resonators","authors":"Y. Mochimaru, M. Toda, T. Ono","doi":"10.1109/NANO.2016.7751555","DOIUrl":"https://doi.org/10.1109/NANO.2016.7751555","url":null,"abstract":"In this paper, thin film diamond resonators on Si wafer for high sensitivity force sensing have been developed. Patterned diamond structures have been formed on Ir/YSZ/Si substrate. The completed diamond resonator of cantilever shows a resonance frequency of 51.0 kHz with a quality factor of 14911. The both clamped resonator shows the force sensitivity of 3.36×10-13 N/Hz0.5 at 229.3 kHz with 23500 of Q factor. While the crystallites and surface roughness are required to be improved, the patterned diamond resonator can be used as a high sensitive physicochemical sensing tool.","PeriodicalId":6646,"journal":{"name":"2016 IEEE 16th International Conference on Nanotechnology (IEEE-NANO)","volume":"70 1","pages":"676-677"},"PeriodicalIF":0.0,"publicationDate":"2016-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"75647802","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
The properties of metamaterials based on gold thin film and nanoparticles 基于金薄膜和纳米颗粒的超材料的性质
Pub Date : 2016-08-01 DOI: 10.1109/NANO.2016.7751475
Zu-Yin Deng, Chin-Wei Lin, Yu-Ting Kuo, Kuen-Lin Chen, Chiu-Hsien Wu
THz metamaterials are designed and fabricated. The resonance frequency of the SRRs (split ring resonators) based on thin film and nanoparticles is studied. Nanoparticle constituted metamaterial has a good absorb of THz spectrum. We compare the properties between thin film metamaterials and nanoparticles metamaterials. The transmission spectra of Au metamaterial was measured. The redshift was obtained when the metamaterials covered semiconductor The redshift phenomenon of absorbed wavelength of nanoparticle will be studied.
设计并制造了太赫兹超材料。研究了基于薄膜和纳米颗粒的劈裂环谐振器的谐振频率。纳米粒子构成的超材料对太赫兹光谱有良好的吸收。我们比较了薄膜超材料和纳米粒子超材料的性能。测量了金超材料的透射光谱。研究了纳米粒子吸收波长的红移现象。
{"title":"The properties of metamaterials based on gold thin film and nanoparticles","authors":"Zu-Yin Deng, Chin-Wei Lin, Yu-Ting Kuo, Kuen-Lin Chen, Chiu-Hsien Wu","doi":"10.1109/NANO.2016.7751475","DOIUrl":"https://doi.org/10.1109/NANO.2016.7751475","url":null,"abstract":"THz metamaterials are designed and fabricated. The resonance frequency of the SRRs (split ring resonators) based on thin film and nanoparticles is studied. Nanoparticle constituted metamaterial has a good absorb of THz spectrum. We compare the properties between thin film metamaterials and nanoparticles metamaterials. The transmission spectra of Au metamaterial was measured. The redshift was obtained when the metamaterials covered semiconductor The redshift phenomenon of absorbed wavelength of nanoparticle will be studied.","PeriodicalId":6646,"journal":{"name":"2016 IEEE 16th International Conference on Nanotechnology (IEEE-NANO)","volume":"30 1","pages":"598-599"},"PeriodicalIF":0.0,"publicationDate":"2016-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"75761958","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
期刊
2016 IEEE 16th International Conference on Nanotechnology (IEEE-NANO)
全部 Acc. Chem. Res. ACS Applied Bio Materials ACS Appl. Electron. Mater. ACS Appl. Energy Mater. ACS Appl. Mater. Interfaces ACS Appl. Nano Mater. ACS Appl. Polym. Mater. ACS BIOMATER-SCI ENG ACS Catal. ACS Cent. Sci. ACS Chem. Biol. ACS Chemical Health & Safety ACS Chem. Neurosci. ACS Comb. Sci. ACS Earth Space Chem. ACS Energy Lett. ACS Infect. Dis. ACS Macro Lett. ACS Mater. Lett. ACS Med. Chem. Lett. ACS Nano ACS Omega ACS Photonics ACS Sens. ACS Sustainable Chem. Eng. ACS Synth. Biol. Anal. Chem. BIOCHEMISTRY-US Bioconjugate Chem. BIOMACROMOLECULES Chem. Res. Toxicol. Chem. Rev. Chem. Mater. CRYST GROWTH DES ENERG FUEL Environ. Sci. Technol. Environ. Sci. Technol. Lett. Eur. J. Inorg. Chem. IND ENG CHEM RES Inorg. Chem. J. Agric. Food. Chem. J. Chem. Eng. Data J. Chem. Educ. J. Chem. Inf. Model. J. Chem. Theory Comput. J. Med. Chem. J. Nat. Prod. J PROTEOME RES J. Am. Chem. Soc. LANGMUIR MACROMOLECULES Mol. Pharmaceutics Nano Lett. Org. Lett. ORG PROCESS RES DEV ORGANOMETALLICS J. Org. Chem. J. Phys. Chem. J. Phys. Chem. A J. Phys. Chem. B J. Phys. Chem. C J. Phys. Chem. Lett. Analyst Anal. Methods Biomater. Sci. Catal. Sci. Technol. Chem. Commun. Chem. Soc. Rev. CHEM EDUC RES PRACT CRYSTENGCOMM Dalton Trans. Energy Environ. Sci. ENVIRON SCI-NANO ENVIRON SCI-PROC IMP ENVIRON SCI-WAT RES Faraday Discuss. Food Funct. Green Chem. Inorg. Chem. Front. Integr. Biol. J. Anal. At. Spectrom. J. Mater. Chem. A J. Mater. Chem. B J. Mater. Chem. C Lab Chip Mater. Chem. Front. Mater. Horiz. MEDCHEMCOMM Metallomics Mol. Biosyst. Mol. Syst. Des. Eng. Nanoscale Nanoscale Horiz. Nat. Prod. Rep. New J. Chem. Org. Biomol. Chem. Org. Chem. Front. PHOTOCH PHOTOBIO SCI PCCP Polym. Chem.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1