Field-effect transistor with recombinant potassium channels: fast and slow response by electrical and chemical interactions

Electrical interfacing of semiconductor devices with ion channels is the basis for a development of neuroelectronic systems and of cell-based biospecific electronic sensors. To elucidate the mechanism of cell–chip coupling, we studied the voltage-gated potassium channel Kv1.3 in HEK 293 cells on field-effect transistors in silicon with a metal-free gate of silicon dioxide. Upon intracellular depolarization there is a positive change of the effective extracellular voltage on the transistor with an amplitude that correlates with the gating of Kv1.3 channels, but with a dynamics that is far slower than channel gating. After repolarization there is a fast negative change of the transistor signal followed by a slow relaxation dynamics without any membrane current. To rationalize the involved transistor response, we propose a concept that combines the electrodiffusion of ions in the cell–chip junction with selective ion binding in the electrical double layer of silicon dioxide. The model implies (i) an electrical charging and discharging of the cell–chip capacitance within a microsecond, (ii) a changing K⁺ concentration in the cell–chip junction within a millisecond and (iii) a changing adsorption of K⁺ and Na⁺ ions within tens of milliseconds. The total transistor signal is a superposition of the changed electrical potential in the extracellular space between cell and chip and of the changed surface potential at the chip surface. PACS 73.40.Mr; 82.45.Vp; 85.30.Tv; 87.16.Uv; 87.19.Nn     

Electrical interfacing of neurotransmitter receptor and field effect transistor

The interfacing of a ligand-gated ion channel to a transistor is studied. It relies on the transduction of ion current to a voltage in a cell-transistor junction. For the first time, a genetically modified cell is used without external driving voltage as applied by a patch-pipette. Using a core-coat conductor model, we show that an autonomous dynamics gives rise to a signal if a driving voltage is provided by potassium channels, and if current compensation is avoided by an inhomogeneous activation of channels. In a proof-of-principle experiment, we transfect HEK293 cells with the serotonin receptor 5-HT3A and the potassium channel Kv1.3. The interfacing is characterized under voltage-clamp with a negative transistor signal for activated 5-HT3A and a positive signal for activated Kv1.3. Without patch-pipette, a biphasic transient is induced by serotonin. The positive wave is assigned to 5-HT3A receptors in the free membrane that drive a potassium outward current through the adherent membrane. The negative wave is attributed to 5-HT3A receptors in the adherent membrane that are activated with a delay due to serotonin diffusion. The implementation of a receptor-cell-transistor device is a fundamental step in the development of biosensors that combine high specificity and universal microelectronic readout.     

非晶硅太阳电池BZO/p-a-SiC:H接触特性改善的研究

采用重掺杂的p型微晶硅来改善前电极掺硼氧化锌 (ZnO:B) 和窗口层p型非晶硅碳 (p-a-SiC) 之间的非欧姆接触特性. 通过优化插入层p型微晶硅的沉积参数 (氢稀释比H₂/SiH₄、硼掺杂比B₂H₆/SiH₄) 获得了较薄厚度下 (20 nm) 暗电导率高达4.2 S/cm的p型微晶硅材料. 在本征层厚度约为150 nm, 仅采用Al背反射电极的情况下,获得了效率6.37%的非晶硅顶电池(V_oc=911 mV, FF=71.7%, J_sc=9.73 mA/cm²), 开路电压V_oc和填充因子FF均较无插入层的电池有大幅提升. 关键词： 氧化锌 p型微晶硅 非晶硅顶电池 非欧姆接触     

Montmorillonite-based ceramic membranes as novel lithium-ion battery separators

Novel montmorillonite-based ceramic membrane (CM) has been prepared with poly(vinylidene fluoride-co-hexafluoropropene) (PVdF-HFP) copolymer as binder. Physical properties such as surface morphology, porosity, liquid electrolyte uptake and thermal stability were analysed. The ceramic membrane was activated by soaking it in a non-aqueous liquid electrolyte (1.0 M LiPF₆ solution in 1/1 v/v ethylene carbonate/diethyl carbonate mixture) for 10 min. The compatibility of the membrane with lithium metal anode as a function of storage time was analysed by assembling a Li/CM/Li symmetric cell. Finally, a lab-scale cell composed of Li/CM/LiFePO₄ is assembled and its cycling performance analysed at different C-rates. Although the ceramic membrane is not flexible, it shows high thermal stability and stable interfacial properties when in contact with the lithium metal anode. A stable cycling behaviour is demonstrated even at 1C-rate with limited fade in capacity.     

Nyquist noise of cell adhesion detected in a neuron-silicon transistor

Interfacing of nerve cells and field-effect transistors is determined by current flow along the electrical resistance of the cell-chip junction. We study the thermal noise of the junction by measuring the fluctuations of extracellular voltage with a low-noise transistor. We find a spectral power density of 5 x 10(-14) V2/Hz and interpret it as Nyquist noise of the cell-chip junction with a resistance of 3 MOhm. The thermal noise allows us to elucidate the properties of cell adhesion and it sets a thermodynamical limit for the signal-to-noise ratio of neuroelectronic interfacing.     

Properties of TiO2 as photoelectrode for hydrogen generation using solar energy

The present paper describes electrochemical characteristics of photo-electrochemical cell during light-on and light-off regimes. The cell involves TiO₂ as photo-anode and Pt as cathode both immersed in a aqueous electrolyte. The photo-voltage was determined for two different cell structures both equipped with TiO₂ as photo-anode. The first cell involved a homogeneous electrolyte system, formed of Na₂SO₄, and photo-anode made of pressed polycrystalline TiO₂. The second cell involved an electrolyte of different pH at both electrodes (ΔpH=14.6) and TiO₂ thin film (deposited in Ti) as photo-anode. Maximum photo-voltage of these cells was 0.7 V and 1.3 V, respectively.     

Function and analytical formula for nanocrystalline dye-sensitization solar cells

Based on the experimental observations that the three-phase nano-TiO₂/F:SnO₂/I^-/I^- ₃ electrolyte front contact has to have pronounced rectifying properties (reverse reaction with electrolyte suppressed) for efficient operation of the dye-sensitization solar cell and plays an active part in the generation of photoelectrochemical energy, an analytical formula is derived which allows the understanding of the relevance and involvement of a variety of kinetic and cell parameters. Essentially, the TiO₂ layer is treated as a photocathode, donating electrons to a kinetically controlled front contact, with the counter-charges being transported by the electrolyte within the pores. The formula was expanded to include photochemical kinetics of the sensitizer, for which photodegradation properties were also calculated. The branching ratio, the ratio of regeneration-rate constant of the sensitizer and of product-formation rate, turned out to be critical for long-term stability. It may have to be improved by one order of magnitude for efficient cells to reach a lifetime of 20 years. The degree of rectifying character of the nano-TiO₂/F:SnO₂/I^-/I^- ₃ electrolyte interface (electric-field-dependent charge transfer to the front contact versus recombination-rate constant with I₃ ^- distinguishes between a low-efficiency (‘dynamic’) Galvani-type solar cell (efficiency determined by photoinduced chemical potential gradients, no rectifying contact) and a more highly efficient ‘junction-type’ solar cell (separation and collection of charges additionally assisted by junction potential). Several controversial subjects are addressed. The key challenges for the improvement of such cells are discussed, especially with respect to photodegradation and to solid-state devices. Received: 18 September 2000 / Accepted: 17 January 2001 / Published online: 20 June 2001     

原位聚合法制备凝胶型离子液体/PMMA聚合物电解质

采用原位聚合法制备了含有N-甲基、丙基哌啶双三氟甲磺酰亚胺离子液体的凝胶型聚合物电解质．利用SEM和XPS测试了电解质膜与LiFePO₄电极的界面状态,充放电循环后,在电解质膜与LiFePO₄之间有一层薄膜,这层薄膜中含有N和S元素．结果表明,随着充放电的不断进行,凝胶型电解质中未聚合的甲基丙烯酸甲酯与电极表面的锂离子之间发生电子转移,形成SEI膜,至少要三个循环后才能形成稳定的SEI膜．随着SEI膜的增厚,放电容量增加,阻碍了电子转移,使系统更加的稳定．在不同     

渐变带隙氢化非晶硅锗薄膜太阳能电池的优化设计

利用一维微电子-光电子结构分析软件(AMPS-1D)在AM1.5G(100 mW/cm2)、室温条件下模拟和比较了有、无渐变带隙氢化非晶硅锗(a-SiGe:H)薄膜太阳能电池的各项性能.计算结果表明:渐变带隙结构电池具有较高的开路电压(V oc)和较好的填充因子(FF),转换效率(E ff)比非渐变带隙电池提高了0.477%.研究了氢化非晶硅(a-Si:H)、氢化非晶碳化硅(a-SiC:H)和氢化纳米晶硅(nc-Si:H)三种不同材料的窗口层对a-SiGe:H薄膜太阳能电池性能的影响.结果显示:在以nc-Si:H为窗口层的电池能带中,费米能级E F已经进入价带,使得窗口层电导率及电池开路电压有所提高,又由于ITO与p-nc-Si:H的接触势垒较低,使得接触处的电场降低,更有利于载流子的收集.另一方面,窗口层与a-SiGe:H薄膜之间存在较大的带隙差,在p/i界面由于能带补偿作用形成了价带势垒(带阶)?E v,阻碍了空穴的迁移,因此我们在p/i界面引入缓冲层,使得能带补偿作用得到释放,更有利于空穴的迁移和收集,得到优化后单结渐变带隙a-SiGe:H薄膜结构太阳能电池的转换效率达到了9.104%.     

Perborate as novel fuel for enhanced performance of membraneless fuel cells

This paper presents the development of membraneless sodium perborate fuel cell using acid/alkaline electrolyte. In the acid/alkaline electrolyte, perborate works both as an oxidant as well as reductant. Sodium perborate affords hydrogen peroxide in aqueous medium. The cell converts the energy released by H₂O₂ decomposition with H⁺ and OH^? ions into electricity and produces water and oxygen. Such a novel design eliminates the need of a membrane, in which acid and alkaline electrolytes contact with each other. At room temperature, the laminar flow-based microfluidic membraneless fuel cell can reach a maximum power density of 34 mW/cm² with the molar ratio of [Perborate]/[NaOH]?=?1 as fuel and [Perborate]/[H₂SO₄]?=?2 as oxidant. The paper reports for the first time the use of sodium perborate as the oxidant and reductant. The developed fuel cell emits no CO₂, features no proton exchange membrane, inexpensive catalysts, and simple planar structure, which enables high design flexibility and easy integration of the microscale fuel cell into actual microfluidic systems and portable power applications.     

Improved electrical properties of silicon-incorporated anodic niobium oxide formed on porous Nb-Si substrate

In the present study, porous Nb-Si alloy films with isolated nano-column morphology have been successfully developed by oblique angle magnetron sputtering on to aluminum substrate with concave cell structure. The deposited films are amorphous with the 15 at% silicon supersaturated into niobium. The porous Nb-15 at% Si films, as well as niobium films with similar morphology, are anodized at several voltages up to 50 V in 0.1 mol dm⁻³ ammonium pentaborate electrolyte. Due to the presence of sufficient gaps between neighboring columns, the gaps are not filled with anodic oxide, despite the large Pilling-Bedworth ratio (for instance, 2.6 for Nb/Nb₂O₅) and hence, a linear correlation between the reciprocal of capacitance and formation voltage is obtained for the Nb-15 at% Si. From the comparison with the anodic films formed on porous niobium films, it has been found that silicon addition improves the thermal stability of anodic niobium oxide; the change in capacitance and increase in leakage current become small for the Nb-Si. The findings indicate the potential of oblique angle deposition to tailor porous non-equilibrium niobium alloy films for high performance niobium-base capacitor.     

All-solid-state lithium-based polymer cells for high-temperature applications

A lithium salt doped siloxane/methacrylate copolymer membrane, prepared by a rapid UV curing process, has been characterised and tested as a fully solid electrolyte in rechargeable lithium test cells using low cost materials as electrodes. In addition, results of a laboratory-scale Li-ion polymer cell, assembled by contacting a LiFePO₄ cathode with a graphite anode and using the solid polymer as electrolyte, are presented. The polymer electrolyte production process is simple and versatile and the highly cross-linked membrane demonstrates mechanical integrity, low T _g and large thermal stability. It is an extra soft, non-crystalline, transparent solid and shows sufficient ionic conductivity (>10⁻⁴ S cm⁻¹ at 60 °C) along with a wide electrochemical stability window and improved interfacial stability with respect to lithium. The performances in Li-based cells have been determined by cycling tests carried out at 80 °C. Good rate capability, along with high charge/discharge efficiency even at 1C-rate, and a satisfactory cyclability have been obtained. These results outline the practical relevance of the use of this solid electrolyte membrane (which serves as the separator simultaneously) in Li-based cells conceived for high-temperature applications.     

Fast voltage transients in capacitive silicon-to-cell stimulation detected with a luminescent molecular electronic probe

The capacitive stimulation of nerve cells from semiconductor chips is a prerequisite for the development of neuroelectronic devices. We report on the primary response of a cell membrane to a voltage step applied to oxidized silicon. It is observed with a luminescent voltage-sensitive dye. We find exponential voltage transients with a time constant of 1-5 micros. We assign the short response to an electrical decoupling by a thin film of electrolyte between oxide and membrane. The high-pass filtering of stimulation is a crucial constraint for the development of silicon-to-neuron interfaces.     

Silicon nitride/silicon oxide interlayers for solar cell passivating contacts based on PECVD amorphous silicon

This Letter demonstrates improved passivating contacts for silicon solar cells consisting of doped silicon films together with tunnelling dielectric layers. An improvement is demonstrated by replacing the commonly used silicon oxide interfacial layer with a silicon nitride/silicon oxide double interfacial layer. The paper describes the optimization of such contacts, including doping of a PECVD intrinsic a‐Si:H film by means of a thermal POCl₃ diffusion process and an exploration of the effect of the refractive index of the SiN_x. The n⁺ silicon passivating contact with SiN_x /SiO_x double layer achieves a better result than a single SiN_x or SiO_x layer, giving a recombination current parameter of ～7 fA/cm² and a contact resistivity of ～0.005 Ω cm², respectively. These self‐passivating electron‐selective contacts open the way to high efficiency silicon solar cells. (© 2015 WILEY‐VCH Verlag GmbH &Co. KGaA, Weinheim)     

Improvement of electrochemical performance for AlF<Subscript>3</Subscript>-coated Li<Subscript>1.3</Subscript>Mn<Subscript>4/6</Subscript>Ni<Subscript>1/6</Subscript>Co<Subscript>1/6</Subscript>O<Subscript>2.40</Subscript> cathode materials for Li-ion batteries

Li-rich layered-layered-Spinel structure spherical Li_1.3Mn_4/6Ni_1/6Co_1/6O_2.40 particles was successfully prepared and coated with a uniform layer by a two-step co-precipitation method and evaluated in lithium cells. The structures and electrochemical properties of pristine Li_1.3Mn_4/6Ni_1/6Co_1/6O_2.40 and AlF₃-coated Li_1.3Mn_4/6Ni_1/6Co_1/6O_2.40 were characterized. When the coating amount was 2 wt%, the cathode showed the best cycling performance and rate capability compared to others. The AlF₃-coated Li_1.3Mn_4/6Ni_1/6Co_1/6O_2.40 Li-ion cell cathode had a capacity retention of 90.07 % after 50 cycles at 0.5 C over 2.0–4.8 V, while the pristine Li_1.3Mn_4/6Ni_1/6Co_1/6O_2.40 exhibited capacity retention of only 80.73 %. Moreover, the rate capability and cyclic performance also improved. Electrochemical impedance spectroscopy testing revealed that the improved electrochemical performance might attribute to the AlF₃ coating layer which can suppress the increase of impedance during the charging and discharging process by preventing direct contact between the highly delithiated active material and electrolyte.     

Charge rate influence on the electrochemical performance of LiFePO<Subscript>4</Subscript> electrode with redox shuttle additive in electrolyte

Overcharge performance of LiFePO₄ cells is investigated through adding 2, 5-ditertbutyl 1, 4-dimethoxybenzene (DDB) as redox shuttle into electrolyte (RS electrolyte) at different charge rate. RS electrolytes with DDB works well as overcharge protection at low charge rate of less than 0.1 C. Novel charge/discharge characteristics are observed when charge rate increases in the cell with RS electrolyte. Especially, larger discharge capacities are obtained at the same discharge rate after charge rate gets higher than 0.1 C rate. Discharge capacity is larger in the cell with RS electrolyte than that in the cell without RS electrolyte at the same charge and discharge rate. At the same charge rate, cells with RS electrolyte have better cycling performances and larger discharge capacity than that with conventional electrolyte. These indicate that DDB accumulates in cathode with cycling and influences electrode–electrolyte interface reactions.     

Electrochemical double layer capacitor based on cellulose-PVA hybrid electrolyte

A polyvinyl alcohol (PVA) cellulose electrolyte was prepared by casting a solution of PVA and H₃PO₄ on both sides of a cellulose membrane (filter paper). The ionic species H⁺ are caused by the H₃PO₄ acid which is entrapped inside the PVA and in the pores of the filter paper. The electrolyte was sandwiched between two carbon electrodes to form an electric double layer capacitor (EDLC). The EDLC exhibits a good charge and discharge characteristics with a capacitance value of 30 Fg⁻¹. Paper presented at the International Conference on Functional Materials and Devices 2005, Kuala Lumpur, Malaysia, June 6 – 8, 2005.     

High-voltage asymmetric supercapacitors operating in aqueous electrolyte

The performance of supercapacitors based on different materials with pseudocapacitive properties such as several conducting polymers (ECPs), amorphous manganese dioxide (a-MnO₂), and activated carbon is reported. Composite electrodes of high resiliency and good electronic conductivity were obtained by mixing the active materials with carbon nanotubes. The various limitations of all the above-mentioned materials, when used as negative and positive electrodes in traditional symmetric systems, are shown. It is demonstrated that a successful application of ECPs and a-MnO₂ in supercapacitor technologies is possible only in an asymmetric configuration, i.e. with electrodes of different nature for positive and negative polarizations. Several types of asymmetric capacitors were developed by combining ECPs, a-MnO₂, and activated carbon and characterized in aqueous electrolyte by galvanostatic charge–discharge, cyclic voltammetry, and impedance spectroscopy. The best device considering the specific energy and power is the asymmetric supercapacitor using a-MnO₂ and poly(3,4-ethylenedioxythiophene) (PEDOT) for the positive and negative electrodes, respectively. It has an operating voltage of 1.8 V, which is attributed to different operating potentials of both electrodes, and good electrochemical stability in neutral aqueous electrolyte. According to the voltage value, the energy density of the asymmetric capacitor at a current density of 250 mA/g is found to be 13.5 W h/kg, which is about ten times more than for a symmetric capacitor based on PEDOT in an aqueous medium. The asymmetric capacitor provides two times higher power than a symmetric capacitor based on activated carbon in organic electrolyte, and is thus extremely promising for the development of environmentally friendly systems. PACS 82.45.Wx; 82.45.Yz; 82.47.Uv; 82.35.Cd     

Analysis of electron recombination in dye-sensitized solar cell

A steady-state numerical model of dye-sensitized solar cell is based on continuity and transport equations for electrons, iodide and triiodide ions. The cell model consists of an active layer, where photovoltaic effect including diffusion of electrons in mesoporous TiO₂ and ions in electrolyte takes place, and a bulk electrolyte layer, where only ions diffuse. Exponential distribution of trap states in TiO₂ and Gaussian distributions of energy levels in the electrolyte within active layer are included in modeling of the recombination dynamics, according to Shockley-Read-Hall statistics and Marcus-Gerischer electron transfer theory. Recombinations at the front contact and a voltage drop at the platinum covered back contact are included in the model. Simulation results are compared with the measured current-voltage characteristics at different light intensities. In particular, light intensity dependence of open circuit voltage is studied over 4 decades. Optimization of cell efficiency regarding active layer and electrolyte layer thickness is carried out. Simulation results show that best efficiency is achieved when electrolyte layer thickness is minimized as much as possible and that active layer thickness is traded off with respect to recombination rates and/or diffusion limited current determined with the selection of the electrolyte.     

Studies on modified anode polymer hydrogen sensor

An improved polymer electrolyte membrane (PEM) fuel cell based amperometric hydrogen sensor that operates at room temperature has been developed. The electrolyte used in the sensor is PVA/H₃PO₄ blend, which is a proton conducting solid polymer electrolyte. A blend of palladium and platinum coated on the membrane is used as anode and platinum as cathode. The sensor functions as a fuel cell, H₂/Pd-Pt//PVA-H₃PO₄//Pt/O₂, and the short circuit current is found to be linearly related to the hydrogen concentration. The present study aims at investigating the dependence of sensor behaviour on the anode composition. Paper presented at the 2nd International Conference on Ionic Devices, Anna University, Chennai, India, Nov. 28–30, 2003.