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Rational design of electrode materials with an excellent structure and morphology is crucial for improving electrochemical properties. Herein, various unique nanostructured Bi2S3 materials with controllable morphology were obtained through a simple and efficient oil bath reaction strategy. Bi2S3 with different morphologies can be obtained by regulating the polarity of solvent, and the lattice spacing can also be adjusted. The Bi2S3 nanomaterials obtained with ethanol as solvent (BS-3) show a three-dimensional nanoflower-like structure assembled with porous layers. The unique structure facilitates the transport of ions and accommodates the volume variation of Bi2S3 during energy storage. Consequently, BS-3 nanoflowers exhibited superior cycling stability and excellent high-rate capability for lithium storage (maintained a high capacity of 923.8 mA h g-1 after 950 cycles at 1.0 A g-1) and excellent sodium storage. We provide guidance for precise synthesis and energy storage application of Bi2S3 nanomaterials.
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Impedance cytometry is wildly used in single-cell detection, and its sensitivity is essential for determining the status of single cells. In this work, we focus on the effect of electrode gap on detection sensitivity. Through comparing the electrode span of 1 µm and 5 µm, our work shows that narrowing the electrode span could greatly improve detection sensitivity. The mechanism underlying the sensitivity improvement was analyzed via numerical simulation. The small electrode gap (1 µm) allows the electric field to concentrate near the detection area, resulting in a high sensitivity for tiny particles. This finding is also verified with the mixture suspension of 1 µm and 3 µm polystyrene beads. As a result, the electrodes with 1 µm gap can detect more 1 µm beads in the suspension than electrodes with 5 µm gap. Additionally, for single yeast cells analysis, it is found that impedance cytometry with 1 µm electrodes gap can easily distinguish budding yeast cells, which cannot be realized by the impedance cytometry with 5 µm electrodes gap. All experimental results support that narrowing the electrode gap is necessary for tiny particle detection, which is an important step in the development of submicron and nanoscale impedance cytometry.
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Poliestirenos , Saccharomyces cerevisiae , Impedância Elétrica , Eletrodos , Análise de Célula ÚnicaRESUMO
The monitoring of currents in the abyssal ocean is an essential foundation of deep-sea research. The state-of-the-art current meter has limitations such as the requirement of a power supply for signal transduction, low pressure resistance, and a narrow measurement range. Here, we report a fully integrated, self-powered, highly sensitive deep-sea current measurement system in which the ultra-sensitive triboelectric nanogenerator harvests ocean current energy for the self-powered sensing of tiny current motions down to 0.02 m/s. Through an unconventional magnetic coupling structure, the system withstands immense hydrostatic pressure exceeding 45 MPa. A variable-spacing structure broadens the measuring range to 0.02-6.69 m/s, which is 67% wider than that of commercial alternatives. The system successfully operates at a depth of 4531 m in the South China Sea, demonstrating the record-deep operations of triboelectric nanogenerator-based sensors in deep-sea environments. Our results show promise for sustainable ocean current monitoring with higher spatiotemporal resolution.
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Two-dimensional molybdenum disulfide (MoS2) is considered as a highly promising anode material for lithium-ion batteries (LIBs) due to its unique layer structure, large plane spacing, and high theoretical specific capacity; however, the overlap of MoS2 nanosheets and inherently low electrical conductivity lead to rapid capacity decay, resulting in poor cycling stability and low multiplicative performance. This severely limits its practical application in LIBs. To overcome the above problems, composite fibers with a core//sheath structure have been designed and fabricated. The sheath moiety of MoS2 nanosheets is uniformly anchored by the hydrothermal treatment of the axial of carbon nanofibers derived from an electrospinning method (CNFs//MoS2). The quantity of the MoS2 nanosheets on the CNFs substrates can be tuned by controlling the amount of utilized thiourea precursor. The influence of the MoS2 nanosheets on the electrochemical properties of the composite fibers has been investigated. The synergistic effect between MoS2 and carbon nanofibers can enhance their electrical conductivity and ionic reversibility as an anode for LIBs. The composite fibers deliver a high reversible capacity of 866.5 mA h g-1 after 200 cycles at a current density of 0.5 A g-1 and maintain a capacity of 703.3 mA h g-1 after a long cycle of 500 charge-discharge processes at 1 A g-1.
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The micro-cantilever-based sensor platform has become a promising technique in the sensing area for physical, chemical and biological detection due to its portability, small size, label-free characteristics and good compatibility with "lab-on-a-chip" devices. However, traditional micro-cantilever methods are limited by their complicated fabrication, manipulation and detection, and low sensitivity. In this research, we proposed a 10 µm thick ultrathin, highly sensitive, and flexible glass cantilever integrated with a strain gauge sensor and presented its application for the measurement of single-cell mechanical properties. Compared to conventional methods, the proposed ultrathin glass sheet (UTGS)-based cantilever is easier to fabricate, has better physical and chemical properties, and shows a high linear relationship between resistance change and applied small force or displacement. The sensitivity of the cantilever is 15 µN µm-1 and the minimum detectable displacement at the current development stage is 500 nm, which is sufficient for cell stiffness measurement. The cantilever also possesses excellent optical transparency that supports real-time observation during measurement. We first calibrated the cantilever by measuring the Young's modulus of PDMS with known specific stiffness, and then we demonstrated the measurement of Xenopus oocytes and fertilized eggs in different statuses. By further optimizing the UTGS-based cantilever, we can extend its applicability to various measurements of different cells.
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Dispositivos Lab-On-A-Chip , Fenômenos Mecânicos , Módulo de ElasticidadeRESUMO
The huge volumetric expansion (>300 %) of Si that occurs during the charge-discharge process makes it to have poor cycling ability and weak stable structure. These factors are considered as critical obstacles to the further development of Si as anode for lithium-ion batteries (LIBs). Herein, novel 3D interpenetrating microspheres, i.e., Si@C-CNTs, which consist of silicon nanoparticles interpenetrated with carbon nanotubes (CNTs) and stuck with amorphous carbon (C) have been designed and prepared via a spray-drying assisted approach. As anode of LIBs, Si@C-CNTs microspheres can achieve high silicon loadings of around 86 % and a high initial coulomb efficiency of 80.8 %. The electrodes maintain a reversible specific capacity of 1585.9mAh/g at 500 mA g-1 after 200 cycles, and deliver an excellent rate capability of 756.4 mAh/g at 5 A g-1. The outstanding performance of Si@C-CNTs can be due to their 3D interpenetrating structure and the synergy effect between the CNTs network and amorphous carbon therein. They synergistically act as conductive matrices which significantly improve the conductivity of the composite; they also act binders and reinforcing skeleton which help the composite spheres to have stable structure. Especially, the latter (reinforcing skeleton) alleviates the volumetric effect induced by the expansion and shrinkage of silicon particles during lithiation. The unique architecture provides an ideal model that can be used to design Si-based composite anode for advanced LIBs.
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The vanadium dioxide (VO2(D)), with ultra-high theoretical capacitance, has been considered as a boon for electrode materials of advanced supercapacitors (SCs). However, the VO2 has a series of shortcomings such as poor electrical conductivity, severe structural damage, and rapid capacity fading during cycles, resulting in unsatisfactory electrochemical performance. Herein, the Co2+ pre-intercalation and amorphous carbon confined vanadium dioxide (CoxVO2@C) with starfruit-like nanostructure is synthesized on a conductive Ni foam substrate via a versatile and cost-effective method. As a cathode for SCs, the obtained CoxVO2@C not only enables a small amount of Co2+ pre-intercalation layer to offer faster ion diffusion kinetics for VO2, but also utilizes a high-conductivity amorphous carbon to protect VO2 from dissolution in an alkaline electrolyte, thereby exhibiting the ultrahigh specific capacitance up to 4440.0 mF cm-2 at 5 mA cm-2 (525.2 F g-1 at 2 A g-1) and the prominent long-term stability performance of the electrode. Benefited from these excellent characteristics, a high-performance CoxVO2@C//V2O3 hybrid supercapacitor (HSC) device with an operating voltage of 1.7 V is further assembled. The HSC device delivers a superior energy density of 102.3 W h kg-1 at a power density of 6.1 kW kg-1, manifesting its practical feasibility.
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The electrical penetration of the cell membrane is vital for determining the cell interior via impedance cytometry. Herein, we propose a method for determining the conductivity of the cell membrane through the tilting levels of impedance pulses. When electrical penetration occurs, a high-frequency current freely passes through the cell membrane; thus, the intracellular distribution can directly act on the high-frequency impedance pulses. Numerical simulation shows that an uneven intracellular component distribution can affect the tilting levels of impedance pulses, and the tilting levels start increasing when the cell membrane is electrically penetrated. Experimental evidence shows that higher detection frequencies (>7 MHz) lead to a wider distribution of the tilting levels of impedance pulses when measuring cell populations with four-frequency impedance cytometry. This finding allows us to determine that a detection frequency of 7 MHz is able to pass through the membrane of Euglena gracilis (E. gracilis) cells. Additionally, we provide a possible application of four-frequency impedance cytometry in the biomass monitoring of single E. gracilis cells. High-frequency impedance (≥7 MHz) can be applied to monitor these biomass changes, and low-frequency impedance (<7 MHz) can be applied to track the corresponding biovolume changes. Overall, this work demonstrates an easy determination method for the electrical penetration of the cell membrane, and the proposed platform is applicable for the multiparameter assessment of the cell state during cultivation.
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Intracellular components (including organelles and biomolecules) at the submicron level are typically analyzed in situ by special preparation or expensive setups. Here, a label-free and cost-effective approach of screening microalgal single-cells at a subcellular resolution is available based on impedance cytometry. To the best of our knowledge, it is the first time that the relationships between impedance signals and submicron intracellular organelles and biomolecules are shown. Experiments were performed on Euglena gracilis (E. gracilis) cells incubated under different incubation conditions (i.e., aerobic and anaerobic) and 15 µm polystyrene beads (reference) at two distinct stimulation frequencies (i.e., 500 kHz and 6 MHz). Based on the impedance detection of tens of thousands of samples at a throughput of about 900 cells per second, three metrics were used to track the changes in biophysical properties of samples. As a result, the electrical diameters of cells showed a clear shrinkage in cell volume and intracellular components, as observed under a microscope. The morphology metric of impedance pulses (i.e., tilt index) successfully characterized the changes in cell shape and intracellular composition distribution. Besides, the electrical opacity showed a stable ratio of the intracellular components to cell volume under the cellular self-regulation. Additionally, simulations were used to support these findings and to elucidate how submicron intracellular components and cell morphology affect impedance signals, providing a basis for future improvements. This work opens up a label-free and high-throughput way to analyze single-cell intracellular components by impedance cytometry.
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Euglena gracilis , Microalgas , Impedância Elétrica , Microscopia , PoliestirenosRESUMO
The benefits of impedance cytometry include high-throughput and label-free detection, while long-term calibration is required to remove the effects of the detection circuits. This study presents a novel impedance cytometry system, called parallel impedance cytometry, to simplify the calibration and analysis of the impedance signals. Furthermore, target objects can be detected even when benchmarked against similar objects. Parallel dual microchannels allow the simultaneous detection of reference and target particles in two separate microchannels, without the premixing of reference and target suspensions. The impedance pulses of both can appear separately on the opposite sides of the same time series, which have been verified via simulation and experimental results. Raw impedance signals can easily distinguish target particles from reference ones. Polystyrene beads with different sizes ranging from nano- to microscale (e.g., 500, 750 nm, 1, 2, 3, and 4.5 µm) confirm the nanosensitivity of the system. In addition, the detection of antibiotic-treated Escherichia coli cells demonstrates that our system can be used for the quantitative assessment of the dielectric properties of individual cells, as well as for the proportion of susceptible cells. Through benchmarking against untreated E. coli cells in the other channel, our method enables the discrimination of susceptible cells from others and the comparison of susceptible and insusceptible cells in the target suspension. Those findings indicate that the parallel impedance cytometry can greatly facilitate the measurement and calibration of the impedances of various particles or cells and provide a means to compare their dielectric properties.
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Bactérias , Escherichia coli , Impedância Elétrica , Poliestirenos , CalibragemRESUMO
In this work, we investigated the ability of impedance flow cytometry to measure the shape of single cells/particles. We found that the impedance pulses triggered by micro-objects that are asymmetric in morphology show a tilting trend, and there is no such a tilting trend for symmetric ones. Therefore, we proposed a new metric, tilt index, to quantify the tilt level of the impedance pulses. Through simulation, we found that the value of tilt index tends to be zero for perfectly symmetrical objects, while the value is greater than zero for asymmetrical ones. Also, this metric was found to be independent on the trajectories (i.e., lateral, and z-direction shift) of the target micro-object. In experiments, we adopted a home-made lock-in amplifier and performed experiments on 10 µm polystyrene beads and Euglena gracilis (E. gracilis) cells with varying shapes. The experimental results coincided with the simulation results and demonstrated that the new metric (tilt index) enables the impedance cytometry to characterize the shape single cells/particles without microscopy or other optical setups.
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Técnicas Biossensoriais , Forma Celular , Impedância Elétrica , Citometria de Fluxo , PoliestirenosRESUMO
A phenomenon that electric current is generated when a pendant water droplet touches an air-electrolyte solution interface is investigated in this paper. A measurement system developed in this study consists of a hollow electrode for droplet generation, a counter electrode immersed in an electrolyte solution, and an electrometer with high precision. Once a droplet touches the air-electrolyte solution interface, it will be pulled into the electrolyte solution and an electric current is produced during this process. Experiments showed that the magnitude of the electric current depends only on the pendant droplet and has nothing to do with the types of the electrolyte solution (with a much larger volume than that of the droplet) below the drop. The electric current is generated by the electric potential difference between the droplet and air-electrolyte solution interface and the liquid bridge formed during droplet coalescence. As a result, the magnitude of the generated electrical current mainly depends on the size, pH, and the type of the solution forming the droplet. Determining the critical micelle concentration using this system was successfully achieved to show the powerfulness of this system.
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Traditionally, a resistive pulse sensor (also known as Coulter counter) works by letting a particle pass through a small orifice in an electrolyte solution. The detection sensitivity mainly relies on the volume ratio of the particle to the orifice. This paper presents a novel resistive pulse sensor which has a sensing orifice located on the side wall of a microchannel. In this way, the sensor can detect and count particles (or cells) without requiring particles (or cells) passing through the sensing gate. An equation was derived to relate the magnitudes of the detected signals and the electrical resistances. Results show that the magnitudes of the detected signals can be increased by applying voltages from more than one voltage input channels simultaneously. Under the same conditions, the magnitudes of the detected signals become larger when the diameters of particles are larger. Higher detection sensitivity can be obtained simply by increasing either the magnitudes of the applied voltages or the number of the voltage input channels, or reducing the opening of the side sensing gate to a size that is even smaller than the diameter of the particle. Due to the high detection sensitivity, detection of 1⯵m particles by a relatively large sensing gate of 5â¯×â¯10â¯×â¯10⯵m (widthâ¯×â¯lengthâ¯×â¯height) was successfully demonstrated with a signal to noise ratio (S/N) of approximately 3. This sensor was also applied to detect and count human red blood cells and lymphocyte cells. Results show that this method can clearly distinguish the cells with different sizes based on the pre-determined-thresholds. Because this sensor does not require cells to pass through the sensing gate, the channel clogging problem can be avoided. More importantly, the detection sensitivity can be tuned by applying different voltages without fabricating a smaller sensing gate.