28 research outputs found

    Nanoscale Triboelectric-Effect-Enabled Energy Conversion for Sustainably Powering Portable Electronics

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    Harvesting energy from our living environment is an effective approach for sustainable, maintenance-free, and green power source for wireless, portable, or implanted electronics. Mechanical energy scavenging based on triboelectric effect has been proven to be simple, cost-effective, and robust. However, its output is still insufficient for sustainably driving electronic devices/systems. Here, we demonstrated a rationally designed arch-shaped triboelectric nanogenerator (TENG) by utilizing the contact electrification between a polymer thin film and a metal thin foil. The working mechanism of the TENG was studied by finite element simulation. The output voltage, current density, and energy volume density reached 230 V, 15.5 μA/cm<sup>2</sup>, and 128 mW/cm<sup>3</sup>, respectively, and an energy conversion efficiency as high as 10–39% has been demonstrated. The TENG was systematically studied and demonstrated as a sustainable power source that can not only drive instantaneous operation of light-emitting diodes (LEDs) but also charge a lithium ion battery as a regulated power module for powering a wireless sensor system and a commercial cell phone, which is the first demonstration of the nanogenerator for driving personal mobile electronics, opening the chapter of impacting general people’s life by nanogenerators

    Nanoscale Triboelectric-Effect-Enabled Energy Conversion for Sustainably Powering Portable Electronics

    No full text
    Harvesting energy from our living environment is an effective approach for sustainable, maintenance-free, and green power source for wireless, portable, or implanted electronics. Mechanical energy scavenging based on triboelectric effect has been proven to be simple, cost-effective, and robust. However, its output is still insufficient for sustainably driving electronic devices/systems. Here, we demonstrated a rationally designed arch-shaped triboelectric nanogenerator (TENG) by utilizing the contact electrification between a polymer thin film and a metal thin foil. The working mechanism of the TENG was studied by finite element simulation. The output voltage, current density, and energy volume density reached 230 V, 15.5 μA/cm<sup>2</sup>, and 128 mW/cm<sup>3</sup>, respectively, and an energy conversion efficiency as high as 10–39% has been demonstrated. The TENG was systematically studied and demonstrated as a sustainable power source that can not only drive instantaneous operation of light-emitting diodes (LEDs) but also charge a lithium ion battery as a regulated power module for powering a wireless sensor system and a commercial cell phone, which is the first demonstration of the nanogenerator for driving personal mobile electronics, opening the chapter of impacting general people’s life by nanogenerators

    Nanoscale Triboelectric-Effect-Enabled Energy Conversion for Sustainably Powering Portable Electronics

    No full text
    Harvesting energy from our living environment is an effective approach for sustainable, maintenance-free, and green power source for wireless, portable, or implanted electronics. Mechanical energy scavenging based on triboelectric effect has been proven to be simple, cost-effective, and robust. However, its output is still insufficient for sustainably driving electronic devices/systems. Here, we demonstrated a rationally designed arch-shaped triboelectric nanogenerator (TENG) by utilizing the contact electrification between a polymer thin film and a metal thin foil. The working mechanism of the TENG was studied by finite element simulation. The output voltage, current density, and energy volume density reached 230 V, 15.5 μA/cm<sup>2</sup>, and 128 mW/cm<sup>3</sup>, respectively, and an energy conversion efficiency as high as 10–39% has been demonstrated. The TENG was systematically studied and demonstrated as a sustainable power source that can not only drive instantaneous operation of light-emitting diodes (LEDs) but also charge a lithium ion battery as a regulated power module for powering a wireless sensor system and a commercial cell phone, which is the first demonstration of the nanogenerator for driving personal mobile electronics, opening the chapter of impacting general people’s life by nanogenerators

    The composition of a protein aggregate modulates the specificity and efficiency of its autophagic degradation

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    <p>The mechanism underlying autophagic degradation of a protein aggregate remains largely unknown. A family of receptor proteins that simultaneously bind to the cargo and the Atg8 family of autophagy proteins (such as the MAP1LC3/LC3 subfamily) has been shown to confer cargo selectivity. The selectivity and efficiency of protein aggregate removal is also modulated by scaffold proteins that interact with receptor proteins and ATG proteins. During <i>C. elegans</i> embryogenesis, autophagic clearance of the cargoes PGL-1 and PGL-3 requires the receptor protein SEPA-1 and the scaffold protein EPG-2. SEPA-1 and EPG-2 also form aggregates that are degraded by autophagy. Here we investigated the effect of composition and organization of PGL granules on their autophagic degradation. We found that depletion of PGL-1 or PGL-3 facilitates the degradation of SEPA-1 and EPG-2. Removal of EPG-2 is also promoted when SEPA-1 is absent. Depletion of PGL-1 or PGL-3 renders the degradation of SEPA-1 independent of EPG-2. We further showed that overexpression of SEPA-1 or EPG-2 as well as SQST-1 or EPG-7 (scaffold protein), which belong to different classes of aggregate, has no evident effect on the degradation of the other type. Our results indicate that the composition and organization of protein aggregates provide another layer of regulation to modulate degradation efficiency.</p

    Motion-Driven Electrochromic Reactions for Self-Powered Smart Window System

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    The self-powered system is a promising concept for wireless networks due to its independent and sustainable operations without an external power source. To realize this idea, the triboelectric nanogenerator (TENG) was recently invented, which can effectively convert ambient mechanical energy into electricity to power up portable electronics. In this work, a self-powered smart window system was realized through integrating an electrochromic device (ECD) with a transparent TENG driven by blowing wind and raindrops. Driven by the sustainable output of the TENG, the optical properties, especially the transmittance of the ECD, display reversible variations due to electrochemical redox reactions. The maximum transmittance change at 695 nm can be reached up to 32.4%, which is comparable to that operated by a conventional electrochemical potentiostat (32.6%). This research is a substantial advancement toward the practical application of nanogenerators and self-powered systems

    Quantitative Measurements of Vibration Amplitude Using a Contact-Mode Freestanding Triboelectric Nanogenerator

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    A vibration sensor is usually designed to measure the vibration frequency but disregard the vibration amplitude, which is rather challenging to be quantified due to the requirement of linear response. Here, we show the application of triboelectric nanogenerator (TENG) as a self-powered tool for quantitative measurement of vibration amplitude based on an operation mode, the contact-mode freestanding triboelectric nanogenerator (CF-TENG). In this mode, the triboelectrically charged resonator can be agitated to vibrate between two stacked stationary electrodes. Under the working principle with a constant capacitance between two electrodes, the amplitudes of the electric signals are proportional to the vibration amplitude of the resonator (provided that the resonator plate is charged to saturation), which has been illuminated both theoretically and experimentally. Together with its capability in monitoring the vibration frequency, the CF-TENG appears as the triboelectrification-based active sensor that can give full quantitative information about a vibration. In addition, the CF-TENG is also demonstrated as a power source for electronic devices

    Pulsed Nanogenerator with Huge Instantaneous Output Power Density

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    A nanogenerator (NG) usually gives a high output voltage but low output current, so that the output power is low. In this paper, we developed a general approach that gives a hugely improved instantaneous output power of the NG, while the entire output energy stays the same. Our design is based on an off–on–off contact based switching during mechanical triggering that largely reduces the duration of the charging/discharge process, so that the instantaneous output current pulse is hugely improved without sacrificing the output voltage. For a vertical contact-separation mode triboelectric NG (TENG), the instantaneous output current and power peak can reach as high as 0.53 A and 142 W at a load of 500 Ω, respectively. The corresponding instantaneous output current and power density peak even approach 1325 A/m<sup>2</sup> and 3.6 × 10<sup>5</sup> W/m<sup>2</sup>, which are more than 2500 and 1100 times higher than the previous records of TENG, respectively. For the rotation disk based TENG in the lateral sliding mode, the instantaneous output current and power density of 104 A/m<sup>2</sup> and 1.4 × 10<sup>4</sup> W/m<sup>2</sup> have been demonstrated at a frequency of 106.7 Hz. The approach presented here applies to both a piezoelectric NG and a triboelectric NG, and it is a major advance toward practical applications of a NG as a high pulsed power source

    Paper-Based Triboelectric Nanogenerators Made of Stretchable Interlocking Kirigami Patterns

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    The development of stretchable energy generation devices is indispensable for achieving stretchable, self-powered electronic systems. In this paper, a type of highly stretchable triboelectric nanogenerators made from conventional, inelastic materials such as paper is presented. It exploits a rationally designed interlocking kirigami structure and is capable of harvesting energy from various types of motions such as stretching, pressing, and twisting owing to the shape-adaptive thin film design. Energy harvested from the as-fabricated devices has been used for powering an LCD screen and lighting LED arrays. Furthermore, the paper-based devices have also been demonstrated for self-powered acceleration sensing and self-powered sensing of book opening and closing. This work introduces traditional kirigami into the development of stretchable triboelectric nanogenerators and verifies its promising applications in both power generation and self-powered sensing

    Quantitative Identification of Basic Growth Channels for Formation of Monodisperse Nanocrystals

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    Different mechanisms are proposed to account formation of monodisperse nanocrystals in literature, each of which is usually proposed to explain one set of experimental observations. Here, a general model based on mass conservation is developed to fully describe all possible channels including free growth by direct incorporation of the monomers converted from the precursors, growth by dissolution of a portion of the regular nanocrystals in solution, and growth by dissolution of the clusters in solution. The new model provides convenient yet quantitative methods to determine the channel ratios at a given time. Experimentally, an automated microreactor system is developed and applied for synthesis of monodisperse CdS nanocrystals, which is coupled with liquid-phase Fourier transform infrared and UV–vis measurements to, respectively, determine precursor conversion and size/concentration of nanocrystals with high reproducibility (<1%) and proper time resolution (<1 s). Different from the most-accepted model for formation of monodisperse nanocrystals, a burst of nucleation followed by growth of all nuclei by direct incorporation of the monomers converted from the precursors (or “focusing of size distribution”), all three basic channels are found to coexist during growth of monodisperse CdS nanocrystals. While the new theory and experimental methods are applied to study growth of monodisperse nanocrystals, they can be extended to offer a full kinetic picture for formation of colloidal nanocrystals
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