Min-Hsin Yeh

Self-powered textile for wearable electronics by hybridizing fiber-shaped nanogenerators, solar cells, and supercapacitors

A hybridized self-powered textile for simultaneously collecting solar energy and random body motion energy was demonstrated. Wearable electronics fabricated on lightweight and flexible substrate are believed to have great potential for portable devices, but their applications are limited by the life span of their batteries. We propose a hybridized self-charging power textile system with the aim of simultaneously collecting outdoor sunshine and random body motion energies and then storing them in an energy storage unit. Both of the harvested energies can be easily converted into electricity by using fiber-shaped dye-sensitized solar cells (for solar energy) and fiber-shaped triboelectric nanogenerators (for random body motion energy) and then further stored as chemical energy in fiber-shaped supercapacitors. Because of the all–fiber-shaped structure of the entire system, our proposed hybridized self-charging textile system can be easily woven into electronic textiles to fabricate smart clothes to sustainably operate mobile or wearable electronics.

Harvesting Low-Frequency (<5 Hz) Irregular Mechanical Energy: A Possible Killer Application of Triboelectric Nanogenerator

Electromagnetic generators (EMGs) and triboelectric nanogenerators (TENGs) are the two most powerful approaches for harvesting ambient mechanical energy, but the effectiveness of each depends on the triggering frequency. Here, after systematically comparing the performances of EMGs and TENGs under low-frequency motion (<5 Hz), we demonstrated that the output performance of EMGs is proportional to the square of the frequency, while that of TENGs is approximately in proportion to the frequency. Therefore, the TENG has a much better performance than that of the EMG at low frequency (typically 0.1-3 Hz). Importantly, the extremely small output voltage of the EMG at low frequency makes it almost inapplicable to drive any electronic unit that requires a certain threshold voltage (∼0.2-4 V), so that most of the harvested energy is wasted. In contrast, a TENG has an output voltage that is usually high enough (>10-100 V) and independent of frequency so that most of the generated power can be effectively used to power the devices. Furthermore, a TENG also has advantages of light weight, low cost, and easy scale up through advanced structure designs. All these merits verify the possible killer application of a TENG for harvesting energy at low frequency from motions such as human motions for powering small electronics and possibly ocean waves for large-scale blue energy.

A highly shape-adaptive, stretchable design based on conductive liquid for energy harvesting and self-powered biomechanical monitoring

Researchers report a scalable approach for highly deformable and stretchable energy harvesters and self-powered sensors. The rapid growth of deformable and stretchable electronics calls for a deformable and stretchable power source. We report a scalable approach for energy harvesters and self-powered sensors that can be highly deformable and stretchable. With conductive liquid contained in a polymer cover, a shape-adaptive triboelectric nanogenerator (saTENG) unit can effectively harvest energy in various working modes. The saTENG can maintain its performance under a strain of as large as 300%. The saTENG is so flexible that it can be conformed to any three-dimensional and curvilinear surface. We demonstrate applications of the saTENG as a wearable power source and self-powered sensor to monitor biomechanical motion. A bracelet-like saTENG worn on the wrist can light up more than 80 light-emitting diodes. Owing to the highly scalable manufacturing process, the saTENG can be easily applied for large-area energy harvesting. In addition, the saTENG can be extended to extract energy from mechanical motion using flowing water as the electrode. This approach provides a new prospect for deformable and stretchable power sources, as well as self-powered sensors, and has potential applications in various areas such as robotics, biomechanics, physiology, kinesiology, and entertainment.

Motion-driven electrochromic reactions for self-powered smart window system.

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.

A composite catalytic film of PEDOT:PSS/TiN–NPs on a flexible counter-electrode substrate for a dye-sensitized solar cell

A composite film of PEDOT:PSS/TiN–NPs, containing poly(3,4-ethylene dioxythiophene):poly(styrene sulfonate) (PEDOT:PSS) and titanium nitride nanoparticles (TiN–NPs), was deposited on a Ti foil by a doctor blade technique. Various weight percentages of TiN–NPs (5, 10, 20, 30 wt%) were used to prepare different composite films. This Ti foil with the composite film was used as the flexible counter-electrode (CE) for a dye-sensitized solar cell (DSSC). Performances of the DSSCs with the platinum-free CEs containing PEDOT:PSS/TiN–NPs with various contents of TiN–NPs were investigated. After the optimization of composition and thickness of the composite film PEDOT:PSS/TiN–NPs, a light-to-electricity conversion efficiency (η) of 6.67% was achieved for the pertinent DSSC, using our synthesized CYC-B1 dye, which was found to be higher than that of a cell with a sputtered-Pt film on its CE (6.57%). The homogeneous nature of the composite film PEDOT:PSS/TiN–NPs, the uniform distribution of TiN–NPs in its polymer matrix, and the large electrochemical surface area of the composite film are seen to be the factors for the best performance of the pertinent DSSC. Scanning electron microscopy (SEM), atomic force microscopy (AFM), transmission electron microscopy (TEM), X-ray diffraction (XRD), and energy dispersive X-ray spectroscopy (EDX) were used to characterize the films. The high efficiency of the cell with PEDOT:PSS/TiN–NPs is explained by cyclic voltammetry (CV), electrochemical impedance spectroscopy (EIS), and incident photon-to-current conversion efficiency (IPCE) curves.

Triboelectrification-Enabled Self-Powered Detection and Removal of Heavy Metal Ions in Wastewater

A fundamentally new working principle into the field of self-powered heavy-metal-ion detection and removal using the triboelectrification effect is introduced. The as-developed tribo-nanosensors can selectively detect common heavy metal ions. The water-driven triboelectric nanogenerator is taken as a sustainable power source for heavy-metal-ion removal by recycling the kinetic energy from flowing wastewater.

Harvesting Broad Frequency Band Blue Energy by a Triboelectric–Electromagnetic Hybrid Nanogenerator

Ocean wave associated energy is huge, but it has little use toward world energy. Although such blue energy is capable of meeting all of our energy needs, there is no effective way to harvest it due to its low frequency and irregular amplitude, which may restrict the application of traditional power generators. In this work, we report a hybrid nanogenerator that consists of a spiral-interdigitated-electrode triboelectric nanogenerator (S-TENG) and a wrap-around electromagnetic generator (W-EMG) for harvesting ocean energy. In this design, the S-TENG can be fully isolated from the external environment through packaging and indirectly driven by the noncontact attractive forces between pairs of magnets, and W-EMG can be easily hybridized. Notably, the hybrid nanogenerator could generate electricity under either rotation mode or fluctuation mode to collect energy in ocean tide, current, and wave energy due to the unique structural design. In addition, the characteristics and advantages of outputs indicate that the S-TENG is irreplaceable for harvesting low rotation speeds (<100 rpm) or motion frequencies (<2 Hz) energy, which fits the frequency range for most of the water wave based blue energy, while W-EMG is able to produce larger output at high frequencies (>10 Hz). The complementary output can be maximized and hybridized for harvesting energy in a broad frequency range. Finally, a single hybrid nanogenerator unit was demonstrated to harvest blue energy as a practical power source to drive several LEDs under different simulated water wave conditions. We also proposed a blue energy harvesting system floating on the ocean surface that could simultaneously harvest wind, solar, and wave energy. The proposed hybrid nanogenerator renders an effective and sustainable progress in practical applications of the hybrid nanogenerator toward harvesting water wave energy offered by nature.

A coral-like film of Ni@NiS with core–shell particles for the counter electrode of an efficient dye-sensitized solar cell

A coral-like film of nickel@nickel sulfide (Ni@NiS) was obtained on a conducting glass through an electrochemical method, in which the Ni functioned as a template. Three types of Ni thin films were electrodeposited on fluorine-doped tin oxide (FTO) substrates by a pulse current technique at the passed charge densities of 100, 200, and 300 mC cm−2, which rendered custard apple-like, coral-like, and cracked nanostructures, respectively. Subsequently, nickel sulfide films were coated on these Ni films by using a pulse potential technique. Due to the template effect of the Ni films, the composite films of Ni@NiS also assumed the same structures as those of their nickel templates. In each case of the films the particle of the film assumed a core–shell structure. The Ni@NiS coated FTO glasses were used as the counter electrodes for dye-sensitized solar cells (DSSCs). The DSSC with the coral-like Ni@NiS film on its counter electrode exhibits the highest power conversion efficiency (η) of 7.84%, while the DSSC with platinum film on its counter electrode shows an η of 8.11%. The coral-like Ni@NiS film exhibits multiple functions, i.e., large surface area, high conductivity, and great electrocatalytic ability for iodine/triiodine (I−/I3−) reduction. X-ray photoelectron spectroscopy (XPS), X-ray diffraction pattern (XRD), scanning electron microscopy (SEM), and four-point probe technique were used to characterize the films. The photovoltaic parameters are substantiated using incident photon-to-current conversion efficiency (IPCE) curves, cyclic voltammetry (CV), electrochemical impedance spectroscopy (EIS), and Tafel polarization plots. The IPCE curves were further used to calculate theoretical short-current densities of the cells.

A novel core–shell multi-walled carbon nanotube@graphene oxide nanoribbon heterostructure as a potential supercapacitor material

A novel core–shell heterostructure with multi-walled carbon nanotubes as the core and graphene oxide nanoribbons as the shell (MWCNT@GONR), fabricated by the facile unzipping of MWCNTs with the help of microwave energy, was used as a supercapacitor (SC) electrode material. Graphene nanopowder (GNP) and multi-walled carbon nanotubes (MWCNTs) have also been applied as SC materials for comparison. A smooth surface and a tube-like structure are found for the GNP and MWCNTs, respectively, while for the MWCNT@GONR material, graphene oxide sheet structures are observed on both sides of central nanotube cores that retain their tube-like structure. The specific capacitance is much better for the SC electrode with the MWCNT@GONR (252.4 F g−1) compared to the SC electrodes with commercial MWCNTs (39.7 F g−1) and GNP (19.8 F g−1), as determined using cyclic voltammetry (CV) at a scan rate of 50 mV s−1, which is due to the defective edges of the nanostructures in the former. The SC electrode with the MWCNT@GONR also exhibits good stability and capacitance retention even after 1000 cycles of galvanostatic charge–discharge testing, indicating its potential as a SC material. CV, galvanostatic charge–discharge (GC/D) and electrochemical impedance spectroscopy (EIS) were applied to analyze the SC performance.

An ultrarobust high-performance triboelectric nanogenerator based on charge replenishment.

Harvesting ambient mechanical energy is a green route in obtaining clean and sustainable electric energy. Here, we report an ultrarobust high-performance triboelectric nanogenerator (TENG) on the basis of charge replenishment by creatively introducing a rod rolling friction in the structure design. With a grating number of 30 and a free-standing gap of 0.5 mm, the fabricated TENG can deliver an output power of 250 mW/m(2) at a rotating rate of 1000 r/min. And it is capable of charging a 200 μF commercial capacitor to 120 V in 170 s, lighting up a G16 globe light as well as 16 spot lights connected in parallel. Moreover, the reported TENG holds an unprecedented robustness in harvesting rotational kinetic energy. After a continuous rotation of more than 14.4 million cycles, there is no observable electric output degradation. Given the superior output performance together with the unprecedented device robustness resulting from distinctive mechanism and novel structure design, the reported TENG renders an effective and sustainable technology for ambient mechanical energy harvesting. This work is a solid step in the development toward TENG-based self-sustained electronics and systems.