Intercalation and exfoliation of lithium: Few-layer-thick inorganic nanosheets (BN, NbSe(2), WSe(2), Sb(2)Se(3), and Bi(2)Te(3)) have been prepared from their layered bulk precursors by using a controllable electrochemical lithium intercalation process. The lithium intercalation conditions, such as cut-off voltage and discharge current, have been systematically studied and optimized to produce high-quality BN and NbSe(2) nanosheets.

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Assembling thermoelectric modules into fabric to harvest energy from body heat could one day power multitudinous wearable electronics. However, the invalid 2D architecture of fabric limits the application in thermoelectrics. Here, we make the valid thermoelectric fabric woven out of thermoelectric fibers producing an unobtrusive working thermoelectric module. Alternately doped carbon nanotube fibers wrapped with acrylic fibers are woven into π-type thermoelectric modules. Utilizing elasticity originating from interlocked thermoelectric modules, stretchable 3D thermoelectric generators without substrate can be made to enable sufficient alignment with the heat flow direction. The textile generator shows a peak power density of 70 mWm −2 for a temperature difference of 44 K and excellent stretchability (~80% strain) with no output degradation. The compatibility between body movement and sustained power supply is further displayed. The generators described here are true textiles, proving active thermoelectrics can be woven into various fabric architectures for sensing, energy harvesting, or thermal management.

The thermoelectric properties of (GeTe)(x)(AgSbTe(2))(100-x) compounds (x = 75, 80, 85 and 90; TAGS-x) have been studied as a function of temperature from 300 to 720 K. At 720 K the dimensionless figure of merit ZT reaches the state-of-the-art value of 1.53 for TAGS-75 and 1.50 for TAGS-80 and TAGS-85 samples, respectively. But the ZT value of the TAGS-90 sample is only 0.50 at 720 K due to the high carrier concentration. Utilizing high-resolution transmission electron microscope and selected area electron diffraction techniques, we identify a considerable number of nanoscale domains with typical size ∼10 nm in the samples that show high ZT values. It is suggested that the presence of nanoscale domains, like the situation in PbTe-AgSbTe(2) compounds, should make a slight contribution to the low lattice thermal conductivity of TAGS compounds due to the enhanced mid-frequency phonon scattering.

A green asymmetric supercapacitor with high energy density has been developed using birnessite-type ultrathin porous MnO(2) nanoflowers (UBMNFs) as positive electrode and functional mesoporous carbon nanotubes (FMCNTs) as negative electrode in 1 M Na(2)SO(4) electrolyte. Both of the electrode materials possess excellent electrochemical performances, with high surface areas and narrow pore size distributions. More significantly, the assembled asymmetric supercapacitor with optimal mass ratio can be cycled reversibly in the high-potential range of 0-2.0 V and exhibits an excellent energy density as high as 47.4 W h kg(-1), which is much higher than those of symmetric supercapacitors based on UBMNFs//UBMNFs and FMCNTs//FMCNTs supercapacitors. Furthermore, our asymmetric supercapacitor (ASC) device also exhibits a superior cycling stability with 90% retention of the initial specific capacitance after 1000 cycles and stable Coulombic efficiency of ~98%. These intriguing results exhibit great potential in developing high energy density "green supercapacitors" for practical applications.