ABSTRACT
Opto-mechanical forces result from the momentum transfer that occurs during light-matter interactions. One of the most common examples of this phenomenon is the radiation pressure that is exerted on a reflective surface upon photon reflection. For an ideal mirror, the radiation pressure is independent of the wavelength of light and depends only on the incident power. Here we consider a different regime where, for a constant input optical power, wavelength-dependent radiation pressure is observed due to coherent thin film Fabry-Perot interference effects. We perform measurements using a Si microcantilever and utilize an in-situ optical transmission technique to determine the local thickness of the cantilever and the light beam's angle of incidence. Although Si is absorptive in the visible part of the spectrum, by exploiting the Fabry-Perot modes of the cantilever, we can determine whether momentum is transferred via reflection or absorption by tuning the incident wavelength by only ~20 nm. Finally, we demonstrate that the tunable wavelength excitation measurement can be used to separate photothermal effects and radiation pressure.
ABSTRACT
Transition metal dichalcogenides hold great promise for a variety of novel electrical, optical and mechanical devices and applications. Among them, molybdenum disulphide (MoS2) is gaining increasing attention as gate dielectrics and semiconductive channels for high-performance field effect transistors. Here we report on the first MoS2 phototransistor built on a flexible, transparent and biodegradable substrate with an electrolyte gate dielectric. We have carried out systematic studies on its electrical and optoelectronic properties. The MoS2 phototransistor exhibited an excellent photoresponsivity of â¼1.5 kA W(-1), about two times higher compared to typical back-gated devices reported in previous studies. The device is highly transparent at the same time with an average optical transmittance of 82%. Successful fabrication of phototransistors on flexible cellulose nanopaper with excellent performance and transparency suggests that it is feasible to achieve an ecofriendly and biodegradable phototransistor with great photoresponsivity, broad spectral range and durable flexibility.
ABSTRACT
The further development of all-solid-state batteries is still limited by the understanding/engineering of the interfaces formed upon cycling. Here, we correlate the morphological, chemical, and electrical changes of the surface of thin-film devices with Al negative electrodes. The stable Al-Li-O alloy formed at the stress-free surface of the electrode causes rapid capacity fade, from 48.0 to 41.5 µAh/cm(2) in two cycles. Surprisingly, the addition of a Cu capping layer is insufficient to prevent the device degradation. Nevertheless, Si electrodes present extremely stable cycling, maintaining >92% of its capacity after 100 cycles, with average Coulombic efficiency of 98%.
ABSTRACT
Various band structure engineering methods have been studied to improve the performance of graphitic transparent conductors; however, none has demonstrated an increase of optical transmittance in the visible range. Here we measure in situ optical transmittance spectra and electrical transport properties of ultrathin graphite (3-60 graphene layers) simultaneously during electrochemical lithiation/delithiation. On intercalation, we observe an increase of both optical transmittance (up to twofold) and electrical conductivity (up to two orders of magnitude), strikingly different from other materials. Transmission as high as 91.7% with a sheet resistance of 3.0 Ω per square is achieved for 19-layer LiC6, which corresponds to a figure of merit σ(dc)/σ(opt) = 1,400, significantly higher than any other continuous transparent electrodes. The unconventional modification of ultrathin graphite optoelectronic properties is explained by the suppression of interband optical transitions and a small intraband Drude conductivity near the interband edge. Our techniques enable investigation of other aspects of intercalation in nanostructures.
