Miniaturization of optical spectrometers has recently drawn a lot of attention due to the increasing needs of portable characterization systems for scientific, industrial, and consumer applications. At the same time, smartphones have technically evolved to become an everyday, ubiquitous device that provides numerous useful applications to consumers. Combining optical spectrometer and smartphone could lead to an explosion of new applications, especially in healthcare, biometrics, and food inspections, and change our daily life, making it more convenient, independent, and hyper-personalized.
In this work, we have developed a smartphone spectrometer in the visible and near infrared (NIR) ranges by directly integrating a 2 dimensional periodic array of band-pass filters on top of the smartphone’s image sensor. Each band pass filter is a silicon resonator consisting of a pair of Si/SiO₂ distributed Bragg reflectors (DBR), where each resonator’s transmitting wavelength is set by adjusting the thickness of the center Si layer. The DBR contains alternating, vertically-stacked TiO2 and SiN films with variable thicknesses while the top and bottom of the DBR were made of Al and Cu or Al reflectors for the visible and NIR ranges, respectively. The fabrication process was completely CMOS-compatible.
Using this smartphone spectrometer, we have proposed the concept of artificial-intelligence-powered spectral barcode for material identification and successfully demonstrated its use in drug identification. The accuracy of correctly identifying the type of drugs was ~99%. In addition, the smartphone spectrometer has also proven to correctly distinguish beef into three different classes according to the freshness.
Wearable devices often employ optical sensors, such as photoplethysmography sensors, for detecting heart rates or other biochemical factors. Pulse waveforms, rather than simply detecting heartbeats, can clarify arterial conditions. However, most optical sensor designs require close skin contact to reduce power consumption while obtaining good quality signals without distortion. We have designed a detection-gap-independent optical sensor array using divergence-beam-controlled slit lasers and distributed photodiodes in a pulse-detection device wearable over the wrist’s radial artery. It achieves high biosignal quality and low power consumption. The top surface of a vertical-cavity surface-emitting laser of 850 nm wavelength was covered by Au film with an open slit of width between 500 nm and 1500 nm, which generated laser emissions across a large divergence angle along an axis orthogonal to the slit direction. The sensing coverage of the slit laser diode (LD) marks a 50% improvement over nonslit LD sensor coverage. The slit LD sensor consumes 100% more input power than the nonslit LD sensor to obtain similar optical output power. The slit laser sensor showed intermediate performance between LD and light-emitting diode sensors. Thus, designing sensors with multiple-slit LD arrays can provide useful and convenient ways for incorporating optical sensors in wrist-wearable devices.
Patterning of colloidal quantum dot (QD) of a nanometer resolution is important for potential applications in micro- or nanophotonics. Several patterning techniques such as polymer composites, molecular key-lock methods, inkjet printing, and the microcontact printing of QDs have been successfully developed and applied to various plasmonic applications. However, these methods are not easily adapted to conventional complementary metal-oxide semiconductor (CMOS)-compatible processes because of either limits in fabrication resolutions or difficulties in sub-100-nm alignment. Here, we present an adaptation of a conventional lift-off method for the patterning of colloidal QDs. This simple method can be later applied to CMOS processes by changing electron beam lithography to photolithography for building up photon-generation elements in various planar geometries. Various shapes formed by colloidal QD clusters such as straight lines, rings, and dot patterns with sub-100-nm size could be fabricated. The patterned structures show sub-10-nm positioning with good fluorescence properties and well-defined sidewall profiles. To demonstrate the applicability of our method, we present a surface plasmon generator from a QD cluster.
The patterning of colloidal quantum dots with nanometer resolution is essential for their application in photonics and plasmonics. Several patterning approaches, such as the use of polymer composites, molecular lock-and-key methods, inkjet printing, and microcontact printing of quantum dots, have limits in fabrication resolution, positioning and the variation of structural shapes. Herein, we present an adaptation of a conventional liftoff method for patterning colloidal quantum dots. This simple method is easy and requires no complicated processes. Using this method, we formed straight lines, rings, and dot patterns of colloidal quantum dots on metallic substrates. Notably, patterned lines approximately 10 nm wide were fabricated. The patterned structures display high resolution, accurate positioning, and well-defined sidewall profiles. To demonstrate the applicability of our method, we present a surface plasmon generator elaborated from quantum dots.
We demonstrate doping-free and adaptive inverter to verify that the single ambipolar SWCNT transistors can be utilized both p- and n-type. Furthermore, we fabricate an adaptive logic circuit that can reveal multifunctions such as NOR and NAND gate using four ambipolar transistors. This new approach is innovative in several aspects, for instance, in improving integration density, simplicity without intentional doping, and its multifunctionality and ensures multidisciplinary interests in materials, physics, mechanics, and electronics areas.
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