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Color QR Codes are often generated to encode digital information, but one also could use colors or to allocate colors in a QR Code to act as a color calibration chart. In this dataset, we present several thousand QR Codes images generated with two different colorization algorithms (random and back-compatible) and several tuning variables in these color encoding. The QR Codes were also exposed to three different channel conditions (empty, augmentation and real-life). Also, we derive the SNR and BER computations for these QR Code in comparison with their black and white versions. Finally, we also show if ZBar, a commercial QR Code scanner, is able to read them.

In this work, nitrogen dioxide (NO2) gas sensors based on zinc oxide nanorods (ZnO NRs) decorated with gold nanoparticles (Au NPs) working under visible-light illumination with different wavelengths at room temperature are presented. The contribution of localized surface plasmon resonant (LSPR) by Au NPs attached to the ZnO NRs is demonstrated. According to our results, the presence of LSPR not only extends the functionality of ZnO NRs towards longer wavelengths (green light) but also increases the response at shorter wavelengths (blue light) by providing new inter-band gap energetic states. Finally, the sensing mechanism based on LSPR Au NPs is proposed.

We report on an inexpensive and very selective gas sensor implemented by simply combining colorimetric indicators casted on top of acetate-based transparent tape, with a commercial microchip adapted here to measure optical reflectance. This sensor can be easily reproduced (leading to quantitatively consistent results), refreshed and reconfigured to sense different target gases replacing only the colorimetric tape. The device may either work as sensor (CO2 and NH3) or dosimeter (Formaldehyde) depending on the targeted gas.

In this work, we present conductometric gas sensors based on p-type calcium iron oxide (CaFe2O4) nanoparticles. CaFe2O4 is a metal oxide (MOx) with a bandgap around 1.9 eV making it a suitable candidate for visible light-activated gas sensors. Our gas sensors were tested under a reducing gas (i.e., ethanol) by illuminating them with different light-emitting diode (LED) wavelengths (i.e., 465−640 nm). Regardless of their inferior response compared to the thermally activated counterparts, the developed sensors have shown their ability to detect ethanol down to 100 ppm in a reversible way and solely with the energy provided by an LED. The highest response was reached using a blue LED (465 nm) activation. Despite some responses found even in dark conditions, it was demonstrated that upon illumination the recovery after the ethanol exposure was improved, showing that the energy provided by the LEDs is sufficient to activate the desorption process between the ethanol and the CaFe2O4 surface.

In this contribution we present a highly miniaturized device that integrates a photoactive material with a highly efficient LED light source. This so-called micro light plate configuration (µLP) allows for maximizing the irradiance impinging on the photoactive material, with a minimum power consumption, excellent uniformity and accurate control of the illumination. We demonstrate that, with the µLP approach, very efficient low power gas sensors can be built, and provide a detailed analysis of the rationales behind such improvement, as well as a quantitative model and a set of design rules to implement it in further integrated applications. As a demonstrator, we will describe a NO2 gas sensor operating in the part per billion range (ppb) with microwatt (µW) power consumption. These are the best figures reported to date in conductometric metal-oxides (MOX) sensors operated with light (instead of heat) at room temperature.

Specificity, or the ability of detecting one single species in the presence of many others, is one ofthe most sought after features in chemical and gas sensors. [...]

Gas sensors based on CaFe2O4 nanopowders, which are p⁻type metal oxide semiconductor (MOX), have been fabricated and assessed for ethanol gas monitoring under visible light activation at room temperature. Regardless of their inferior sensitivity compared to thermally activated counterparts, the developed sensors have shown responsive sensing behavior towards ethanol vapors confirming the ability of using visible light for sensor activation. LEDs with different wavelengths (i.e., 465⁻590 nm) were employed. The highest sensitivity (3.7%) was reached using green LED activation that corresponds to the band gap of CaFe2O4.

Self-heating operation, or the use of the resistance-probing signal to warm up and control the temperature of nanowire devices, has been the subject of research for more than a decade. The state-of-the-art shows that this approach is serving to lower the power demand in temperature-activated devices, especially in conductometric gas sensors, but the simplicity of eliminating the heating element comes with the complexity of integrating 1-dimensional nanomaterials in electronic devices. The advantages of the efficient self-heating effect in nanowires have already been probed in a broad range of systems and materials. But when it comes to transfer this operating principle to new systems and materials natural doubts arise: how to do it?, how much savings in power will be achieved? We will address these questions in this review contribution.

Arrays of 1D-vertically arranged gallium nitride (GaN) nanorods (NRs) are fabricated on sapphire and connected to both bottom and freestanding top contacts. This shows a fully validated top-down method to obtain ordered arrays of high-surface-to-volume elements that can be electrically interrogated and used, e.g., for sensing applications. Specifically, these will be used as highly integrated heating elements for conductometric gas sensors in self-heating operation. Detailed fabrication and processing steps involving inductively coupled plasma reactive ion etching (ICP-RIE), KOH-etching, interspace filling, and electron-beam physical vapor deposition technologies are discussed, in which they can be well adjusted and combined to obtain vertical GaN NRs as thin as 300 nm in arbitrarily large and regular arrays (e.g., 1 × 1, 3 × 3, 9 × 10 elements). These developed devices are proposed as a novel sensor platform for temperature-activated measurements that can be produced at a large scale offering low-power, and very stable temperature control.

We developed an integrated platform to build up conductometric sensors with controlled illumination. Our device contains a miniaturized indium gallium nitride (InGaN) LED as a light source, and a set of interdigitated electrodes (IDEs) in close contact with the LED. The sensor material is later deposited on top of the IDE, to monitor its resistance. In this configuration, all the light emitted by the LED is collected by the sensor material, leading to a very efficient photoexcitation. We demonstrate the effectiveness of the approach building a photoactivated gas sensor based on ZnO operating with as little as 100 μW.

We present a simple an inexpensive method to implement a Griess-Saltzman-type reaction that combines the advantages of the liquid phase method (high specificity, fast response time) with the benefits of a solid implementation (easy to handle). We demonstrate that the measurements can be carried out using conventional RGB sensors; circumventing all the limitations around the measurement of the samples with spectrometers. We also present a method to optimize the measurement protocol and target a specific range of NO2 concentrations. We demonstrate that it is possible to measure the concentration of NO2 from 50 ppb to 300 ppm with high specificity and without modifying the sensing elements.