Researchers at UCI have developed a method for enhancing existing hydrogen gas sensors, leading to as much as a 20-fold improvement in sensor response and recovery times.
In the push toward utilizing hydrogen gas (H2) as a clean energy alternative, the ability to rapidly detect minute quantities of leaked H2 has become increasingly important due to its high combustibility at concentrations >4% volume in air. According to the US Department of Energy, H2 sensors should have rapid response times, detecting 1% volume of H2 within one minute. Many commercial H2 sensors are chemiresistors, which display an increase in resistance upon adsorption of certain gases. Though sensor architecture has evolved over the years, palladium (Pd) has remained one of the most commonly studied sensor materials due to its high H2 sensitivity, simple preparation, and operability at room temperature. In particular, Pd nanowires (NWs) have demonstrated remarkable sensitivity to the presence of H2 due to their high surface area, which increases the number of H2 adsorption sites. Despite these advantages, Pd NWs have found limited application in actual hydrogen sensors due to their affinity for other air-based species, including oxygen and nitrogen, which dramatically limit the ability of the NWs to detect H2.
To combat this lack of H2 selectivity, researchers at UCI have developed a protective filter layer that is easily added to Pd NWs. The filter layer is based on a common metal organic framework motif, whose pore sizes (0.34 nm) allow for the diffusion of H2 (0.289 nm) through the layer, while simultaneously blocking the larger oxygen (0.345 nm) and nitrogen (0.364 nm) molecules. Such functionalized Pd NWs display an improved response and recovery time, able to detect 1% H2 within 7s compared to the 164 s response time of bare Pd NWs.
For the rapid and selective detection of molecular hydrogen gas.
Functionalized Pd NWs have been fabricated and used to detect a range of concentrations of H2 (0.1-1%).