Abstract
Achieving high sensitivity and selective detection at low temperature is of great significance for hydrogen leakage monitoring and early warning. As a very promising hydrogen sensitive material, In2O3 still faces great challenges in achieving high-performance hydrogen sensing at low temperatures due to inherent defects such as low specific surface area and limited active sites. Here, we prepared Ni-doped In2O3 mesoporous nanomaterials using metal organic framework (MOF) as sacrificial templates. The prepared Ni-doped In2O3 exhibited mesoporous structures with small diameters (2–3 nm), which could be used as effective molecular sieves for the selective detection of hydrogen. The high specific surface area (72.0 m²/g) provided numerous active sites for surface redox reactions, resulting in a remarkable hydrogen sensing response. Notably, gas sensitivity tests demonstrated that the Ni-doped In2O3 gas sensor achieved optimal hydrogen detection performance at 100°C. Particularly, the 3 at% Ni-doped In2O3 nanomaterials exhibited a high response of 12.5–100 ppm hydrogen, along with favorable response/recovery time and a practical limit of detection down to 5 ppm. Furthermore, the Ni-doped In2O3 sensor exhibited excellent reversibility, reproducibility, selectivity and long-term stability. In addition, simulation calculations based on molecular dynamics (MD) and density functional theory (DFT) show that molecular sieve effect is the main reason for the enhanced selectivity, and Ni doping induced oxygen vacancy (OV) defects could enhance gas adsorption. This work could provide technical support for leak detection and warning during hydrogen use, storage and transportation in the future.
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.