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April 27, 2026ACS Sensors2 citations

Morphology-Engineered Pd−SnO 2 Porous Networks for Enhanced Hydrogen Detection

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RBReza BehboodianXZXiaoran ZhengLHLong Hu

Key Points

  • The aim is to enhance hydrogen detection sensitivity and selectivity using Pd-functionalized SnO2 porous networks.
  • Utilized flame spray pyrolysis to create SnO2 films followed by Pd drop-casting to produce porous structures.
  • Characterized the sensor response at 200 °C with 400 ppm hydrogen exposure.
  • Evaluated selectivity against common gases like CO, CH4, and CO2.
  • The Pd-functionalized sensor showed an 18.5 response to 400 ppm hydrogen, significantly higher than the 1.4 response of pristine SnO2.
  • High selectivity demonstrated with cross-responses of ≤1.8 to CO, CH4, and CO2.
  • DFT calculations confirmed stronger hydrogen adsorption on Pd-SnO2 compared to other gases.

Abstract

Hydrogen (H2) is a critical clean energy carrier, yet its flammability demands sensors that are both highly sensitive and selective. SnO2-based semiconductors show promise but typically suffer from poor selectivity, high operating temperatures, and complex fabrication methods. We report a simplified and reproducible two-step integration of flame spray pyrolysis (FSP)-derived SnO2 films with capillary-force-assisted drop-casting of 1 wt % Pd. This yields porous films with well-dispersed Pd that enhance catalytic activity and gas diffusion, while toluene-induced capillary forces promote nanoparticle necking and cluster formation, refining the microstructure. The Pd-functionalized sensor (1% Pd@M-SnO2) exhibits a strong response of ∼18.5 toward 400 ppm H2 at 200 °C, representing approximately 13- and 6-fold enhancements over pristine SnO2 (P-SnO2, ∼1.4) and surface-modified SnO2 (M-SnO2, ∼3), respectively. High H2 selectivity is further evidenced by the low cross-responses to CO, CH4, and CO2 (≤1.8 at 40 ppm and 150 °C), consistent with DFT results showing stronger H2 adsorption on Pd-SnO2 (Eads = -1.12 eV; H-H = 0.89 Å) than CO (-0.69 eV), CO2 (-0.15 eV), or CH4 (-0.13 eV). This approach bridges scalable nanomaterial synthesis with precision surface functionalization, offering a versatile route for next-generation hydrogen sensors.

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Cite This Study

Behboodian et al. (2026) studied this question.

synapsesocial.com/papers/69eefcf4fede9185760d3a9chttps://doi.org/10.1021/acssensors.5c04184
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