Synthesis of SnS2 modified to sulfated tin oxide by electrochemical method and VOC sensing properties


ŞAHİN A. N., Altındal A., GÜVEN ÖZDEMİR Z.

Micro and Nanostructures, cilt.212, 2026 (SCI-Expanded, Scopus) identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 212
  • Basım Tarihi: 2026
  • Doi Numarası: 10.1016/j.micrna.2026.208570
  • Dergi Adı: Micro and Nanostructures
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Anahtar Kelimeler: Electrochemical, SnS2, SO42−/SnO2, VOC sensor
  • Yıldız Teknik Üniversitesi Adresli: Evet

Özet

This study investigates the room-temperature gas-sensing performance of next-generation sensors fabricated by electrochemically transforming 2D SnS2 films into SO42−/SnO2 structures. The sensors were prepared on an interdigital transducer via the spin-coating method, followed by low-potential electrochemical oxidation in a sulfuric acid–methanol medium to form a 3D SO42−/SnO2 structure. Unlike conventional high-temperature oxidation or chemical etching methods that cause bulk degradation, this study employs a low-potential electrochemical oxidation–sulfation strategy to controllably convert the SnS2 surface into SO42−/SnO2 while preserving the nanostructure. While the Sn core structure remained intact, FTIR, EDX, and XPS analyses confirmed the successful surface sulfation and the formation of sulfate-related chemical states on the SnO2 surface. XRD analysis verified crystalline-level structural transformation, and SEM imaging revealed distinct surface morphology changes. The gas-sensing performance was systematically evaluated against VOC's vapors over a concentration range of 50–350 ppm, enabling a comprehensive assessment of sensitivity and selectivity. Results showed that the SnS2-based sensor exhibited high sensitivity to acetone, whereas the SO42−/SnO2 structure demonstrated nearly tenfold enhanced responsiveness to NH3 vapor. Sulfate functionalization introduced Lewis acidic surface sites, strengthening interactions with NH3 and enabling nA-level responses. Although increased humidity (30–90 % RH) reduced response amplitude, reliable NH3 sensing was maintained, with interference tests at 50 % RH confirming robust performance. Furthermore, stable and repeatable signals over 10 days demonstrated excellent durability. These results highlight electrochemical surface engineering as an effective strategy to develop metal oxide– and chalcogenide-based NH3 sensors with improved selectivity, humidity tolerance, and long-term stability.