Wei Wang, Li Chen, Leif Riemenschneider, Chenchen Wang, Luis-Antonio Panes-Ruiz, Martin Hantusch, Yunxu Chen, Jianjun Zhang, Shivam Singh, Yana Vaynzof, Markus Löffler, Arezoo Dianat, Naisa Chandrasekhar, Shirong Huang, Gianaurelio Cuniberti
High Resolution Image Download MS PowerPoint Slide High sensitivity and selectivity are never-ending points of interest in the gas sensing field. Herein, the novel functionalized N-doped graphitic carbon is derived from Zn-MOF by modulating the pyrolysis temperature toward H 2 S sensing application. The results demonstrate excellent sensing performance toward H 2 S gas with a limit of detection (LOD) of 56.9 ppb, faster response and recovery time (18 and 29 s), and high selectivity with a 20-fold response difference than other interfering gases. The expected stability with stable multiple consecutive responses and a strong response toward 1 ppm of H 2 S after 4 months were reached. Functionalized groups pyridinic nitrogen (PD-N) and pyrrolic nitrogen (PR-N) that make MOF-derived carbon stand out in H 2 S gas sensing are mainly attributed to dual active sites: (i) N–C bonds on graphitic carbon undergo surface redox reactions, forming oxidized carbon species (C═O or C═S), and (ii) PD/PR-N-Zn coordination centers facilitate the formation of SO 4 2– -based surface complexes through reaction with H 2 S and adsorbed oxygen. Notably, DFT calculation was employed to confirm both PR-N and PD-N bonding with zinc, yielding the largest charge transfer and binding energy among simulated factors, which attributes to the generation of significant sensing performance for H 2 S. Consequently, this work will provide a novel strategy for the advancement of gas sensing applications.