Strontium doped Fe-based porous carbon for highly efficient electrocatalytic ORR and MOR reactions.

The catalytic activity improvement of Fe-based active sites derived from metal organic frameworks toward oxygen reduction reaction (ORR) and methanol oxidation reaction (MOR) remains a major challenge. In this study, the growth of strontium decorated 2-methylimidazole zinc salt (Sr/ZIF-8) is prepared as a carrier to vapor deposited iron formation Sr doped Fe-based nitrogen-doped carbon framework (named as Sr/FeNC). After high-temperature pyrolysis and vapor deposition, strontium carbonate nanocrystals are evenly dispersed on the shrunk dodecahedron carbon frame and multitudinous Fe-based active catalytic sites are embedded in carbon skeleton. The optimal Sr/FeNC-2 catalyst demonstrates the outstanding ORR performance in terms of a half-wave potential of 0.851 V and an onset potential of 0.90 V, while Sr/FeNC-2 exhibits a high current density of 18.2 mA cm-2 and a lower Tafel slope of 21 mV dec-1 in MOR. The exceptional catalytic activity could be ascribed to the synergistic coupling effect of strontium compounds with Fe-based catalytic sites (Fe-Nx, Fe, and iron oxide). In particular, the formation of SrCO3 affects the bonding configuration of the iron species sites, leading to an optimization of the electronic structure within the multihole carbon matrix. The synthetic approach presents a prospective strategy for future endeavors in developing innovative and advanced bifunctional catalysts for ORR and MOR.

Boosting activity on copper functionalized biomass graphene by coupling nanocrystalline Nb2O5 as impressive rate capability for supercapacitor and outstanding catalytic activity for oxygen reduction.

A novel and hierarchical porous but cross-linked copper-doped biomass graphene (Cu@HPBG) combined with Nb2O5 (denoted as Nb2O5/Cu@HPBG) is successfully fabricated on a large-scale using fig peels as biomass carbon and copper as the graphitization catalyst. During the synthesis process, basic copper carbonate serves dual functions of pore-forming agent, as well as homogeneous copper provider, and NH3 is employed as a defect-forming agent and N dopant. Owing to the porous hierarchical structure increased availability of contact interface and pseudo capacitance active sites provided by copper and Nb2O5, the assembled asymmetrical supercapacitor (ASC) employing Nb2O5/Cu@HPBG as positive electrode and HPBG as negative electrode can not only widen the stability window range of 0～1.9 V, but also deliver a maximum gravimetric energy density of 82.8 W h kg-1 at the power density of 950.0 W kg-1 and maintain a remarkable cycling stability of 97.1% after 15,000 cycles. Impressively, due to the synergistic enhancement of Cu@HPBG and Nb2O5, the resulting Nb2O5/Cu@HPBG hybrid displays more positive half wave potential (∼0.85 V) and a long-life stability than Pt/C electrode toward oxygen reduction reaction (ORR). Our research provides a feasible strategy to fabricate renewable biomass graphene electroactive composites for large-scale supercapacitor electrodes and efficient ORR catalysts toward energy applications.