Porous Co9S8/Nitrogen, Sulfur-Doped Carbon@Mo2C Dual Catalyst for Efficient Water Splitting.

Abstract

The exploration of highly efficient and stable bifunctional electrocatalysts for overall water splitting is currently of extreme interest for the efficient conversion of sustainable energy sources. Herein, we provide an earth-abundant, low-cost, and highly efficient bifunctional electrocatalyst composed of cobalt sulfide (Co9S8) and molybdenum carbide (Mo2C) nanoparticles anchored to metal-organic frameworks (MOFs)-derived nitrogen, sulfur-codoped graphitic carbon (Co9S8-NSC@Mo2C). The new composite mode of the electrocatalyst was realized through simple pyrolysis processes. The composite electrocatalyst shows outstanding hydrogen evolution reaction (HER) performance and excellent stability over the entire pH range. For example, it has a lower overpotential of 74, 89, and 121 mV with the Tafel slopes of 69.3, 86.7, and 106.4 mV dec-1 to achieve a current density of 10 mA cm-2 in 0.5 M H2SO4, 1.0 M KOH, and 1.0 M phosphate-buffered saline solutions, respectively. Moreover, it shows a small overpotential of 293 mV with a Tafel slope of 59.7 mV dec-1 to reach 10 mA cm-2 for the oxygen evolution reaction (OER) in 1.0 M KOH. The significantly enhanced HER and OER activities of Co9S8-NSC@Mo2C are mainly attributable to the electron transfer from Co to Mo2C, resulting in a lower Mo valence and a higher Co valence in Co9S8-NSC@Mo2C. Furthermore, using the Co9S8-NSC@Mo2C bifunctional electrocatalyst as both the anode for the OER and the cathode for the HER for overall water splitting, a cell voltage of only 1.61 V is needed to derive a current density of 10 mA cm-2. This interesting work offers a general method for designing and fabricating highly efficient and stable non-noble electrocatalysts for promising energy conversion.