Electrochemically active and robust cobalt doped copper phosphosulfide electro-catalysts for hydrogen evolution reaction in electrolytic and photoelectrochemical water splitting.

The area of non-noble metals based electro-catalysts with electrochemical activity and stability similar or superior to that of noble metal electro-catalyst for efficient hydrogen production from electrolytic and photoelectrochemical (PEC) water splitting is a subject of intense research. In the current study, exploiting theoretical first principles study involving determination of hydrogen binding energy to the surface of the electro-catalyst, we have identified the (Cu 0.83 Co 0.17 ) 3 P: x at. % S system displaying excellent electrochemical activity for hydrogen evolution reaction (HER). Accordingly, we have experimentally synthesized (Cu 0.83 Co 0.17 ) 3 P: x at. % S (x = 10, 20, 30) demonstrating excellent electrochemical activity with an onset overpotential for HER similar to Pt/C in acidic, neutral as well as basic media. The highest electrochemical activity is exhibited by (Cu 0.83 Co 0.17 ) 3 P:30 at. % S nanoparticles (NPs) displaying overpotential to reach 100 mA cm −2 in acidic, neutral and basic media similar to Pt/C. The (Cu 0.83 Co 0.17 ) 3 P:30 at. % S NPs also display excellent electrochemical stability in acidic media for long term electrolytic and PEC water splitting process [using our previously reported (Sn 0.95 Nb 0.05 ) O 2 : N-600 nanotubes (NTs) as the photoanode]. The applied bias photon-to-current efficiency obtained using (Cu 0.83 Co 0.17 ) 3 P:30 at. % S NPs as the cathode electro-catalyst for HER in an H-type PEC water splitting cell (∼4%) is similar to that obtained using Pt/C (∼4.1%) attesting to the promise of this exciting non-noble metal containing system. [ABSTRACT FROM AUTHOR]