Integrating Electrochemical CO2 Reduction on α-NiS with the Water or Organic Oxidations by Its Electro-Oxidized NiO(OH) Counterpart to an Artificial Photosynthetic Scheme

Avinava Kundu, Brajesh Kumar, Anubha Rajput, Biswarup Chakraborty

Research output: Contribution to journalArticlepeer-review

21 Scopus citations

Abstract

Efficient hydrogen production, biomass up-conversion, and CO2-to-fuel generation are the key challenges of the present decade. Electrocatalysis in aqueous electrolytes by choosing suitable transition-metal-based electrode materials remains the green approach for the trio of sustainable developments. Given that, finding electrode materials with multifunctional capability would be beneficial. Herein, the nanocrystalline α-NiS, synthesized solvothermally, has been chosen as an electrode material. As the first step to construct an electrolyzer, α-NiS deposited on conducting nickel foam (NF) has been used as an anode, and under the anodic potential, the α-NiS particles have lost sulfides to the electrolyte and transform to amorphous electro-derived NiO(OH) (NiO(OH)ED), confirmed by different spectroscopic and microscopic studies. In situ transformation of α-NiS to amorphous NiO(OH)ED results in an enhancement of the electrochemical surface area and not only becomes active toward oxygen evolution reaction (OER) at a moderate overpotential of 264 mV (at 20 mA cm-2) but also can convert a series of biomass-derived organic compounds, namely, 2-hydroxymethylfurfural (HMF), 2-furfural (FF), ethylene glycol (EG), and glycerol (Gly), to industrially relevant feedstocks with a high (∼96%) Faradaic efficiency. During these organic oxidations, NiO(OH)ED/NF participate in the multiple-electron oxidation process (up to 8e-) including C-C bond cleavages of EG and Gly. During the cathodic performance of the α-NiS/NF, the structural integrity has been retained and the unaltered α-NiS/NF electrode remains more effective cathode for alkaline hydrogen evolution reaction (HER) and CO2 reduction (CO2R) compared to its in situ-derived NiO(OH)ED/NF. α-NiS/NF can reduce the CO2 predominantly to CO even at a higher potential like −0.8 V (vs RHE). The fabricated cell with α-NiS and its electro-oxidized NiO(OH)ED counterpart, α-NiS/NF(−)/(+)NiO(OH)ED/NF, is able to show an artificial photosynthetic scheme in which the NiO(OH)ED/NF anode oxidizes water to O2 and the α-NiS cathode reduces CO2 majorly to CO in a moderate cell potential. In this study, α-NiS has been utilized as a single electrode material to perform multiple sustainable transformations.

Original languageEnglish
Pages (from-to)8010-8021
Number of pages12
JournalACS Applied Materials and Interfaces
Volume15
Issue number6
DOIs
StatePublished - 15 Feb 2023
Externally publishedYes

Keywords

  • CO reduction
  • NiO(OH)
  • artificial photosynthetic scheme
  • electro-activation
  • organic electro-oxidation
  • water splitting
  • α-NiS electrode

ASJC Scopus subject areas

  • General Materials Science

Fingerprint

Dive into the research topics of 'Integrating Electrochemical CO2 Reduction on α-NiS with the Water or Organic Oxidations by Its Electro-Oxidized NiO(OH) Counterpart to an Artificial Photosynthetic Scheme'. Together they form a unique fingerprint.

Cite this