Abstract

AbstractElectrocatalytic biomass valorization coupled with hydrogen production provides an efficient and economical way to achieve a zero‐carbon economy. Ni‐based electrocatalysts are promising candidates due to their intrinsic redox capabilities, but the rational design of active Ni site coordination is still a huge challenge. Herein, the combined strategies of surface reconstruction and heteroatom doping are adopted to modify Ni3S2 pre‐catalysts and the obtained bimetallic catalyst exhibits superior electrocatalytic performance toward 5‐hydroxymethylfurfural (HMF) oxidation to 2,5‐furanedicarboxylic acid (FDCA). Specifically, the oxysulfide‐coordinated amorphous NiOOH (NiOOH‐SOx) active phase is in situ constructed following the anionic regulation mechanism, which endows numerous defects and unsaturated sites for anodic HMF oxidation. Cu heteroatom doping further modulates the electronic structure of active sites with abundant Lewis acidic sites, offering advanced capability for HMF adsorption. Several operando characterization techniques (in situ Raman, infrared, and electrochemical impedance spectroscopies) are performed to disclose the reaction pathway and structure‐activity‐potential relationship. Theoretical results further demonstrate that Cu doping and oxyanionic regulation effectively modulate the local coordination environment of Ni sites and correspondingly tailor the intermediate adsorption behavior and then promote the reaction kinetics. Moreover, a two‐electrode system is assembled to pair HMF oxidation with cathode hydrogen production, demonstrating better energy conversion efficiency.

Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.