摘要
The dynamic evolution of catalyst structures during the electrocatalytic reaction has seriously hindered our comprehensive understanding of catalytic processes and pathways. In this work, we report that the metal-sulfide (ReS 2 /Co 9 S 8 ) heterostructure has multiple synergistic effects, enhancing the furfural oxidation reaction (FOR) coupling with hydrogen evolution (HER). Under cathodic reduction conditions, H 2 production can be promoted at specific active sites by the original heterostructure of ReS 2 /Co 9 S 8 . Under anodic oxidation conditions, a new heterointerface of ReS 2 /Co 9 S 8 -Co(OH) 2 is in-situ reconstructed based on the original ReS 2 /Co 9 S 8 heterostructure. The new ReS 2 /Co 9 S 8 -Co(OH) 2 heterointerface induced by this ReS 2 /Co 9 S 8 heterostructure significantly enhances FOR performance in an indirect way at 1.33–1.53 V RHE , resulting in a 86.3 % faradaic efficiency (FE). The optimized composite of ReS 2 /Co 9 S 8 with different molar ratios in a two-electrode system exhibits superior performance toward HER||FOR, achieving a smaller cell voltage of 1.43 V to reach 10 mA cm −2 compared to ReS 2 ||Co 9 S 8 (1.69 V). This work verifies the reconstructed heterointerface of ReS 2 /Co 9 S 8 -Co(OH) 2 for FOR and identifies the distinct catalytic mechanisms for FOR and HER.
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