In situ structural evolution of BiOCOOH nanowires and their performance towards electrocatalytic CO_(2)reduction

Bismuth-based materials have attracted broad research interest as catalysts for electrocatalytic CO_(2)reduction(ECR)to formate in recent years.Most studies have been focused on exploring materials with high activity,selectivity,durability,while little attention has been paid to the catalysts structure stability especially under working conditions of CO_(2)electrolysis.Here,starting from the precursor of bismuth oxide formate nanowires(BiOCOOH NWs),it was found that BiOCOOH NWs were easy to electrochemically evolve into two-dimensional sheet structure in CO_(2)-saturated KHCO3 solution and would further reconstitute into larger ultrathin bismuth nanosheets covered with amorphous oxide thin layer(Bi/BiO_(x)NSs).However,in Ar-saturated HCOONa solution,the one-dimensional structure could be maintained and reconstructed into rough porous bismuth nanowires(Bi NWs).Bi NWs showed less stability during ECR,which also generated surface amorphous oxide layer and further fragmentated into nanoparticles or nanosheets.Bi/BiO_(x)NSs showed better activity,selectivity,stability than Bi NWs,thanks to the high exposing active sites,enhancing CO_(2)adsorption and charge transfer.The demonstrated electrolyte dependence of structure evolution for bismuth-based catalysts and their performance for CO_(2)electroreduction could provide guidance for the design and synthesis of efficient catalysts.