TY - JOUR
T1 - Density functional theory study of furfural electrochemical oxidation on the Pt (1 1 1) surface
AU - Gong, Li
AU - Agrawal, Naveen
AU - Roman, Alex
AU - Holewinski, Adam
AU - Janik, Michael J.
N1 - Funding Information:
L. Gong acknowledges scholarship from the China Scholarship Council for a joint PhD student. Financial support from the National Science Foundation , Grant # 1665155 is acknowledged. This work used the Extreme Science and Engineering Discovery Environment (XSEDE), supported by National Science Foundation grant number ACI – 1053575. N. A. acknowledges training provided by the Computational Materials Education and Training (CoMET) NSF Research Traineeship (Grant No. DGE-1449785 ).
Publisher Copyright:
© 2019 Elsevier Inc.
PY - 2019/5
Y1 - 2019/5
N2 - Electro-oxidation of furfural may allow for tunability of product selectivity by varying the electrode potential. We have applied density functional theory (DFT) to investigate the electrocatalytic oxidation mechanism on the Pt (1 1 1) surface. The potential-dependent reaction free energy profiles for furfural electrocatalytic oxidation to furoic acid, succinic acid, maleic acid, and maleic anhydride are reported. After comparing several possible furfural oxidation paths, we conclude that the electro-oxidation of furfural preferentially proceeds to furoic acid, with further oxidation slowed by difficult C[sbnd]C bond dissociation. Oxidation beyond furoic acid can proceed to succinic acid via 2(3H)-furanone as an intermediate and to maleic acid and maleic anhydride via 2(5H)-furanone as an intermediate. The rate of these processes is likely limited by the decarboxylation of furoic acid. DFT analysis of elementary step thermodynamics and kinetics suggests that the selectivity between furoic acid, succinic acid, maleic acid, or other oxidized products is tunable by varying the electrode potential. Initial experimental results show furoic acid as the most significant product (>80% selectivity) at 0.9 V-RHE on a Pt electrode, in agreement with DFT results. These results broaden our fundamental understanding into electrocatalytic oxidation of furfural, which is applicable in upgrading renewable biomass derivatives.
AB - Electro-oxidation of furfural may allow for tunability of product selectivity by varying the electrode potential. We have applied density functional theory (DFT) to investigate the electrocatalytic oxidation mechanism on the Pt (1 1 1) surface. The potential-dependent reaction free energy profiles for furfural electrocatalytic oxidation to furoic acid, succinic acid, maleic acid, and maleic anhydride are reported. After comparing several possible furfural oxidation paths, we conclude that the electro-oxidation of furfural preferentially proceeds to furoic acid, with further oxidation slowed by difficult C[sbnd]C bond dissociation. Oxidation beyond furoic acid can proceed to succinic acid via 2(3H)-furanone as an intermediate and to maleic acid and maleic anhydride via 2(5H)-furanone as an intermediate. The rate of these processes is likely limited by the decarboxylation of furoic acid. DFT analysis of elementary step thermodynamics and kinetics suggests that the selectivity between furoic acid, succinic acid, maleic acid, or other oxidized products is tunable by varying the electrode potential. Initial experimental results show furoic acid as the most significant product (>80% selectivity) at 0.9 V-RHE on a Pt electrode, in agreement with DFT results. These results broaden our fundamental understanding into electrocatalytic oxidation of furfural, which is applicable in upgrading renewable biomass derivatives.
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U2 - 10.1016/j.jcat.2019.04.012
DO - 10.1016/j.jcat.2019.04.012
M3 - Article
AN - SCOPUS:85064565144
SN - 0021-9517
VL - 373
SP - 322
EP - 335
JO - Journal of Catalysis
JF - Journal of Catalysis
ER -
