Amorphous NiB as an electrocatalyst: from KA oil to succinic acid

Succinic acid (SA), a vital C4 building block, is predominantly produced <i>via</i> biological fermentation and chemical processes. Herein, we report an efficient electrocatalytic strategy for succinic acid production from KA oil (cyclohexanol/cyclohexanone mixture) oxidation using amorphous NiB as the catalyst under mild conditions. Modification of NiOOH active sites within the amorphous NiB structure <i>via</i> B doping significantly shifts the catalyst selectivity toward SA as the primary product, contrasting with previous reports where adipic acid (AA) is the dominant product. Density functional theory (DFT) calculations both mapped the reaction pathway and elucidated the origin of this selectivity shift. Our proposed mechanism identifies 1,4-cyclohexanedione as a key intermediate, which undergoes two sequential C-C cleavage events to yield SA.

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Publication Details

Journal
Physical Chemistry Chemical Physics
Published
2026-01-01
DOI
https://doi.org/10.1039/d5cp03623b
Primary Topic
Catalysis for Biomass Conversion
Type
article
Field-Weighted Citation Impact
0.00
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article

Amorphous NiB as an electrocatalyst: from KA oil to succinic acid

Yulin Zhou, Jun Chai, Hangjia Shen, Wenbin Jiang et al.
Physical Chemistry Chemical Physics
Catalysis for Biomass Conversion
article

Amorphous NiB as an electrocatalyst: from KA oil to succinic acid

Yulin Zhou, Jun Chai, Hangjia Shen, Wenbin Jiang, Xiaohong Tao, Lei Zhu
article en

Abstract

Succinic acid (SA), a vital C4 building block, is predominantly produced <i>via</i> biological fermentation and chemical processes. Herein, we report an efficient electrocatalytic strategy for succinic acid production from KA oil (cyclohexanol/cyclohexanone mixture) oxidation using amorphous NiB as the catalyst under mild conditions. Modification of NiOOH active sites within the amorphous NiB structure <i>via</i> B doping significantly shifts the catalyst selectivity toward SA as the primary product, contrasting with previous reports where adipic acid (AA) is the dominant product. Density functional theory (DFT) calculations both mapped the reaction pathway and elucidated the origin of this selectivity shift. Our proposed mechanism identifies 1,4-cyclohexanedione as a key intermediate, which undergoes two sequential C-C cleavage events to yield SA.

Physical Chemistry Chemical PhysicsVol. 28(6)
Samjin Pharm (South Korea) (KR), Quzhou University (CN)
Openalex Percentile: Top 93%
Catalysis for Biomass Conversion
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