TY - JOUR
T1 - Efficient Self-Driven Adipic Acid Production with Bioelectricity Generation
AU - Bu, Yifan
AU - Li, Chao
AU - Deng, Ziliang
AU - Li, Shiyun
AU - Zhao, Zipeng
AU - Xie, Jisheng
AU - Zhou, Jihan
AU - Xiao, Hai
AU - Lv, Ximin
AU - Zhang, Xueqiang
AU - Yang, Wulin
AU - Li, Mufan
N1 - Publisher Copyright:
© 2026 The Authors. Published by American Chemical Society
PY - 2026/4/27
Y1 - 2026/4/27
N2 - Electrocatalysis offers a sustainable route for producing value-added chemicals, yet its widespread adoption is limited by low turnover frequency (TOF) and electron efficiency (EE). Here, we unveil a promotion effect in molecular phthalocyanine catalysts, enabling synergistic oxygen reduction reaction (ORR) and cyclohexanone oxidation (CyO). This mechanism bypasses the kinetic limitations of ORR steps and the overpotential penalties of CyO, achieving a record TOF of 1711 h–1 with superior EE (∼100% at 0.5 VRHE) for adipic acid production. Near-ambient pressure X-ray photoelectron spectroscopy reveals that this remarkable activity arises from interactions between *OOH intermediates at metal centers and substrates on neighboring nitrogen atoms. Integrating this design into microbial fuel cell reactors enables self-driven adipic acid synthesis alongside spontaneous bioelectricity generation, i.e., the system operates without any external power input. Life cycle assessment shows a 43% reduction in CO2 emissions, surpassing conventional adipic acid production methods. This self-driven strategy establishes a new paradigm for coupling energy generation with chemical synthesis, offering highly efficient and environmentally sustainable models for industrial processes.
AB - Electrocatalysis offers a sustainable route for producing value-added chemicals, yet its widespread adoption is limited by low turnover frequency (TOF) and electron efficiency (EE). Here, we unveil a promotion effect in molecular phthalocyanine catalysts, enabling synergistic oxygen reduction reaction (ORR) and cyclohexanone oxidation (CyO). This mechanism bypasses the kinetic limitations of ORR steps and the overpotential penalties of CyO, achieving a record TOF of 1711 h–1 with superior EE (∼100% at 0.5 VRHE) for adipic acid production. Near-ambient pressure X-ray photoelectron spectroscopy reveals that this remarkable activity arises from interactions between *OOH intermediates at metal centers and substrates on neighboring nitrogen atoms. Integrating this design into microbial fuel cell reactors enables self-driven adipic acid synthesis alongside spontaneous bioelectricity generation, i.e., the system operates without any external power input. Life cycle assessment shows a 43% reduction in CO2 emissions, surpassing conventional adipic acid production methods. This self-driven strategy establishes a new paradigm for coupling energy generation with chemical synthesis, offering highly efficient and environmentally sustainable models for industrial processes.
KW - adipic acid production
KW - cyclohexanone oxidation
KW - near-ambient pressure XPS
KW - oxygen reduction reaction
KW - self-driven chemical synthesis
KW - single-atom catalysis
UR - https://www.scopus.com/pages/publications/105037163773
U2 - 10.1021/jacsau.6c00186
DO - 10.1021/jacsau.6c00186
M3 - Article
AN - SCOPUS:105037163773
SN - 2691-3704
VL - 6
SP - 2559
EP - 2568
JO - JACS Au
JF - JACS Au
IS - 4
ER -