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Efficient Self-Driven Adipic Acid Production with Bioelectricity Generation

  • Yifan Bu
  • , Chao Li
  • , Ziliang Deng
  • , Shiyun Li
  • , Zipeng Zhao
  • , Jisheng Xie
  • , Jihan Zhou
  • , Hai Xiao
  • , Ximin Lv
  • , Xueqiang Zhang*
  • , Wulin Yang*
  • , Mufan Li*
  • *Corresponding author for this work
  • Peking University
  • Beijing Institute of Technology
  • Tsinghua University

Research output: Contribution to journalArticlepeer-review

Abstract

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.

Original languageEnglish
Pages (from-to)2559-2568
Number of pages10
JournalJACS Au
Volume6
Issue number4
DOIs
Publication statusPublished - 27 Apr 2026
Externally publishedYes

Keywords

  • adipic acid production
  • cyclohexanone oxidation
  • near-ambient pressure XPS
  • oxygen reduction reaction
  • self-driven chemical synthesis
  • single-atom catalysis

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