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Nitrate reduction to ammonia catalyzed by GaN/Si photoelectrodes with metal clusters

Author

Listed:
  • Wan Jae Dong

    (University of Michigan
    Korea University)

  • Jan Paul Menzel

    (Yale University)

  • Kejian Li

    (University of Michigan)

  • Zhengwei Ye

    (University of Michigan)

  • Zhuoran Long

    (Yale University)

  • Ishtiaque Ahmed Navid

    (University of Michigan)

  • Ke R. Yang

    (Yale University)

  • Yixin Xiao

    (University of Michigan)

  • Victor S. Batista

    (Yale University)

  • Zetian Mi

    (University of Michigan)

Abstract

The development of photoelectrochemical cells for reduction of nitrate to ammonia under solar light is of significant interest for the production of clean chemicals and fuels but has remained a daunting challenge. Here, we investigate various metal catalysts supported on GaN nanowires grown on n+-p Si wafer – an emerging functional platform for scalable artificial photosynthesis – and demonstrate highly stable and efficient photoelectrochemical nitrate reduction reaction. We find that Co and Ni catalysts on GaN/Si exhibit the best performance, with an onset potential >0.3 VRHE and a faradaic efficiency of NH3 of 99% at 0.2 VRHE. These results highlight the advantage of photoelectrochemical system in achieving efficient nitrate reduction under more positive potentials. In-situ measurements and theoretical calculations reveal that the binding modes of the $${{{\rm{NO}}}}_{2}^{{-}}$$ NO 2 − intermediate play a key role in the NH3 synthetic process. These results demonstrate that the rational design of catalysts on photoelectrodes can construct synergistic metal-semiconductor interactions for efficient and stable photoelectrochemical NH3 synthesis.

Suggested Citation

  • Wan Jae Dong & Jan Paul Menzel & Kejian Li & Zhengwei Ye & Zhuoran Long & Ishtiaque Ahmed Navid & Ke R. Yang & Yixin Xiao & Victor S. Batista & Zetian Mi, 2025. "Nitrate reduction to ammonia catalyzed by GaN/Si photoelectrodes with metal clusters," Nature Communications, Nature, vol. 16(1), pages 1-11, December.
  • Handle: RePEc:nat:natcom:v:16:y:2025:i:1:d:10.1038_s41467-025-58372-7
    DOI: 10.1038/s41467-025-58372-7
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