Chinese Journal of Catalysis ›› 2027, Vol. 92: 365-375.DOI: 10.1016/S1872-2067(26)65241-2

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Co(OH)2/Cu NWs with interface modification of hypophosphite ions for sustainable ammonia synthesis from nitrate at ~2.8 A·cm-2

Ruihan Zhoua, Tixuan Xiaa, Yingchen Yanga, Dongbo Xua,b,*(), Weidong Shia,c,*()   

  1. a School of Chemistry and Chemical Engineering, Jiangsu University, Zhenjiang 212013, Jiangsu, China
    b Jiangsu Key Laboratory of Advanced Structural Materials and Application Technology, Nanjing Institute of Technology, Nanjing 211167, Jiangsu, China
    c School of Environmental and Chemical Engineering, Jiangsu University of Science and Technology, Zhenjiang 212100, Jiangsu, China
  • Received:2026-02-28 Accepted:2026-05-15 Online:2027-01-02 Published:2026-10-30
  • Contact: *E-mail: xudb39@ujs.edu.cn (D. Xu),
    swd1978@ujs.edu.cn (W. Shi).
  • Supported by:
    National Natural Science Foundation of China(22225808);National Natural Science Foundation of China(U24A20551);Natural Science Foundation of Jiangsu Province(BK20230551);Opening Project of Jiangsu Key Laboratory of Advanced Structural Materials and Application Technology(ASMA202503)

Abstract:

Ammonia production via nitrate electroreduction (NO3RR) offers an environmentally benign alternative, yet it is still extremely difficult to simultaneously attain superior Faradaic efficiency and long-lasting durability when operating at the high current densities. Herein, we report a self-supporting electrode comprising Cu nanowires uniformly coated with cobalt hydroxide incorporating surface-coordinated hypophosphite ions (H2PO2-) (denoted as P-Co(OH)2/Cu NWs), directly fabricated on Cu foam. The P-Co(OH)2/Cu NWs catalyst exhibited remarkable NO3RR performance in 0.1 mol·L-1 NaNO3/1 mol·L-1 NaOH, producing NH3 at a rate of 204.3 mg·h-1·cm-2 (-1.0 V) with a peak Faradaic efficiency of 96.8% (-0.7 V), both potentials referenced to RHE. Notably, the electrode maintains stable electroactivity and NH3 selectivity over 20 consecutive test cycles (1 h per cycle) under approximately 2.8 A·cm-2. In-situ attenuated total reflection Fourier transform infrared spectroscopy reveals that the P-Co(OH)2/Cu NWs electrode promotes enhanced deoxygenation of *NO3 and deep hydrogenation of *NOx intermediates. Cyclic voltammetry test and In-situ Raman spectroscopy demonstrate that the incorporated H2PO2- induce and stabilize the in-situ formation of metallic Co0 phase under operative electrolysis conditions. Density functional theory calculations further elucidate that the metallic Co0 phase, generated in situ during NO3RR, optimizes the adsorption energetics of *NOH, thereby substantially facilitating the energy-demanding step (*NO → *NOH) relative to Co(OH)2, while concurrently strengthening *H adsorption. This work presents a viable electrode design strategy for securing efficient and stable electrocatalytic NO3--to-NH3 conversion under high-rate operation.

Key words: Nitrate reduction, Industrial current density, Hypophosphite ion, Ammonia, Interface modification