Chinese Journal of Catalysis ›› 2024, Vol. 56: 25-50.DOI: 10.1016/S1872-2067(23)64576-0
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Yunrui Tiana, Haotian Tana, Xia Lia, Jingjing Jiaa, Zixian Maoa, Jian Liub, Ji Lianga,*()
Received:
2023-08-29
Accepted:
2023-11-24
Online:
2024-01-18
Published:
2024-01-10
About author:
Prof. Ji Liang received his Ph.D. degree from the University of Adelaide in 2014. After a T. S. Ke Fellowship and an ARC DECRA fellowship, he joined the School of Materials Science and Engineering, Tianjin University. His research interests are the design of functional carbon-based materials for electrochemical catalysis and energy storage applications.
Supported by:
Yunrui Tian, Haotian Tan, Xia Li, Jingjing Jia, Zixian Mao, Jian Liu, Ji Liang. Metal-based electrocatalysts for ammonia electro-oxidation reaction to nitrate/nitrite: Past, present, and future[J]. Chinese Journal of Catalysis, 2024, 56: 25-50.
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URL: https://www.cjcatal.com/EN/10.1016/S1872-2067(23)64576-0
Fig. 7. (a) Schematic illustration of the AOR reaction mechanism. CV measurement with 1 mol L?1 KOH (b) and 1 mol L?1 KOH + 0.5 mol L?1 NH4OH (c) electrolyte. Schematic representation of two proposed pathways for the copper-catalyzed AOR. Reprinted with permission from Ref. [32]. Copyright 2023, Elsevier Ltd.
Fig. 8. (a) Homogeneous electrocatalytic (mediated) oxidation, where the primary product is NO2-. (b) Direct heterogeneous electrocatalytic oxidation of NH3, where the primary product is NO3-. Reprinted with permission from Ref. [2]. Copyright 2021, Wiley-VCH.
Fig. 11. Top: Free energy diagrams of NO3? formation from ammonia via Nads (a) and NHOHads (b) intermediates at equilibrium (red trace) and limiting (blue trace) potentials computed using the computational hydrogen electrode at pH 11. (c) Bottom, top and side views of the lowest energy configurations for AOR intermediates in the path toward NO3?; Reprinted with permission from Ref. [46]. Copyright 2021, Wiley-VCH.
Fig. 12. (a) CV for NiCuBO/NF at 5 mV s?1. (b) In-situ electrochemical Raman spectra during forward scan from low to high potential. (c) From high to low potential for NiCuBO/NF. Reprinted with permission from Ref. [49]. Copyright 2023, Elsevier Ltd. (d) Cyclic voltammograms collected on the Ir film electrode. (e) ATR-SEIRA spectra obtained on Ir surface as applied potential positive scanning from 0 to 1.2?V, taken the single-beam spectrum at 1.2? and 0 V as the reference spectrum, respectively. (f) Potential-dependent intensity variation of Ir-Hads, N2Hx+y,ads, NOads, NO2? and NO3?; Reprinted with permission from Ref. [52]. Copyright 2021, Elsevier Ltd.
Electrode | pH | Potential (V vs. RHE) | Current density (mA cm-2) | Net yield reaction rate (mmol L-1 h-1 cm-2) | NO2- selectivity (%) | Ref. |
---|---|---|---|---|---|---|
Ru-Ir/TiO2 | 6.5 | — | 9 | — | 1 | [ |
Ni(OH)2 | 13 | 1.51 | — | — | 26.4 | [ |
Ni/Ni(OH)2 | 11 | — | 20 | 0.14 | 47 | [ |
Ni(OH)2/Ni | 11 | 1.64 | — | — | 80 | [ |
Table 1 Comparing ammonia electrochemical oxidation rates.
Electrode | pH | Potential (V vs. RHE) | Current density (mA cm-2) | Net yield reaction rate (mmol L-1 h-1 cm-2) | NO2- selectivity (%) | Ref. |
---|---|---|---|---|---|---|
Ru-Ir/TiO2 | 6.5 | — | 9 | — | 1 | [ |
Ni(OH)2 | 13 | 1.51 | — | — | 26.4 | [ |
Ni/Ni(OH)2 | 11 | — | 20 | 0.14 | 47 | [ |
Ni(OH)2/Ni | 11 | 1.64 | — | — | 80 | [ |
Fig. 14. Percentage of Pt(111) and Pt(100) sites for Typea, b, and c nanoparticles and ammonia oxidation on Pt nanoparticles of type c (solidline), type b (dashed line), and type a (dotted line) in 0.2 mol L?1 NaOH and 0.1 mol L?1 NH3. The sweep rate is 10 mV s?1. Reprinted with permission from Ref. [56]. Copyright 2004, American Chemical Society.
Fig. 15. SEM images of the surface morphologies of Pt particles electrodeposited on the ITO substrates at current densities of 0.2 (a), 0.5 (b), 1 (c) mA cm?2. Reprinted with permission from Ref. [57]. Copyright 2012, Elsevier Ltd.
Electrocatalyst | Carrier material | Ref. |
---|---|---|
CNT/NCNT@MOF | carbon paper | [ |
1-Cu’ | carbon paper | [ |
CuO-Cu2O | glassy carbon | [ |
Pt/glassy carbon | nickel foam | [ |
Ni(OH)2-decorated Pt NCs/C | glassy carbon | [ |
(Mn, Fe, Co, Ni, Cu)3O4 | carbon fiber paper | [ |
NiCo2N | carbon fiber paper | [ |
Table 2 Summarize the exemplary results as well as the catalytic performance of different electrocatalyst substrates in the literature.
Electrocatalyst | Carrier material | Ref. |
---|---|---|
CNT/NCNT@MOF | carbon paper | [ |
1-Cu’ | carbon paper | [ |
CuO-Cu2O | glassy carbon | [ |
Pt/glassy carbon | nickel foam | [ |
Ni(OH)2-decorated Pt NCs/C | glassy carbon | [ |
(Mn, Fe, Co, Ni, Cu)3O4 | carbon fiber paper | [ |
NiCo2N | carbon fiber paper | [ |
Fig. 16. STEM images of the NiCu/CP electrode before (a) and after (b) ammonia electrolysis tests. (c) The LSVs data of NiCu anode and Pt/C anode. Reprinted with permission from Ref. [41]. Copyright 2018, Elsevier Ltd. (d) CV curves in Ar-saturated 0.1 mol L?1 NH3 + 1.0 mol L?1 KOH at 5 mV s?1 (inset is TEM images and corresponding 3D models of PtIrCu HCOND). Reprinted with permission from Ref. [18]. Copyright 2021, Elsevier Ltd.
Fig. 17. SEM (a) and TEM (b) images of Cu@Pt/PGE at various magnifications. Reprinted with permission from Ref. [73]. Copyright 2021, The Royal Society of Chemistry. (c) Schematic of Ni(OH)2-Cu2O@CuO with dual-interface structure. Reprinted with permission from Ref. [61]. Copyright 2020, American Chemical Society.
Fig. 18. (a) HRTEM image of Ni(OH)2-Cu2O@CuO. (b) CVs of Ni(OH)2-Cu2O@CuO acquired. Reprinted with permission from Ref. [61]. Copyright 2020, American Chemical Society.
Fig. 19. (a) A schematic illustration of selective NH3-to-N2 oxidation over Cu/NCNT via the i-SCR mechanism. (b) XPS Cu 2p3/2 spectra for Cu/NCNT catalysts with different surface N contents (Cu 2 wt% for all the catalysts). (c) Concentrations of the reactants and products in NH3-SCO over Cu/NCNT with different concentrations of NO in the reaction mixture at 120 °C. Reprinted with permission from Ref. [77]. Copyright 2022, American Chemical Society.
Fig. 20. (a) HRTEM images of Ce-NR. (b) NH3-TPD profiles of the as-synthesized catalysts. (c) Corresponding peak intensity ratios of I1226/I1117 and the amounts of relevant desorbed-NH3 species (peak β + γ) over the Cu/Ce-NR and Cu/Ce-NC catalysts. Reprinted with permission from Ref. [81]. Copyright 2023, American Chemical Society.
Fig. 21. (a) CV curves at the potential range from 0 to 0.6 V vs. Hg/HgO. (b) Atomic structures of CuO with oxygen vacancies. (c) Free energy diagrams of oxidation on the Vo-free and Vo-rich CuO(111) surface. Reprinted with permission from Ref. [42].Copyright 2022, Springer-Verlag.
Fig. 22. (a) Preparation and evolution of the host-guest Cu catalyst through metal ion deposition and in situ clustering routes. (b) In situ XANES. (c) FE-EXAFS at the Cu K-edge for 1-Cu. Reprinted with permission from Ref. [27] Copyright 2022, American Chemical Society.
Electrocatalyst | Structural characteristics | Test environment | Performancea (Peak current density) | Ref. |
---|---|---|---|---|
Pt-Rh/carbon fiber | continuous Pt-Rh layer on carbon fibers | 1.03 mmol L-1 NH3 + 0.1 mol L-1 KOH | 15 mA cm-2 (10 mV s-1) | [ [ |
Pt/graphite | Pt layer consisting of aggregates | 0.1 mol L-1 NH3 + 0.2 mol L-1 NaOH | 32 mA (20 mV s-1) | |
Pt/Ni | submicron-sized Pt particles | 0.1 mol L-1 NH3 + 0.2 mol L-1 NaOH | 1 mA cm-2 (5 mV s-1) | [ |
Pt/glassy carbon | Pt nanoparticles/Pt nanosheetsata | 0.075-1.5mmol L-1 NH3 + 1 mol L-1 KOH | 4.6 mA (10 mV s-1) | [ |
Pt-Ir/Pt or Au | Fcc Pt70Ir30 alloy | 0.005 mmol L-1 NH3 + 0.1 mmol L-1 KOH | 25mA cm-2 (10 mV s-1) | [ |
Pt black | Pt film | 0.1 mol L-1 NH3+1 mol L-1 NaClO4 | 22.5 mA (5 mV s-1) | [ |
Pt | coral-like Pt nanowires | 0.05 mol L-1 (NH4)2SO4 + 1 mol L-1 KOH | 72 mA cm-2 (10 mV s-1) | [ |
NiCu@NiCuOOH | core-shell NiCu@NiCuOOH | 0.5 mol L-1 NaOH + 0.015 mol L-1 NH4Cl | — | [ |
NiCu-S/DSA | particulate metal oxides | 0.5 mol L-1 NaOH + 0.015 mol L-1 NH4Cl | — | [ |
Table 3 Summarizes the exemplary results of electrodeposition in the literature for the preparation of electrocatalysts, as well as their structural features and catalytic performance.
Electrocatalyst | Structural characteristics | Test environment | Performancea (Peak current density) | Ref. |
---|---|---|---|---|
Pt-Rh/carbon fiber | continuous Pt-Rh layer on carbon fibers | 1.03 mmol L-1 NH3 + 0.1 mol L-1 KOH | 15 mA cm-2 (10 mV s-1) | [ [ |
Pt/graphite | Pt layer consisting of aggregates | 0.1 mol L-1 NH3 + 0.2 mol L-1 NaOH | 32 mA (20 mV s-1) | |
Pt/Ni | submicron-sized Pt particles | 0.1 mol L-1 NH3 + 0.2 mol L-1 NaOH | 1 mA cm-2 (5 mV s-1) | [ |
Pt/glassy carbon | Pt nanoparticles/Pt nanosheetsata | 0.075-1.5mmol L-1 NH3 + 1 mol L-1 KOH | 4.6 mA (10 mV s-1) | [ |
Pt-Ir/Pt or Au | Fcc Pt70Ir30 alloy | 0.005 mmol L-1 NH3 + 0.1 mmol L-1 KOH | 25mA cm-2 (10 mV s-1) | [ |
Pt black | Pt film | 0.1 mol L-1 NH3+1 mol L-1 NaClO4 | 22.5 mA (5 mV s-1) | [ |
Pt | coral-like Pt nanowires | 0.05 mol L-1 (NH4)2SO4 + 1 mol L-1 KOH | 72 mA cm-2 (10 mV s-1) | [ |
NiCu@NiCuOOH | core-shell NiCu@NiCuOOH | 0.5 mol L-1 NaOH + 0.015 mol L-1 NH4Cl | — | [ |
NiCu-S/DSA | particulate metal oxides | 0.5 mol L-1 NaOH + 0.015 mol L-1 NH4Cl | — | [ |
Fig. 23. Schematic illustration of Pt NPs morphology variations depends on EL of 0.05, ?0.2, ?0.35, and ?0.5 V. Reprinted with permission from Ref. [98]. Copyright 2023, Elsevier Ltd.
Fig. 24. (a) The formation diagram of NiCu@NiCuOOH-NF core-shell electrode. (b) SEM images of NiCu@NiCuOOH-NF. (c) The comparison of i-t curves at 0.6 V vs. SCE between 2 mol L?1 NaOH + 0.4 NH4Cl and 2 mol L?1 NaOH. Reprinted with permission from Ref. [99]. Copyright 2022, Elsevier Ltd.
Fig. 25. (a) Magnified TEM image. (b) Size distribution histogram. (c) Chronoamperometry curves of Pt-NCs and Pt-NPs-JM in 1 mol L?1 KOH solution containing 0.1 mol L?1 NH4OH at 0.6 V potential. Reprinted with permission from Ref. [107]. Copyright 2020, Elsevier Ltd.
Fig. 26. Schematic representation of the relative orientation of (003), (012), and (100) facets for CuFeO2 (a) and (012), (104), and (212?1) facets for CuFeO2-NH3 (b). (c) Calculated free energy profile for AOR processes on CuFeO2 (212?1) and CuFeO2 (212?1) @Cu-FeOOH (adsorption sites*). The inset is the charge density difference of *NH3 models. Isosurface is 0.003 e ??1. Reprinted with permission from Ref. [108]. Copyright 2023, Wiley-VCH.
Fig. 27. (a) HAADF-STEM images of individual PtIrCu RDNF-HNDs-2, and corresponding 3D models of respectively. (b) CV curves in Ar-saturated 0.1 mol L?1 NH3 and 1.0 mol L?1 KOH at 5 mV s?1. (c) Free energy diagrams of NH3 dehydrogenation at 0.3 V vs. RHE. Reprinted with permission from Ref. [109]. Copyright 2023, Elsevier Ltd.
Fig. 28. (a) TEM pictures of colloidal Pt nanoparticles. (b) Cyclic voltammograms of voltammetric profiles of Pt(100), Pt(110), Pt(111) and polyoriented Pt single crystal in 0.1 mol L?1 NaOH and 10?3 mol L?1 NH3. Scan rate 10 mV s?1. (c) Ammonia oxidation on hydrazine-Pt, borohydride-Pt, and colloidal Pt nanoparticles and polyoriented platinum in 0.2 mol L?1 NaOH and 0.1 mol L?1 NH3. Scan rate 10 mV s?1. Reprinted with permission from Ref. [110]. Copyright 2004, Elsevier Ltd.
Fig. 29. (a) Preparation schematic diagram of PtZn-P-300. (b) Cyclic voltammograms of HRTEM false color images of PtZn-P-300. (c) CV curves in 1.0 mol L?1 KOH with 0.1 mol L?1 NH3·H2O solution at 10 mV s?1. Reprinted with permission from Ref. [111]. Copyright 2023, Elsevier Ltd.
Fig. 30. The effect of NH3 concentration on the AOR. (a) LSV curves of α-Fe2O3 in the 0.1 mol L?1 NaClO4 electrolytes with different NH3 concentrations. (b) The FEs and the average current density at 1.3 V. Reprinted with permission from Ref. [118]. Copyright 2022, Wiley-VCH.
Strategy | Reaction | αin ($) | Produced fertilizer | N-P-K-(S) ratio | αout ($) | δ ($) |
---|---|---|---|---|---|---|
Acid-base reaction | 2NH3 (0.3 mol L-1) + H2SO4 (0.15 mol L-1) → (NH4)2SO4 (0.15 mol L-1) | 0.4 | (NH4)2SO4 | 21-0-0-(24) | 1.7 | 1.3 |
Acid-base reaction | NH3 (0.3 mol L-1) + HNO3 (0.3 mol L-1) → NH4NO3 (0.3 mol L-1) | 1.7 | NH4NO3 | 35-0-0-(0) | 2.1 | 0.3 |
Electrolysis in 0.1 mol L-1 K2SO4 | 2NH3 (0.3 mol L-1) + 3H2O → NH4NO3 (0.15 mol L-1) + 4H2 | 3.6 | NH4NO3 + K2SO4 (3:2) | 14-0-32-(11) | 4.6 | 1.0 |
Electrolysis in 0.1 mol L-1 K2HPO4 | 2NH3 (0.3 mol L-1) + 3H2O → NH4NO3 (0.15 mol L-1) + 4H2 | 6.7 | NH4NO3 + K2HPO4 (3:2) | 14-24-32-(0) | 7.7 | 1.0 |
Table 4 Assessment of several waste-ammonia-to-fertilizer recovery strategies [6]. a
Strategy | Reaction | αin ($) | Produced fertilizer | N-P-K-(S) ratio | αout ($) | δ ($) |
---|---|---|---|---|---|---|
Acid-base reaction | 2NH3 (0.3 mol L-1) + H2SO4 (0.15 mol L-1) → (NH4)2SO4 (0.15 mol L-1) | 0.4 | (NH4)2SO4 | 21-0-0-(24) | 1.7 | 1.3 |
Acid-base reaction | NH3 (0.3 mol L-1) + HNO3 (0.3 mol L-1) → NH4NO3 (0.3 mol L-1) | 1.7 | NH4NO3 | 35-0-0-(0) | 2.1 | 0.3 |
Electrolysis in 0.1 mol L-1 K2SO4 | 2NH3 (0.3 mol L-1) + 3H2O → NH4NO3 (0.15 mol L-1) + 4H2 | 3.6 | NH4NO3 + K2SO4 (3:2) | 14-0-32-(11) | 4.6 | 1.0 |
Electrolysis in 0.1 mol L-1 K2HPO4 | 2NH3 (0.3 mol L-1) + 3H2O → NH4NO3 (0.15 mol L-1) + 4H2 | 6.7 | NH4NO3 + K2HPO4 (3:2) | 14-24-32-(0) | 7.7 | 1.0 |
Strategy | Reaction | αin ($) | Produced fertilizer | N-P-K-(S) ratio | αout ($) | δ ($) | ||
---|---|---|---|---|---|---|---|---|
Acid-base reaction | 2NH3 (0.3 mol L-1) + H2SO4 (0.15 mol L-1) → (NH4)2SO4 (0.15 mol L-1) | 0.15 | (NH4)2SO4 | 21-0-0-(24) | 0.66 | 0.51 | ||
Acid-base reaction | NH3 (0.3 mol L-1) + HNO3 (0.3 mol L-1) → NH4NO3 (0.3 mol L-1) | 1.00 | NH4NO3 | 35-0-0-(0) | 1.18 | 0.18 | ||
Electrolysis in 0.1 mol L-1 K2SO4 | 2NH3 (0.3 mol L-1) + 3H2O → NH4NO3 (0.15 mol L-1) + 4H2 | 1.90 | NH4NO3 + K2SO4 (3:2) | 14-0-32-(11) | 2.49 | 0.59 |
Table 5 Assessment of several waste-ammonia-to-fertilizer recovery strategies [6].
Strategy | Reaction | αin ($) | Produced fertilizer | N-P-K-(S) ratio | αout ($) | δ ($) | ||
---|---|---|---|---|---|---|---|---|
Acid-base reaction | 2NH3 (0.3 mol L-1) + H2SO4 (0.15 mol L-1) → (NH4)2SO4 (0.15 mol L-1) | 0.15 | (NH4)2SO4 | 21-0-0-(24) | 0.66 | 0.51 | ||
Acid-base reaction | NH3 (0.3 mol L-1) + HNO3 (0.3 mol L-1) → NH4NO3 (0.3 mol L-1) | 1.00 | NH4NO3 | 35-0-0-(0) | 1.18 | 0.18 | ||
Electrolysis in 0.1 mol L-1 K2SO4 | 2NH3 (0.3 mol L-1) + 3H2O → NH4NO3 (0.15 mol L-1) + 4H2 | 1.90 | NH4NO3 + K2SO4 (3:2) | 14-0-32-(11) | 2.49 | 0.59 |
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