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Explora: Environment
            and Resource                                                     Electrocatalyst for ammonia oxidation reaction



            concentration of 450 μL of H PtCl ·6H O (0.1 moL/L) and   3. Results and discussion
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            1,050 μL of deionized water, the temperature of the water
            bath was controlled at 30°C, 40°C, and 50°C, with heating   In this work, ammonium chloride (NH Cl) was used as the
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            maintained for 8 h. The obtained samples were named as   ammonia source. The cyclic voltammetry (CV) technique
            Pt-(NiCo-LDH)-X (X = 5, 6, 7). In addition, the sample   was employed to analyze the electrochemical reactions
            prepared without H PtCl ·6H O (0.1 moL/L) was named   based on the peak current, peak potential, and related
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                                    2
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            NiCo-LDH-8,  the  sample  prepared  without  NiCo-LDH   parameters.  The oxidation peak current is one  of the
            was named Pt-NF-9, and the NF was designated NF-10.   important parameters to evaluate the activity of catalysts.
            Figure 1 shows the synthesis process of NiCo-LDH and   Higher peak currents indicate better catalytic activity,
            Pt-(NiCo-LDH)-X.                                   characterized by faster electron transfer, accelerated
                                                               electrode reaction rates, and lower reaction resistance.
                                                               To select the best synthesis condition of the catalyst, the
                                                               CV technique was conducted on all catalysts for the AOR.
                                                               The oxidation reaction peak currents were collected and
                                                               used as a key parameter to evaluate the catalyst activity.
                                                               In addition, to obtain an electrocatalyst with excellent
                                                               catalytic performance, the volume of H PtCl   6H O and
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                                                               the reaction temperatures of H PtCl   6H O and NiCo-
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                                                               LDH were regulated.
                                                                 First, the concentrations of H PtCl  6H O were studied.
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                                                               Figure  2A-D shows the CV curves of the Pt-(NiCo-
                                                               LDH)-X (X = 1, 2, 3, 4) catalysts synthesized with H PtCl
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                                                               6H O volumes ranging from 0.15 mL to 0.60 mL. In the
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            Figure  1. The synthesis process of nickel (Ni)–cobalt layered double   1 M potassium hydroxide (KOH) and 1 M KOH + 0.1 M
            hydroxide and platinum–(Ni–cobalt layered double hydroxide)-X  NH Cl solutions, a distinct oxidation peak emerged at
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                        A                                    B








                         C                                   D


















            Figure  2. The cyclic voltammetry curves of platinum–(nickel–cobalt layered double hydroxide)-X (Pt-[NiCo-LDH]-X). (A) Pt-(NiCo-LDH)-1,
            (B) Pt-(NiCo-LDH)-2, (C) Pt-(NiCo-LDH)-3, and (D) Pt-(NiCo-LDH)-4 catalysts in 1 M potassium hydroxide (KOH) and 1 M KOH + 0.1 M ammonium
            chloride (NH4Cl) solutions. Hg/HgO refers to mercury/mercury oxide used as the reference.


            Volume 2 Issue 3 (2025)                         3                           doi: 10.36922/EER025170033
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