Iranna
Udachyan
a,
Jayesh T.
Bhanushali
a,
Tomer
Zidki
a,
Amir
Mizrahi
b and
Dan
Meyerstein
*ac
aDepartment of Chemical Sciences, and The Radical Research Center, Ariel University, Ariel, Israel. E-mail: danm@ariel.ac.il
bChemistry Department, Nuclear Research Centre Negev, Beer-Sheva 8419001, Israel
cDepartment of Chemistry, Ben-Gurion University, Beer-Sheva, Israel
First published on 24th May 2024
In pursuing green hydrogen fuel, electrochemical water-splitting emerges as the optimal method. A critical challenge in advancing this process is identifying a cost-effective electrocatalyst for oxygen evolution on the anode. Recent research has demonstrated the efficacy of first-row transition metal carbonates as catalysts for various oxidation reactions. In this study, Earth-abundant first-row transition metal carbonates were electrodeposited onto nickel foam (NF) electrodes and evaluated for their performance in the oxygen evolution reaction. The investigation compares the activity of these carbonates on NF electrodes against bare NF electrodes. Notably, Fe2(CO3)3/NF exhibited superior oxygen evolution activity, characterized by low overpotential values, i.e. Iron is master of them all (R. Kipling, Cold Iron, Rewards and Fairies, Macmillan and Co. Ltd., 1910). Comprehensive catalytic stability and durability tests also indicate that these transition metal carbonates maintain stable activity, positioning them as durable and efficient electrocatalysts for the oxygen evolution reaction.
To date, noble metal oxides, notably IrO2 and RuO2, have been recognized for their efficiency as catalysts for the oxygen evolution reaction (OER). However, their commercial viability is hindered by the prohibitive cost and limited availability of noble metals.7,8 Consequently, substantial efforts are underway to design catalysts with advanced materials using Earth-abundant transition metals.9–12
Recent studies have identified first-row transition metal carbonates as promising catalysts for electrochemical oxidation processes.13–22 These metal carbonates, widely employed in industrial applications such as plastics, paper, paint, and rubber industries, have shown utility in various electrochemical catalytic reactions.23–26 Metal carbonates are widely used in solid oxide fuel cells, batteries, and supercapacitors.27–29 Notably, the carbonate's role as σ-donor ligand stabilizes high oxidation states of metals like MnIII, FeIV/III, CoV/IV/III, NiIII, and CuIV/III, facilitating the stabilization of metal complexes’ high oxidation states and partial radicalization of the carbonate ligand.16,17,30–32 In the high oxidation states of these complexes, the carbonate functions as an electron donor to the central metal cation, stabilizing the high oxidation states of metal complexes while also inducing partial radicalization of the carbonate ligand.18,19 Additionally, metal complex intermediates in higher oxidation states boost electrochemical reactions.
The report by Chen et al. shows that incorporating Fe in NiFeOx catalysts enhances the water oxidation activity and delivers a stable current density of 100 mA cm−2 in an alkaline media.31 Building on this background, the present study demonstrates a series of first-row transition metal carbonates as effective OER catalysts and identifies the most potent catalyst among them. Electrochemical deposition of the metal carbonate complexes onto Ni foam substrate (NF) was accomplished through anodization in aqueous electrolytes. The synthesized catalysts were comprehensively analyzed for their chemical and physical properties through various spectroscopic techniques. Subsequently, the activity of the deposited metal carbonate complexes on the NF electrode in the electrochemical OER was determined and compared.
The experimental procedures for the electrochemical deposition of metal carbonates, their respective characterization, and electrochemical activity are described in the ESI.†
Fig. 1 SEM images of NF (a), Mn2(CO3)3/NF (b), Fe2(CO3)3/NF (c), Co2(CO3)3/NF (d), Ni2(CO3)3/NF (e), Cu(CO3)/NF (f). |
The interaction type between the metal and carbonate was explored by ATR-IR spectroscopy. The IR spectrum of Mn2(CO3)3/NF is presented in Fig. 2a. The peak at 1713 cm−1 is ascribed to CO stretching. Further, 1410, 864, and 718 cm−1 peaks are characteristic Mn2(CO3)3 peaks,34 corresponding to asymmetric stretching of CO32−, out-of-plane, and in-plane bending vibrations, respectively.35,36 Similarly, the other metal carbonates showed similar IR spectra, which are presented in the ESI (Fig. S1†).
Fig. 2 ATR spectrum of Mn2(CO3)3 (a), XPS spectra of Fe 2p for Fe2(CO3)3/NF (b), Ni 2p for Ni2(CO3)3/NF (c) and Cu 2p for Cu(CO3)/NF (d). |
XPS analysis of the metal carbonates on the NF electrode was performed to determine the elemental composition and their oxidation states. The obtained XPS spectra are presented in Fig. 2b–d. Fe2(CO3)3/NF showed the presence of Fe in +2 and +3 oxidation states, as noted from the Fe 2p3/2 (712.1 eV) and Fe 2p1/2 (725.0 eV) peaks and their respective satellite peaks (714.9 and 727.8 eV) (Fig. 2b).37 Similarly, Ni2(CO3)3/NF and Cu(CO3)/NF displayed the presence of Ni in +2, +3 oxidation states (Fig. 2c)38 and Cu in +2 oxidation state (Fig. 2d)39 by the Ni 2p3/2 (855.4 eV), Ni 2p1/2 (873.3 eV), Cu 2p3/2 (934.9 eV), and Cu 2p1/2 (954.6) peaks along with their respective satellite peaks (Ni 2p3/2 861.8 eV, Ni 2p1/2 879.2 eV, Cu 2p3/2 943.4 eV and Cu 2p1/2 962.7). The data corresponding to other metal carbonates, namely, Co2(CO3)3/NF and Mn2(CO3)3/NF, are presented in Fig. S2.† In addition, carbon and oxygen signals were detected in the XPS analysis of the metal carbonates, as seen in Fig. S2f–j.†
The electrochemically deposited Mn2(CO3)3/NF, Fe2(CO3)3/NF, Co2(CO3)3/NF, Ni2(CO3)3/NF, and Cu(CO3)/NF were investigated for the oxygen evolution reaction in 1.0 M KOH N2-purged solutions using the standard three-electrode system with a scan rate of 20 mV s−1. Fig. 3a shows the LSV curves (without IR correction) for Mn2(CO3)3/NF, Fe2(CO3)3/NF, Co2(CO3)3/NF, Ni2(CO3)3/NF, Cu(CO3)/NF, CO3/NF, and NF. To begin with, the highest electrocatalytic activity for oxygen evolution was observed for the Fe2(CO3)3/NF electrode with 10 mA cm−2 current density at a low overpotential of 310 mV (1.54 V vs. RHE), which is much lower in comparison with the other metal carbonates. Also, the other catalysts achieved 10 mA cm−2 current densities at low over potential values namely, Mn2(CO3)3/NF at 360 mV (1.59 V vs. RHE), Co2(CO3)3/NF at 390 mV (1.62 V vs. RHE), Ni2(CO3)3/NF at 350 mV (1.58 V vs. RHE), Cu(CO3)/NF at 400 mV (1.63 V vs. RHE), CO3/NF at 460 mV (1.69 V vs. RHE), and bare NF at 520 mV (1.75 V vs. RHE), respectively. These results indicate that first-row transition metal carbonates are active electrocatalysts for the OER. Among these metal carbonates, the Fe2(CO3)3/NF showed superior electrocatalytic behavior with the lowest overpotential. Furthermore, all the metal carbonates show multiple oxidation peaks before the sharp catalytic current peak for water oxidation, as was observed from the respective cyclic voltammograms, Fig. 3b. Additional results obtained are explained in the ESI.† Moreover, a comparative study was performed between the metal carbonates and the substrates used for the deposition of these metal carbonates to determine the effect on the OER activity. The results thus obtained are presented in the ESI.†
Additionally, Tafel curves were used to study the kinetics of the OER; the data is provided in Fig. 3c. The corresponding Tafel slope curves were fitted with the Tafel equation (η = blogj + a, η = overpotential, j = current density, b = Tafel slope).40,41 From Fig. 3b, Fe2(CO3)3/NF displayed the lowest Tafel slope of 86 mV dec−1 compared to the other metal carbonates. Correspondingly, Mn2(CO3)3/NF, Co2(CO3)3/NF, Ni2(CO3)3/NF, Cu(CO3)/NF, CO3/NF, and NF displayed Tafel slopes of 106 mV dec−1, 96 mV dec−1, 110 mV dec−1, 112 mV dec−1, 112 mV dec−1 and 122 mV dec−1, respectively. The results indicate that metal carbonates show rapid reaction kinetics for oxygen evolution.42,43
Moreover, the electron transfer kinetics for the OER were determined by electrochemical impedance spectroscopy (EIS). Fig. S4† shows the EIS-Nyquist plot of the metal carbonates. The experiments relating to EIS were carried out at constant potential for oxygen evolution, as mentioned in the caption of Fig. S4.† All the metal carbonates exhibited smaller charge transfer resistance (Rct) than NF and CO3/NF. Interestingly, Co2(CO3)3/NF showed a bit higher charge transfer resistance; the values are given in Table S1.† These metal carbonates may be considered suitable electron transfer catalysts and exhibit good conductivity towards electrochemical OER.44–46
Further, the key factor for a catalyst to be applied depends on its long-term stability and durability. Therefore, chronoamperometric analysis was carried out in 1.0 M KOH for the metal carbonates/NF with CO3/NF to determine their stability for a duration of 15 h; the results are presented in Fig. 3d. Mn2(CO3)3/NF, Fe2(CO3)3/NF, Co2(CO3)3/NF, Ni2(CO3)3/NF and CO3/NF showed good electrocatalytic stability whereas, Cu(CO3)/NF showed decrement in electrocatalytic stability. The analysis was performed for all catalysts at their respective electrocatalytic oxygen evolution potentials. The results indicate no significant change in catalytic current density after 15 h except for a slight decay in the catalytic current density in the initial stage of the experiment for Fe2(CO3)3/NF, Co2(CO3)3/NF, Ni2(CO3)3/NF and Cu(CO3)/NF. After one h, the current density stabilized for Fe2(CO3)3/NF, whereas Cu(CO3)/NF exhibited slight decay in the catalytic current density throughout the analysis.
Footnote |
† Electronic supplementary information (ESI) available. See DOI: https://doi.org/10.1039/d4dt00708e |
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