RESUMEN
Organic polymers have attracted considerable interest in designing a multifunctional electrocatalyst. However, the inferior electro-conductivity of such metal-free polymers is often regarded as a shortcoming. Herein, a nitrogen- and phosphorus-rich polymer with phosphamide functionality (PAP) in the repeating unit has been synthesized from diaminopyridine (DAP) and phenylphosphonic dichloride (PPDC) precursors. The presence of phosphamide oxygen and pyridine nitrogen in the repeating unit of PAP leads to the coordination of the CuII ion and the incorporation of 3.29 wt % in the polymer matrix (Cu30@PAP) when copper salt is used to impregnate the polymer. Combined with a spectroscopic, microscopic, and DFT study, the coordination and geometry of copper in the PAP matrix has been established to be a distorted square planar CuII in a N2O2 ligand environment where phosphamide oxygen and pyridine nitrogen of the PAP coordinate to the metal center. The copper incorporation in the PAP modulates its electrocatalytic activity. On the glassy carbon electrode, PAP shows inferior activity toward the hydrogen evolution reaction (HER) in 0.5 M H2SO4 while 3 wt % copper incorporation (Cu30@PAP) significantly improves the HER performance with an overpotential of 114 mV at 10 mA cm-2. The notable electrochemical activity with Cu30@PAP occurs due to the impregnation of Cu(II) in PAP, improved electro-kinetics, and better charge transfer resistance (Rct). When changing the electrolyte from H2SO4 to CO2-saturated bicarbonate solution at nearly neutral pH, PAP shows HER as the dominant pathway along with the partial reduction of CO2 to formate. Moreover, the use of Cu30@PAP as an electrolcatalyst could not alter the predominant HER path, and only 20% Faradaic efficiency for the CO2 reduced products has been achieved. Post-chronoamperometric characterization of the recovered catalyst suggests an unaltered valence state of the copper ion and the intact chemical structure of PAP. DFT studies unraveled that the copper sites of Cu30@PAP promote water adsorption while phosphamide-NH of the PAP can weakly hold the CO2 adduct via a hydrogen bonding interaction. A detailed calculation has pointed out that the tetra-coordinated copper centers present in the PAP frame are the reactive sites and that the formation of the [CuI-H] intermediate is the rate-limiting step for both HER and its competitive side reaction, i.e., CO2 reduction to formate or CO formation. The high proton concentration in the electrolyte of pH < 7 leads to HER as the predominant pathway. This combined experimental and theoretical study has highlighted the crucial role of copper sites in electrocatalysis, emphasizing the plausible reason for electrocatalytic selectivity.
RESUMEN
Nickel-based bimetallic oxides such as NiMoO4 and NiWO4, when deposited on the electrode substrate, show remarkable activity toward the electrocatalytic oxygen evolution reaction (OER). The stability of such nanostructures is nevertheless speculative, and catalytically active species have been less explored. Herein, NiMoO4 nanorods and NiWO4 nanoparticles are prepared via a solvothermal route and deposited on nickel foam (NF) (NiMoO4/NF and NiWO4/NF). After ensuring the chemical and structural integrity of the catalysts on electrodes, an OER study has been performed in the alkaline medium. After a few cyclic voltammetry (CV) cycles within the potential window of 1.0-1.9 V (vs reversible hydrogen electrode (RHE)), ex situ Raman analysis of the electrodes infers the formation of NiO(OH)ED (ED: electrochemically derived) from NiMoO4 precatalyst, while NiWO4 remains stable. A controlled study, stirring of NiMoO4/NF in 1 M KOH without applied potential, confirms that NiMoO4 hydrolyzes to the isolable NiO, which under a potential bias converts into NiO(OH)ED. Perhaps the more ionic character of the Ni-O-Mo bond in the NiMoO4 compared to the Ni-O-W bond in NiWO4 causes the transformation of NiMoO4 into NiO(OH)ED. A comparison of the OER performance of electrochemically derived NiO(OH)ED, NiWO4, ex-situ-prepared Ni(OH)2, and NiO(OH) confirmed that in-situ-prepared NiO(OH)ED remained superior with a substantial potential of 238 (±6) mV at 20 mA cm-2. The notable electrochemical performance of NiO(OH)ED can be attributed to its low Tafel slope value (26 mV dec-1), high double-layer capacitance (Cdl, 1.21 mF cm-2), and a low charge-transfer resistance (Rct, 1.76 Ω). The NiO(OH)ED/NF can further be fabricated as a durable OER anode to deliver a high current density of 25-100 mA cm-2. Post-characterization of the anode proves the structural integrity of NiO(OH)ED even after 12 h of chronoamperometry at 1.595 V (vs reversible hydrogen electrode (RHE)). The NiO(OH)ED/NF can be a compatible anode to construct an overall water splitting (OWS) electrolyzer that can operate at a cell potential of 1.64 V to reach a current density of 10 mA cm-2. Similar to that on NF, NiMoO4 deposited on iron foam (IF) and carbon cloth (CC) also electrochemically converts into NiO(OH) to perform a similar OER activity. This work understandably demonstrates monoclinic NiMoO4 to be an inherently unstable electro(pre)catalyst, and its structural evolution to polycrystalline NiO(OH)ED succeeding the NiO phase is intrinsic to its superior activity.
RESUMEN
In the present era, electrochemical water splitting has been showcased as a reliable solution for alternative and sustainable energy development. The development of a cheap, albeit active, catalyst to split water at a substantial overpotential with long durability is a perdurable challenge. Moreover, understanding the nature of surface-active species under electrochemical conditions remains fundamentally important. A facile hydrothermal approach is herein adapted to prepare covellite (hexagonal) phase CuS nanoplates. In the covellite CuS lattice, copper is present in a mixed-valent state, supported by two different binding energy values (932.10 eV for CuI and 933.65 eV for CuII) found in X-ray photoelectron spectroscopy analysis, and adopted two different geometries, that is, trigonal planar preferably for CuI and tetrahedral preferably for CuII. The as-synthesized covellite CuS behaves as an efficient electro(pre)catalyst for alkaline water oxidation while deposited on a glassy carbon and nickel foam (NF) electrodes. Under cyclic voltammetry cycles, covellite CuS electrochemically and irreversibly oxidized to CuO, indicated by a redox feature at 1.2 V (vs the reversible hydrogen electrode) and an ex situ Raman study. Electrochemically activated covellite CuS to the CuO phase (termed as CuSEA) behaves as a pure copper-based catalyst showing an overpotential (η) of only 349 (±5) mV at a current density of 20 mA cm-2, and the TOF value obtained at η349 (at 349 mV) is 1.1 × 10-3 s-1. A low Rct of 5.90 Ω and a moderate Tafel slope of 82 mV dec-1 confirm the fair activity of the CuSEA catalyst compared to the CuS precatalyst, reference CuO, and other reported copper catalysts. Notably, the CuSEA/NF anode can deliver a constant current of ca. 15 mA cm-2 over a period of 10 h and even a high current density of 100 mA cm-2 for 1 h. Post-oxygen evolution reaction (OER)-chronoamperometric characterization of the anode via several spectroscopic and microscopic tools firmly establishes the formation of crystalline CuO as the active material along with some amorphous Cu(OH)2 via bulk reconstruction of the covellite CuS under electrochemical conditions. Given the promising OER activity, the CuSEA/NF anode can be fabricated as a water electrolyzer, Pt(-)//(+)CuSEA/NF, that delivers a j of 10 mA cm-2 at a cell potential of 1.58 V. The same electrolyzer can further be used for electrochemical transformation of organic feedstocks like ethanol, furfural, and 5-hydroxymethylfurfural to their respective acids. The present study showcases that a highly active CuO/Cu(OH)2 heterostructure can be constructed in situ on NF from the covellite CuS nanoplate, which is not only a superior pure copper-based electrocatalyst active for OER and overall water splitting but also for the electro-oxidation of industrial feedstocks.
RESUMEN
Transition metal-based ABO4-type materials have now been paid significant attention due to their excellent electrochemical activity. However, a detailed study to understand the active species and its electro-evolution pathway is not traditionally performed. Herein, FeAsO4, a bimetallic ABO4-type oxide, has been prepared solvothermally. In-depth microscopic and spectroscopic studies showed that the as-synthesized cocoon-like FeAsO4 microparticles consist of several small individual nanocrystals with a mixture of monoclinic and triclinic phases. While depositing FeAsO4 on three-dimensional nickel foam (NF), it can show oxygen evolution reaction (OER) in a moderate operating potential. During the electrochemical activation of the FeAsO4/NF anode through cyclic voltammetric (CV) cycles prior to the OER study, an exponential increment in the current density (j) was observed. An ex situ Raman study with the electrode along with field emission scanning electron microscopy imaging showed that the pronounced OER activity with increasing number of CV cycles is associated with a rigorous morphological and chemical change, which is followed by [AsO4]3- leaching from FeAsO4. A chronoamperometric study and subsequent spectro- and microscopic analyses of the isolated sample from the electrode show an amorphous γ-FeO(OH) formation at the constant potential condition. The in situ formation of FeO(OH)ED (ED indicates electrochemically derived) shows better activity compared to pristine FeAsO4 and independently prepared FeO(OH). Tafel, impedance spectroscopic study, and determination of electrochemical surface area have inferred that the in situ formed FeO(OH)ED shows better electro-kinetics and possesses higher surface active sites compared to its parent FeAsO4. In this study, the electrochemical activity of FeAsO4 has been correlated with its structural integrity and unravels its electro-activation pathway by characterizing the active species for OER.
RESUMEN
Due to poor conductivity, the electrocatalytic performance of independently prepared iron oxy-hydroxide (FeO(OH)) is inferior whereas FeO(OH) derived in situ from the iron based electro(pre)catalyst shows superior performance in the oxygen evolution reaction (OER). Use of mixed phase FeO(OH) and/or incorporation of CoII/NiII metal into the FeO(OH) structure has also been demonstrated as a convenient approach to achieve high OER activity. Nevertheless, preparation of phase-pure, albeit active FeO(OH) material with fair electrochemical performance remains a perdurable challenge. Moreover, the role of the crystalline phase and its surface structure in controlling the OER activity is still unclear. Herein, a simple synthetic protocol has been developed to prepare a series of phase-pure α-FeO(OH) (goethite) and γ-FeO(OH) (lepidocrocite) materials. By changing the reaction conditions such as iron salt and reaction temperature, the crystallinity as well as the phase of the oxy-hydroxide material have been varied. The isolated α- and γ-FeO(OH) materials with different crystallinity were thereafter deposited on nickel foam (NF) for alkaline OER study. The recorded overpotential value at 10 mA cm-2 has been found to be dependent on the phase and crystallinity of the FeO(OH) materials. The partially crystalline γ-FeO(OH) isolated at room temperature (γ-FeO(OH)@RT) turns out to be the most active with a lowest overpotential of 260 mV at 10 mA cm-2 and a long term stability of 12 h. The γ-FeO(OH)@RT/NF anode can furnish high current densities like 50-100 mA cm-2 which makes this anode distinct from the previously reported FeO(OH) materials. Detailed electrochemical study suggested that the fair activity of the γ-FeO(OH)@RT arises due to a facile electrokinetics as evident from the small Tafel slope and charge transfer resistance (Rct value from the Nyquist plot). Owing to the superior activity of the γ-FeO(OH)@RT/NF, the anode can further be incorporated into an overall water splitting electrolyzer that can operate at a cell potential of 1.68 V. The microscopic characterization provides concrete evidence in support of the polycrystallinity of the γ-FeO(OH)@RT. The superior activity of the γ-FeO(OH)@RT perhaps can be correlated to its polycrystalline nature with more defect edges, the presence of a large exposed surface and random atomic arrangements. The highest degree of multiple surface active terminals (-O, -OH and -Fe) available in this polycrystalline γ-FeO(OH) perhaps makes the catalyst more active compared to the crystalline FeO(OH) analogue with a limited number of surface terminals. From a comparative study with a series of FeO(OH) materials, this work highlights a direct relationship between the surface functionality and the electrochemical activity of the FeO(OH) material.