Search

Figure S 1. SEM images of (a) CoFe/NC10% , (b) CoFe/NC20% , and (c) CoFe/NC40%. Figure S 2.TEM images of (a) CoFe/NC10% , (b) CoFe/NC20% , and (c) CoFe/NC40%. Figure S 3. Particle size distribution of the various electrocatalyst: (a) CoFe2O4, (b) CoFe/NC10% , (c) CoFe/NC20% ,(d) CoFe/NC30% , and (e) CoFe/NC40% . Table S 1. Amount of CoFe alloys and oxides in the composite samples, determined from the XRD analysis. Figure S 4. XPS high resolution spectra of (a) Fe 2p, (b) Co 2p, for all electrocatalysts. Table S 2. XPS analysis results of the electrocatalysts. Table S 3. Elemental composition of the prepared electrocatalysts. Table S 4. Specific capacitance and ECSA values for the various eletrocataysts. Table S 5. Charge transfer resistance (Rct) and solution resistance (Rs) determined from EIS measurement. Figure S 5. ECSA-normalized polarization curve.

Designing and developing affordable, high-performance, and stable electrocatalysts for oxygen evolution reaction (OER) is decisive for pragmatic water electrolysis to produce green hydrogen energy. In this work, we report cobalt and iron incorporated in phosphorus and nitrogen co-doped carbon foam (CF) derived from petroleum pitch as a promising electrocatalyst for alkaline OER. The P, N heteroatoms co-doped carbon foam (PN-CF) was first synthesized via thermo-chemical treatment of low-cost petroleum pitch in the presence of melamine (N source) and sodium hypophosphite (P source) precursors, followed by carbonization. Then, mono and bimetals of Co and Fe were impregnated into the as-prepared composite carbon foam (PN-CF) substrate, followed by further carbonization. Among the different catalysts, the bimetallic CoFe integrated with the PN-CF (CoFe@PN-CF) reveals an outstanding electrocatalytic activity (320 mV overpotential at j = 10 mA·cm-2), low Tafel slope (48 mV·dec-1), and excellent durability during OER measurement in 1 M KOH aqueous solution. The superb performance of the CoFe@PN-CF catalyst stems from the synergetic effect of the bimetals confined on phosphorus and nitrogen co-doped carbon foam support with high specific surface area, highly porous structure, and formation of graphitic domains, which enhances the electrical conductivity. This work sheds light on the potential for valorizing petroleum pitch and provides a facile synthesis approach to synthesizing a low-cost, high-performance, and durable electrocatalyst for alkaline OER.

Electrochemical water splitting is an environmentally benign technology employed for H2 production; however, it is critically hampered by the sluggish kinetics of the oxygen evolution reaction (OER) at the positive electrode. In this work, nitrogen-doped carbon-coated CoFe electrocatalysts were synthesized via a three-step route comprising (1) hydrothermal reaction, (2) in-situ polymerization of dopamine and (3) carbonization. The effect of carbonized polydopamine on the overall physicochemical properties and electrochemical activity of CoFe catalysts was systematically studied. By controlling and optimizing the ratio of CoFe2O4 and dopamine contents, a transformation of the CoFe2O4 structure to CoFe alloy was observed. It was found that CoFe/NC30% (prepared with 30% dopamine) exhibits an excellent catalytic activity towards OER. A small overpotential of 340 mV was required to generate a current density of 10 mA cm-2 in a 1.0 M KOH electrolyte. More importantly, the CoFe/NC30% catalyst reflected exceptional durability for at least 24 h. This research sheds light on the development of affordable, highly efficient, and durable electrocatalysts for OER.

High performance, durable and affordable electrocatalyst for Oxygen Evolution Reaction (OER) is of great importance for tenable hydrogen production via water electrolysis. Although spinel oxide-based electrocatalysts (AB2O4, A, B = metal) represent a class of promising candidates for OER, their intrinsically poor electrical conductivity impacts their electrochemical performance. To overcome these bottlenecks, heteroatom-doped carbon structures can be used to improve the conductivity, adjust the electronic structure, durability and also boost the charge transfer, leading to enhanced electrochemical water oxidation [1]. In this work, a selection of nitrogen doped carbon decorated NiFe2O4 composites derived of polydopamine for OER in alkaline medium have been investigated.

High performance, durable and inexpensive electrocatalyst for oxygen evolution reaction (OER) is of great importance for tenable hydrogen production via water electrolysis. Although spinel oxides (AB2O4, A, B = metal) represent a class of promising candidates for OER, their intrinsically poor electrical conductivity impacts their electrochemical performance. Herein, we employed a facile approach to transform an intrinsically low active NiFe2O4 into nitrogen-doped carbon decorated Ni3Fe@Fe3O4 catalyst with improved activity and stability for alkaline OER. Initially, a pristine NiFe2O4 octahedron-like structure was synthesized by a hydrothermal route. Then, series electrocatalysts were prepared by incorporating the pristine NiFe2O4 with different dopamine concentrations via in-situ polymerizations of dopamine followed by carbonization. The morphology, crystalline structure, and chemical composition of the catalysts were characterized by scanning electron microscopy (SEM), transmission electron microscopy (TEM), X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), and inductively coupled plasma (ICP). The OER electrocatalysis performance was measured in a standard three-electrode system. The effect of the carbonized dopamine on the electrocatalytic activity and structure of the NiFe2O4 precursor was systematically investigated. Among several NiFe electrocatalysts, the one with 10 wt% of dopamine (NiFe/NC10%) exhibited a relatively higher catalytic activity for OER tested in 1.0 M KOH; unveiled low overpotential (350 mV at 10 mAcm−2 current density), a low Tafel slope (56 mVdec−1), low charge transfer resistance, relatively higher electrochemically active surface area. Most prominently, it remained stable for at least 12 h. This work provides a new perspective for functionalizing metal oxides and affords a facile synthesis approach, low-cost, high-performance, and robust electrocatalyst for alkaline OER electrodes.

The stainless steel mesh (SSM) has received remarkable attention for hydrogen and oxygen evolution reactions. It was demonstrated that the SSM exhibits admirable performance towards oxygen evolution reaction (OER) electrocatalysis, while its catalytic activity for hydrogen evolution reaction (HER) remains quite low. This obstructs the utilization of SSM-based catalysts for sustainable complete water electrolysis. In this study, a facile hydrothermal route followed by a phosphorization process was adopted to transform commercially available SSM materials into high-performance and stable electrocatalysts for alkaline HER. We report an interconnected NiCoP-CoP sponge-like structure on SSM substrate without polymer binder. Benefiting from the 3D construction with high exposed surface area, close contact between electroactive species and conductive surface, and facilitated infiltration of electrolyte, the as-prepared NiCoP@SSM electrocatalyst brought an improved catalytic activity for HER, required a low overpotential of 138 mV to derive a current density of 10 mAcm−2 in 1.0 M KOH aqueous solution. The high performance of the NiCoP@SSM catalyst has also unveiled fast reaction kinetics (presents a small Tafel slope of 74 mV/dec), a relatively large electrochemical active surface area (ECSA), and small charge transfer resistance. Furthermore, the NiCoP@SSM electrode also presented excellent stability during long-term measurements, making it one of the most encouraging HER electrodes to date. This research study paves the way for the development of HER-active electrocatalysts made from SSMs that are commercially available, low-cost, and highly active.

The deployment of hydrogen as an energy carrier is found to be a vital alternative fuel for the future. It is expected that water electrolysis, powered by renewable energy sources, be able to scale‐up hydrogen production. However, the reaction kinetic of oxygen evolution reaction (OER) is a sluggish process, which predominantly limits the efficiency of water electrolysis. This review recapitulates the recent progress and efforts made in the design and development of two selected earth-abundant bimetallic electrocatalysts (NiCo and CoFe) for alkaline OER. Each bimetal electrocatalyst is thoroughly outlined and discussed in five sub-sections, including bimetal (oxy) hydroxides, Layered double hydroxides (LDHs) structures, oxides, composites, alloy and nanostructured electrocatalysts, and assembled with heteroatoms. Furthermore, a brief introduction to an in situ/operando characterization techniques and advantages for monitoring the structure of the electrocatalysts is provided. Finally, a summary outlining the challenges and conceivable approaches to advance OER performance is highlighted and discussed.

Ethiopia is one of the fastest-growing economies in the world despite immense challenges towards access to sustainable energy supplies and modern energy technologies. The country is undertaking great effort towards the development of renewable energy technologies and green legacy. However, the largest share of energy consumption (≈87%) in Ethiopia is dominated by traditional fuels (charcoal, fuel wood, dung cakes, and agricultural residues) which pose various health and environmental risks. The country has an enormous amount of renewable energy potentials (e.g., solar, hydro, wind and geothermal), but only 5% of its full hydropower potential is exploited and others are not fully harvested or not well developed to date. This review paper provides a comprehensive assessment on renewable energy availability, potential, opportunity, and challenges in Ethiopia. We believe the information provided in this review will enlighten the current and future prospects of renewable energy deployment in Ethiopia.