Electrochemically Fabricated NiW on a Cu Nanowire as a Highly Porous Non-Precious-Metal Cathode Catalyst for a Proton Exchange Membrane Water Electrolyzer
Abstract:A hierarchical Ni
x
W100–x
/Cu nanowire (NW)
catalyst for the acidic hydrogen evolution reaction was electrochemically
fabricated on carbon paper (CP) for practical applications of a proton
exchange membrane water electrolyzer (PEMWE). The Ni and W contents
in the catalysts were controlled by adjusting the concentration of
Ni and W precursors during electrodeposition. The as-prepared catalyst
had an amorphous structure due to the addition of W. The activities
of Ni
x
W100–x
/Cu NW/CP catalysts were evaluated f… Show more
“…Therefore, welldefined nanostructure fabrication has garnered much attention recently. [4][5][6][7][8] Although different solution-based metal nanoparticle syntheses and their assemblies have been developed successfully and used in diverse applications, the fabrication process requires multiple steps and/or linker molecules. [9] These linker molecules and capping agents for the preparation of nanostructure could potentially affect the surface morphology and electroanalytical activities.…”
Section: Introductionmentioning
confidence: 99%
“…The fabrication process can control the shapes and sizes of metal nanostructures, which provide unique physical and chemical properties. Therefore, well‐defined nanostructure fabrication has garnered much attention recently [4–8] . Although different solution‐based metal nanoparticle syntheses and their assemblies have been developed successfully and used in diverse applications, the fabrication process requires multiple steps and/or linker molecules [9] .…”
Christmas-tree-shaped Pd nanostructures were synthesized using a simple one-step electrodeposition method with no additives on a glassy carbon electrode (GCE) surface. Growth of the hierarchical nanostructures was optimized through the applied potential, deposition time, and precursor concentration. Comprehensive characterization techniques such as scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDX), X-ray photoelectron spectroscopy (XPS), Xray powder diffraction (XRD), and cyclic voltammetry (CV) were used to characterize structural features of the Christmas-treeshaped Pd nanostructures. Our Christmas-tree-shaped Pd nanostructures showed excellent catalytic activity for ascorbic acid (AA) electro-oxidation in the alkaline condition. The modified electrode exhibited current density of 4.5 mA cm À 2 : much higher than that of unmodified GCE (0.6 mA cm À 2 ). This simple electrodeposition technique with well-defined hierarchical Pd nanostructures is expected to offer new perspectives using Pdbased nanostructured surfaces in different research areas.
“…Therefore, welldefined nanostructure fabrication has garnered much attention recently. [4][5][6][7][8] Although different solution-based metal nanoparticle syntheses and their assemblies have been developed successfully and used in diverse applications, the fabrication process requires multiple steps and/or linker molecules. [9] These linker molecules and capping agents for the preparation of nanostructure could potentially affect the surface morphology and electroanalytical activities.…”
Section: Introductionmentioning
confidence: 99%
“…The fabrication process can control the shapes and sizes of metal nanostructures, which provide unique physical and chemical properties. Therefore, well‐defined nanostructure fabrication has garnered much attention recently [4–8] . Although different solution‐based metal nanoparticle syntheses and their assemblies have been developed successfully and used in diverse applications, the fabrication process requires multiple steps and/or linker molecules [9] .…”
Christmas-tree-shaped Pd nanostructures were synthesized using a simple one-step electrodeposition method with no additives on a glassy carbon electrode (GCE) surface. Growth of the hierarchical nanostructures was optimized through the applied potential, deposition time, and precursor concentration. Comprehensive characterization techniques such as scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDX), X-ray photoelectron spectroscopy (XPS), Xray powder diffraction (XRD), and cyclic voltammetry (CV) were used to characterize structural features of the Christmas-treeshaped Pd nanostructures. Our Christmas-tree-shaped Pd nanostructures showed excellent catalytic activity for ascorbic acid (AA) electro-oxidation in the alkaline condition. The modified electrode exhibited current density of 4.5 mA cm À 2 : much higher than that of unmodified GCE (0.6 mA cm À 2 ). This simple electrodeposition technique with well-defined hierarchical Pd nanostructures is expected to offer new perspectives using Pdbased nanostructured surfaces in different research areas.
“…For hydrogen production in PEMWEs, platinum group metals (PGMs) have been commonly used as the cathode catalyst owing to their high corrosion resistance and superior catalytic activity . However, to reduce the cost of catalysts, alloy or compound catalysts based on non‐noble metals (Ni, Co, Mo, W, Cu, etc) have been extensively studied as potential substitutes . Among non‐noble‐metal‐based catalysts, Co‐based catalysts, which are well known to have relatively high catalytic activities for the hydrogen evolution reaction (HER), are expected to replace PGM‐based catalysts .…”
Section: Introductionmentioning
confidence: 99%
“…[22][23][24][25][26][27][28][29] However, to reduce the cost of catalysts, alloy or compound catalysts based on non-noble metals (Ni, Co, Mo, W, Cu, etc) have been extensively studied as potential substitutes. [30][31][32][33][34][35][36][37] Among non-noble-metal-based catalysts, Co-based catalysts, which are well known to have relatively high catalytic activities for the hydrogen evolution reaction (HER), are expected to replace PGM-based catalysts. 32,38,39 However, the catalytic activity of Co is significantly lower than that of Pt; furthermore, Co could dissolve in acidic solution because its standard reduction potential is −0.277 V vs the normal hydrogen electrode (NHE), resulting in poor durability.…”
Summary
To realize nonprecious‐metal catalysts with practical applicability for the hydrogen evolution reaction (HER), improved corrosion resistance and catalytic activity are required. In this study, composition‐controlled Co‐Cu alloys were fabricated by electrodeposition for use as HER catalysts in proton exchange membrane water electrolyzers (PEMWEs). As the Cu content in the alloy increased, the morphology changed from needle‐shaped particles to small round particles. Furthermore, a phase transition from a hexagonal close‐packed structure to a face‐centered cubic structure occurs because the latter structure is stabilized by adding Cu to Co. The optimum catalyst composition for the HER was found to be Co59Cu41, which had an overpotential of 342 mV at −10 mA cm−2. This catalyst exhibited excellent durability, showing a potential reduction of approximately 100 mV over 12 hours under a constant current density. This superior performance was attributed to the increase in the electrochemical surface area resulting from the addition of Cu, as confirmed by electrochemical double layer capacitance measurements, in addition to a counterbalance between the hydrogen adsorption energies of Co and Cu. Finally, the application of the Co‐Cu alloy catalyst as a cathode catalyst in a PEMWE resulted in excellent performance of 1.2 A cm−2 at 2.0 Vcell.
“…For the water cycle, the transformation of renewable electricity into chemical energy in the form of covalent bonds of H 2 and O 2 via water electrolyzers largely depends on the OER at the anode. [ 24–26 ] The ORR is crucial for the subsequent electricity generation and H 2 O production via PEMFCs. [ 10,27,28 ] For the nitrogen cycle, NRR and AOR catalytic processes relate to the breaking and forming of NN bonds, [ 29 ] respectively, ideal for electrochemical ammonia (NH 3 ) synthesis from N 2 and DAFCs via utilizing NH 3 as a carbon‐free fuel.…”
Clean and efficient energy storage and conversion via sustainable water and nitrogen reactions have attracted substantial attention to address the energy and environmental issues due to the overwhelming use of fossil fuels. These electrochemical reactions are crucial for desirable clean energy technologies, including advanced water electrolyzers, hydrogen fuel cells, and ammonia electrosynthesis and utilization. Their sluggish reaction kinetics lead to inefficient energy conversion. Innovative electrocatalysis, i.e., catalysis at the interface between the electrode and electrolyte to facilitate charge transfer and mass transport, plays a vital role in boosting energy conversion efficiency and providing sufficient performance and durability for these energy technologies. Herein, a comprehensive review on recent progress, achievements, and remaining challenges for these electrocatalysis processes related to water (i.e., oxygen evolution reaction, OER, and oxygen reduction reaction, ORR) and nitrogen (i.e., nitrogen reduction reaction, NRR, for ammonia synthesis and ammonia oxidation reaction, AOR, for energy utilization) is provided. Catalysts, electrolytes, and interfaces between the two within electrodes for these electrocatalysis processes are discussed. The primary emphasis is device performance of OER‐related proton exchange membrane (PEM) electrolyzers, ORR‐related PEM fuel cells, NRR‐driven ammonia electrosynthesis from water and nitrogen, and AOR‐related direct ammonia fuel cells.
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