Electrocatalyst For Oxidation Research Articles

Ag–Ru interface for highly efficient hydrazine assisted water electrolysis

Ru decorated Ag nanoparticles are designed as highly effective bifunctional electrocatalysts for hydrazine oxidation and hydrogen evolution reactions, enabling a hydrazine assisted water electrolyser with greatly increased current density.

High-entropy layered hydroxide for efficient and sustainable seawater oxidation

High-entropy NiCrCoFeMo layered hydroxide has been identified as a potential electrocatalyst for sustainable seawater oxidation with high activity and great corrosion resistance ability.

CuO-Ni(OH)2 heterostructure nanosheets: a high-performance electrocatalyst for 5-hydroxymethylfurfural oxidation.

CuO-Ni(OH)2 heterostructure nanosheets were designed for efficient electrocatalytic oxidation of 5-hydroxymethylfurfural (HMF) to 2,5-furanedioic acid (FDCA). The CuO-Ni(OH)2 nanosheets exhibited impressive performance, achieving 100% HMF conversion, 99.8% FDCA yield, and 98.4% faradaic efficiency.

Scalable production of bifunctional ordered PtFe alloy electrocatalysts for efficient methanol oxidation and hydrogen evolution

Sub-5 nm sized ordered PtFe alloys encapsulated with thin N-doped carbon (NC) shells exhibit remarkable electrochemical performance both toward methanol oxidation and hydrogen evolution reactions.

Investigation of electrocatalytic oxygen evolution reaction (OER) selectivity against methanol oxidation on stainless steel

Stainless steel (SS) is a cost-effective, stable, and sustainable electrocatalyst for water oxidation.

Electrifying oxidation of ethylene and propylene.

Ethylene and propylene, as essential precursors in the chemical industry, have been playing a pivotal role in the production of various value-added chemicals that find wide applications in diverse sectors, such as polymer synthesis, lithium-ion battery electrolytes, antifreeze agents and pharmaceuticals. Nevertheless, traditional methods for olefin functionalization including chlorohydrination and epoxidation involve energy-intensive steps and environment-detrimental by-products. In contrast, electrocatalysis is emerging as a promising and sustainable approach for olefin oxidation via utilizing renewable electricity. Recent advancements in energy storage and conversion technologies have intensified the research efforts toward designing efficient electrocatalysts for the selective oxidation of ethylene and propylene, highlighting the shift towards more sustainable production methods. Herein, we summarize recent progress in the electrocatalytic oxidation of ethylene and propylene, focusing on achievement in catalyst design, reaction system selection and mechanism exploration. We figure out the advantages of different oxidation methods for improved performance and discuss the various types of catalysts like noble metals, non-noble metals, metal oxides and carbon-based materials, in facilitating the electrochemical oxidation of ethylene and propylene. Finally, we also provide an overview of current challenges and problems requiring further works.

Soluble Gd6Cu24 clusters: effective molecular electrocatalysts for water oxidation.

The water oxidation half reaction in water splitting for hydrogen production is extremely rate-limiting. This study reports the synthesis of two heterometallic clusters (Gd6Cu24-IM and Gd6Cu24-AC) for application as efficient water oxidation catalysts. Interestingly, the maximum turnover frequency of Gd6Cu24-IM in an NaAc solution of a weak acid (pH 6) was 319 s-1. The trimetallic catalytic site, H2O-GdIIICuII2-H2O, underwent two consecutive two-electron two-proton coupled transfer processes to form high-valent GdIII-O-O-CuIII2 intermediates. Furthermore, the O-O bond was formed via intramolecular interactions between the CuIII and GdIII centers. The results of this study revealed that synergistic catalytic water oxidation between polymetallic sites can be an effective strategy for regulating O-O bond formation.

2D petal-like PdAg nanosheets promote efficient electrocatalytic oxidation of ethanol and methanol.

The development of efficient alcohol electrooxidation catalysts is of vital importance for the commercialization of direct liquid fuel cells. As emerging advanced catalysts, two-dimensional (2D) noble metal nanomaterials have attracted much research attention due to their intrinsic structural advantages. Herein, we report the synthesis of petal-like PdAg nanosheets (NSs) with an ultrathin 2D structure and jagged edges via a facile wet-chemical approach, combining doping engineering and morphology tuning. Notably, the highly active sites and Pd-Ag composition endowed PdAg NSs with improved toxicity tolerance and substantially improved the durability toward the ethanol/methanol oxidation reaction (EOR/MOR). Moreover, the electronic effect and synergistic effect significantly enhanced the EOR and MOR activities in comparison with Pd NSs and commercial Pd/C. This work provides efficient catalysts for fuel electrooxidations and deep insight into the rational design and fabrication of novel 2D nanoarchitecture.

Robust Nanoporous NiMn oxide Electrocatalysts for Oxygen Evolution Reaction through Defect Engineering

The sluggish oxygen evolution reaction (OER) remains a major bottleneck in hydrogen generation through electrolysis, particularly at large current operations. Thus, there is a huge interest in the development of...

Decrypting the hydrogen evolution in alkaline water with novel magnetoactive cobalt(II) complex-driven cobalt oxide electrocatalysts.

Under the gravity of future socio-economic development, the viability of water electrolysis still hinges on the accessibility of stable earth-abundant electrocatalysts and net energy efficiency. This work emphasizes the design and synthesis of two newly developed cobalt(II) complexes, [Co(HL)2(NCS)2] (Comono) and [Co2(L)3(CH3OH)]ClO4 (Codi), with a (N,O)-donor ligand, HL (2-methoxy-6-(((2-methoxyphenyl)imino)methyl)phenol). The study delves into understanding their structural, morphological, magnetic, and charge transport characteristics. Moreover, the study explores the potential of these complexes in catalyzing hydrogen production through heterogeneous electrocatalysis. The X-ray crystal structure of Comono reveals the octahedral geometry of the Co(II) ion, adopting two HL units and two NCS- units. The Codi complex exhibits a doubly-phenoxo-O-bridged (μ1,1) dinuclear complex, forming a typical octahedral geometry for both the Co(II) centres in coupling with three units of L-. Temperature-dependent magnetic susceptibility measurements showed that all of the Co(II) ion in Comono shows a typical paramagnetic behaviour for high spin octahedral Co(II) ions while the Co(II) centres in Codi are coupled with doubly-phenoxo-bridges bearing weak ferromagnetic characteristics at low temperature. Electron transport properties of the Co(II) complex-mediated Schottky device address the superior carrier mobility (μ) for Codi (9.21 × 10-5) over Comono (2.02 × 10-5 m2 v-1 s-1) with respective transit times of 1.70 × 10-9 and 7.77 × 10-9 s. Additionally, electron impedance spectral analysis supports the lower electrical transport resistance of Codi relative to Comono. The heterogeneous electrocatalytic HER activity of Codi and Comono in 0.1 M KOH shows excellent electrocatalytic efficiency in terms of the various electrochemical parameters. Constant potential electrolysis, multi-cycle CVs, and post-HER analysis reveal the pre-catalytic nature of the complexes, which in turn delivers Co3O4 nanoparticles as the active catalysts for efficient hydrogen evolution.

Recent advances in ambient electrochemical methane conversion to oxygenates using metal oxide electrocatalysts

In this review, the recent developments in the electrocatalytic conversion of methane under ambient conditions, with focus on metal oxide catalysts, are examined. The commonly employed strategies are systematically reviewed.

Universal synthesis strategy for preparation of transition metal oxide electrocatalysts doped with noble metal single atoms for oxygen evolution reaction

A universal salt-template method for the preparation of various noble metals-doped 3d-transition metal oxides electrocatalysts was developed.

NiSe2/CeO2 catalysts from Ce-UiO-66 metal-organic skeletons and their electrocatalytic oxidation of methanol, urea and glycerol.

Hydrogen is a viable alternative energy source to fossil fuels. In order to manufacture enough hydrogen to meet the needs of social growth, finding an alternate energy source that is more effective is essential. Electrochemical water cracking is a more appropriate method for producing hydrogen. The methanol oxidation reaction (MOR), urea oxidation reaction (UOR) and glycerol oxidation reaction (GOR) can be used to replace the anodic oxygen evolution reaction (OER) and indirectly accelerate the hydrogen evolution reaction (HER), which has the advantages of saving energy and reducing environmental pollution. In this study, Ni/CeO2 catalysts were prepared by thermal annealing of MOFs (Ce-UiO-66) containing nickel species and NiSe2/CeO2 nanocrystalline catalysts were obtained through the selenation reaction at different temperatures. The NiSe2/CeO2-450 °C catalysts exhibited superior catalytic performance for the MOR, UOR, and GOR. The MOR showed a peak current density of roughly 186.68 mA cm-2 and a low oxidation potential of around 1.34 V. Similarly, the UOR demonstrated a peak current density of approximately 142.28 mA cm-2 and a low oxidation potential of around 1.32 V. Furthermore, the GOR exhibited a peak current density of approximately 82.56 mA cm-2 and a low oxidation potential of around 1.37 V. NiSe2/CeO2-450 °C could improve electrocatalytic performance for the MOR, UOR, and GOR, which is attributed to the more active sites that were exposed as a result of utilizing MOFs (Ce-UiO-66) as a precursor. Additionally, selenation increased the ability to transfer electrons. This research is crucial for the production of inexpensive, easily accessible transition metals in place of expensive noble metals, for the reduction of wastewater pollution from methanol and urea, and for the creation of effective anodic oxidation electrocatalysts.

Research progress on layered metal oxide electrocatalysts for an efficient oxygen evolution reaction.

Hydrogen, highly valued for its pristine cleanliness and remarkable efficiency as an emerging energy source, is anticipated to ascend to a preeminent status within the forthcoming energy landscape. Electrocatalytic water splitting is considered a pivotal, eco-friendly, and sustainable strategy for hydrogen production. The substantial energy consumption stemming from oxygen evolution side reactions significantly impedes the commercial viability of water electrolysis. Consequently, the pursuit of a cost-effective and efficacious oxygen evolution reaction (OER) catalyst stands as an imperative strategy for realizing hydrogen production via water electrolysis. Layered metal oxides, owing to their robust anisotropic properties, versatile adjustability, and extensive surface area, have emerged as suitable candidates for OER catalysts. However, owing to the distinctive attributes of layered metal oxides, ongoing investigations into these materials are slightly fragmented, lacking universal consensus. This article comprehensively surveys the recent advancements in layered metal oxide-based OER catalysts, categorized into single metal oxides, alkali cobalt oxides, perovskites, and miscellaneous metal oxides. Initially, the main OER intermediate reaction steps of layered metal oxides are scrutinized. Subsequently, the design, mechanism, and application of several pivotal layered metal oxides in the OER are systematically delineated. Finally, a summary is provided, alongside the proposal of future research trajectories and challenges encountered by layered metal oxides, with the aspiration that this paper may serve as a valuable reference for scholars in the field.

P-incorporated CuO/Cu2S heteronanorods as efficient electrocatalysts for the glucose oxidation reaction toward highly sensitive and selective glucose sensing.

Currently, tremendous efforts have been made to explore efficient glucose oxidation electrocatalysts for enzymeless glucose sensors to meet the urgent demands for accurate and fast detection of glucose in the fields of health care and environmental monitoring. In this work, an advanced nanostructured material based on the well-aligned CuO/Cu2S heteronanorods incorporated with P atoms is successfully synthesized on a copper substrate. The as-synthesized material shows high catalytic behavior accompanied by outstanding electrical conductivity. This, combined with the unique morphology of unstacked nanorod arrays, which endow the entire material with a greater number of exposed active sites, make the proposed material act as a highly efficient electrocatalyst for the glucose oxidation reaction. Density functional theory calculations demonstrate that P doping endows P-doped CuO/Cu2S with excellent electrical conductivity and glucose adsorption capability, significantly improving its catalytic performance. As a result, a non-enzymatic glucose sensor fabricated based on our proposed material exhibits a broad linear detection range (0.02-8.2 mM) and a low detection limit (0.95 μM) with a high sensitivity of 2.68 mA mM-1 cm-2 and excellent selectivity.

The mechanism of water oxidation using transition metal-based heterogeneous electrocatalysts.

The water oxidation reaction, a crucial process for solar energy conversion, has garnered significant research attention. Achieving efficient energy conversion requires the development of cost-effective and durable water oxidation catalysts. To design effective catalysts, it is essential to have a fundamental understanding of the reaction mechanisms. This review presents a comprehensive overview of recent advancements in the understanding of the mechanisms of water oxidation using transition metal-based heterogeneous electrocatalysts, including Mn, Fe, Co, Ni, and Cu-based catalysts. It highlights the catalytic mechanisms of different transition metals and emphasizes the importance of monitoring of key intermediates to explore the reaction pathway. In addition, advanced techniques for physical characterization of water oxidation intermediates are also introduced, for the purpose of providing information for establishing reliable methodologies in water oxidation research. The study of transition metal-based water oxidation electrocatalysts is instrumental in providing novel insights into understanding both natural and artificial energy conversion processes.

Hydrogen oxidation electrocatalysts for anion-exchange membrane fuel cells: activity descriptors, stability regulation, and perspectives

The general principles in terms of reactivity and stability to design efficient electrocatalysts for the alkaline hydrogen oxidation reaction are reviewed. The performance of catalysts in anion-exchange membrane fuel cells is further discussed.

Electronic Structure Effect of PtCo Alloy with Adjustable Compositions for Efficient Methanol Electrooxidation.

Various efficient strategies have been developed to overcome the anodic electrocatalyst issue of methanol-based fuel cells owing to their complicated methanol electrooxidation mechanism. In this work, PtCo nanoparticles with adjustable compositions supported on multiwalled carbon nanotubes (Pt1Cox/MWCNTs) through the adsorbing-coating-annealing-etching route were synthesized. Compared with the Pt/C catalyst, Pt1Co3/MWCNTs exhibit better electrocatalytic MOR activity in both activity and durability. Notably, the electrochemical mass and specific activity of the as-prepared catalyst are 1.04 mA μg-1Pt and 2.18 mA cm-2, respectively, which are higher than those of the Pt/C catalyst. Moreover, the as-prepared sample revealed lower onset potential during the CO stripping test. Furthermore, the Pt1Co3/MWCNTs possess a lower current density decrease rate in chronoamperometry and cyclic durability tests. The enhancement of activity and stability of Pt1Co3/MWCNTs could be ascribed to their ordered morphological structure, the electronic interaction between MWCNTs and PtCo nanoparticles, and the suitable electronic structure effect between Pt/Co ratios. The concept of the catalyst design in this study offers a different guideline for constructing the novel methanol electrooxidation catalyst, which will accelerate the widespread fuel cell practical application.

CuTe supported on graphitic carbon nitride nanocomposite as an effective electrocatalyst for oxidation of water in basic media

For the purpose of using water electrolysis to yield hydrogen and to solve this issue of energy shortage, the highly active electrocatalysts for water (H2O) oxidation must be developed. For this purpose, the potential of copper-based nanomaterials electrocatalysts are completely investigated due to its good conductivity. In this study, we account the hydrothermal synthesis of novel hierarchical CuTe-gCN nanocomposite, and numerous characterization techniques are utilized to check the crystal structure, morphology, textual properties and oxidation states as well. On the other hand, the electrocatalytic performance and durability for OER in basic conditions are confirmed by different electrochemical testing. Furthermore, among all the CuTe-gCN nano-catalyst have exceptional electrocatalytic performance, like, a less overpotential around 277 mV, that is less than 312 and 326 mV for CuTe and gCN, respectively to get a current density (Cd) around 10 mAcm−2. On the other hand, it is also showing results almost similar to RuO2 having overpotential of 269 mV as well. In addition, the as prepared CuTe-gCN nanohybrid shows an impressively smaller Tafel value of 53 mVdec-1 to show the fast electron transfer process. Hence, the remarkable results are because of large surface area, accessible mesoporous structure, the remarkable electrical conductivity of gCN shows synergistic effect with CuTe was responsible for high catalytic performance, and may be useful for many other applications in future.

Investigation of the performance of (4-(3-iodobenzo[b]thiophen-2-yl)-N,N-dimethyllaniline as an anode catalyst for glucose electrooxidation

In this study (4-(3-iodobenzo[b]thiophen-2-yl)-N,N-dimethyllaniline (4), Sonagashira Coupling Reaction was synthesized using Electrophilic Cyclization Reactions. Then, the anode catalyst performance for glucose electrooxidation was investigated. The electrocatalytic activities of the organic catalyst were investigated by CV, CA and EIS measurements in 1 M KOH + 0.5 M C6H12O6 solution. Interestingly, electrochemical depositing on organic catalyst by Pd metal increased the specific activity, and it was calculated as 0.61 mA/cm2 Consequently, Pd@4 catalyst will be used as an electrocatalyst with high specific and stability and low charge transfer activity.