“…[ 174 ] Some metal phosphides showed good alkaline HER performance, and also good oxidation resistance in both the acidic and alkaline electrolytes owing to relatively strong bonds between the metal and phosphide atoms. [ 173–176 ] Nevertheless, metal phosphides are typically nonlayered materials which increases the materials usage in the catalysis. The full exposure and participation of the surface and edges in the HER render particular advantages of 2D TMDs, although significant modifications of the materials (e.g., doping and hybrid structure) and relating engineering works of the electrode (e.g., 3D electrode) are still required to improve the HER performance.…”
Section: Comparison With Other Her Catalystsmentioning
Tackling global climate change and the energy crisis requires novel approaches in clean energy generation and efficient manufacturing. [1] Hydrogen (H 2 ) is one of the most popular clean energy sources, providing the highest energy outputThe hydrogen evolution reaction (HER) is an emerging key technology to provide clean, renewable energy. Current state-of-the-art catalysts still rely on expensive and rare noble metals, however, the relatively cheap and abundant transition metal dichalcogenides (TMDs) have emerged as exceptionally promising alternatives. Early studies in developing TMD-based catalysts laid the groundwork in understanding the fundamental catalytically active sites of different TMD phases, enabling a toolbox of physical, chemical, and electronic engineering strategies to improve the HER catalytic activity of TMDs. This report focuses on recent progress in improving the catalytic properties of TMDs toward highly efficient production of H 2 . Combining theoretical and experimental considerations, a summary of the progress to date is provided and a pathway forward for viable hydrogen evolution from TMD driven catalysis is concluded.
“…[ 174 ] Some metal phosphides showed good alkaline HER performance, and also good oxidation resistance in both the acidic and alkaline electrolytes owing to relatively strong bonds between the metal and phosphide atoms. [ 173–176 ] Nevertheless, metal phosphides are typically nonlayered materials which increases the materials usage in the catalysis. The full exposure and participation of the surface and edges in the HER render particular advantages of 2D TMDs, although significant modifications of the materials (e.g., doping and hybrid structure) and relating engineering works of the electrode (e.g., 3D electrode) are still required to improve the HER performance.…”
Section: Comparison With Other Her Catalystsmentioning
Tackling global climate change and the energy crisis requires novel approaches in clean energy generation and efficient manufacturing. [1] Hydrogen (H 2 ) is one of the most popular clean energy sources, providing the highest energy outputThe hydrogen evolution reaction (HER) is an emerging key technology to provide clean, renewable energy. Current state-of-the-art catalysts still rely on expensive and rare noble metals, however, the relatively cheap and abundant transition metal dichalcogenides (TMDs) have emerged as exceptionally promising alternatives. Early studies in developing TMD-based catalysts laid the groundwork in understanding the fundamental catalytically active sites of different TMD phases, enabling a toolbox of physical, chemical, and electronic engineering strategies to improve the HER catalytic activity of TMDs. This report focuses on recent progress in improving the catalytic properties of TMDs toward highly efficient production of H 2 . Combining theoretical and experimental considerations, a summary of the progress to date is provided and a pathway forward for viable hydrogen evolution from TMD driven catalysis is concluded.
“…It is pertinent mention here that it is a well-known and reported fact that CO 2 saturation makes the aqueous electrolyte solutions more acidic. It is also well known that hydrogen evolution becomes more prevalent in acidic solutions 19,26,27 Hence, the production of H 2 gas is increased in presence of CO 2 as compared to that in presence of Ar. However, the competitive production H 2 can be suppressed over the certain electro-catalyst surfaces that are less active for hydrogen evolution but highly active for ECR.…”
Herein, we present fabrication of graphene oxide supported Cu/CuxO nano-electrodeposits which efficiently and selectively can electroreduce CO2 into ethylene with a faradaic efficiency of 34% and conversion rate of 194 mmol g−1 h−1 at −0.985 V vs. RHE.
“…It is a gigantic challenge for the research community to produce energy via adapting the green route. , Consequently, all over the world, researchers are regularly working on alternative green energy sources. − In this context, water splitting is an important alternative found to be more efficient toward sustainable energy development and storage. − Electrochemical water splitting is a combination of the oxygen evolution reaction (OER) and the hydrogen evolution reaction (HER), which take place at the anode and cathode, respectively. , Sustainable H 2 production depends upon the sluggish OER process during water splitting. Moreover, it is evident that the anodic OER process is the rate-determining step and it requires a high overpotential in both acidic and alkaline conditions. − Currently, alkaline water electrolysis is the point of interest because hydroxide anions (OH – ) are the major charge carriers in liquid ion-conducting electrolytes. , Hence, the water electrolysis performance and its competency directly depend upon the electrocatalyst used for this purpose. Therefore, OER electrocatalysts must be highly efficient and stable in alkaline medium and oxidative environmental conditions without weathering and dissolution. − …”
Section: Introductionmentioning
confidence: 99%
“…3−5 Electrochemical water splitting is a combination of the oxygen evolution reaction (OER) and the hydrogen evolution reaction (HER), which take place at the anode and cathode, respectively. 5,6 Sustainable H 2 production depends upon the sluggish OER process during water splitting. Moreover, it is evident that the anodic OER process is the rate-determining step and it requires a high overpotential in both acidic and alkaline conditions.…”
The unique atomic arrangement and excellent charge transfer properties of two-dimensional (2D) metal chalcogenides (MX 2 ; M = transition metal, X = S, Se) make them effective electrocatalysts toward water splitting. But, so far, none of them have been able to replace noble-metal catalysts for the oxygen evolution reaction (OER), and it remains a great challenge to develop these catalysts. Specifically, cost-effective and earth-abundant FeS 2 has shown potential, but it is less acknowledged due to the associated weathering process. Here, we report a spin-coated TiO 2 layer on hydrothermally synthesized 2D-FeS 2 nanoplates to control weathering through physical barricading at the nanoscale. Notably, the electrochemical and chemical weathering studies suggest that the TiO 2 layer stabilized FeS 2 oxidation in alkaline solution, while the latter gets oxidized without TiO 2 overlayers. To the best of our knowledge, this would be the first report on an FeS 2 /TiO 2 photoanode for efficient and stable OER without any composite or doping. It displayed improved long-term durability of OER activity. Moreover, the annealed crystalline leaky TiO 2 layer (∼72 nm) remarkably displayed enhanced charge transfer at the FeS 2 /TiO 2 interface. Also, Mott−Schottky measurements confirmed that the leaky TiO 2 served as a protective layer (physical barrier) against the weathering of FeS 2 . The current study may provide new insights into the rational design of low-cost FeS 2 /TiO 2 layered electrocatalysts for OER and renewable energy applications.
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