Fabrication and Characterization of Amorphous Cobalt-Doped Molybdenum Sulfide for Hydrogen Evolution Reaction

2015 ◽  
Vol 15 (10) ◽  
pp. 8257-8262 ◽  
Author(s):  
Dongwook Lim ◽  
Hyein Hwang ◽  
Taewoo Kim ◽  
Sang Eun Shim ◽  
Sung-Hyeon Baeck
Keyword(s):  
Electron Microscopy ◽  
Hydrogen Evolution ◽  
Hydrogen Evolution Reaction ◽  
Photoelectron Spectroscopy ◽  
Water Electrolysis ◽  
Molybdenum Sulfide ◽  
Intrinsic Activity ◽  
Metal Catalyst ◽  
Alkaline Water Electrolysis ◽  
Catalytic Hydrogen Evolution

In the present study, hydrogen evolution reaction (HER) by alkaline water electrolysis was conducted without using a precious metal catalyst. We synthesized an amorphous cobalt-doped molybdenum sulfide by electrodeposition using different cobalt loadings. The amorphous Co-MoSx produced was characterized by scanning electron microscopy, transmission electron microscopy, and X-ray photoelectron spectroscopy. The cobalt doping and sulfidation procedure resulted in the successful fabrication of a candidate catalyst for the catalytic hydrogen evolution in alkaline solution with high intrinsic activity. Cobalt incorporated amorphous MoSx exhibited 3 times higher HER activity than non-promoted MoSx.

scholarly journals Electrochemically Induced In-Situ Generated Co(OH)2 Nanoplates to Promote the Volmer Process Toward Efficient Alkaline Hydrogen Evolution Reaction

2020 ◽  
Author(s):  
Hong Liu ◽  
Jian-Jun Wang ◽  
Li-Wen Jiang ◽  
Yuan Huang ◽  
Bing Bing Chen ◽  
...  
Keyword(s):  
Hydrogen Evolution ◽  
Hydrogen Evolution Reaction ◽  
Active Sites ◽  
Water Electrolysis ◽  
Water Dissociation ◽  
Alkaline Water Electrolysis ◽  
Additional Water ◽  
Dissociation Step ◽  
Insight Into

<p>Hydrogen production via alkaline water electrolysis is of significant interest. However, the additional water dissociation step makes the Volmer step a relatively more sluggish kinetics and consequently leads to a slower reaction rate than that in acidic solution. Herein, we demonstrate an effective strategy that Co(OH)<sub>2</sub> can promote the Volmer process by accelerating water dissociation and enhance the electrocatalytic performance of CoP toward alkaline hydrogen evolution reaction. The Co(OH)<sub>2</sub> nanoplates are electrochemically induced in-situ generated to form a nanotree-like structure with porous CoP nanowires, endowing the hybrid electrocatalyst with superior charge transportation, more exposed active sites, and enhanced reaction kinetics. This strategy may be extended to <a></a><a>other phosphides and chalcogenides </a>and provide insight into the design and fabrication of efficient alkaline HER catalysts.</p>

scholarly journals Amorphous Ni x Co y P-supported TiO2 nanotube arrays as an efficient hydrogen evolution reaction electrocatalyst in acidic solution

2019 ◽  
Vol 10 ◽  
pp. 62-70 ◽  
Author(s):  
Yong Li ◽  
Peng Yang ◽  
Bin Wang ◽  
Zhongqing Liu
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Hydrogen Evolution ◽  
Hydrogen Evolution Reaction ◽  
Photoelectron Spectroscopy ◽  
Electrochemical Impedance ◽  
Nanotube Arrays ◽  
Active Surface Area ◽  
X Ray ◽  
Transmission Electron

Bimetallic phosphides have been attracting increasing attention due to their synergistic effect for improving the hydrogen evolution reaction as compared to monometallic phosphides. In this work, NiCoP modified hybrid electrodes were fabricated by a one-step electrodeposition process with TiO2 nanotube arrays (TNAs) as a carrier. X-ray diffraction, transmission electron microscopy, UV–vis diffuse reflection spectroscopy, X-ray photoelectron spectroscopy and scanning transmission electron microscopy/energy-dispersive X-ray spectroscopy were used to characterize the physiochemical properties of the samples. The electrochemical performance was investigated by cyclic voltammetry, linear sweep voltammetry, and electrochemical impedance spectroscopy. We show that after incorporating Co into Ni–P, the resulting Ni x Co y P/TNAs present enhanced electrocatalytic activity due to the improved electron transfer and increased electrochemically active surface area (ECSA). In 0.5 mol L−1 H2SO4 electrolyte, the Ni x Co y P/TNAs (x = 3.84, y = 0.78) demonstrated an ECSA value of 52.1 mF cm−2, which is 3.8 times that of Ni–P/TNAs (13.7 mF cm−2). In a two-electrode system with a Pt sheet as the anode, the Ni x Co y P/TNAs presented a bath voltage of 1.92 V at 100 mA cm−2, which is an improvment of 79% over that of 1.07 V at 10 mA cm−2.

Hydrothermal Synthesis of Few-Layer and Edge-Rich Cobalt-Doped Molybdenum Selenide/Nitrogenated Graphene Composite and Investigation of Its Electrocatalytic Activity for Hydrogen Evolution Reaction

NANO ◽  
2016 ◽  
Vol 11 (10) ◽  
pp. 1650107 ◽  
Author(s):  
Ming Ou ◽  
Lin Ma ◽  
Limei Xu ◽  
Zhuomei Yang ◽  
Haizhen Li
Keyword(s):  
Electron Microscopy ◽  
Hydrogen Evolution ◽  
Hydrogen Evolution Reaction ◽  
Photoelectron Spectroscopy ◽  
Hydrothermal Route ◽  
X Ray ◽  
Graphene Composite ◽  
Molybdenum Selenide ◽  
Nitrogen Doped Graphene ◽  
Doped Graphene

Cobalt-doped MoSe2/nitrogenated graphene composite has been successfully synthesized via a facile hydrothermal route and is investigated as an electrocatalyst for hydrogen evolution reaction (HER). The as-prepared samples are well characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), high-resolution transmission electron microscopy (HRTEM), X-ray photoelectron spectroscopy (XPS) and Raman spectrum. The results reveal that Co-doped MoSe2 nanosheets which are characteristic of few layers (2–4 layers) and abundant exposed active edge sites are well anchored on the nitrogen-doped graphene sheets to constitute robust composites. When evaluated as catalysts for HER, the obtained composites demonstrate superior electrocatalytic activities toward HER.

scholarly journals MoSe2-GO/rGO Composite Catalyst for Hydrogen Evolution Reaction

Polymers ◽  
2018 ◽  
Vol 10 (12) ◽  
pp. 1309 ◽  
Author(s):  
Wenwu Guo ◽  
Quyet Le ◽  
Amirhossein Hasani ◽  
Tae Lee ◽  
Ho Jang ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Graphene Oxide ◽  
Hydrogen Evolution ◽  
Hydrogen Evolution Reaction ◽  
Photoelectron Spectroscopy ◽  
Transition Metal Dichalcogenides ◽  
Catalytic Performance ◽  
Composite Catalyst ◽  
X Ray ◽  
Molybdenum Selenide

There has been considerable research to engineer composites of transition metal dichalcogenides with other materials to improve their catalytic performance. In this work, we present a modified solution-processed method for the formation of molybdenum selenide (MoSe2) nanosheets and a facile method of structuring composites with graphene oxide (GO) or reduced graphene oxide (rGO) at different ratios to prevent aggregation of the MoSe2 nanosheets and hence improve their electrocatalytic hydrogen evolution reaction performance. The prepared GO, rGO, and MoSe2 nanosheets were characterized by X-ray powder diffraction, Raman spectroscopy, X-ray photoelectron spectroscopy, transmission electron microscopy, energy-dispersive X-ray spectroscopy, and scanning electron microscopy. The electrocatalytic performance results showed that the pure MoSe2 nanosheets exhibited a somewhat high Tafel slope of 80 mV/dec, whereas the MoSe2-GO and MoSe2-rGO composites showed lower Tafel slopes of 57 and 67 mV/dec at ratios of 6:4 and 4:6, respectively. We attribute the improved catalytic effects to the better contact and faster carrier transfer between the edge of MoSe2 and the electrode due to the addition of GO or rGO.

scholarly journals Electrochemically Induced In-Situ Generated Co(OH)2 Nanoplates to Promote the Volmer Process Toward Efficient Alkaline Hydrogen Evolution Reaction

2020 ◽  
Author(s):  
Hong Liu ◽  
Jian-Jun Wang ◽  
Li-Wen Jiang ◽  
Yuan Huang ◽  
Bing Bing Chen ◽  
...  
Keyword(s):  
Hydrogen Evolution ◽  
Hydrogen Evolution Reaction ◽  
Active Sites ◽  
Water Electrolysis ◽  
Water Dissociation ◽  
Alkaline Water Electrolysis ◽  
Additional Water ◽  
Dissociation Step ◽  
Insight Into

<p>Hydrogen production via alkaline water electrolysis is of significant interest. However, the additional water dissociation step makes the Volmer step a relatively more sluggish kinetics and consequently leads to a slower reaction rate than that in acidic solution. Herein, we demonstrate an effective strategy that Co(OH)<sub>2</sub> can promote the Volmer process by accelerating water dissociation and enhance the electrocatalytic performance of CoP toward alkaline hydrogen evolution reaction. The Co(OH)<sub>2</sub> nanoplates are electrochemically induced in-situ generated to form a nanotree-like structure with porous CoP nanowires, endowing the hybrid electrocatalyst with superior charge transportation, more exposed active sites, and enhanced reaction kinetics. This strategy may be extended to <a></a><a>other phosphides and chalcogenides </a>and provide insight into the design and fabrication of efficient alkaline HER catalysts.</p>

Two-Dimensional WS2/g-C3N4 Layered Heterostructures With Enhanced Pseudocapacitive and Electrocatalytic Properties

2020 ◽  
Author(s):  
Oluwafunmilola Ola ◽  
Yanqiu Zhu
Keyword(s):  
Electron Microscopy ◽  
Hydrogen Evolution ◽  
Hydrogen Evolution Reaction ◽  
Photoelectron Spectroscopy ◽  
Carbon Nitride ◽  
Graphitic Carbon ◽  
Hybrid Nanocomposites ◽  
Graphitic Carbon Nitride ◽  
Electrochemical Performances ◽  
X Ray

Abstract In this work, tungsten-based hybrid nanocomposites were grown on interconnected, macroscopic graphitic carbon nitride scaffold after solvothermal treatment followed by sulfidation to attain multifunctional composite electrocatalysts. The physicochemical properties of the obtained samples were characterized by scanning electron microscopy (SEM), transmission electron microscopy (TEM), Raman spectroscopy, X-ray diffraction (XRD) and X-ray photoelectron spectroscopy (XPS). The tungsten-based composites were tested as electrodes for pseudocapacitors and as electrocatalysts for hydrogen evolution reaction, to take advantage of their porous graphitic carbon nitride features which would be beneficial for optimal ion transport to tungsten-based nanoparticles. These unique physicochemical features endow these composites with excellent electrochemical performances to reach a current density of 10 mA/cm2 for the hydrogen evolution reaction. In addition to demonstrating excellent specific capacitance, these hybrid nanocomposites also possess good stability after 8 hours of testing.

Sacrificial Species Approach to Designing Robust Transition Metal Phosphide Cathodes for Alkaline Water Electrolysis in Discontinuous Operation

2021 ◽  
Author(s):  
Ik-Sun Kim ◽  
Hyun-Seok Cho ◽  
MinJoong Kim ◽  
Hyung-Jung Oh ◽  
Sang-Yeon Lee ◽  
...  
Keyword(s):  
Transition Metal ◽  
Hydrogen Evolution ◽  
Hydrogen Evolution Reaction ◽  
Water Electrolysis ◽  
Alkaline Water Electrolysis ◽  
Metal Phosphide ◽  
Alkaline Water ◽  
Electrolysis Cells ◽  
Transition Metal Phosphide

The degradation of amorphous cobalt phosphides (CoPx) as electrocatalyst for hydrogen evolution reaction (HER) is studied in the discontinuous operation of alkaline water electrolysis cells (AWEs). Although amorphous CoPx shows...

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