scholarly journals Targeted Assembly of Ultrathin NiO/MoS2 Electrodes for Electrocatalytic Hydrogen Evolution in Alkaline Electrolyte

Nanomaterials ◽  
2020 ◽  
Vol 10 (8) ◽  
pp. 1547
Author(s):  
Kai Xia ◽  
Meiyu Cong ◽  
Fanfan Xu ◽  
Xin Ding ◽  
Xiaodong Zhang
Keyword(s):  
Current Density ◽  
Active Sites ◽  
Nickel Foam ◽  
Active Surface ◽  
Alkaline Media ◽  
Water Dissociation ◽  
Alkaline Electrolyte ◽  
Active Surface Area ◽  
Dissociation Step ◽  
A Current

The development of non-noble metal catalysts for hydrogen revolution in alkaline media is highly desirable, but remains a great challenge. Herein, synergetic ultrathin NiO/MoS2 catalysts were prepared to improve the sluggish water dissociation step for HER in alkaline conditions. With traditional electrode assembly methods, MoS2:NiO-3:1 exhibited the best catalytic performance; an overpotential of 158 mV was required to achieve a current density of 10 mA/cm2. Further, a synergetic ultrathin NiO/MoS2/nickel foam (NF) electrode was assembled by electrophoretic deposition (EPD) and post-processing reactions. The electrode displayed higher electrocatalytic ability and stability, and an overpotential of only 121 mV was needed to achieve a current density of 10 mA/cm2. The improvement was ascribed to the better catalytic environment, rather than a larger active surface area, a higher density of exposed active sites or other factors. DFT calculations indicated that the hybrid NiO/MoS2 heterostuctured interface is advantageous for the enhanced water dissociation step and the corresponding lower kinetic energy barrier—from 1.53 to 0.81 eV.

MOF-derived hierarchical 3D bi-doped CoP nanoflower eletrocatalyst for hydrogen evolution reaction in both acidic and alkaline media

2020 ◽  
Vol 56 (56) ◽  
pp. 7702-7705 ◽  
Author(s):  
Lei Guo ◽  
Xue Bai ◽  
Hui Xue ◽  
Jing Sun ◽  
Tianshan Song ◽  
...  
Keyword(s):  
Hydrogen Evolution ◽  
Hydrogen Evolution Reaction ◽  
Current Density ◽  
Alkaline Media ◽  
Alkaline Electrolyte ◽  
Acidic Electrolyte ◽  
Acidic And Alkaline Media ◽  
A Current

A 3D hierarchical Bi-doped CoP nanoflowers electrocatalyst is developed based on a MOF self-sacrifice strategy. The 3% Bi/CoP catalyst delivers a current density of 10 mA cm−2 at low overpotentials of 122 mV in alkaline electrolyte and 150 mV in acidic electrolyte.

scholarly journals Zn- and Ti-Doped SnO2 for Enhanced Electroreduction of Carbon Dioxide

Materials ◽  
2021 ◽  
Vol 14 (9) ◽  
pp. 2354
Author(s):  
Katarzyna Bejtka ◽  
Nicolò B. D. Monti ◽  
Adriano Sacco ◽  
Micaela Castellino ◽  
Samuele Porro ◽  
...  
Keyword(s):  
Formic Acid ◽  
Current Density ◽  
Photoelectron Spectroscopy ◽  
Active Sites ◽  
Active Surface ◽  
Active Surface Area ◽  
Co2 Conversion ◽  
Hydrogen Electrode ◽  
Faradaic Efficiency ◽  
Wet Impregnation

The electrocatalytic reduction of CO2 into useful fuels, exploiting rationally designed, inexpensive, active, and selective catalysts, produced through easy, quick, and scalable routes, represents a promising approach to face today’s climate challenges and energy crisis. This work presents a facile strategy for the preparation of doped SnO2 as an efficient electrocatalyst for the CO2 reduction reaction to formic acid and carbon monoxide. Zn or Ti doping was introduced into a mesoporous SnO2 matrix via wet impregnation and atomic layer deposition. It was found that doping of SnO2 generates an increased amount of oxygen vacancies, which are believed to contribute to the CO2 conversion efficiency, and among others, Zn wet impregnation resulted the most efficient process, as confirmed by X-ray photoelectron spectroscopy analysis. Electrochemical characterization and active surface area evaluation show an increase of availability of surface active sites. In particular, the introduction of Zn elemental doping results in enhanced performance for formic acid formation, in comparison to un-doped SnO2 and other doped SnO2 catalysts. At −0.99 V versus reversible hydrogen electrode, the total faradaic efficiency for CO2 conversion reaches 80%, while the partial current density is 10.3 mA cm−2. These represent a 10% and a threefold increases for faradaic efficiency and current density, respectively, with respect to the reference un-doped sample. The enhancement of these characteristics relates to the improved charge transfer and conductivity with respect to bare SnO2.

scholarly journals A Superaerophobic Bimetallic Selenides Heterostructure for Efficient Industrial-Level Oxygen Evolution at Ultra-High Current Densities

2020 ◽  
Vol 12 (1) ◽  
Author(s):  
Jiaxin Yuan ◽  
Xiaodi Cheng ◽  
Hanqing Wang ◽  
Chaojun Lei ◽  
Sameer Pardiwala ◽  
...  
Keyword(s):  
Oxygen Evolution ◽  
Active Sites ◽  
Electronic Conductivity ◽  
Three Dimensional ◽  
Active Surface ◽  
Alkaline Media ◽  
Active Surface Area ◽  
High Current ◽  
High Electronic Conductivity ◽  
Current Densities

AbstractCost-effective and stable electrocatalysts with ultra-high current densities for electrochemical oxygen evolution reaction (OER) are critical to the energy crisis and environmental pollution. Herein, we report a superaerophobic three dimensional (3D) heterostructured nanowrinkles of bimetallic selenides consisting of crystalline NiSe2 and NiFe2Se4 grown on NiFe alloy (NiSe2/NiFe2Se4@NiFe) prepared by a thermal selenization procedure. In this unique 3D heterostructure, numerous nanowrinkles of NiSe2/NiFe2Se4 hybrid with a thickness of ~ 100 nm are grown on NiFe alloy in a uniform manner. Profiting by the large active surface area and high electronic conductivity, the superaerophobic NiSe2/NiFe2Se4@NiFe heterostructure exhibits excellent electrocatalytic activity and durability towards OER in alkaline media, outputting the low potentials of 1.53 and 1.54 V to achieve ultra-high current densities of 500 and 1000 mA cm−2, respectively, which is among the most active Ni/Fe-based selenides, and even superior to the benchmark Ir/C catalyst. The in-situ derived FeOOH and NiOOH species from NiSe2/NiFe2Se4@NiFe are deemed to be efficient active sites for OER.

Pt Nanoparticles Decorated on Fe2O3/N, P-Doped Mesoporous Carbon for Enhanced Oxygen Reduction Activity and Durability

2020 ◽  
Vol 18 (2) ◽  
Author(s):  
Sabarinathan Ravichandran ◽  
Narayanamoorthy Bhuvanendran ◽  
Kai Peng ◽  
Weiqi Zhang ◽  
Qian Xu ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Oxygen Reduction ◽  
Photoelectron Spectroscopy ◽  
Active Sites ◽  
Chemical Reduction ◽  
Pt Nanoparticles ◽  
Active Surface ◽  
Alkaline Media ◽  
Active Surface Area ◽  
X Ray

Abstract The Pt–Fe2O3 nanoparticles embedded over N, P-doped carbon (Pt–Fe2O3/NPC) was successfully synthesized by chemical reduction method demonstrating an enhanced electrocatalytic efficacy in alkaline media toward oxygen reduction reaction (ORR). The surface morphology of Pt–Fe2O3/NPC has been characterized by electron microscopy scanning, X-ray diffraction, electron microscopy transmission, Raman spectra, and X-ray photoelectron spectroscopy. The ORR electrocatalytic activity of Pt–Fe2O3/NPC was found to be the superior mass activity of 0.120 mA µg−1, which are almost twice higher than those for Pt–Fe2O3/VC (0.068 mA µg−1) and Pt/C (0.061 mA µg−1) catalysts. The durability tests revealed that the Pt–Fe2O3/NPC exhibited enhanced stability observed from the order of electrochemical active surface area (ECA) loss determined as Pt–Fe2O3/NPC (45.67%) <Pt–Fe2O3/VC (62.5%) <(Pt/C (72.13%) after 5000 cycles. This present investigation unveiled a facile approach to develop the number of active sites with the combination between P–Fe2O3 and N, P-doped carbon for improved electrocatalytic performance toward ORR.

scholarly journals Non-Enzymatic Glucose Detection Based on NiS Nanoclusters@NiS Nanosphere in Human Serum and Urine

Micromachines ◽  
2021 ◽  
Vol 12 (4) ◽  
pp. 403
Author(s):  
Mani Arivazhagan ◽  
Yesupatham Manova Santhosh ◽  
Govindhan Maduraiveeran
Keyword(s):  
Human Serum ◽  
Active Sites ◽  
Electrode Materials ◽  
Limit Of Detection ◽  
Nickel Foam ◽  
Active Surface ◽  
Glucose Sensing ◽  
Active Surface Area ◽  
Serum Samples ◽  
Serum And Urine

Herein, we report a non-enzymatic electrochemical glucose sensing platform based on NiS nanoclusters dispersed on NiS nanosphere (NC-NiS@NS-NiS) in human serum and urine samples. The NC-NiS@NS-NiS are directly grown on nickel foam (NF) (NC-NiS@NS-NiS|NF) substrate by a facile, and one-step electrodeposition strategy under acidic solution. The as-developed nanostructured NC-NiS@NS-NiS|NF electrode materials successfully employ as the enzyme-mimic electrocatalysts toward the improved electrocatalytic glucose oxidation and sensitive glucose sensing. The NC-NiS@NS-NiS|NF electrode presents an outstanding electrocatalytic activity and sensing capability towards the glucose owing to the attribution of great double layer capacitance, excessive electrochemical active surface area (ECASA), and high electrochemical active sites. The present sensor delivers a limit of detection (LOD) of ~0.0083 µM with a high sensitivity of 54.6 µA mM−1 cm−2 and a wide linear concentration range (20.0 µM–5.0 mM). The NC-NiS@NS-NiS|NF-based sensor demonstrates the good selectivity against the potential interferences and shows high practicability by glucose sensing in human urine and serum samples.

scholarly journals Superior FexN electrocatalyst derived from 1,1′-diacetylferrocene for oxygen reduction reaction in alkaline and acidic media

2020 ◽  
Vol 9 (1) ◽  
pp. 843-852
Author(s):  
Hunan Jiang ◽  
Jinyang Li ◽  
Mengni Liang ◽  
Hanpeng Deng ◽  
Zuowan Zhou
Keyword(s):  
Oxygen Reduction Reaction ◽  
Oxygen Reduction ◽  
Current Density ◽  
Active Sites ◽  
Reduction Reaction ◽  
Alkaline Media ◽  
Acidic Media ◽  
Onset Potential ◽  
Acidic And Alkaline Media ◽  
The Stability

AbstractAlthough Fe–N/C catalysts have received increasing attention in recent years for oxygen reduction reaction (ORR), it is still challenging to precisely control the active sites during the preparation. Herein, we report FexN@RGO catalysts with the size of 2–6 nm derived from the pyrolysis of graphene oxide and 1,1′-diacetylferrocene as C and Fe precursors under the NH3/Ar atmosphere as N source. The 1,1′-diacetylferrocene transforms to Fe3O4 at 600°C and transforms to Fe3N and Fe2N at 700°C and 800°C, respectively. The as-prepared FexN@RGO catalysts exhibited superior electrocatalytic activities in acidic and alkaline media compared with the commercial 10% Pt/C, in terms of electrochemical surface area, onset potential, half-wave potential, number of electrons transferred, kinetic current density, and exchange current density. In addition, the stability of FGN-8 also outperformed commercial 10% Pt/C after 10000 cycles, which demonstrates the as-prepared FexN@RGO as durable and active ORR catalysts in acidic media.

Hollow structure engineering of FeCo alloy nanoparticles electrospun in nitrogen-doped carbon enables high performance flexible all-solid-state zinc–air batteries

2020 ◽  
Vol 4 (4) ◽  
pp. 1747-1753 ◽  
Author(s):  
Yuanyuan Ma ◽  
Wenjie Zang ◽  
Afriyanti Sumboja ◽  
Lu Mao ◽  
Ximeng Liu ◽  
...  
Keyword(s):  
Active Sites ◽  
High Performance ◽  
Hollow Structure ◽  
Active Surface ◽  
Oxygen Electrode ◽  
Active Surface Area ◽  
Active Components ◽  
Nitrogen Doped Carbon ◽  
Structure Engineering ◽  
Kinetics Of

Hollow structuring of active components is an effective strategy to improve the kinetics of oxygen electrode catalysts, arising from the increased the active surface area, the defects on the exposed surface, and the accessible active sites.

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>

CO2 electrolysis to multicarbon products in strong acid

Science ◽  
2021 ◽  
Vol 372 (6546) ◽  
pp. 1074-1078
Author(s):  
Jianan Erick Huang ◽  
Fengwang Li ◽  
Adnan Ozden ◽  
Armin Sedighian Rasouli ◽  
F. Pelayo García de Arquer ◽  
...  
Keyword(s):  
Carbon Dioxide ◽  
Hydrogen Evolution ◽  
Current Density ◽  
Carbon Emissions ◽  
Active Sites ◽  
Cell Voltage ◽  
Strong Acid ◽  
Electrochemically Active ◽  
Co2 Electrolysis ◽  
A Current

Carbon dioxide electroreduction (CO2R) is being actively studied as a promising route to convert carbon emissions to valuable chemicals and fuels. However, the fraction of input CO2 that is productively reduced has typically been very low, <2% for multicarbon products; the balance reacts with hydroxide to form carbonate in both alkaline and neutral reactors. Acidic electrolytes would overcome this limitation, but hydrogen evolution has hitherto dominated under those conditions. We report that concentrating potassium cations in the vicinity of electrochemically active sites accelerates CO2 activation to enable efficient CO2R in acid. We achieve CO2R on copper at pH <1 with a single-pass CO2 utilization of 77%, including a conversion efficiency of 50% toward multicarbon products (ethylene, ethanol, and 1-propanol) at a current density of 1.2 amperes per square centimeter and a full-cell voltage of 4.2 volts.

Permeation of Electrolytically Generated Hydrogen and Tritium Atoms through Lead

1971 ◽  
Vol 49 (14) ◽  
pp. 2406-2411 ◽  
Author(s):  
Bansi L. Muju ◽  
Frank R. Smith
Keyword(s):  
Current Density ◽  
Separation Factor ◽  
Room Temperature ◽  
Alkaline Media ◽  
Gas Evolution ◽  
Hydrogen Atoms ◽  
Metal Lattice ◽  
Acidic And Alkaline Media ◽  
A Current ◽  
Lead Foil

Radiochemical and electrochemical evidence is presented that electrochemically generated tritium and hydrogen atoms permeate through lead foil at measureable rates at room temperature. The permeation process is controlled by diffusion through the metal lattice, Fick's First Law being obeyed by both H and 3H atoms. Using earlier measurements of the diffusivity of H in Pb, H and 3H concentrations of 4 × 10−7 and 9 × 10−13 g-atom cm−3 are computed for a current density of 53 mA cm−2 at the Pb cathode surface.The overall hydrogen-tritium separation factor, ST is apparently 0.3 ± 0.15, in contrast to Bockris and Srinivasan's 6.7 and 7.2 for cathodic gas evolution from acidic and alkaline media, respectively. Reasons are suggested for this large difference.

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