Topic
Overpotential
About: Overpotential is a research topic. Over the lifetime, 16474 publications have been published within this topic receiving 616632 citations.
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TL;DR: Porous CoFe2 O4 /C NRAs supported on nickel foam@NC are directly fabricated by the carbonization of bimetal-organic framework NRAs grown on NF@poly-aniline(PANI), and they exhibit high electrocatalytic activity, low overpotential, and high stability for the oxygen evolution reaction in alkaline media.
Abstract: Porous CoFe2 O4 /C NRAs supported on nickel foam@NC (denoted as NF@NC-CoFe2 O4 /C NRAs) are directly fabricated by the carbonization of bimetal-organic framework NRAs grown on NF@poly-aniline(PANI), and they exhibit high electrocatalytic activity, low overpotential, and high stability for the oxygen evolution reaction in alkaline media.
666 citations
TL;DR: In this paper, the authors summarized and divided recent intensification technologies of water electrolysis into three categories: external field, new electrolyte composition, and new thermodynamic reaction system.
Abstract: Water electrolysis derived by renewable energy such as solar energy and wind energy is a sustainable method for hydrogen production due to high purity, simple and green process. One of the challenges is to reduce energy consumption of water electrolysis for large-scale application in future. Cell voltage, an important criterion of energy consumption, consists of theoretical decomposition voltage (U-theta), ohmic voltage drop (i*Sigma R) and reaction overpotential (eta). The kinetic and thermodynamic roots of high cell voltage are analyzed systemically in this review. During water electrolysis, bubble coverage on electrode surface and bubble dispersion in electrolyte, namely bubble effect, result in high ohmic voltage drop and large reaction overpotential. Bubble effect is one of the most key factors for high energy consumption. Based on the theoretical analysis, we summarize and divide recent intensification technologies of water electrolysis into three categories: external field, new electrolyte composition and new thermodynamic reaction system. The fundamentals and development of these intensification technologies are discussed and reviewed. Reaction overpotential and ohmic voltage drop are improved kinetically by external field or new electrolyte composition. The thermodynamic decomposition voltage of water is also reduced by new reaction systems such as solid oxide electrolysis cell (SOEC) and carbon assisted water electrolysis (CAWE). (C) 2013 Elsevier Ltd. All rights reserved.
665 citations
TL;DR: In this paper, single Ru sites supported on N-doped porous carbon greatly promoted electroreduction of aqueous N2 selectively to NH3, affording an NH3 formation rate of 3.665 m g N H 3 h − 1 m g Ru − 1 at −0.21 V versus the reversible hydrogen electrode.
661 citations
TL;DR: It is found that zinc-doped MoS2 (Zn-MoS2) exhibits superior electrochemical activity toward HER as evidenced by the positively shifted onset potential to -0.13 V vs RHE.
Abstract: Water-splitting devices for hydrogen generation through electrolysis (hydrogen evolution reaction, HER) hold great promise for clean energy. However, their practical application relies on the development of inexpensive and efficient catalysts to replace precious platinum catalysts. We previously reported that HER can be largely enhanced through finely tuning the energy level of molybdenum sulfide (MoS2) by hot electron injection from plasmonic gold nanoparticles. Under this inspiration, herein, we propose a strategy to improve the HER performance of MoS2 by engineering its energy level via direct transition-metal doping. We find that zinc-doped MoS2 (Zn-MoS2) exhibits superior electrochemical activity toward HER as evidenced by the positively shifted onset potential to -0.13 V vs RHE. A turnover of 15.44 s-1 at 300 mV overpotential is achieved, which by far exceeds the activity of MoS2 catalysts reported. The large enhancement can be attributed to the synergistic effect of electronic effect (energy level matching) and morphological effect (rich active sites) via thermodynamic and kinetic acceleration, respectively. This design opens up further opportunities for improving electrocatalysts by incorporating promoters, which broadens the understanding toward the optimization of electrocatalytic activity of these unique materials.
654 citations
TL;DR: In this article, a highly active and stable electrocatalyst for hydrogen evolution is developed based on the in situ formation of MoS2 nanoparticles on mesoporous graphene foams (MoS2/MGF).
Abstract: A highly active and stable electrocatalyst for hydrogen evolution is developed based on the in situ formation of MoS2 nanoparticles on mesoporous graphene foams (MoS2/MGF). Taking advantage of its high specific surface area and its interconnected conductive graphene skeleton, MGF provides a favorable microenvironment for the growth of highly dispersed MoS2 nanoparticles while allowing rapid charge transfer kinetics. The MoS2/MGF nanocomposites exhibit an excellent electrocatalytic activity for the hydrogen evolution reaction with a low overpotential and substantial apparent current densities. Such enhanced catalytic activity stems from the abundance of catalytic edge sites, the increase of electrochemically accessible surface area and the unique synergic effects between the MGF support and active catalyst. The electrode reactions are characterized by electrochemical impedance spectroscopy. A Tafel slope of ≈42 mV per decade is measured for a MoS2/MGF modified electrode, suggesting the Volmer-Heyrovsky mechanism of hydrogen evolution.
654 citations