Abstract:Large-scale,
clean, efficient, and sustainable hydrogen production
from water is one of the major goals in solar-to-fuel conversion as
the sun and water represent the two most abundant and geographically
balanced free resources available on earth. Considering that most
of the liquid water available on the earth’s surface is present
in the form of seawater, H2 generation from seawater splitting
is highly desirable for large-scale practical and economical application.
Herein, we report on the first demonstration… Show more
“…Therefore, these 3 samples had similar behaviors, without plateau photocurrents, that show they are eligible for use PEC in seawater. Previous works reported that the generation of oxygen can occur by 2 major reactions: the OER from water oxidation and photodissociation of hypochlorite (HClO), which was produced from the reaction between water and chlorine (Cl 2 ) dissolved in seawater . For instance, it was verified that a small fraction of Cl − remained in solution and it was suggested that the chlorine oxidation reaction may be an intermediate process for seawater splitting .…”
Section: Resultsmentioning
confidence: 99%
“…Previous works reported that the generation of oxygen can occur by 2 major reactions: the OER from water oxidation and photodissociation of hypochlorite (HClO), which was produced from the reaction between water and chlorine (Cl 2 ) dissolved in seawater. [34,35] For instance, it was verified that a small fraction of Cl À remained in solution and it was suggested that the chlorine oxidation reaction may be an intermediate process for seawater splitting. [34] These reports used an artificial solution and a filtrated natural seawater where the pH was 6.5, the same used in this work.…”
Section: Photoelectrochemistry and Eismentioning
confidence: 99%
“…[34,35] For instance, it was verified that a small fraction of Cl À remained in solution and it was suggested that the chlorine oxidation reaction may be an intermediate process for seawater splitting. [34] These reports used an artificial solution and a filtrated natural seawater where the pH was 6.5, the same used in this work. [34][35][36] At this condition, it is known that there is the highest chlorine oxidation reaction.…”
Section: Photoelectrochemistry and Eismentioning
confidence: 99%
“…[34] These reports used an artificial solution and a filtrated natural seawater where the pH was 6.5, the same used in this work. [34][35][36] At this condition, it is known that there is the highest chlorine oxidation reaction. Hence, this may be the reason why the photocurrent density has a lower value in comparison to the experiment using Na 2 SO 4 as electrolyte -the major contribution in this case is the chlorine reaction, but still there is oxygen evolution.…”
Herein, a detailed investigation of the surface modification of a zinc oxide (ZnO) nanorod electrode with FeOOH nanoparticles dispersed in glycine was conducted to improve the water oxidation reaction assisted by sunlight. The results were systematically analysed in terms of the general parameters (light absorption, charge separation, and surface for catalysis) that govern the photocurrent density response of metal oxide as photoanode in a photoelectrochemical (PEC) cell. ZnO electrodes surface were modified with different concentration of FeOOH nanoparticles using the spin‐coating deposition method, and it was found that 6‐layer deposition of glycine‐FeOOH nanoparticles is the optimum condition. The glycine plays an important role decreasing the agglomeration of FeOOH nanoparticles over the ZnO electrode surface and increasing the overall performance. Comparing bare ZnO electrodes with the ones modified with glycine‐FeOOH nanoparticles an enhanced photocurrent density can be observed from 0.27 to 0.57 mA/cm2 at 1.23 VRHE under sunlight irradiation. The impedance spectroscopy data aid us to conclude that the higher photocurrent density is an effect associated with more efficient surface for chemical reaction instead of electronic improvement. Nevertheless, the charge separation efficiency remains low for this system. The present discovery shows that the combination of glycine‐FeOOH nanoparticle is suitable and environmentally‐friend cocatalyst to enhance the ZnO nanorod electrode activity for the oxygen evolution reaction assisted by sunlight irradiation.
“…Therefore, these 3 samples had similar behaviors, without plateau photocurrents, that show they are eligible for use PEC in seawater. Previous works reported that the generation of oxygen can occur by 2 major reactions: the OER from water oxidation and photodissociation of hypochlorite (HClO), which was produced from the reaction between water and chlorine (Cl 2 ) dissolved in seawater . For instance, it was verified that a small fraction of Cl − remained in solution and it was suggested that the chlorine oxidation reaction may be an intermediate process for seawater splitting .…”
Section: Resultsmentioning
confidence: 99%
“…Previous works reported that the generation of oxygen can occur by 2 major reactions: the OER from water oxidation and photodissociation of hypochlorite (HClO), which was produced from the reaction between water and chlorine (Cl 2 ) dissolved in seawater. [34,35] For instance, it was verified that a small fraction of Cl À remained in solution and it was suggested that the chlorine oxidation reaction may be an intermediate process for seawater splitting. [34] These reports used an artificial solution and a filtrated natural seawater where the pH was 6.5, the same used in this work.…”
Section: Photoelectrochemistry and Eismentioning
confidence: 99%
“…[34,35] For instance, it was verified that a small fraction of Cl À remained in solution and it was suggested that the chlorine oxidation reaction may be an intermediate process for seawater splitting. [34] These reports used an artificial solution and a filtrated natural seawater where the pH was 6.5, the same used in this work. [34][35][36] At this condition, it is known that there is the highest chlorine oxidation reaction.…”
Section: Photoelectrochemistry and Eismentioning
confidence: 99%
“…[34] These reports used an artificial solution and a filtrated natural seawater where the pH was 6.5, the same used in this work. [34][35][36] At this condition, it is known that there is the highest chlorine oxidation reaction. Hence, this may be the reason why the photocurrent density has a lower value in comparison to the experiment using Na 2 SO 4 as electrolyte -the major contribution in this case is the chlorine reaction, but still there is oxygen evolution.…”
Herein, a detailed investigation of the surface modification of a zinc oxide (ZnO) nanorod electrode with FeOOH nanoparticles dispersed in glycine was conducted to improve the water oxidation reaction assisted by sunlight. The results were systematically analysed in terms of the general parameters (light absorption, charge separation, and surface for catalysis) that govern the photocurrent density response of metal oxide as photoanode in a photoelectrochemical (PEC) cell. ZnO electrodes surface were modified with different concentration of FeOOH nanoparticles using the spin‐coating deposition method, and it was found that 6‐layer deposition of glycine‐FeOOH nanoparticles is the optimum condition. The glycine plays an important role decreasing the agglomeration of FeOOH nanoparticles over the ZnO electrode surface and increasing the overall performance. Comparing bare ZnO electrodes with the ones modified with glycine‐FeOOH nanoparticles an enhanced photocurrent density can be observed from 0.27 to 0.57 mA/cm2 at 1.23 VRHE under sunlight irradiation. The impedance spectroscopy data aid us to conclude that the higher photocurrent density is an effect associated with more efficient surface for chemical reaction instead of electronic improvement. Nevertheless, the charge separation efficiency remains low for this system. The present discovery shows that the combination of glycine‐FeOOH nanoparticle is suitable and environmentally‐friend cocatalyst to enhance the ZnO nanorod electrode activity for the oxygen evolution reaction assisted by sunlight irradiation.
“…Moreover,operando ambient pressure X-ray photoelectron spectroscopy (APXPS) has also show groundbreaking ability for instanceb ys patially-resolvingt he surfacechemical states of aworkingsolid state electrochemical cell (SOC), providing critical understanding for the rational design of such devices. [75] Finally,t he combinationo fn ovel and smart energy materials design studied at atomics cale and in "real" operating conditions by operando X-ray spectroscopies at synchrotron radiation facilities worldwide is an ideal situation for the current and future generation of scientists to unravel new phenomena as well as establishing quantitative correlations between structural properties, electronic structure and physical/chemical properties of materials [76][77][78] to not only improveour fundamental knowledge but also going beyond as imple incremental increase of device efficiency by breakthrough fundamental and appliedd iscoveries in materials science, condensed matter physics,c hemistry and biology.S uch advances in energy materials, characterizations techniques as wella sb etter fundamental and applied understanding should allow scientists and engineers of all origins to efficiently contribute( and potentially solve) current societal and environmental crucial issues that is, novel carbon-zero sustainable energy resources such as stable and efficient hydrogen generation from (sea)water splitting [79,80] for ac leanerand safer world.…”
Issues relatedt oe nergy and the environment have now become of central and crucial importance in our societies. Low-carbon green energy will have ac ritical role in an ecessary third industrial revolution.T or educe global greenhouse gas emissions in response to globalization and increasingly stringent carbone mission policies, large scale green energy production technologiesm ust be established worldwide. An ew age of human demandf or green energy is thus cominga nd scientists are focusedo nf inding new functional efficient and low-cost materialst ogenerate clean and sustainable energy.I mproving the energy conversion, generation, and storagee fficiency of energy materials has always been ad aunting challenge. For many important energy materials ystems, such as nanostructured catalysts, artificial photosynthetic systems, smart energy saving materials, and energy storaged evices, monitoring the atomica nd electronic structures close to the interfacial region in ar eal working environment is of paramount importance.D esigning ab etter-performing materialw ithoutc omprehendingi ts fundamentalp roperties such as chemical states, atomica nd electronic structures and how they are altered close to the interfacial regions during the physical and chemicalr eactions involved in their applications is very challenging. Understanding, controlling and tuning the interfaces in energy conversion and storagem aterials requires in situ/operando characterization tools, of which synchrotron X-ray spectroscopies, whichh ave severalu nique features, are very suitable ones. X-ray absorption spectroscopy can be used to elucidate the local unoccupied electronic structure in the con-ductionb and, and X-ray emission spectroscopy can be used to characterizet he occupied electronic structurei nt he valence band. The derived resonanti nelastic X-ray scattering reveals inter-and/ori ntra-electric transitions (i.e. d-d, f-f excitation and charge-transfer excitation) that reflect intrinsic chemicala nd physicalp roperties. Scanning transmission Xray microscopy is ac hemicalm apping technique with elemental sensitivity and spatial selectivity,w hich can therefore yield information about chemical composition in various spatialr egions. This unique characteristic makest he method effectivef or investigating interfacial phenomena (such as electront ransport, interface formation/deformation,d efects, doping etc.). In situ/operandoa pproaches have made the probinga nd understanding of changes in the atomica nd electronic structures of energy materials in an operational environment feasible. This article presentsaperspective of the pioneering developments as wella st he recent achievements in in situ/operando synchrotron X-ray spectroscopies for the advanced investigationo fe nergy materials. Four major energy materials ystems are identified:e nergy storage, energy generation,e nergy conversion,a nd energy saving materials ystems. Selected representative investigations of each systems are showcased and discussed demonstratingt hat in situ/operando sy...
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