共查询到20条相似文献,搜索用时 31 毫秒
1.
Photocatalytic water splitting using semiconductor photocatalysts has been considered as a “green” process for converting solar energy into hydrogen. The pioneering work on electrochemical photolysis of water at TiO2 electrode, reported by Fujishima and Honda in 1972, ushered in the area of solar fuel. As the real ultimate solution for solar fuel‐generation, overall water splitting has attracted interest from researchers for some time, and a variety of inorganic photocatalysts have been developed to meet the challenge of this dream reaction. To date, high‐efficiency hydrogen production from pure water without the assistance of sacrificial reagents remains an open challenge. In this Focus Review, we aim to provide a whole picture of overall water splitting and give an outlook for future research. 相似文献
2.
Earth‐Abundant Oxygen Evolution Catalysts Coupled onto ZnO Nanowire Arrays for Efficient Photoelectrochemical Water Cleavage
下载免费PDF全文
![点击此处可从《Chemistry (Weinheim an der Bergstrasse, Germany)》网站下载免费的PDF全文](/ch/ext_images/free.gif)
Chaoran Jiang Dr. Savio J. A. Moniz Dr. Majeda Khraisheh Dr. Junwang Tang 《Chemistry (Weinheim an der Bergstrasse, Germany)》2014,20(40):12954-12961
ZnO has long been considered as a model UV‐driven photoanode for photoelectrochemical water splitting, but its performance has been limited by fast charge‐carrier recombination, extremely poor stability in aqueous solution, and slow kinetics of water oxidation. These issues were addressed by applying a strategy of optimization and passivation of hydrothermally grown 1D ZnO nanowire arrays. The length and diameter of bare ZnO nanowires were optimized by varying the growth time and precursor concentration to achieve optimal photoelectrochemical performance. The addition of earth‐abundant cobalt phosphate (Co‐Pi) and nickel borate (Ni‐B) oxygen evolution catalysts onto ZnO nanowires resulted in substantial cathodic shifts in onset potential to as low as about 0.3 V versus the reversible hydrogen electrode (RHE) for Ni‐B/ZnO, for which a maximum photocurrent density of 1.1 mA cm?2 at 0.9 V (vs. RHE) with applied bias photon‐to‐current efficiency of 0.4 % and an unprecedented near‐unity incident photon‐to‐current efficiency at 370 nm. In addition the potential required for saturated photocurrent was dramatically reduced from 1.6 to 0.9 V versus RHE. Furthermore, the stability of these ZnO nanowires was significantly enhanced by using Ni‐B compared to Co‐Pi due to its superior chemical robustness, and it thus has additional functionality as a stable protecting layer on the ZnO surface. These remarkable enhancements in both photocatalytic activity and stability directly address the current severe limitations in the use of ZnO‐based photoelectrodes for water‐splitting applications, and can be applied to other photoanodes for efficient solar‐driven fuel synthesis. 相似文献
3.
Xiang Qin LIN Liang Dong FENG 《中国化学快报》2006,17(5):703-706
It is well known that the iR compensation is very important in electrochemistry, especially in fast, ultra-fast and transient voltammetry for kinetic and mechanistic studies. The modern design of potentiostat is usually of the three-electrode system, in w… 相似文献
4.
Dr. Jin‐Song Zhao Jin‐He Wang Wen‐Bin He Yi‐Bin Ruan Prof. Dr. Yun‐Bao Jiang 《Chemistry (Weinheim an der Bergstrasse, Germany)》2012,18(12):3631-3636
The induced aggregation of achiral building blocks by a chiral species to form chiral aggregates with memorized chirality has been observed for a number of systems. However, chiral memory in isolated aggregates of achiral building blocks remains rare. One possible reason for this discrepancy could be that not much is understood in terms of designing these chiral aggregates. Herein, we report a strategy for creating such isolable chiral aggregates from achiral building blocks that retain chiral memory after the facile physical removal of the chiral templates. This strategy was used for the isolation of chiral homoaggregates of neutral achiral π‐conjugated carboxylic acids in pure aqueous solution. Under what we have termed an “interaction–substitution” mechanism, we generated chiral homoaggregates of a variety of π‐conjugated carboxylic acids by using carboxymethyl cellulose (CMC) as a mediator in acidic aqueous solutions. These aggregates were subsequently isolated from the CMC templates whilst retaining their memorized supramolecular chirality. Circular dichroism (CD) spectra of the aggregates formed in the acidic CMC solution exhibited bisignated exciton‐coupled signals of various signs and intensities that were maintained in the isolated pure homoaggregates of the achiral π‐conjugated carboxylic acids. The memory of the supramolecular chirality in the isolated aggregates was ascribed to the substitution of COOH/COOH hydrogen‐bonding interaction between the carboxylic acid groups within the aggregates for the hydrogen‐bonding interactions between the COOH groups of the building blocks and the chiral templates. We expect that this “interaction–substitution” procedure will open up a new route to isolable pure chiral aggregates from achiral species. 相似文献
5.
Meng Li Li-Qing Jiang Lin Lin Yong-Feng Li Ding-Ling Yu Li-Li Cui Xing-Quan He 《Journal of Solid State Electrochemistry》2014,18(10):2743-2753
A novel high-performance non-noble metal electrocatalyst for the oxygen reduction reaction (ORR) was fabricated by anchoring cobalt tetraferrocenylporphyrin (CoFcP) onto poly(sodium-p-styrenesulfonate) modified graphene (PSS-Gr) through solvothermally assisted π–π assembling method. The morphology of the assembled composite was characterized by scanning electron microscopy (SEM) and transmission electron microscopy (TEM). The interactions between CoFcP moieties and graphene sheets were confirmed by UV–Vis absorption spectroscopy and X-ray photoelectron spectroscopy. The electrocatalytic properties of the CoFcP/PSS-Gr catalyst towards the oxygen reduction reaction were assessed using rotating disk electrode (RDE) and rotating ring-disk electrode (RRDE) measurements in both alkaline and acidic media. In addition, cyclic voltammetry and chronoamperometric measurements were utilized to evaluate the catalytic activity and stability of the CoFcP/PSS-Gr composite in alkaline solution. The results showed that CoFcP supported on graphene exhibited an outstanding electrocatalytic performance towards the ORR comparable with commercial Pt/C catalyst in alkaline media, such as high onset potential (0.889 V vs. reversible hydrogen electrode, RHE), half wave potential (0.789 V vs. RHE), better tolerance to methanol, excellent stability (84.1 %, retention after 10000 s), and efficient four-electron pathway. Moreover, the proposed hybrid presented excellent catalytic activity in terms of onset potential (0.72 V vs. RHE) and high-electron transfer number compared with Pt/C in acidic media. 相似文献
6.
Xien Liu Haeseong Jang Ping Li Jia Wang Qing Qin Min Gyu Kim Guangkai Li Jaephil Cho 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2019,131(38):13463-13468
A nanocomposite of PC/Sb/SbPO4 (PC, phosphorus‐doped carbon) exhibits a high activity and an excellent selectivity for efficient electrocatalytic conversion of N2 to NH3 in both acidic and neutral electrolytes under ambient conditions. At a low reductive potential of ?0.15 V versus the reversible hydrogen electrode (RHE), the PC/Sb/SbPO4 catalyst achieves a high Faradaic efficiency (FE) of 31 % for ammonia production in 0.1 m HCl under mild conditions. In particular, a remarkably high FE value of 34 % is achieved at a lower reductive potential of ?0.1 V (vs. RHE) in a 0.1 m Na2SO4 solution, which is better than most reported electrocatalysts towards the nitrogen reduction reaction (NRR) in neutral electrolyte under mild conditions. The change in surface species and electrocatalytic performance before and after N2 reduction is explored by an ex situ method. PC and SbPO4 are both considered as the active species that enhanced the performance of NRR. 相似文献
7.
Andrzej Lewandowski Monika Osińska Agnieszka Swiderska‐Mocek Maciej Galinski 《Electroanalysis》2008,20(17):1903-1908
The cryptate electrode (Ag/Ag+222), prepared by immersing silver wire in a solution of silver(I) salt and the cryptand 222 (4,7,13,16,21,24‐hexaoxa‐1,10‐diazabicyclo[8.8.8]hexacosane) in ionic liquids have been studied. The potential of the electrode is stabilized by the equilibrium of the Ag+ ion complexation by the cryptand, similarly to the potential stabilization by the ionic product of slightly soluble salts, used in aqueous electrodes of the second kind. The Ag/Ag+222 cryptate electrode (concentration of the cryptate was much higher than the silver(I) cation concentration, [222]>[Ag+]) may be used as a reference electrode in room temperature ionic liquids. The potential of the Ag/Ag+222 electrode is less sensitive to the presence of impurities, such as halides or water, in comparison to the Ag/Ag+ electrode. After anodic or cathodic polarization, the potential of the Ag/Ag+222 electrode comes back to the initial open circuit potential quickly. Preparation of the Ag/Ag+222 reference electrode is very easy: a silver wire is immersed in a solution of Ag+ salt and cryptand 222 (both available commercially) in the ionic liquid under study. 相似文献
8.
Surface Pourbaix diagrams and oxygen reduction activity of Pt, Ag and Ni(111) surfaces studied by DFT 总被引:1,自引:0,他引:1
Based on density functional theory calculations we investigate the electrochemically most stable surface structures as a function of pH and electrostatic potential for Pt(111), Ag(111) and Ni(111), and we construct surface Pourbaix diagrams. We study the oxygen reduction reaction (ORR) on the different surface structures and calculate the free energy of the intermediates. We estimate their catalytic activity for ORR by determining the highest potential at which all ORR reaction steps reduce the free energy. We obtain self-consistency in the sense that the surface is stable under the potential at which that particular surface can perform ORR. Using the self consistent surfaces, the activity of the very reactive Ni surface changes dramatically, whereas the activity of the more noble catalysts Pt and Ag remains unchanged. The reason for this difference is the oxidation of the reactive surface. Oxygen absorbed on the surface shifts the reactivity towards the weak binding region, which in turn increases the activity. The oxidation state of the surface and the ORR potential are constant versus the reversible hydrogen electrode (RHE). The dissolution potential in acidic solution, on the other hand, is constant vs. the standard hydrogen electrode (SHE). For Ag, this means that where the potential for dissolution and ORR are about the same at pH = 0, Ag becomes more stable relative to RHE as pH is increased. Hence the pH dependent stability offers an explanation for the possible use of Ag in alkaline fuel cell cathodes. 相似文献
9.
In this work, the electrochemical behavior of ferrocene (Fc) was investigated by cyclic voltammetry (CV) in room temperature ionic liquids (RTILs) of 1‐ethyl‐3‐methylimidazolium tetrafluoroborate (EMIBF4) on glass carbon (GC), edge plane pyrolytic graphite (EPPG) and multi‐walled carbon nanotube (MWCNTs)‐modified EPPG electrodes, respectively. The results demonstrated that on GC electrode, pairs of well‐defined reversible peaks were observed, while for the electrode of EPPG, the peak potential separation (ΔEp) is obviously larger than the theoretical value of 59 mV, hinting that the electrode of EPPG is distinguished from the commonly used electrode, consistent with the previous proposition that EPPG has many “defects”. To obtain an improved electrochemical response, multi‐walled carbon nanotubes (MWCNTs) were modified on the electrode of EPPG; the increased peak current and promoted peak potential separation not only proved the existence of “defects” in MWCNTs, but also supported that “creating active points” on an electrode is the main contribution of MWCNTs. Initiating the electrochemical research of Fc on the MWCNTs‐modified EPPG electrode in RTILs and verifying the presence of “defects” on both EPPG and MWCNTs using cyclic voltammograms (CVs) of Fc obtained in RTILs of EMIBF4, is the main contribution of this preliminary work. 相似文献
10.
11.
新式夹心型光透薄层光谱电化学电解池 总被引:1,自引:0,他引:1
本文设计了一种新式夹心型光透薄层紫外-可见光谱电化学池。该池采用铂网工作电极,两侧平行放置铂片为对极置于同一石英窗口夹层中,同时以聚四氟乙烯隔离膜作为边际限制器,结合池内小孔道设置内参比点进行精确的电位控制,具有理想的光谱电化学响应。利用循环伏安、循环电位-吸收、恒电位现场光谱、双电位跃-计时电量、双电位跃-计时吸收等技术,对铁氰化钾在氯化钾溶液中的行为进行了表征。 相似文献
12.
《中国化学快报》2023,34(1):107480
Organic semiconductors are promising candidates as photoactive layers for photoelectrodes used in photoelectrochemical (PEC) cells due to their excellent light absorption and efficient charge transport properties with the help of interfacial materials. However, the use of multilayers will make the charge transfer mechanism more complicated and decrease the PEC performance of the photoelectrode caused by the increased contact resistance. In this work, a PM6:Y6 bulk heterojunction (BHJ)-based photocathode is fabricated for efficient PEC hydrogen evolution reaction (HER) in an acidic aqueous solution. With RuO2 as an interfacial modification layer, the photocathode with a simple structure (fluorine-doped tin oxide (FTO)/PM6:Y6/RuO2) generates a maximum photocurrent density up to ?15 mA/cm2 at 0 V vs. reference hydrogen electrode (RHE), outperforming all previously reported BHJ-based photocathodes in terms of PEC performance. The highest ratiometric power-saved efficiency of 3.7% is achieved at 0.4 V vs. RHE. 相似文献
13.
Efficient and Stable MoS2/CdSe/NiO Photocathode for Photoelectrochemical Hydrogen Generation from Water
下载免费PDF全文
![点击此处可从《化学:亚洲杂志》网站下载免费的PDF全文](/ch/ext_images/free.gif)
Yuming Dong Yanmei Chen Pingping Jiang Guangli Wang Xiuming Wu Ruixian Wu Chi Zhang 《化学:亚洲杂志》2015,10(8):1660-1667
A novel CdSe/NiO heteroarchitecture was designed, prepared, and used as a photocathode for hydrogen generation from water. The composite films were structurally, optically, and photoelectrochemically characterized. The deposition of CdSe on the NiO film enhanced light harvesting in the visible‐light region and photoelectrochemical properties. Moreover, the CdSe/NiO photoelectrode showed superior stability both in nitrogen‐saturated and air‐saturated neutral environments. The CdSe/NiO photoelectrode after MoS2 modification retained the stability of the CdSe/NiO electrode and exhibited higher photocatalytic and photoelectrochemical performances than the unmodified CdSe/NiO electrode. In pH 6 buffer solution, an average hydrogen‐evolution rate of 0.52 μmol h?1 cm?2 at ?0.131 V (versus reversible hydrogen electrode, RHE) was achieved on a MoS2/CdSe/NiO photocathode, with almost 100 % faradaic efficiency. 相似文献
14.
Nongnoot Wongkaew Stefanie E. K. Kirschbaum Werasak Surareungchai Richard A. Durst Antje J. Baeumner 《Electroanalysis》2012,24(10):1903-1908
A new strategy of three‐electrode system fabrication in polymer‐based microfluidic systems is described here. Standard lithography, hot embossing and UV‐assisted thermal bonding were employed for fabrication and assembly of the microfluidic chip. For the electrode design the gold working (WE) and counter electrodes (CE) are placed inside a main channel through which the sample solution passes. A silver reference electrode (RE) is embedded in a small side channel containing KCl solution that is continuously pushed into the main channel. In the present work, the overall electrochemical set up and its microfabrication is described. Conditions including silver ion concentration, cyclic voltammetry (CV) settings, and the flow rate of KCl solution in the RE channel were optimized. The electrochemical performance of the three‐electrode system was evaluated by CV and also by amperometric oxidation of ferro hexacyanide ([Fe(CN)6]4?) and ruthenium bipyridyl ([Ru(bipy)3]2+) at 400 mV and 1200 mV, respectively. CV analysis using ferri/ferro hexacyanide showed a stable, quasi‐reversible redox reaction at the electrodes with 96 mV peak separation and an anodic/cathodic peak ratio of 1. Amperometric analysis of the electrochemical species resulted in linear correlation between analyte concentration and current response in the range of 0.5–15 µM for [Fe(CN)6]4?, and 0–1000 µM for [Ru(bipy)3]2+. Upon the given experimental conditions, the limit of detection was found to be 3.15 µM and 24.83 µM for [Fe(CN)6]4? and [Ru(bipy)3]2+, respectively. As a fully integrated three‐electrode system that is fabricated on polymer substrates, it has great applications in microfluidic‐based systems requiring stable electrochemical detection. 相似文献
15.
This work demonstrates the performance of a bio‐inspired iron/sulfur/graphene nanocomposite as a non‐platinum electrocatalyst for the oxygen reduction reaction (ORR) in an alkaline medium. The catalyst shows the most positive ORR onset potential (1.1 V vs. RHE) according to its unique structure in the alkaline medium (KOH solution, pH = 13) at low temperature (T = 298 K). The catalyst is evaluated by the rotating‐disk electrode (RDE) method under various rotating speeds (0–2,000 rpm) in the potential range ?0.02–1.18 V vs. a rechargeable hydrogen electrode (RHE). The number of transferred electrons, as one of the most important parameters, is almost constant over a wide range of potentials (0.1–0.8 V), which indicates a more efficient four‐electron pathway from O2 to H2O on the FePc‐S‐Gr surface. The mean size of catalyst centers are in the nanoscale (<10 nm). The estimated Tafel slope in the appropriate range is about ?110 mV per decade at low current density, and E1/2 of FePc‐S‐Gr displays a negative shift of only 7.1 mV after 10,000 cycles. 相似文献
16.
Ana T. Simonović Marija B. Petrović Milan B. Radovanović Snežana M. Milić Milan M. Antonijević 《Chemical Papers》2014,68(3):362-371
This investigation aimed to study a “green” non-toxic biodegradable copper corrosion inhibitor in an acidic sodium sulphate solution. The methods used in the investigation of cysteine as a copper corrosion inhibitor in an acidic sodium sulphate solution were: potentiodynamic measurements, open circuit potential measurements, and chronoamperometric measurements. Optical microscopy was used in addition to electrochemical methods. Potentiodynamic measurements show that cysteine has good inhibitory properties in an acidic medium. Polarisation curves indicate that the presence of cysteine in a sulphate solution decreases the current density and that using various cysteine concentrations results in the formation of a protective film on the surface of the electrode due to the formation of the Cu(I)-cys complex. These results are confirmed by chronoamperometric measurements. Furthermore, it is clear from microphotographs that a protective film does form on copper electrode in the presence of cysteine. The Langmuir adsorption isotherm indicates that cysteine is chemisorbed on the surface of the electrode. 相似文献
17.
(Ni-Co)-WC复合电极的析氢催化性能 总被引:12,自引:0,他引:12
采用 复合电沉 积方法获 得了( Ni Co) W C 复合电极 ,考 察了 复合 电极 在弱 酸性、碱性 和中性介质 中的析 氢电催化 性能,并 在弱酸性 介质中 进行了电 化学稳定 性实验 . 结果 表明,复 合电极具有优越 的析氢 电催化性 能和良好 的电化 学稳定性 . 相似文献
18.
Jie Yu Congliang Wang Dr. Wenjing Yuan Prof. Yuhua Shen Prof. Anjian Xie 《Chemistry (Weinheim an der Bergstrasse, Germany)》2019,25(11):2877-2883
Herein, an ordinary and mass-production approach is reported to synthesize boron (B) and nitrogen (N) co-doped three-dimensional (3D) carbon aerogels (CA) by using glucose and borax as the raw materials by a simple hydrothermal method and then carbonization in NH3 atmosphere. The porous material (BN-CA-900) possesses a large specific surface area (1032 m2 g−1) and high contents of doped pyridinic N and graphitic N. The onset potential (0.91 V vs. reversible hydrogen electrode, RHE), half-wave potential (0.77 V vs. RHE), and current density (5.70 mA cm−2 at 0.2 V vs. RHE) of BN-CA-900 for ORR are similar to those of commercial Pt/C, indicating that BN-CA-900 has a comparable catalytic activity with Pt/C in alkaline media. The number of electron transfer is 3.86–3.99 and the yield of hydrogen peroxide is less than 6.8 %. BN-CA-900 also presents decent catalytic performance in acidic medium. Moreover, the stability and methanol tolerance of BN-CA-900 are superior to commercial Pt/C in both alkaline and acidic media. The prepared BN-CA-900 is a promising candidate that may be applied in other areas, such as the adsorption of pollution, porous conductive electrodes, and lithium-ion batteries. 相似文献
19.
A microelectrode array microprobe with a choline sensing site and an on‐probe reference electrode was constructed by depositing permselective polymer films and choline oxidase (ChOx) on one microelectrode, and iridium oxide (IrOx) on another, both of which were coated previously with a nanostructured Pt deposit. Scanning electron microscopy (SEM) of the nanostructured Pt layer revealed a unique pillar‐like, “nanograss” structure. Polyphenylenediamine (PPD) and Nafion were coated sequentially on the working (i. e. sensing) electrode surface to serve as the permselective polymer films. The microsensor exhibited high sensitivity to choline (123±13 μA mM?1 cm?2), low detection limit (3.2±0.8 μM), and fast response time (3–5 s). The choline sensor also was tested at physiological concentrations of electroactive interfering species common to brain extracellular fluid (i. e. ascorbic acid, dopamine, DOPA, and DOPAC) and showed excellent selectivity. Selectivity likely was aided by the relatively low potential of 0.35 V vs. IrOx that was made possible by the enhanced H2O2 electrooxidation activity of the underlying nanostructured Pt‐coated working electrode. Thus, Pt “nanograss” appears to be an excellent electrode surface modification for creation of high performance electroenzymatic biosensors. 相似文献
20.
Osamu Yamazaki Hideaki Yoshitake Nobuyuki Kamiya Ken-ichiro Ota 《Journal of Electroanalytical Chemistry》1995,390(1-2)
The amount of electrochemically absorbed hydrogen and lithium in a Pd cathode during electrolysis was measured quantitatively in LiOH solution. The electrode potential was also measured by the current interruption method. Inclusion of Li in Pd was found even at the potential of −0.22 V vs. RHE. This potential is far more positive than the reported UPD potential. Since Li was detected up to a depth of 200 nm, this phenomenon is not a simple UPD. The deposition of Li onto Pd and the formation of Pd---Li alloy are likely to occur at a much more positive potential than expected. The [H]/[Pd] ratio decreased gradually after 50 h electrolysis at a current density greater than 5 mA cm−2. 相似文献