A review of understanding electrocatalytic reactions in energy conversion and energy storage systems via scanning electrochemical microscopy

To address climate change and promote environmental sustainability,electrochemical energy conversion and storage systems emerge as promising alternative to fossil fuels,catering to the escalating demand for energy.Achieving optimal energy efficiency and cost competitiveness in these systems requires the strategic design of electrocatalysts,coupled with a thorough comprehension of the underlying mechanisms and degradation behavior occurring during the electrocatalysis processes.Scanning electrochemical microscopy(SECM),an analytical technique for studying surface electrochemically,stands out as a powerful tool offering electrochemical insights.It possesses remarkable spatiotemporal resolution,enabling the visualization of the localized electrochemical activity and surface topography.This review compiles crucial research findings and recent breakthroughs in electrocatalytic processes utilizing the SECM methodology,specifically focusing on applications in electrolysis,fuel cells,and metal–oxygen batteries within the realm of energy conversion and storage systems.Commencing with an overview of each energy system,the review introduces the fundamental principles of SECM,and aiming to provide new perspectives and broadening the scope of applied research by describing the major research categories within SECM.

The Study on the Self-assembled Monolayer(SAMs)of Porphyrin with Different Chain Length by Scanning Electrochemical Microscopy(SECM)

The thiol-porphyrins were prepared to investigate the effect of spacer length on the gold electrode. These measurements showed that as the length of the spacers increases, the SAMs tend to form highly ordered structures on the gold electrodes. In addition, the structures of the monoalyers vary depending on the even and odd number of the methylene spacers （n）.

Corrosion behavior of aluminum alloys in Na_2SO_4 solution using the scanning electrochemical microscopy technique

The corrosion behavior of aluminum alloys 1060 and 2A12 in a 10 mM Na2SO4＋5 mM KI solution was investigated by scanning electrochemical microscopy （SECM） and scanning electron microscopy （SEM）. The potential topography and corrosion morphology results show that the potential of the sample surface over the same area changes with the increase of immersion time. The corrosion area becomes large, and the potential becomes more negative. The corrosion potential of the 2A12 alloy surface is lower than that of 1060 aluminum, and 2A12 alloy becomes easily corrosive. This is the reason that preferential dissolution in the boundary region of some intermetallic particles （IMPs） occurs and different dissolution behaviors are associated with different types of IMPs because of different potentials.

Imaging of Activity of Horseradish Peroxidase at β-Cyclodextrin Polymer by Scanning Electrochemical Microscopy

The activity of horseradish peroxidase at b-cyclodextrin polymer was imaged by scanning electrochemical microscopy using 3, 3', 5, 5'-tetramethylbenzide and H2O2 as the substrates.

Modern applications of scanning electrochemical microscopy in the analysis of electrocatalytic surface reactions

Development of reaction-tailored electrocatalysts is becoming increasingly important as energy and environment are among key issues governing our sustainable future.Electrocatalysts are inherently optimized for application towards reactions of interest in renewable energy,such as those involved in water splitting and artificial photosynthesis,owing to its energy efficiency,simple fabrication,and ease of operation.In this view,it is important to secure logical design principles for the synthesis of electrocatalysts for various reactions of interest,and also understand their catalytic mechanisms in the respective reactions for improvements in further iterations.In this review,we introduce several key methods of scanning electrochemical microscopy(SECM)in its applications towards electrocatalysis.A brief history and a handful of seminal works in the SECM field is introduced in advancing the synthetic designs of electrocatalysts and elucidation of the operating mechanism.New developments in nano-sizing of the electrodes in attempts for improved spatial resolution of SECM is also introduced,and the application of nanoelectrodes towards the investigation of formerly inaccessible single catalytic entities is shared.

Mapping the kinetics of hydrogen evolution reaction on Ag via pseudo-single-crystal scanning electrochemical cell microscopy

Elucidating the structure-activity relationship in electrocatalysis is of fundamental interest for electrochemical energy conversion and storage.However,the heterogeneity in the surface structure of electrocatalysts,including the presence of various facets,poses an analytical challenge in revealing the true structure-activity relationship because the activity is conventionally measured on ensemble,resulting in an averaged activity that cannot be unequivocally associated with a single structural motif.Scanning electrochemical cell microscopy(SECCM)[1]combined with colocalized electron backscatter diffraction(EBSD)offers a direct way to reveal the correlative local electrochemical and structural information.Herein,we measured the hydrogen evolution reaction(HER)activity on Ag and its dependence on the crystal orientation.From the combined EBSD and SECCM mapping,it is found that Ag grains closer to{111}show a higher exchange current density,while those closer to{110}show a lower Tafel slope.The Tafel slope is also found to decrease with the step density increase.The ability to measure the electrocatalytic activity under a high mass-transfer rate allows us to reveal the activity difference at a high current density(up to 200 mA/cm^(2)).The approach reported here can be expanded to other systems to reveal the nature of active sites of electrocatalysis.

Electrochemical Scanning Tunneling Microscopy──An Ex－situ Study of the Growth of Polypyrrole Films on Electrodes

his paper covers the electropolymerized polypyrrole doped with p-toluenesul-fonate studied using scanning tunneling microscope. The growth processes of polypyrrole films on the electrode surface were observed. Polypyrrole chain struc-ture with many separated micro-holes of 0. 15 nm diameter at the initial state ofelectropolymerization can be seen from obtained STM images. This structure is ex-tremely similar to the pioneer-proposed ideal structure of polypyrrole chains. Thereexisted some helical structure and simple strands on the electrode surface, which isdue to different existing states of polypyrrole chains on electrode surface. STM ex-periments showed that polypyrrole chains were firstly formed on the electrode sur-face, then, they growed gradually by 3-dimensional mode during slow oxidation toform many separated micro-islands. Finally, a large corrugation area of polymerfilms occurred on the electrodes.

FABRICATION OF THE TIP FOR ELECTROCHEMICAL SCANNING TUNNELING MICROSCOPY

A nover technique for the fabrication of the tip for e tectrochemical scanning tunneting microscopy(ECSTM)is presented. The curvature radius of the fabricated tip is smatter than 1 μM. Faradaic leakage current is tess than 0.1nA in the sotution of 1 mol/L NaCl. The atomic image of highty oriented pyrotytic graphite (HOPG)has been taken using the prepared tip.

Dye Regeneration Kinetics of Sensitized Nickel Oxide Films under Illumination Investigated by Scanning Electrochemical Microscopy

Scanning electrochemical microscopy (SECM) feedback mode has been used to investigate regeneration kinetics on P1 (4-(bis-{4-[5-(2,2-dicyanovinyl) thiophene-2-yl] pH-enyl} amino) benzoic acid) dye sensitized nickel oxide (NiO) electrodes in contact with reduced iodide liquid electrolyte in different electrolyte solvents. We were used acetonitrile, ethanol, methanol and propylene carbonate solvents for comparison under illumination of different wavelengths. We found significant variation of regeneration kinetics parameters such as regeneration rate constant (keff), the reduction rate constant (kred) and absorption cross-section (Φhv) in different illumination intensity and different solvents.

Corrosion Investigation by Scanning Electrochemical Microscopy of AISI 446 and Ti-Coated AISI 446 Ferritic Stainless Steel as Potential Material for Bipolar Plate in PEMWE

The components of proton exchange membrane water electrolysers frequently experience corrosion issues, especially at high anodic polarization, that restrict the use of more affordable alternatives to titanium. Here, we investigate localized corrosion processes of bare and Ti-coated AISI 446 ferritic stainless steel under anodic polarization by scanning electrochemical microscopy (SECM) in sodium sulphate and potassium chloride solutions. SECM approach curves and area scans measured at open-circuit potential (OCP) of the samples in the feedback mode using a redox mediator evidence a negative feedback effect caused by the surface passive film. For the anodic polarization of the sample, the substrate generation-tip collection mode enables to observe local generation of iron (II) ions, as well as formation of molecular oxygen. For the uncoated AISI 446 sample, localized corrosion is detected in sodium sulphate solution simultaneously with oxygen formation at anodic potentials of 1.0 V vs. Ag/AgCl, whereas significant pitting corrosion is observed even at 0.2 V vs. Ag/AgCl in potassium chloride solution. The Ti-coated AISI 446 sample reveals enhanced corrosion resistance in both test solutions, without any evidence of iron (II) ions generation at anodic potentials of 1.2 V vs. Ag/AgCl, where only oxygen formation is observed.

Assessing the dynamics of O_(2) desorption from cobalt phthalocyanine by in situ electrochemical scanning tunneling microscopy

We report here the in situ electrochemical scanning tunneling microscopy(ECSTM) study of cobalt phthalocyanine(CoPc)-catalyzed O_(2) evolution reaction(OER) and the dynamics of CoPc-O_(2) dissociation.The self-assembled CoPc monolayer is fabricated on Au(111) substrate and resolved by ECSTM in 0.1 M KOH electrolyte.The OH^(-)adsorption on CoPc prior to OER is observed in ECSTM images.During OER,the generated O_(2) adsorbed on Co Pc is observed in the CoPc monolayer.Potential step experiment is employed to monitor the desorption of OER-generated O_(2) from CoPc,which results in the decreasing surface coverage of CoPc-O_(2) with time.The rate constant of O_(2) desorption is evaluated through data fitting.The insights into the dynamics of Co-O_(2) dissociation at the molecular level via in situ imaging help understand the role of Co-O_(2) in oxygen reduction reaction(ORR) and OER.

Fast Scan mode of scanning electrochemical microscopy:In-situ characterization of phase transition and mapping the hydrogen evolution activity for MoS_(2)

Scanning electrochemical microscopy(SECM)is an attractive technology to in-situ characterize the structural evolution and catalytic performance for various electrocatalysts.However,spatial and temporal resolution coupling are still the obstacles that limit its wide applications.Herein,a new operation mode,Fast Scan mode,was developed by improving the dual-pass scan mode,designing novel hardware structure,and employing thermal drift calibration software to achieve a high spatial and temporal resolution simultaneously.The temporal speed can achieve 4 Hz for a high spatial resolution(less than 30 nm)image.This operation mode was employed to dynamically track the phase transition process of molybdenum disulfide(MoS_(2))over time and characterize the hydrogen evolution reaction(HER)catalytic activity on the edge of semiconducting MoS_(2)quantitatively while minimizing the diffusional broadening effect and total amount of catalytic products generated above the surface.This new approach should be useful for in-situ tracking dynamic electrochemical processes,establishing the structure-activity relationship for structural complex electrocatalysts,and offering a strategy for high-speed scanning with other electrochemical imaging techniques.

Elucidating the electronic metal-support interaction enhanced hydrogen evolution activity on Ti_(3)C_(2)T_(x)MXene basal plane by scanning electrochemical microscopy

MXene,a family of two-dimensional(2D)transition metal carbides and nitrides,has intriguing electrochemical energy storage and electrocatalysis applications.Introducing the electronic metal-support interaction(EMSI)effect is one effective strategy to optimize the catalytic efficiency for MXene-based composites.However,most of the studies concentrate on optimizing the performance of metals rather than supported substrates by using this strategy.In this work,we mainly investigate the influence of an EMSI effect on the performance of the supported substrate(Ti_(3)C_(2)T_(x)MXene).Detailed scanning electrochemical microscopy and numerical simulations results reveal that the charge distribution on the Ti_(3)C_(2)T_(x)basal plane(approximate 100 nm-radius)surrounding Au nanoparticles(20 nm-radius)was significantly enhanced as a result of-O being the majority surface functional group on Ti_(3)C_(2)T_(x)that was attached to Au nanoparticle,and the related hydrogen evolution reaction(HER)activity was much better than that of the unaffected Ti_(3)C_(2)T_(x)basal plane,which even can be comparable to that of Au.This finding will be helpful for designing new strategies to enhance the overall catalytic performance of various MXene-based composites.

Electrochemical performance of a nickel-rich LiNi0.6Co0.2Mn0.2O2 cathode material for lithium-ion batteries under different cut-off voltages

A spherical-like Ni0.6Co0.2Mn0.2(OH)2precursor was tuned homogeneously to synthesize LiNi0.6Co0.2Mn0.2O2as a cathode material for lithium-ion batteries. The effects of calcination temperature on the crystal structure, morphology, and the electrochemical performance of the as-prepared LiNi0.6Co0.2Mn0.2O2were investigated in detail. The as-prepared material was characterized by X-ray diffraction, scanning electron microscopy, laser particle size analysis, charge–discharge tests, and cyclic voltammetry measurements. The results show that the spherical-like LiNi0.6Co0.2Mn0.2O2material obtained by calcination at 900°C displayed the most significant layered structure among samples calcined at various temperatures, with a particle size of approximately 10 μm. It delivered an initial discharge capacity of 189.2 mAh•g−1at 0.2C with a capacity retention of 94.0% after 100 cycles between 2.7 and 4.3 V. The as-prepared cathode material also exhibited good rate performance, with a discharge capacity of 119.6 mAh•g−1at 5C. Furthermore, within the cut-off voltage ranges from 2.7 to 4.3, 4.4, and 4.5 V, the initial discharge capacities of the calcined samples were 170.7, 180.9, and 192.8 mAh•g−1, respectively, at a rate of 1C. The corresponding retentions were 86.8%, 80.3%, and 74.4% after 200 cycles, respectively. © 2017, University of Science and Technology Beijing and Springer-Verlag Berlin Heidelberg.

Galvanic corrosion behavior of plain carbon steel-B_4C composite in 3.5% NaCl solution with electrochemical noise

The galvanic corrosion behavior of metal-matrix composite plain carbon steel/boron carbide （B4C） in 3.5% NaCl solution was studied. The composite was locally produced as a weld band on carbon steel by means of the gas tungsten arc welding process and using nickel as the wetting agent. Samples from the weld band, heat-affected zone and parent metal region were extracted precisely and DC/AC electrochemical tests in combination with techniques such as scanning electron microcopy and energy dispersive spectrometry were conducted. The results of the electrochemical tests show that the corrosion resistance of the parent metal sample is higher than that of the welded composite and the HAZ samples. However, as the corrosion potential （Eco^r） of the parent metal is more positive than other two samples, this becomes the cathode in galvanic couples with two other samples. On the other hand, the weld composite sample is also cathodic due to its more positive Ecorr compared to HAZ sample. This means that the HAZ can be particularly at risk of preferential dissolution. The approach can be used in specific areas on plain carbon steel to locally increase hardness and resistance to abrasion and reduce manufacturing costs.

Quantitative micro-electrochemical study of duplex stainless steel 2205 in 3.5wt%NaCl solution

Duplex stainless steels(DSSs)are suffering from various localized corrosion attacks such as pitting,selective dissolution,crevice corrosion during their service period.It is of great value to quantitatively analyze and grasp the micro-electrochemical corrosion behavior and related mechanism for DSSs on the micrometer or even smaller scales.In this work,scanning Kelvin probe force microscopy(SKPFM)and energy dispersive spectroscopy(EDS)measurements were performed to reveal the difference between the austenite phase and ferrite phase in microregion of DSS 2205.Then traditional electrochemical impedance spectroscopy(EIS)and potentiodynamic polarization(PDP)tests were employed for micro-electrochemical characterization of DSS 2205 with different proportion phases inϕ40 andϕ10μm micro holes.Both of them can only be utilized for qualitative or semi-quantitative micro-electrochemical characterization of DSS 2205.Coulostatic perturbation method was employed for quantitative micro-electrochemical characterization of DSS 2205.What is more,the applicable conditions of coulostatic perturbation were analyzed in depth by establishing a detailed electrochemical interface circuit.A series of microregion coulostatic perturbations for DSS 2205 with different proportion phases inϕ10μm micro holes showed that as the austenite proportion increases,the corresponding polarization resistance of microregion increases linearly.

杂质镓对纯铝表面锆钛转化膜的组织及耐腐蚀性能的影响

目的探究杂质镓对纯铝锆钛转化膜的生长规律和防护性能的影响。方法采用扫描电化学显微镜(SECM)技术表征了含镓纯铝表面锆钛转化膜在3.5%(质量分数)NaCl溶液中局部腐蚀的演变过程,结合X射线衍射仪(XRD)、X射线光电子能谱(XPS)、扫描电镜(SEM)等技术分析了镓对纯铝锆钛转化膜的组织及成分的影响规律,采用开路电位法(OCP)、电化学阻抗技术(EIS)以及极化曲线(Tafel)等探究了杂质镓对纯铝表面转化膜的生长和耐腐蚀性能的影响规律。结果锆钛转化膜主要由冰晶石Na3AlF6、氧化物(如TiO_(2)、ZrO_(2)、Al_(2)O_(3))和有机金属络合物组成;杂质镓的添加会抑制铝表面转化膜的生长,破坏膜层的完整性。随镓含量(质量分数)从0%增大到0.5%,锆钛转化膜阻抗值从4.75×10^(4)Ω·cm^(2)不断减小到2.49×10^(3)Ω·cm^(2),自腐蚀电流密度由0.45μA增加到13.4μA,腐蚀电位从-0.485 V降低到-0.890 V,耐腐蚀性能逐渐降低。在锆钛转换膜的SECM微区腐蚀演变过程中,膜层自修复行为会降低膜层的被腐蚀倾向,但富集在表面的镓会抑制自修复膜层的形成,导致基体被严重腐蚀。结论铝中的杂质镓能够直接影响锆钛膜的完整性,降低对铝基体的保护,导致了铝基体局部腐蚀溶解的发生。

Scanning electrochemical microscopy-development of instrumentation utilizing piezo-bimorph X-Y scanners

The development of the instrumentation of a scanning electrochemical microscopy (SECM) is presented. The core of the SECM sensing system is constructed based on piezo-bimorph scanners, a mechanical micropositioner of multi-dimensional adjustment and ultramicroelectrodes. The control of the electrochemical cell and the SECM system is realized by a battery powered bipoteniostat and analog control circuits respectively with the control of a microcomputer work station. The demonstrations of SECM experiments are given on both a standard IDA sample and a silver electrode. Discussions on the resolution and quality of SECM image are made.

Prospective Roles of Scanning Photoelectrochemical Microscopy in Microbial Hybrid Photosynthesis

Microbial hybrid photosynthesis has attracted great interests in recent years since it integrates the advantages of natural and artificial photosynthesis for solar-to-chemical conversion. Coupling a light source with scanning electrochemical microscopy, scanning photoelectrochemical microscopy (SPECM) shows great potential in investigating the interfacial reactions of microbial hybrid photosynthesis. In this Emerging Topic, the potential roles of SPECM in revealing biotic–abiotic interfacial electron transfer mechanisms and calculating electrode process kinetics are proposed for hybrid photosynthesis, and this will also inspire the applications of SPECM in the fields including biomineralization, photocatalytic-biodegradation and microbial photoelectrochemical systems.

SECM基本原理及其在金属腐蚀中的应用

扫描电化学显微镜(SECM)是一种具有较高空间分辨率的化学显微镜,在成像和动力学研究已经广泛应用.本文简要介绍SECM基本原理,综述2009年以来SECM在腐蚀方面的应用,包括扫描成像和异相电子转移化学活性的研究,并简要介绍了作者课题组在SECM方面的研究工作,展望SECM在腐蚀研究的应用.