Electrodes Toward(电极朝向)研究综述
Electrodes Toward 电极朝向 - Until now, tremendous efforts have been dedicated to the development of cathode materials with innovative characteristics, while scarce efforts have been concentrated on the study of the catalyst layer aiming at maximizing the performance of the electrodes toward the CO2RR. [1] Here, we show that the push process, in which molecular junctions are formed by bringing the electrodes towards each other, allows the fabrication of molecular junction structures that are not necessarily formed in the pull process. [2] The cyclic voltammetry (CV) analysis revealed the superior electrochemical performance of Ag 2TiO3 than other electrodes towards metronidazole (MTZ) detection. [3] To demonstrate this methodology, we proceed as follows: after assessing the basic electrochemical properties of a-C films, we investigate the effect of short HNO3 treatment on the sensitivity of these electrodes towards an inner sphere redox probe (ISR) dopamine (DA) to gain knowledge about the influence of altered surface chemistry to observed electrochemical performance. [4] This work supply an effective but facile strategy to enhance the performance of carbon-based electrodes towards 2eORR by regulating the micro-environment of electrodes. [5] Finally, a preliminary investigation of the photoelectrodes towards benzyl alcohol oxidation is presented, achieving photocurrent density up to 90 μA/cm2 in acetonitrile in the presence of N-hydroxysuccinimide and pyridine as redox mediator and base, respectively. [6] The responses of oxidized Zn–In electrodes towards different cholesterol concentration (01 μM – 9 mM) have been recorded by cyclic voltammetry (CV) and amperometry in phosphate buffer solution without using any enzymes. [7] The coatings were evaluated as photoelectrodes towards thiosulfate oxidation and oxygen reduction. [8] The performance of both electrodes towards nitrite oxidation was tested and it was found that GC/Au/Cu-YBDC exhibited a better electrocatalytic behavior toward the oxidation of nitrite than GC/Cu-YBDC with enhanced catalytic currents and a reduced nitrite overpotential from 1. [9] The performance of electrodes towards detection and quantification of CHL was investigated through square wave voltammetry. [10] Photoredution and micro-nanostructuring of GO using laser holography may hold great promise for production of effective carbon-based electrodes towards practical applications in energy storage devices. [11] The feasibility of the developed micro PFC with dual photoelectrodes toward the applications of using solar energy to remove organic pollutants contained in wastewater and simultaneously generate electricity is demonstrated in this work. [12] Especially, it provides a superior way to design photoelectrodes towards PEC application. [13] Herein, an attempt is made to investigate how certain carbon features determine the properties and the performance of electrodes towards the HER. [14]到目前为止，人们一直致力于开发具有创新特性的正极材料，而很少有精力集中在催化剂层的研究上，旨在最大限度地提高电极对 CO2RR 的性能。 [1] 在这里，我们展示了推动过程，其中通过使电极彼此靠近来形成分子结，允许制造在拉过程中不一定形成的分子结结构。 [2] 循环伏安法 (CV) 分析表明，Ag 2TiO3 在检测甲硝唑 (MTZ) 方面的电化学性能优于其他电极。 [3] 为了证明这种方法，我们进行如下：在评估 a-C 薄膜的基本电化学特性后，我们研究了短 HNO3 处理对这些电极对内球氧化还原探针 (ISR) 多巴胺 (DA) 敏感性的影响，以获得知识关于改变的表面化学对观察到的电化学性能的影响。 [4] 这项工作提供了一种有效但简便的策略，通过调节电极的微环境来提高碳基电极对 2eORR 的性能。 [5] 最后，介绍了光电极对苯甲醇氧化的初步研究，在 N-羟基琥珀酰亚胺和吡啶作为氧化还原介质和碱的情况下，在乙腈中分别实现了高达 90 μA/cm2 的光电流密度。 [6] 在不使用任何酶的情况下，通过循环伏安法 (CV) 和安培法在磷酸盐缓冲溶液中记录了氧化 Zn-In 电极对不同胆固醇浓度 (01 μM – 9 mM) 的响应。 [7] 涂层被评估为对硫代硫酸盐氧化和氧还原的光电极。 [8] 测试了两个电极对亚硝酸盐氧化的性能，发现 GC/Au/Cu-YBDC 对亚硝酸盐的氧化表现出比 GC/Cu-YBDC 更好的电催化行为，具有增强的催化电流和从 1 降低的亚硝酸盐过电位。 [9] 通过方波伏安法研究了电极对 CHL 的检测和定量的性能。 [10] 使用激光全息术对 GO 进行光还原和微纳米结构化可能对生产有效的碳基电极在储能设备中的实际应用具有很大的前景。 [11] 这项工作证明了开发的具有双光电极的微型 PFC 在利用太阳能去除废水中含有的有机污染物并同时发电的应用中的可行性。 [12] 特别是，它为设计用于 PEC 应用的光电极提供了一种优越的方法。 [13] 在此，试图研究某些碳特征如何决定电极对 HER 的特性和性能。 [14]
oxygen reduction reaction
The electrocatalytic activity of the electrodes towards the oxygen reduction reaction (ORR) was studied as a function of pH using cyclic voltammetry with a rotating disk electrode. [1] As a result, an enhanced activity of BL30-BL70 electrodes towards oxygen reduction reaction is detected in comparison to LSCF or BSCF pure powders. [2] Electrocatalytic activity of both TNT and NP electrodes toward oxygen reduction reaction (ORR) has been examined by cyclic voltammetry (CV). [3]使用带有旋转圆盘电极的循环伏安法研究了电极对氧还原反应 (ORR) 的电催化活性作为 pH 值的函数。 [1] 结果，与 LSCF 或 BSCF 纯粉末相比，检测到 BL30-BL70 电极对氧还原反应的活性增强。 [2] TNT 和 NP 电极对氧还原反应 (ORR) 的电催化活性已通过循环伏安法 (CV) 进行了检测。 [3]
hydrogen evolution reaction 析氢反应
In this work, atomic layer deposition (ALD) was exploited for the deposition of MoS2 onto 3D-printed metallic electrodes toward hydrogen evolution reaction (HER) under the acidic condition. [1]在这项工作中，原子层沉积 (ALD) 被用于在酸性条件下将 MoS2 沉积到 3D 打印的金属电极上进行析氢反应 (HER)。 [1]
Modified Electrodes Toward 修饰电极
The electrochemical response characteristics of the modified electrodes toward glucose were investigated by cyclic voltammetry (CV) and chronoamperometry (CA). [1] Electrochemical characterization indicates higher activity for the GTO(S)-Gr composite modified electrode than the individual graphene, GTO(S) and GTO(H) component modified electrodes towards DA and ACE sensing. [2] The prepared MIP/ErGO/GCE exhibited better analytical performance than other modified electrodes toward NVP detection. [3] Results showed that the 3D structure of rGO clusters greatly increased its effective surface area and improved the electronic transmission efficiency of the composite nanomaterial thus the Pt/PANI/rGO/CuO modified electrodes displayed much higher electrocatalytic activity than the Pt/PANI/CuO modified electrodes towards glucose, exhibiting a high sensitivity of 1252 μA mM−1 cm−2, a fast response time of l -ascorbic acid (AA), acetaminophen (AP) and uric acid (UA) and retained ~ 90% of its initial sensitivity after 15 days. [4] The deposition methods of NiCo2O4 MSs were found to affect the electrochemical behavior of the modified electrodes towards the oxidation of venlafaxine (VEN), an anti-depressant drug. [5] The as-prepared materials were first screened and optimized, and then, a series of characterizations and electrochemical measurements of modified electrodes towards glycerol were performed. [6] The Au nanostructures on rGO-$$\hbox {MnFe}_{{2}}\hbox {O}_{4}$$MnFe2O4 improved the electrocatalytic activity of the rGO-$$\hbox {MnFe}_{{2}}\hbox {O}_{{4}}$$MnFe2O4@Au composite-materials-modified electrodes towards glucose oxidation. [7] The time and potential of MnO2 electrodeposition influenced the electrocatalytic properties of the modified electrodes towards H2O2. [8]通过循环伏安法（CV）和计时电流法（CA）研究了修饰电极对葡萄糖的电化学响应特性。 [1] 电化学表征表明，GTO(S)-Gr 复合修饰电极比单独的石墨烯、GTO(S) 和 GTO(H) 组分修饰电极对 DA 和 ACE 传感具有更高的活性。 [2] nan [3] 结果表明，rGO簇的3D结构大大增加了其有效表面积并提高了复合纳米材料的电子传输效率，因此Pt/PANI/rGO/CuO修饰电极比Pt/PANI/CuO修饰电极表现出更高的电催化活性。对葡萄糖，表现出 1252 μA mM-1 cm-2 的高灵敏度，L-抗坏血酸 (AA)、对乙酰氨基酚 (AP) 和尿酸 (UA) 的快速响应时间，并在之后保留了约 90% 的初始灵敏度15天。 [4] 发现 NiCo2O4 MSs 的沉积方法会影响修饰电极对抗抑郁药物文拉法辛 (VEN) 氧化的电化学行为。 [5] nan [6] nan [7] nan [8]
Advanced Electrodes Toward 先进的电极
Our doping-induced polymorph engineering may be applicable to other advanced electrodes toward energy storage applications. [1] Carbon based metal-free materials owing to their abundance, electrical conductivity, porosity, structural modification at the molecular levels and exceptional stability under harsh conditions are emerging as advanced electrodes toward the design of high-performance oxygen electrocatalysts. [2] Moreover, the unique natural three-dimensional structure and moderate graphitization degree of leaf-based carbon facilitate Na+/e− transport to activate selenium which can guarantee a high utilization of the selenium during discharge/charge process, demonstrating a promising strategy to fabricate advanced electrodes toward the sodium-selenium batteries. [3]我们的掺杂诱导多晶型工程可能适用于其他先进的能量存储应用电极。 [1] 碳基无金属材料由于其丰度、导电性、孔隙率、分子水平的结构改性以及在恶劣条件下的出色稳定性，正在成为设计高性能氧电催化剂的先进电极。 [2] nan [3]
Posterior Electrodes Toward
The patterns differences were minor and concerned stronger propagation from the posterior electrodes towards the frontal ones during the visual task and from the temporal sites to the frontal ones during the auditory task, which can be explained as bottom-up communication from specific sensory sites. [1] The differences between the patterns of transmission between the visual and auditory versions of working memory tasks were subtle and involved bigger propagation from the posterior electrodes towards the frontal ones during the visual task as well as from the temporal sites to the frontal ones during the auditory task. [2]模式差异很小，并且涉及在视觉任务期间从后部电极向额部电极的更强传播，以及在听觉任务期间从颞部到额部的更强传播，这可以解释为来自特定感觉部位的自下而上的通信。 [1] 工作记忆任务的视觉和听觉版本之间的传输模式之间的差异是微妙的，并且涉及在视觉任务期间从后部电极到额叶的更大传播，以及在听觉任务期间从颞部到额叶的更大传播. [2]
Carbon Electrodes Toward
Electrocatalytic activity of chromium-carbon electrodes towards hydrogen evolution reaction was studied in this work. [1] Herein, the reactivity of iodophenyl and ethynylphenyl-terminated carbon electrodes towards the Sonogashira coupling with ethynylferrocene and iodoferrocene was examined and multilayer and monolayer underlying chemically addressable platforms were compared. [2]本工作研究了铬碳电极对析氢反应的电催化活性。 [1] 在此，研究了碘苯基和乙炔基苯基封端的碳电极对与乙炔基二茂铁和碘二茂铁偶联的 Sonogashira 的反应性，并比较了底层的化学可寻址平台的多层和单层。 [2]
Two Electrodes Toward
Photocurrent measurements (1C) are made applying bias between two electrodes toward the CdSe-rich end of a typical nanowire photodetector array, under the labelled irradiances by 490 nm light. [1] The catalytic activities of these two electrodes towards methanol oxidation were determined by cyclic voltammetry (CV) testing, and a superior electrocatalytic activity and poisoning tolerance were detected for the electrode prepared by pulse deposition. [2]光电流测量 (1C) 是在两个电极之间向典型纳米线光电探测器阵列的富含 CdSe 的一端施加偏压，在 490 nm 光的标记辐照度下进行的。 [1] 通过循环伏安法（CV）测试确定了这两种电极对甲醇氧化的催化活性，并检测到脉冲沉积制备的电极具有优异的电催化活性和抗中毒能力。 [2]
Composite Electrodes Toward
The superior sensitivity of these modified composite electrodes towards lead and copper ions has largely been attributed to its enhanced surface area, electronic conductivity, and enhanced electron transport rate which eventually results in better catalytic response of the target species. [1] All the above results demonstrate the feasibility of using sustainable nanocellulose as a nanoscale carbon substrate for the synthesis of hybrid composite electrodes toward renewable supercapacitor applications. [2]这些改性复合电极对铅和铜离子的卓越灵敏度很大程度上归因于其增强的表面积、电子导电性和增强的电子传输速率，最终导致目标物质的催化响应更好。 [1] 所有上述结果都证明了使用可持续纳米纤维素作为纳米级碳基底来合成用于可再生超级电容器应用的混合复合电极的可行性。 [2]
Type Electrodes Toward 类型电极朝向
Herein, through insertion of 1D core‐shell conductive BC@PPy nanofibers between MXene nanosheets, an interlayer structure engineering technique for MXene/BC@PPy capacitor‐type electrodes towards ZHMSCs is presented. [1] The structural evolution addressed in the study updates the understanding of conversion reactions and sheds light on novel types of conversion-type electrodes towards the full-cell application of conversion-reaction electrodes. [2]在此，通过在 MXene 纳米片之间插入一维核壳导电 BC@PPy 纳米纤维，提出了一种面向 ZHMSCs 的 MXene/BC@PPy 电容器型电极的层间结构工程技术。 [1] 该研究中涉及的结构演变更新了对转化反应的理解，并揭示了新型转化型电极在转化反应电极的全电池应用中的应用。 [2]
electrodes toward high
This study provides a novel strategy for constructing thick electrodes toward high energy density LIBs. [1] Furthermore, research directions of anodes, electrolytes, and air electrodes toward high-performance HSABs are proposed. [2]该研究为构建厚电极以实现高能量密度锂离子电池提供了一种新策略。 [1] nan [2]
electrodes toward pec
These results provide an efficient way to design and develop high-performance photoelectrodes toward PEC hydrogen evolution. [1] Here, an innovative charge-transfer manipulation concept based on the aligned hole transport across the interface has been realized to enhance the photostability of In2S3 electrodes toward PEC solar hydrogen production. [2]这些结果为设计和开发用于 PEC 析氢的高性能光电极提供了一种有效的方法。 [1] 在这里，已经实现了基于跨界面对齐空穴传输的创新电荷转移操作概念，以提高 In2S3 电极对 PEC 太阳能制氢的光稳定性。 [2]
electrodes toward oxygen
The results of electrochemical tests demonstrated that thus-prepared NPG possesses higher electrocatalytic activity than other types of gold electrodes toward oxygen reduction in alkaline media. [1] Electrocatalytic activity of both TNT and NP electrodes toward oxygen reduction reaction (ORR) has been examined by cyclic voltammetry (CV). [2]电化学测试结果表明，由此制备的 NPG 比其他类型的金电极对碱性介质中的氧还原具有更高的电催化活性。 [1] TNT 和 NP 电极对氧还原反应 (ORR) 的电催化活性已通过循环伏安法 (CV) 进行了检测。 [2]