Triboelectric nanogenerators (TENGs) based on sliding metal–semiconductor junctions are an emerging technology that can efficiently convert mechanical into electrical energy. These miniature autonomous power sources can output large direct current (DC) densities, but often suffer from limited durability; hence, their practical scope remains uncertain. Herein, through a combination of conductive atomic force microscopy (C-AFM) and photocurrent decay (PCM) experiments, we explored the underlying cause of surface wear during the operation of DC-TENGs. Using monolayer-functionalized Si(211) surfaces as the model system, we demonstrate the extent to which surface damage develops during TENG operation. We reveal that the introduction of surface defects (oxide growth) during TENG operation is not caused by the passage of the rather large current densities (average output of ~2 × 106 A/m2); it is instead mainly caused by the large pressure (~GPa) required for the sliding Schottky diode to output a measurable zero-bias current. We also discovered that the drop in output during operation occurs with a delay in the friction/pressure event, which partially explains why such deterioration of DC-TENG performance is often underestimated or not reported.
{"title":"Oxidative Damage during the Operation of Si(211)-Based Triboelectric Nanogenerators","authors":"Carlos Hurtado, S. Ciampi","doi":"10.3390/surfaces6030020","DOIUrl":"https://doi.org/10.3390/surfaces6030020","url":null,"abstract":"Triboelectric nanogenerators (TENGs) based on sliding metal–semiconductor junctions are an emerging technology that can efficiently convert mechanical into electrical energy. These miniature autonomous power sources can output large direct current (DC) densities, but often suffer from limited durability; hence, their practical scope remains uncertain. Herein, through a combination of conductive atomic force microscopy (C-AFM) and photocurrent decay (PCM) experiments, we explored the underlying cause of surface wear during the operation of DC-TENGs. Using monolayer-functionalized Si(211) surfaces as the model system, we demonstrate the extent to which surface damage develops during TENG operation. We reveal that the introduction of surface defects (oxide growth) during TENG operation is not caused by the passage of the rather large current densities (average output of ~2 × 106 A/m2); it is instead mainly caused by the large pressure (~GPa) required for the sliding Schottky diode to output a measurable zero-bias current. We also discovered that the drop in output during operation occurs with a delay in the friction/pressure event, which partially explains why such deterioration of DC-TENG performance is often underestimated or not reported.","PeriodicalId":22129,"journal":{"name":"Surfaces","volume":"2005 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2023-08-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"89872095","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Talita A. Vida, Clarissa Cruz, A. Barros, N. Cheung, C. Brito, Amauri Garcia
The development of biodegradable Zn-based alloys for implants that effectively mimic the functionality of native bone throughout the healing process is a multifaceted challenge; this is particularly evident in the task of achieving appropriate corrosion rates. This work explores the incorporation of 0.5wt.%Mn into a Zn−1wt.%Mg alloy, with focus on the relationship between corrosion behavior and microstructure. Electrochemical corrosion tests were carried out in a 0.06 M NaCl solution using as-solidified samples with two distinct microstructural length scales. Mn addition was found to induce significant electrochemical active behavior. Localized corrosion was predominant in interdendritic regions, with the ternary alloy exhibiting a higher susceptibility. For both alloys, the coarsening of the microstructure promoted a slight inclination to accelerate the corrosion rates in both biodegradable Zn alloys. The corrosion rate showed an increase of about nine-times with Mn addition for coarser eutectic spacings, while for finer ones, the increase was by about 22 times.
生物可降解的锌基合金种植体在整个愈合过程中有效地模仿天然骨的功能是一个多方面的挑战;这在实现适当腐蚀速率的任务中尤为明显。这项工作探讨了0.5wt的合并。%Mn变成Zn - 1wt。%镁合金，重点研究腐蚀行为与微观组织的关系。采用两种不同显微组织长度尺度的凝固试样，在0.06 M NaCl溶液中进行电化学腐蚀试验。发现Mn的加入诱导了显著的电化学活性行为。局部腐蚀主要发生在枝晶间，三元合金表现出较高的腐蚀敏感性。对于这两种合金，组织的粗化促进了腐蚀速率的轻微倾向。对于较粗的共晶间距，Mn的腐蚀速率提高了约9倍，而对于较细的共晶间距，Mn的腐蚀速率提高了约22倍。
{"title":"Biodegradable Zn−1wt.%Mg(−0.5wt.%Mn) Alloys: Influence of Solidification Microstructure on Their Corrosion Behavior","authors":"Talita A. Vida, Clarissa Cruz, A. Barros, N. Cheung, C. Brito, Amauri Garcia","doi":"10.3390/surfaces6030019","DOIUrl":"https://doi.org/10.3390/surfaces6030019","url":null,"abstract":"The development of biodegradable Zn-based alloys for implants that effectively mimic the functionality of native bone throughout the healing process is a multifaceted challenge; this is particularly evident in the task of achieving appropriate corrosion rates. This work explores the incorporation of 0.5wt.%Mn into a Zn−1wt.%Mg alloy, with focus on the relationship between corrosion behavior and microstructure. Electrochemical corrosion tests were carried out in a 0.06 M NaCl solution using as-solidified samples with two distinct microstructural length scales. Mn addition was found to induce significant electrochemical active behavior. Localized corrosion was predominant in interdendritic regions, with the ternary alloy exhibiting a higher susceptibility. For both alloys, the coarsening of the microstructure promoted a slight inclination to accelerate the corrosion rates in both biodegradable Zn alloys. The corrosion rate showed an increase of about nine-times with Mn addition for coarser eutectic spacings, while for finer ones, the increase was by about 22 times.","PeriodicalId":22129,"journal":{"name":"Surfaces","volume":"69 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2023-08-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"82892048","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
We measured spectra of low energy electrons emitted in the interaction of singly charged Ne+ ions with the Mg surface at incident ion energies ranging from 50 eV to 4 keV. The study examines issues related to the excitation of both the surface and the bulk plasmons of the target. We will also focus on the dynamics of the production of the singlet Ne2p4(1D)3s2 and triplet Ne2p4(3P)3s2 autoionizing states of projectiles scattered in a vacuum. The threshold behavior of the autoionization lines show that double excitation occurs simultaneously in a single scattering. The predominant excitation of the triplet state indicates the importance of charge rearrangement and the electron correlation effects during the collisional excitation.
{"title":"Spectra of Low Energy Electrons Emitted in the Interaction of Slow Ne+ Ions with Mg Surfaces","authors":"P. Riccardi, C. Dukes","doi":"10.3390/surfaces6030018","DOIUrl":"https://doi.org/10.3390/surfaces6030018","url":null,"abstract":"We measured spectra of low energy electrons emitted in the interaction of singly charged Ne+ ions with the Mg surface at incident ion energies ranging from 50 eV to 4 keV. The study examines issues related to the excitation of both the surface and the bulk plasmons of the target. We will also focus on the dynamics of the production of the singlet Ne2p4(1D)3s2 and triplet Ne2p4(3P)3s2 autoionizing states of projectiles scattered in a vacuum. The threshold behavior of the autoionization lines show that double excitation occurs simultaneously in a single scattering. The predominant excitation of the triplet state indicates the importance of charge rearrangement and the electron correlation effects during the collisional excitation.","PeriodicalId":22129,"journal":{"name":"Surfaces","volume":"50 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2023-08-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"73613970","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
A flexible chitin nanofiber (ChNF) film with a thin fiber morphology, named, scaled-down (SD)-ChNF film, was previously found to be formed via successive partial deacetylation of the parent self-assembled ChNFs, cationization/dispersion via electrostatic repulsion in aqueous acetic acid, and suction filtration/drying. In this study, acetylation of a SD-ChNF film using acetic anhydride in pyridine was carried out to improve the mechanical properties. The FT-IR spectra of the acetylated SD-ChNF films suggested that acetylation progressed from the surface to the interior of the films with the increasing amounts of pyridine and elevating temperatures. The degrees of acetylation (DA) strongly affected the chitin crystallinity and surface morphology of the acetylated SD-ChNF films. Tensile testing of the acetylated SD-ChNF films indicated that the mechanical properties were improved by adjusting the DA values of the films. For example, the acetylated SD-ChNF film with an 1.84 DA value on surface showed values of 44.1 MPa and 24.9% for tensile strength and elongation at break, respectively.
{"title":"Acetylation of Scaled-Down Chitin Nanofiber Films to Improve Mechanical Properties","authors":"J. Kadokawa, Chiharu Iiyama, Aoi Nakashima","doi":"10.3390/surfaces6030017","DOIUrl":"https://doi.org/10.3390/surfaces6030017","url":null,"abstract":"A flexible chitin nanofiber (ChNF) film with a thin fiber morphology, named, scaled-down (SD)-ChNF film, was previously found to be formed via successive partial deacetylation of the parent self-assembled ChNFs, cationization/dispersion via electrostatic repulsion in aqueous acetic acid, and suction filtration/drying. In this study, acetylation of a SD-ChNF film using acetic anhydride in pyridine was carried out to improve the mechanical properties. The FT-IR spectra of the acetylated SD-ChNF films suggested that acetylation progressed from the surface to the interior of the films with the increasing amounts of pyridine and elevating temperatures. The degrees of acetylation (DA) strongly affected the chitin crystallinity and surface morphology of the acetylated SD-ChNF films. Tensile testing of the acetylated SD-ChNF films indicated that the mechanical properties were improved by adjusting the DA values of the films. For example, the acetylated SD-ChNF film with an 1.84 DA value on surface showed values of 44.1 MPa and 24.9% for tensile strength and elongation at break, respectively.","PeriodicalId":22129,"journal":{"name":"Surfaces","volume":"1 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2023-07-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"88870979","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Flexible and binderless electrodes have become a promising candidate for the next generation of flexible power storage devices. However, developing high-performance electrode materials with high energy density and a long cycle life remains a serious challenge for sodium-ion batteries (SIBs). The main issue is the large volume change in electrode materials during the cycling processes, leading to rapid capacity decay for SIBs. In this study, flexible electrodes for a SnSb alloy–carbon nanofiber (SnSb@NC) membrane were successfully synthesized with the aid of hydrothermal, electrospinning and annealing processes. The as-prepared binderless SnSb@NC flexible anodes were investigated for the storage properties of SIBs at 500 °C, 600 °C and 700 °C (SnSb@NC-500, SnSb@NC-600 and SnSb@NC-700), respectively. And the flexible SnSb@NC-700 electrode displayed the preferable SIB performances, achieving 240 mAh/g after 100 cycles at 0.1 A g−1. In degree-dependent I-V curve measurements, the SnSb@NC-700 membrane exhibited almost the same current at different bending degrees of 0°, 45°, 90°, 120° and 175°, indicating the outstanding mechanical properties of the flexible binderless electrodes.
柔性和无粘结电极已成为下一代柔性电力存储设备的有前途的候选者。然而，开发具有高能量密度和长循环寿命的高性能电极材料仍然是钠离子电池(sib)面临的严峻挑战。主要问题是在循环过程中电极材料的体积变化很大，导致sib的容量快速衰减。本研究通过水热法、静电纺丝法和退火法成功地合成了SnSb合金-碳纳米纤维(SnSb@NC)薄膜的柔性电极。研究了制备的无粘结剂SnSb@NC柔性阳极在500°C、600°C和700°C (SnSb@NC-500、SnSb@NC-600和SnSb@NC-700)下SIBs的存储性能。在0.1 A g−1下循环100次后，柔性SnSb@NC-700电极显示出较好的SIB性能，达到240 mAh/g。在不同弯曲度(0°、45°、90°、120°和175°)的I-V曲线测量中，SnSb@NC-700膜在不同弯曲度(0°、45°、90°、120°和175°)下表现出几乎相同的电流，表明柔性无粘结剂电极具有优异的力学性能。
{"title":"Using Highly Flexible SbSn@NC Nanofibers as Binderless Anodes for Sodium-Ion Batteries","authors":"Jiaojiao Liang, Gengkun Fang, Xinmiao Niu, Zhi Zhang, Yufei Wang, Lingyuan Liao, Xiaoming Zheng, Di Huang, Yuehua Wei","doi":"10.3390/surfaces6030016","DOIUrl":"https://doi.org/10.3390/surfaces6030016","url":null,"abstract":"Flexible and binderless electrodes have become a promising candidate for the next generation of flexible power storage devices. However, developing high-performance electrode materials with high energy density and a long cycle life remains a serious challenge for sodium-ion batteries (SIBs). The main issue is the large volume change in electrode materials during the cycling processes, leading to rapid capacity decay for SIBs. In this study, flexible electrodes for a SnSb alloy–carbon nanofiber (SnSb@NC) membrane were successfully synthesized with the aid of hydrothermal, electrospinning and annealing processes. The as-prepared binderless SnSb@NC flexible anodes were investigated for the storage properties of SIBs at 500 °C, 600 °C and 700 °C (SnSb@NC-500, SnSb@NC-600 and SnSb@NC-700), respectively. And the flexible SnSb@NC-700 electrode displayed the preferable SIB performances, achieving 240 mAh/g after 100 cycles at 0.1 A g−1. In degree-dependent I-V curve measurements, the SnSb@NC-700 membrane exhibited almost the same current at different bending degrees of 0°, 45°, 90°, 120° and 175°, indicating the outstanding mechanical properties of the flexible binderless electrodes.","PeriodicalId":22129,"journal":{"name":"Surfaces","volume":"55 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2023-07-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"83886499","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Elisa Tosin, T. Gatti, S. Agnoli, L. Calvillo, E. Menna
The search of active, stable and low costs catalysts for the oxygen reduction reaction (ORR) is crucial for the extensive use of fuel cells and metal–air batteries. The development of metal-free catalysts, instead of platinum-based materials, can dramatically reduce the cost and increase the efficiency of these devices. In this work, carbon nanohorns (CNHs) have been covalently functionalized with N-containing heterocycles by the Tour reaction protocol and tested as metal-free ORR catalysts. The insertion of N-functionalities favored the complete reduction of oxygen to hydroxyl ions, while their absence favored the production of hydrogen peroxide. With the aim of determining the N-species responsible for the ORR activity of CNHs, photoemission and electrochemical measurements were combined. Results suggest that protonated N is the main species involved in the ORR process, facilitating the adsorption of oxygen, with their consequent reduction to neutral hydrogenated N species.
{"title":"Nitrogen- and Fluorine-Doped Carbon Nanohorns as Efficient Metal-Free Oxygen Reduction Catalyst: Role of the Nitrogen Groups","authors":"Elisa Tosin, T. Gatti, S. Agnoli, L. Calvillo, E. Menna","doi":"10.3390/surfaces6030015","DOIUrl":"https://doi.org/10.3390/surfaces6030015","url":null,"abstract":"The search of active, stable and low costs catalysts for the oxygen reduction reaction (ORR) is crucial for the extensive use of fuel cells and metal–air batteries. The development of metal-free catalysts, instead of platinum-based materials, can dramatically reduce the cost and increase the efficiency of these devices. In this work, carbon nanohorns (CNHs) have been covalently functionalized with N-containing heterocycles by the Tour reaction protocol and tested as metal-free ORR catalysts. The insertion of N-functionalities favored the complete reduction of oxygen to hydroxyl ions, while their absence favored the production of hydrogen peroxide. With the aim of determining the N-species responsible for the ORR activity of CNHs, photoemission and electrochemical measurements were combined. Results suggest that protonated N is the main species involved in the ORR process, facilitating the adsorption of oxygen, with their consequent reduction to neutral hydrogenated N species.","PeriodicalId":22129,"journal":{"name":"Surfaces","volume":"32 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2023-07-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"79969936","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
V. Tarasenko, D. Beloplotov, A. N. Panchenko, D. Sorokin
Features of the nanosecond discharge development in a non-uniform electric field are studied experimentally. High spatial resolution imaging showed that thin luminous tracks of great length with a cross-section of a few microns are observed against the background of discharge glow in air and argon. It has been established that the detected tracks are adjacent to brightly luminous white spots on the electrodes or in the vicinity of these spots, and are associated with the flight of small particles. It is shown that the tracks have various shapes and change from pulse to pulse. The particle tracks may look like curvy or straight lines. In some photos, they can change their direction of movement to the opposite. It was found that the particle’s track abruptly breaks and a bright flash is visible at the break point. The color of the tracks differs from that of the spark leaders, while the bands of the second positive nitrogen system dominate in the plasma emission spectra during the existence of a diffuse discharge. Areas of blue light are visible near the electrodes as well. The development of glow and thin luminous tracks in the gap during its breakdown is revealed using an ICCD camera. Physical reasons for the observed phenomena are discussed.
{"title":"Thin Luminous Tracks of Particles Released from Electrodes with A Small Radius of Curvature in Pulsed Nanosecond Discharges in Air and Argon","authors":"V. Tarasenko, D. Beloplotov, A. N. Panchenko, D. Sorokin","doi":"10.3390/surfaces6020014","DOIUrl":"https://doi.org/10.3390/surfaces6020014","url":null,"abstract":"Features of the nanosecond discharge development in a non-uniform electric field are studied experimentally. High spatial resolution imaging showed that thin luminous tracks of great length with a cross-section of a few microns are observed against the background of discharge glow in air and argon. It has been established that the detected tracks are adjacent to brightly luminous white spots on the electrodes or in the vicinity of these spots, and are associated with the flight of small particles. It is shown that the tracks have various shapes and change from pulse to pulse. The particle tracks may look like curvy or straight lines. In some photos, they can change their direction of movement to the opposite. It was found that the particle’s track abruptly breaks and a bright flash is visible at the break point. The color of the tracks differs from that of the spark leaders, while the bands of the second positive nitrogen system dominate in the plasma emission spectra during the existence of a diffuse discharge. Areas of blue light are visible near the electrodes as well. The development of glow and thin luminous tracks in the gap during its breakdown is revealed using an ICCD camera. Physical reasons for the observed phenomena are discussed.","PeriodicalId":22129,"journal":{"name":"Surfaces","volume":"7 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2023-06-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"73248274","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Marlena Gęca, A. Khalil, Mengqi Tang, A. Bhakta, Y. Snoussi, P. Nowicki, M. Wiśniewska, M. Chehimi
In recent years, biochar has emerged as a remarkable biosourced material for addressing global environmental, agricultural, biomedical, and energy challenges. However, the performances of biochar rest in part on finely tuning its surface chemical properties, intended to obtain specific functionalities. In this review, we tackle the surface treatment of biochar with silane and other coupling agents such as diazonium salts, titanates, ionic/non-ionic surfactants, as well as nitrogen-containing (macro)molecules. We summarize the recent progress achieved mostly in the last five years and correlate the nature and extent of functionalization to eye-catchy end applications of the surface-engineered biochar.
{"title":"Surface Treatment of Biochar—Methods, Surface Analysis and Potential Applications: A Comprehensive Review","authors":"Marlena Gęca, A. Khalil, Mengqi Tang, A. Bhakta, Y. Snoussi, P. Nowicki, M. Wiśniewska, M. Chehimi","doi":"10.3390/surfaces6020013","DOIUrl":"https://doi.org/10.3390/surfaces6020013","url":null,"abstract":"In recent years, biochar has emerged as a remarkable biosourced material for addressing global environmental, agricultural, biomedical, and energy challenges. However, the performances of biochar rest in part on finely tuning its surface chemical properties, intended to obtain specific functionalities. In this review, we tackle the surface treatment of biochar with silane and other coupling agents such as diazonium salts, titanates, ionic/non-ionic surfactants, as well as nitrogen-containing (macro)molecules. We summarize the recent progress achieved mostly in the last five years and correlate the nature and extent of functionalization to eye-catchy end applications of the surface-engineered biochar.","PeriodicalId":22129,"journal":{"name":"Surfaces","volume":"28 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2023-06-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"83593235","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
M. Iioka, W. Kawanabe, Tatsuya Kobayashi, I. Shohji, Kota Sakamoto
In this study, the fabrication of nickel (Ni)-cellulose nanofiber (CNF) composite electroplating films was attempted using sodium carboxymethyl cellulose (CMC) and 2,2,6,6-tetramethylpiperidine 1-oxyl (TEMPO)-oxidized CNF as CNF introduced with carboxy groups. As a result, co-deposition was confirmed for both CNFs, and the former showed 82% improvement in surface Vickers hardness compared to the plated film deposited from a conventional Watts bath without CNF. Although the latter showed slightly inferior 71% improvement, the surface roughness measurement showed a smoother surface than that of the plated copper material C1100. On the other hand, the film with CMC had a rough surface. The image analysis showed that the distance between co-deposited CNF on the surface of the plated film was 40% shorter on the specimen with TEMPO CNF than CMC, indicating that a fine dispersion was obtained. In addition, a co-deposition model was proposed in which Ni is deposited from the chelate complex formed between the carboxylate of CNF and Ni ions. CNF is fixed to the plated film surface by Ni deposition and the simultaneous bond of hydrogen ions to the carboxylate, resulting in a return to the carboxy group.
{"title":"Fabrication of Electroplated Nickel Composite Films Using Cellulose Nanofibers Introduced with Carboxy Groups as Co-Deposited Materials","authors":"M. Iioka, W. Kawanabe, Tatsuya Kobayashi, I. Shohji, Kota Sakamoto","doi":"10.3390/surfaces6020012","DOIUrl":"https://doi.org/10.3390/surfaces6020012","url":null,"abstract":"In this study, the fabrication of nickel (Ni)-cellulose nanofiber (CNF) composite electroplating films was attempted using sodium carboxymethyl cellulose (CMC) and 2,2,6,6-tetramethylpiperidine 1-oxyl (TEMPO)-oxidized CNF as CNF introduced with carboxy groups. As a result, co-deposition was confirmed for both CNFs, and the former showed 82% improvement in surface Vickers hardness compared to the plated film deposited from a conventional Watts bath without CNF. Although the latter showed slightly inferior 71% improvement, the surface roughness measurement showed a smoother surface than that of the plated copper material C1100. On the other hand, the film with CMC had a rough surface. The image analysis showed that the distance between co-deposited CNF on the surface of the plated film was 40% shorter on the specimen with TEMPO CNF than CMC, indicating that a fine dispersion was obtained. In addition, a co-deposition model was proposed in which Ni is deposited from the chelate complex formed between the carboxylate of CNF and Ni ions. CNF is fixed to the plated film surface by Ni deposition and the simultaneous bond of hydrogen ions to the carboxylate, resulting in a return to the carboxy group.","PeriodicalId":22129,"journal":{"name":"Surfaces","volume":"763 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2023-05-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"76919486","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Microfluidic devices are increasingly utilized in numerous industries, including that of medicine, for their abilities to pump and mix fluid at a microscale. Within these devices, microchannels paired with microelectrodes enable the mixing and transportation of ionized fluid. The ionization process charges the microchannel and manipulates the fluid with an electric field. Although complex in operation at the microscale, microchannels within microfluidic devices are easy to produce and economical. This paper uses simulations to convey helpful insights into the analysis of electrokinetic microfluidic device phenomena. The simulations in this paper use the Navier–Stokes and Poisson Nernst–Planck equations solved using COMSOL to determine the maximum attainable fluid velocity with an electric potential applied to the microchannel and the most suitable frequency or voltage to use for transporting the fluid. Alternating current electroosmosis (ACEO) directs and provides velocity to the ionized fluid. ACEO can also mix the fluid at low frequencies for the purpose of dispersing particles. DC electroosmosis (DCEO) applies voltage along the microchannel to create an electric field that ionizes fluid within the microchannel, making it a cost-effective method for transporting fluid. This paper explores a method for an alternate efficient utilization of microfluidic devices for efficient mixing and transportation of ionized fluid and analyzes the electrokinetic phenomena through simulations using the Navier–Stokes and Poisson Nernst–Planck equations. The results provide insights into the parameters at play for transporting the fluid using alternating current electroosmosis (ACEO) and DC electroosmosis (DCEO).
{"title":"Long-Range ACEO Phenomena in Microfluidic Channel","authors":"D. Dutta, K. Smith, X. Palmer","doi":"10.3390/surfaces6020011","DOIUrl":"https://doi.org/10.3390/surfaces6020011","url":null,"abstract":"Microfluidic devices are increasingly utilized in numerous industries, including that of medicine, for their abilities to pump and mix fluid at a microscale. Within these devices, microchannels paired with microelectrodes enable the mixing and transportation of ionized fluid. The ionization process charges the microchannel and manipulates the fluid with an electric field. Although complex in operation at the microscale, microchannels within microfluidic devices are easy to produce and economical. This paper uses simulations to convey helpful insights into the analysis of electrokinetic microfluidic device phenomena. The simulations in this paper use the Navier–Stokes and Poisson Nernst–Planck equations solved using COMSOL to determine the maximum attainable fluid velocity with an electric potential applied to the microchannel and the most suitable frequency or voltage to use for transporting the fluid. Alternating current electroosmosis (ACEO) directs and provides velocity to the ionized fluid. ACEO can also mix the fluid at low frequencies for the purpose of dispersing particles. DC electroosmosis (DCEO) applies voltage along the microchannel to create an electric field that ionizes fluid within the microchannel, making it a cost-effective method for transporting fluid. This paper explores a method for an alternate efficient utilization of microfluidic devices for efficient mixing and transportation of ionized fluid and analyzes the electrokinetic phenomena through simulations using the Navier–Stokes and Poisson Nernst–Planck equations. The results provide insights into the parameters at play for transporting the fluid using alternating current electroosmosis (ACEO) and DC electroosmosis (DCEO).","PeriodicalId":22129,"journal":{"name":"Surfaces","volume":"101 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2023-04-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"78703060","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
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