Chia-Yu Chang , Wei-Hsiang Huang , Meng-Che Tsai , Chih-Wen Pao , Jeng-Lung Chen , Masato Yoshimura , Nozomu Hiraoka , Chi-Liang Chen , Bing Joe Hwang , Wei-Nien Su
{"title":"Turning natural copper phthalocyanine into high-loading single-atom catalysts using an electrochemically-generated template and cationic substitution","authors":"Chia-Yu Chang , Wei-Hsiang Huang , Meng-Che Tsai , Chih-Wen Pao , Jeng-Lung Chen , Masato Yoshimura , Nozomu Hiraoka , Chi-Liang Chen , Bing Joe Hwang , Wei-Nien Su","doi":"10.1016/j.mtnano.2024.100466","DOIUrl":"10.1016/j.mtnano.2024.100466","url":null,"abstract":"<div><p>Phthalocyanine (PC) has a unique N<sub>4</sub>-coordinated structure that offers an inherent advantage with respect to the accommodation of metal ions. This feature can help overcome the limitations of many single-atom electrocatalysts, <em>i.e</em>. low loading and poor stability. Here, we detail the development of a universal electrochemical template and a cationic substitution synthesis protocol for preparing various single-atom catalysts with high-loading (≌ 8.6 wt%) from commercial copper phthalocyanine (CuPC). Commercial CuPC is transformed into Cu NPs and vacant N<sub>4</sub>-sites are created during applied potential cycling. The generated vacant N<sub>4</sub>-sites, with strong negative charges, can take-up Pd<sup>2+</sup> ions from a precursor solution to create single-atom catalysts with Pd high-loadings. The material’s structural transformation and cationic substitution mechanism were investigated by <em>in situ</em> X-ray absorption spectroscopy (XAS). We also demonstrate the viability of extending the proposed electrochemical template synthesis method to the development of other high-loading transition metal single-atom catalysts, <em>e.g</em>., Ni, Co, and Fe.</p></div>","PeriodicalId":48517,"journal":{"name":"Materials Today Nano","volume":"25 ","pages":"Article 100466"},"PeriodicalIF":10.3,"publicationDate":"2024-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140008887","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Alexander Yu. Polyakov , Serge Al Bacha , Waleed M.A. El Rouby , Battulga Munkhbat , Loïc Assaud , Pierre Millet , Björn Wickman , Timur O. Shegai
{"title":"Top-down nanostructured multilayer MoS2 with atomically sharp edges for electrochemical hydrogen evolution reaction","authors":"Alexander Yu. Polyakov , Serge Al Bacha , Waleed M.A. El Rouby , Battulga Munkhbat , Loïc Assaud , Pierre Millet , Björn Wickman , Timur O. Shegai","doi":"10.1016/j.mtnano.2024.100467","DOIUrl":"10.1016/j.mtnano.2024.100467","url":null,"abstract":"<div><p>Cost-efficient and readily scalable platinum-free electrocatalysts are crucial for a smooth transition to future renewable energy systems. Top-down activation of MoS<sub>2</sub> promises the production of sustainable hydrogen evolution electrocatalysts from the Earth-abundant molybdenite ore. Here, the deterministic nanopatterning of multilayer MoS<sub>2</sub> with numerous zigzag edges is explored as a pathway to enhance hydrogen evolution reaction (HER). Nanopatterned single-nanosheet MoS<sub>2</sub> electrodes are assessed by two highly localized electrochemical techniques: selected area voltammetry (with lithography-defined regions of electrode-electrolyte contact) and Scanning ElectroChemical Microscopy (SECM). The nanopatterning effect is the most pronounced after prolonged electrochemical cycling in an acidic electrolyte. The electrocatalytic hydrogen evolution activity of edge-enriched electrodes is dramatically enhanced: the maximum electrochemical current density (<em>j</em><span><math><msub><mrow></mrow><mrow><mi>m</mi><mi>a</mi><mi>x</mi></mrow></msub></math></span>) achieved at -510 mV <em>vs.</em> reversible hydrogen electrode (mV<span><math><msub><mrow></mrow><mrow><mi>R</mi><mi>H</mi><mi>E</mi></mrow></msub></math></span>) is increased by two orders of magnitude, reaching >300 mA⋅cm<sup>−2</sup>. Both the <span><math><msub><mrow><mi>η</mi></mrow><mrow><mn>10</mn></mrow></msub></math></span> and <span><math><msub><mrow><mi>η</mi></mrow><mrow><mn>100</mn></mrow></msub></math></span> overpotentials are significantly reduced as well. Meanwhile, pristine MoS<sub>2</sub> shows just ≈6 times <em>j</em><span><math><msub><mrow></mrow><mrow><mi>m</mi><mi>a</mi><mi>x</mi></mrow></msub></math></span> increase (≈30 mA⋅cm<sup>−2</sup>) after the very same cycling. The increased electrocatalytic activity comes with electrode morphology degradation, evidenced by <em>ex-situ</em> scanning electron microscopy. SECM directly visualizes stronger HER activity in the regions with densely located zigzag edges. Intense white light illumination significantly boosts HER on MoS<sub>2</sub> electrodes due to the photo-enhanced MoS<sub>2</sub> conductivity. These results improve the understanding and reveal the limitations of MoS<sub>2</sub>-based electrocatalytic water splitting.</p></div>","PeriodicalId":48517,"journal":{"name":"Materials Today Nano","volume":"25 ","pages":"Article 100467"},"PeriodicalIF":10.3,"publicationDate":"2024-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2588842024000178/pdfft?md5=4ee03064602381d88478f916af8fef0f&pid=1-s2.0-S2588842024000178-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140046313","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Yuta Aida , Yasuhiro Nakagawa , Tetsuo Kishi , Masaki Takeguchi , Yoshihiro Nemoto , Yasutaka Anraku , Toshiyuki Ikoma
{"title":"Growth mechanism of star-shaped Au–Ag nanoparticles synthesized by ascorbic acid reduction and underpotential deposition","authors":"Yuta Aida , Yasuhiro Nakagawa , Tetsuo Kishi , Masaki Takeguchi , Yoshihiro Nemoto , Yasutaka Anraku , Toshiyuki Ikoma","doi":"10.1016/j.mtnano.2024.100468","DOIUrl":"https://doi.org/10.1016/j.mtnano.2024.100468","url":null,"abstract":"<div><p>The growth mechanism of star-shaped Au–Ag nanoparticles, which is important for improving the absorption efficiency of nanoparticles in the near-infrared region, remains to be clarified. In this study, the growth mechanism by stabilizing certain facets of Au in spines by underpotential deposition of Ag was investigated. The nanoparticles were analyzed primarily by scanning transmission electron microscopy (STEM) and energy dispersive X-ray spectroscopy. Analysis of spines on nanoparticles synthesized with an Au/Ag ratio of 18/4 revealed that approximately 1 nm of Ag was deposited on the topmost surface of Au, and the growth direction of spines was <200>. Underpotential deposition of Ag nanolayers on specific facets of the spines on nanoparticles was observed for the first time by elemental mapping and high-angle annular dark-field STEM tomography. These findings are expected to contribute to the morphology control of plasmonic nanoparticles.</p></div>","PeriodicalId":48517,"journal":{"name":"Materials Today Nano","volume":"25 ","pages":"Article 100468"},"PeriodicalIF":10.3,"publicationDate":"2024-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140030347","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Surface modification by CO2 plasma boosting core shells structural Fe/Fe3C/FeN @ graphite carbon nanoparticles toward high performance microwave absorber","authors":"Xiaoqiang Li, Qun Wang, Yunfei Yu","doi":"10.1016/j.mtnano.2024.100465","DOIUrl":"10.1016/j.mtnano.2024.100465","url":null,"abstract":"<div><p>The surface modification of three-dimensional (3D) materials is an efficient method for adjusting their interfacial defect concentration, electronic conductivity and content of functional groups with extensive applications in catalysis, electrode materials and bioengineering. In this work, a multiphase iron nanocrystals consisting of Fe<sub>3</sub>C, Fe and FeN nanoparticles encapsulated in hierarchical structure of graphite carbon (denoted as Fe/Fe<sub>3</sub>C/FeN@GC) is synthesized for the first time by a novel high temperature plasma method. Meanwhile, more defects and functional groups are introduced by surface modification of graphite carbon layer of Fe/Fe<sub>3</sub>C/FeN@GC with controllable CO<sub>2</sub> (low temperature) plasma. Benefiting from the advantages of multiple heterogenous interface and the abundant interfacial polarization relaxation that represent strong electromagnetic (EM) wave dissipation as well as an applicable impedance matching, the optimized Fe/Fe<sub>3</sub>C/FeN@GC demonstrate superior microwave absorption (MA) properties. The minimum reflection loss (RL) achieves −54.4 dB (more than 99.9% MA) at 17.6 GHz with a thin thickness of 1.8 mm, and the maximum effective absorption bandwidth (EAB, RL < −10 dB) is up to 6.2 GHz (11.8–18.0 GHz) at 2.0 mm. The above results reveal that the optimized Fe/Fe<sub>3</sub>C/FeN@GC composites with strong absorption, broad EAB, light mass (only filling content of 30 wt%) and ultrathin thickness are prospective candidate for high performance EM wave absorbers.</p></div>","PeriodicalId":48517,"journal":{"name":"Materials Today Nano","volume":"25 ","pages":"Article 100465"},"PeriodicalIF":10.3,"publicationDate":"2024-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140046419","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Hao Wang , Jiheng Ding , Hongran Zhao , Qinchao Chu , Mohammad Raza Miah , Jinggang Wang , Jing Chen , Jin Zhu
{"title":"Preparing strong, tough, and high-barrier biobased polyester composites by regulating interfaces of carbon nanotubes","authors":"Hao Wang , Jiheng Ding , Hongran Zhao , Qinchao Chu , Mohammad Raza Miah , Jinggang Wang , Jing Chen , Jin Zhu","doi":"10.1016/j.mtnano.2024.100463","DOIUrl":"10.1016/j.mtnano.2024.100463","url":null,"abstract":"<div><p>Carbon nanotubes (CNTs) have been regarded as ideal functional fillers for enhancing superior mechanical properties of polymer composites. However, the performances of CNTs-based composites are well below the theoretical values, due to the poor dispersion of inert CNTs and weak interfacial interaction with the polymer matrix. Herein, “hydrothermal and <em>in-situ</em> growth” approach is induced to synthesize multiscale TiO<sub>2</sub>@CNTs functional fillers. Such the TiO<sub>2</sub>@CNTs show excellent dispersibility and strong interfacial bonding with matrix. The biobased TiO<sub>2</sub>@CNTs/poly (ethylene furandicarboxylate) (TCP) composite films are prepared via loading a small amount (0.05–0.2 wt%) of TiO<sub>2</sub>@CNTs. When the mass content of fillers is 0.2 wt%, TCP composite film exhibits the optimal of strength (80 MPa), Young's modulus (4.12 GPa), and toughness (1.2 MJ/m<sup>3</sup>). Moreover, the presence of TiO<sub>2</sub> nanoparticles endow the films with excellent oxygen barrier and UV-shielding properties. We believe these composite films promise a spread application potential in high-performance food packing materials.</p></div>","PeriodicalId":48517,"journal":{"name":"Materials Today Nano","volume":"25 ","pages":"Article 100463"},"PeriodicalIF":10.3,"publicationDate":"2024-02-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139950369","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Andreas Rosenkranz , Bo Wang , Dario Zambrano , Javier Marqués Henríquez , Jose Y. Aguilar-Hurtado , Edoardo Marquis , Paolo Restuccia , Brian C. Wyatt , M. Clelia Righi , Babak Anasori
{"title":"Solid-lubrication performance of Ti3C2Tx - Effect of tribo-chemistry and exfoliation","authors":"Andreas Rosenkranz , Bo Wang , Dario Zambrano , Javier Marqués Henríquez , Jose Y. Aguilar-Hurtado , Edoardo Marquis , Paolo Restuccia , Brian C. Wyatt , M. Clelia Righi , Babak Anasori","doi":"10.1016/j.mtnano.2024.100464","DOIUrl":"10.1016/j.mtnano.2024.100464","url":null,"abstract":"<div><p>Multi-layer Ti<sub>3</sub>C<sub>2</sub>T<sub><em>x</em></sub> coatings have demonstrated an outstanding wear performance with excellent durability due to beneficial tribo-layers formed. However, the involved formation processes dependent on the tribological conditions and coating thickness are yet to be fully explored. Therefore, we spray-coated Ti<sub>3</sub>C<sub>2</sub>T<sub><em>x</em></sub> multi-layer particles onto stainless steel substrates to create coatings with two different thicknesses and tested their solid lubrication performance with different normal loads (100 and 200 mN) and sliding frequencies (1 and 2.4 Hz) using linear-reciprocating ball-on-disk tribometry. We demonstrate that MXenes’ tribological performance depends on their initial state (delaminated few-layer vs. multi-layer particles), coating thickness, applied load and sliding frequency. Specifically, the best behavior is observed for thinner multi-layer coatings tested at the lower frequency. In contrast, coatings made of delaminated few-layer MXene are not as effective as their multi-layer counterparts. Our high-resolution interface characterization by transmission electron microscopy revealed unambiguous differences regarding the uniformity and chemistry of the formed tribo-layers as well as the degree of tribo-induced MXenes’ exfoliation. Atomistic insights into the exfoliation process and molecular dynamic simulations quantitatively backed up our experimental results regarding coating thickness and velocity dependency. This ultimately demonstrates that MXenes’ tribological performance is governed by the underlying tribo-chemistry and their exfoliation ability during rubbing.</p></div>","PeriodicalId":48517,"journal":{"name":"Materials Today Nano","volume":"25 ","pages":"Article 100464"},"PeriodicalIF":10.3,"publicationDate":"2024-02-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139950596","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Xiaobin Xie, Alfons van Blaaderen, Marijn A. van Huis
{"title":"Thermally stimulated structural evolution of bimetallic nanoplatelets - Changing from core-shell to alloyed to Janus nanoplatelets","authors":"Xiaobin Xie, Alfons van Blaaderen, Marijn A. van Huis","doi":"10.1016/j.mtnano.2024.100462","DOIUrl":"10.1016/j.mtnano.2024.100462","url":null,"abstract":"<div><p>Gold-based bimetallic nanostructures exhibit unique optical and catalytic properties that are strongly dependent on their composition and nanoscale geometry. Here we show the nano-structural transformation of mesoporous-silica-coated Au-M (Ag, Pd, Pt) core-shell nanoplatelets (NPLs) with a triangular shape to alloyed platelets at temperatures at least 300 °C below the lowest melting point of the metals while still retaining the out-of-equilibrium triangular shape and intact mesoporous shell. Before the alloying started the rough core-shell morphology of the Au–Pd and Au–Pt NPL systems were first observed to relax into a much smoother core-shell morphology. The alloying temperature was found to be related to the melting points and atom fractions of the shell metals; the higher the melting point and atomic fraction of the shell metal, the higher the temperature required for alloying. The highest alloying temperature was found for the Au–Pt system (650 °C), which is still hundreds of degrees below the bulk melting points. Surprisingly, a phase separation of Au and Pt, and of Au and Pd, was observed at 1100 °C while both systems still had an anisotropic plate-like shape, which resulted in Janus-like morphologies where the pure Pt and pure Pd ended up on the tips of the NPLs as revealed via in-situ heating in the scanning transmission electron microscope (STEM). The Janus-type morphologies obtained at elevated temperatures for the NPLs composed of combinations of Au–Pt and Au–Pd, and the smooth core-shell morphologies before alloying, are very interesting for investigating how differences in the bi-metallic morphology affect plasmonic, catalytic and other properties.</p></div>","PeriodicalId":48517,"journal":{"name":"Materials Today Nano","volume":"25 ","pages":"Article 100462"},"PeriodicalIF":10.3,"publicationDate":"2024-02-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2588842024000129/pdfft?md5=049211b6f935ddb599a1bdf36f15c7ba&pid=1-s2.0-S2588842024000129-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139925386","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Jiaqi Han, Ziyang Yan, Ya Lin, Ye Tao, Xuanyu Shan, Zhongqiang Wang, Xiaoning Zhao, Haiyang Xu, Yichun Liu
{"title":"Humidity-mediated synaptic plasticity in Ag loaded porous SiOx based memristor for multimodal neuromorphic sensory system","authors":"Jiaqi Han, Ziyang Yan, Ya Lin, Ye Tao, Xuanyu Shan, Zhongqiang Wang, Xiaoning Zhao, Haiyang Xu, Yichun Liu","doi":"10.1016/j.mtnano.2024.100461","DOIUrl":"https://doi.org/10.1016/j.mtnano.2024.100461","url":null,"abstract":"<div><p>Neuromorphic sensory system plays a critical role for human being to perceive, interact and even deduce with the external environment. Multimodal plasticity implementation of neuromorphic sensory system that can learn with diversified information empowers the development of environment-interactive artificial intelligence. In this work, we demonstrated a multimodal neuromorphic sensory system based on Ag loaded porous SiO<sub>x</sub> based memristor. The humidity-mediated synaptic plasticity behaviors were detailedly analyzed in the range of 10–90% relative humidity (RH). The humidity-mediated silver ion migration in porous SiO<sub>x</sub> memristors was studied by theoretical and experimental methods, and the mechanism of synergistic effect between porous micro-structure and ambient humidity was elucidated. A multimodal neuromorphic sensory system was finally constructed and the adaptive behavior of the human eye was also successfully simulated by taking advantage of this well-designed Au/Ag-SiO<sub>x</sub>/ITO memristor. The biomimetic intelligence demonstrated in our multimodal neuromorphic sensory devices and systems shows its potential in promoting the advancement in brain-like artificial intelligence.</p></div>","PeriodicalId":48517,"journal":{"name":"Materials Today Nano","volume":"25 ","pages":"Article 100461"},"PeriodicalIF":10.3,"publicationDate":"2024-02-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139914505","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Philip Anggo Krisbiantoro , Tzu-Jung Kuo , Yu-Chia Chang , Weisheng Liao , Jih-Peng Sun , Chun-Yen Yang , Yuichi Kamiya , Fa-Kuen Shieh , Chia-Chin Chen , Kevin C.-W Wu
{"title":"PET-derived bis(2-hydroxyethyl) terephthalate as a new linker source for solvent-free and hydrothermal synthesis of BDC-based MOFs","authors":"Philip Anggo Krisbiantoro , Tzu-Jung Kuo , Yu-Chia Chang , Weisheng Liao , Jih-Peng Sun , Chun-Yen Yang , Yuichi Kamiya , Fa-Kuen Shieh , Chia-Chin Chen , Kevin C.-W Wu","doi":"10.1016/j.mtnano.2024.100459","DOIUrl":"https://doi.org/10.1016/j.mtnano.2024.100459","url":null,"abstract":"<div><p>To date, the high cost of organic linkers and the energy-consuming synthesis processes remain two of the main challenges for the commercialization of metal-organic frameworks (MOFs). Herein, we demonstrate that polyethylene terephthalate (PET)-derived bis(2-hydroxyethyl) terephthalate (BHET) is a new linker source that enables the facile solvent-free and hydrothermal synthesis of BDC-based MOFs. Using BHET as a linker source, UiO-66(Zr) was rapidly synthesized via a solvent-free “grind and bake” technique, while Ca-BDC and Ba-BDC were easily obtained by using hydrothermal synthesis. We found that the hydrolysis of BHET to terephthalate anion (BDC<sup>2−</sup>) over proton produced from the hydrolysis/clustering of Zr precursor and hydroxyl anion produced from the dissolution of M(OH)<sub>2</sub> (M = Ca or Ba) was the key to the crystal growth of solvent-free synthesized UiO-66(Zr) and hydrothermally synthesized M-BDC (M = Ca or Ba), respectively. While the as-synthesized UiO-66(Zr) was highly active for the esterification of lactic acid (LA) with ethanol (EtOH), Ca-BDC and Ba-BDC exhibited remarkable electrochemical performance for lithium storage. Our strategy provides a major step towards realizing the idea of a more facile, green, and low-cost synthesis of PET-derived MOFs compared to prior arts applicable for catalysis and energy applications.</p></div>","PeriodicalId":48517,"journal":{"name":"Materials Today Nano","volume":"25 ","pages":"Article 100459"},"PeriodicalIF":10.3,"publicationDate":"2024-02-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139732746","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Shuangyue Wang , Mengyao Li , Yang Liu , Junjie Shi , Ashraful Azam , Xiaotao Zu , Liang Qiao , Peter Reece , John Stride , Jack Yang , Danyang Wang , Sean Li
{"title":"Fabrication of transferable ultrathin Au films with eminent thermal stability via a nanocrystalline MoS2 interlayer","authors":"Shuangyue Wang , Mengyao Li , Yang Liu , Junjie Shi , Ashraful Azam , Xiaotao Zu , Liang Qiao , Peter Reece , John Stride , Jack Yang , Danyang Wang , Sean Li","doi":"10.1016/j.mtnano.2024.100460","DOIUrl":"https://doi.org/10.1016/j.mtnano.2024.100460","url":null,"abstract":"<div><p>Ultrathin gold (Au) films are a critical component in plasmonics, metal optics, and nano-electronics devices. However, fabricating ultrathin Au films faces a great challenge due to the dewetting behavior of Au when being deposited onto an oxide (such as SiO<sub>2</sub>/Si or Al<sub>2</sub>O<sub>3</sub>) substrate. This problem is often relieved by introducing a metal or an organic adhesion layer to bind the Au film with the substrate. While the interdiffusion and thermal instability of the adhesion layers often negatively affect the physical properties of the films. Besides, this kind of Au film is usually untransferable due to the strong chemical bonding at the interfaces. Herein, we demonstrate a new strategy of utilizing a nanocrystalline MoS<sub>2</sub> layer as the adhesion interlayer to stabilize the Au film. The atomically thin nanocrystalline MoS<sub>2</sub> with abundant fresh edges enhances the wetting of Au films and allows for the ultra-smoothness and a few nanometers in thickness of the Au films without interdiffusion. The resulting ultrathin Au films possess superior electrical conductivity, high optical transmittance, and eminent thermal stability, which are much better than those utilizing Cu or Ti as the adhesion layers. Moreover, these Au films can be easily transferred to arbitrary substrates. Our method provides a new benchmark in the fabrication of transferable ultrathin and thermally stable Au films.</p></div>","PeriodicalId":48517,"journal":{"name":"Materials Today Nano","volume":"25 ","pages":"Article 100460"},"PeriodicalIF":10.3,"publicationDate":"2024-02-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2588842024000105/pdfft?md5=78d942e7da1cfb68709834b153284e42&pid=1-s2.0-S2588842024000105-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139749191","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}