ACS Applied Engineering Materials最新文献

{"title":"ACS Applied Materials & Interfaces Family Early Career Forum 2024","authors":"Xing Yi Ling, ","doi":"10.1021/acsaenm.4c0076610.1021/acsaenm.4c00766","DOIUrl":"https://doi.org/10.1021/acsaenm.4c00766https://doi.org/10.1021/acsaenm.4c00766","url":null,"abstract":"","PeriodicalId":55639,"journal":{"name":"ACS Applied Engineering Materials","volume":"2 12","pages":"2719–2721 2719–2721"},"PeriodicalIF":0.0,"publicationDate":"2024-12-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143126662","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}

{"title":"Surface-Treated Three-Dimensional Boron Nitride Epoxy Composite Dielectric for Smartphone-Printed Circuit Board Application","authors":"Jae Man Park,&nbsp;Tae Hyun Kwon,&nbsp;Young Jo Kim* and Moon Sung Kang*,&nbsp;","doi":"10.1021/acsaenm.4c0070110.1021/acsaenm.4c00701","DOIUrl":"https://doi.org/10.1021/acsaenm.4c00701https://doi.org/10.1021/acsaenm.4c00701","url":null,"abstract":"<p >With the increasing need for efficient heat dissipation in high-end smartphones, the development of dielectric materials for printed circuit boards (PCBs) with high thermal conductivity, a low dielectric constant, and strong adhesion characteristics is crucial. This study aims to design a composite dielectric addressing these often-conflicting properties and to examine its heat dissipation characteristics within an operating smartphone. The composite is formulated using a resin mixture of diglycidyl thioetherdiphenyl, ortho-phenyl phenol novolac glycidyl ether, and bisphenol A diglycidyl ether, combined with surface-treated three-dimensional boron nitride fillers (<i>surf</i>-3D BN fillers). The <i>surf</i>-3D BN fillers, formed from aggregated two-dimensional boron nitride plates, address issues arising from the anisotropic thermal conductivity in individual components. Their surface treatment ensures seamless integration with the native resin network enhancing both thermal and mechanical performance. By carefully adjusting the resin composition and utilizing <i>surf</i>-3D BN fillers, the composite achieves a high thermal conductivity of 5.4 W/m·K, a low dielectric constant of 3.59, and a peel strength of 0.72 kgf/cm. Furthermore, replacing a fraction of the BN fillers with cost-effective SiO₂ fillers maintained the performance while reducing material costs. The composite passed ion migration tests and exhibited superior heat dissipation in smartphone testbeds, making it a promising candidate for next-generation PCB materials in advanced electronic devices.</p>","PeriodicalId":55639,"journal":{"name":"ACS Applied Engineering Materials","volume":"3 1","pages":"178–186 178–186"},"PeriodicalIF":0.0,"publicationDate":"2024-12-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143086565","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}

{"title":"Upcycling Discarded Polyethylene Terephthalate Plastic into Highly Valuable Flexible Materials with Good Tensile Strength, Weather, and Corrosion Resistance via Molecular Structure Reconstruction","authors":"Bingying Gao,&nbsp;Yunyun Sun,&nbsp;Xuzhang Sun,&nbsp;Chao Yao and Linqiang Mao*,&nbsp;","doi":"10.1021/acsaenm.4c0074310.1021/acsaenm.4c00743","DOIUrl":"https://doi.org/10.1021/acsaenm.4c00743https://doi.org/10.1021/acsaenm.4c00743","url":null,"abstract":"<p >The chemical conversion of discarded poly(ethylene terephthalate) (dPET) into functional materials presents a promising approach to waste disposal. However, the loss of flexibility and tensile strength significantly limits the practical application of these fabricated materials. This work aims to develop a simple and effective approach to convert dPET into functional materials with flexible properties through molecular structure reconstruction. Molecular structures─C₁₀H₁₁ClO₃, (C₇H₄O₂)_<i>n</i>, and C₁₅H₁₄O₃─were formed through the introduction of styrene butadiene styrene block polymer to react with dPET. These three products were embedded into a viscous fluid in rodlike or sheet-like shapes, and homogeneous and stable cross-linked structures were formed by physical and chemical bonds rather than a simple physical mixture, which is responsible for the good tensile strength, corrosion resistance, and weather resistance properties of the flexible material. The resulting flexible material had a tensile strength of up to 4.2 MPa. Even after 50 cycles of stretching at 80% elongation without a dwell time, the sample retained its resilience. The material also exhibited good corrosion and weather resistance, with no deformation or dissolution observed even after 30 h of exposure to harsh environments, including strong acids, alkalis, and salt solutions. When exposed to simulated sunlight for 6 h, the sample exhibited a strong resistance in the 200–340 nm range. Overall, the successful fabrication of dPET into flexible materials presents a simple and effective approach to the high-value disposal of waste plastic. The resulting samples show potential applications in various areas such as soft joints, shock absorbers, and pipe shock absorbers.</p>","PeriodicalId":55639,"journal":{"name":"ACS Applied Engineering Materials","volume":"3 1","pages":"233–242 233–242"},"PeriodicalIF":0.0,"publicationDate":"2024-12-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143086235","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}

{"title":"Viscoelastic Fluid Stresses in the Formation and Shaping of Melt-Spun Hollow Fibers","authors":"Himendra S. Perera,&nbsp;Katherine J. Ernst,&nbsp;Hooman V. Tafreshi and Saad A. Khan*,&nbsp;","doi":"10.1021/acsaenm.4c0055110.1021/acsaenm.4c00551","DOIUrl":"https://doi.org/10.1021/acsaenm.4c00551https://doi.org/10.1021/acsaenm.4c00551","url":null,"abstract":"<p >Hollow fibers are considered for a wide range of applications as their inherent internal void geometry enhances functionality and reduces material need. This study examines how stresses in polymer melts affect fiber void space and cross-sectional shapes during 4-C segmented arc melt spinning, a process where polymer extruded through four C-shaped arcs coalesce after extrusion to form a single hollow fiber. We conducted spinning trials under various conditions and analyzed hollow fiber cross sections by measuring circularity and hollowness, defined as the volume fraction of the fiber’s hollow core relative to the total fiber volume. Rheological properties of different polypropylene melts at the temperature and conditions of spinning are related to the final fiber properties to show that the processing parameters of spinning temperature and flow rate are of significance. Experiments maintaining constant denier, or linear density, reveal that hollowness and circularity are related to the flow behavior through the Weissenberg number (Wi). At low Wi, hollowness increases with Wi; however, as Wi exceeds unity, the polymer takes on more elastic characteristics and the fiber transitions to constant hollowness, followed by instability at higher Wi values. Computational fluid dynamics (CFD) simulations using the Giesekus model allow for the analysis of stresses present during extrusion, revealing that uneven stress distributions at high Wi lead to a decrease in the circularity of the inside of the fiber. At low Wi, the extruded polymer melt has more viscous character and more time to resolve stresses in the melt before solidification, creating a fiber that retains less hollowness but more shape uniformity. A generalized inverse relationship between fiber circularity and hollowness is also observed across various polymer samples, flow rates, and temperatures. These findings provide valuable insights on hollow fiber spinning and predictions of hollow fiber geometry based on the viscoelastic properties of the polymer melt.</p>","PeriodicalId":55639,"journal":{"name":"ACS Applied Engineering Materials","volume":"3 1","pages":"75–84 75–84"},"PeriodicalIF":0.0,"publicationDate":"2024-12-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143086540","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}

{"title":"Electronic Modulation of Interfacial Engineering Co2P@FeP-FeP4 Nanoframe Heterostructures Boosting Overall Water Splitting","authors":"Xuan Wu,&nbsp;Thangavelu Dhanasekaran*,&nbsp;Wei Han,&nbsp;Yimin Gao,&nbsp;Yuhang Li,&nbsp;Dan Zhao,&nbsp;Guiling Wang and Jing Zhao*,&nbsp;","doi":"10.1021/acsaenm.4c0068010.1021/acsaenm.4c00680","DOIUrl":"https://doi.org/10.1021/acsaenm.4c00680https://doi.org/10.1021/acsaenm.4c00680","url":null,"abstract":"<p >The development of bifunctional electrocatalysts using renewable electricity for sustainable green energy industrial production is a potential method. As a result, numerous standard methodologies investigate developing electrocatalysts that naturally alter the electronic structure and minimize kinetic barriers. This study developed a promising method for engineering interfacial heterostructure nanoframes (Co₂P/FeP-FeP₄, hereafter denoted as CFP-8) deposited on nickel foam using hydrothermal and low-temperature phosphorization techniques. However, the improved CFP-8 electrocatalyst was exposed to abundant active sites and nanocrystals that remained intact. Importantly, P incorporation plays a crucial role in creating a P vacancy defect, which contributes to the thermodynamic favoring of the electrocatalysis of the oxygen evolution reaction (OER) and intrinsically enhances the hydrogen adsorption-free energy in hydrogen evolution reactions (HERs), due to the interconnected arrangement of CFP-8 nanoframes via the synergistic and strain-induced effect. Therefore, enclosed CFP-8 nanoframes demonstrate good performance and display low overpotential with high current densities (HER, η₁₀ = 97 mV, η₂₀ = 131 mV, η₅₀ = 186 mV; OER, η₁₀ = 230 mV, η₂₀ = 247 mV, η₅₀ = 280 mV) with a minimal Tafel value of η₁₀ = 111 mV/dec and η₁₀ = 74 mV/dec for HER and OER under alkaline medium, superior to benchmark electrocatalysts. Also, CFP-8 demonstrated remarkable stability over 50 h, utilizing chronoamperometry (CA) and chronopotentiometry (CP). In addition, an integrated electrolyzer using CFP-8/NF electrodes (polymeric binder-free electrodes) delivered a cell voltage of 1.65 V with a current density of 20 mA cm^–2 with accelerated kinetics and improved stability, outperforming Pt/C (cathode)||RuO₂ (anode) for overall water splitting reactions (OWSRs). The coexistence of Co, Fe, and P elements may accelerate electron and mass movement, improving the high current density electrocatalytic performance. This method paves the way for further research into low-cost transition metal-based phosphides for bifunctional energy applications.</p>","PeriodicalId":55639,"journal":{"name":"ACS Applied Engineering Materials","volume":"3 1","pages":"158–170 158–170"},"PeriodicalIF":0.0,"publicationDate":"2024-12-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143085715","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}

{"title":"Development of White Light-Emitting Textiles Using Inorganic Phosphor-Loaded Photopolymers for Potential Lighting Applications","authors":"Jessica Plé,&nbsp;Anthony Barros,&nbsp;Damien Boyer,&nbsp;Geneviève Chadeyron,&nbsp;Didier Zanghi and Lavinia Balan*,&nbsp;","doi":"10.1021/acsaenm.4c0062710.1021/acsaenm.4c00627","DOIUrl":"https://doi.org/10.1021/acsaenm.4c00627https://doi.org/10.1021/acsaenm.4c00627","url":null,"abstract":"<p >The development of flexible textile-based lighting systems remains challenging, usually requiring the combination of light-emitting diodes (LEDs) with polymer optical fibers to achieve larger emission areas. However, the overall emission remains point-based, leading to possible glare issues and shadowed zones. In this context, the present work proposes the development of light-emitting textiles that uniformly distribute white light when excited by a blue LED source. Simple cotton substrates were coated with a flexible photoluminescent phosphor-loaded polymer composite. The yellow and/or red phosphors were efficiently incorporated into the polymer matrix via a fast and easy-to-implement UV-induced polymerization reaction, conducted in air and in the absence of any toxic organic solvents. Under blue light, the yellow phosphor-coated textile produced cold white light, but the color temperature was easily tuned to warmer nuances by adjusting the amount of red-emitting phosphor, with high color rendering index (&gt;70) and luminance values over 500 cd/m². Stability and structural measurements were then carried out to assess possible scale-up options. The versatility of the polymer matrix also expanded the possible applications to 2D surface functionalization and 3D printing.</p>","PeriodicalId":55639,"journal":{"name":"ACS Applied Engineering Materials","volume":"3 1","pages":"118–127 118–127"},"PeriodicalIF":0.0,"publicationDate":"2024-12-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143085562","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}

{"title":"Viability of Additively Manufactured Electrodes for Lithium-Ion Batteries","authors":"Nicholas R. Cross,&nbsp;Hanyu Li,&nbsp;Thomas Roy,&nbsp;Victoria M. Ehlinger,&nbsp;Tiras Y. Lin,&nbsp;Nicholas W. Brady,&nbsp;Swetha Chandrasekaran,&nbsp;Marcus A. Worsley and Giovanna Bucci*,&nbsp;","doi":"10.1021/acsaenm.4c0071710.1021/acsaenm.4c00717","DOIUrl":"https://doi.org/10.1021/acsaenm.4c00717https://doi.org/10.1021/acsaenm.4c00717","url":null,"abstract":"<p >As the global economy becomes increasingly electrified, the demand for batteries and energy storage is expected to rise significantly, particularly in the transportation and electricity sectors. Lithium-ion batteries (LIBs) are currently the most advanced and widely used technology in this field. Traditionally, LIBs are manufactured using simple 2D planar geometries to maximize production efficiency and minimize costs. However, this approach limits energy density due to the restricted design flexibility of the electrodes. Additive manufacturing (AM) offers a promising solution to enhance the energy density and efficiency of LIBs by enabling the design of architectures that reduce diffusive losses and allow for a greater amount of active material to be incorporated within the same device footprint, thereby minimizing the use of inactive materials. Different AM techniques come with their own set of limitations, including printing speed, material compatibility, and scale, which must be considered when designing electrodes. Scalable and cost-effective methods are particularly important for electric vehicle batteries, while achieving higher energy densities in microbatteries is crucial for the miniaturization of wearable electronics and medical devices. In this study, we simulate various 3D porous electrode designs for LIBs using graphite and nickel manganese cobalt oxide (NMC) electrodes. These designs are selected to represent structures that could be produced using different AM techniques, such as direct ink writing, fused deposition modeling, and stereolithography. Our results indicate that at higher charging rates and increased areal mass loading, 3D structures can outperform traditional 2D electrodes, although the benefits may diminish with more complex designs that are harder to manufacture. The observed gains in energy density are attributed to improved electrode utilization and reduced diffusive energy losses. This comprehensive analysis of structure–performance relationships will provide valuable insights to guide future research on 3D designs, material selection, and AM techniques for additively manufactured battery electrodes.</p>","PeriodicalId":55639,"journal":{"name":"ACS Applied Engineering Materials","volume":"3 1","pages":"214–224 214–224"},"PeriodicalIF":0.0,"publicationDate":"2024-12-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143085816","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}

{"title":"Synthesis and Properties Study of a Multifunctional Polymethacrylate Viscosity Index Improver","authors":"Weiyan Liao,&nbsp;Chao Ju,&nbsp;Qin Zhao,&nbsp;Wenjing Lou,&nbsp;Xiaobo Wang* and Shengmao Zhang*,&nbsp;","doi":"10.1021/acsaenm.4c0062410.1021/acsaenm.4c00624","DOIUrl":"https://doi.org/10.1021/acsaenm.4c00624https://doi.org/10.1021/acsaenm.4c00624","url":null,"abstract":"<p >This paper reports on the design, preparation, and characterization of a multifunctional polymethacrylate (PMA) viscosity index improver (VII) that exhibits high oxidative stability and shear stability, which imparts multifunctionality to the viscosity index improver through the introduction of a disulfide pentacyclic ring in lipoic acid. The resulting polymers were added to base oils to investigate their physicochemical and frictional properties. The results demonstrated that, in addition to a significant increase in the viscosity index and high shear stability, the polymers exhibited notable improvements in extreme pressure performance up to 900 N as well as improved antioxidant stability, antiwear, and friction reduction properties. These enhancements were evidenced by a significant reduction in the coefficient of friction and wear volume of the polymers, which decreased by 40% and 92.01%, respectively. Additionally, the polymers exhibited low corrosiveness compared to those of both the base oils and commercial products. Analysis of wear scars revealed that the main formations of protective films were Fe-oxides and Fe-sulfides. This methodology demonstrates the versatility and low corrosiveness of the 1,2-dithiolane-containing viscosity index improver.</p>","PeriodicalId":55639,"journal":{"name":"ACS Applied Engineering Materials","volume":"3 1","pages":"108–117 108–117"},"PeriodicalIF":0.0,"publicationDate":"2024-12-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143085288","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}

{"title":"Bimetallic Conductive Metal Organic Framework Nanorods with Atomically Dispersed Fe and Co Sites for Efficient Oxygen Evolution","authors":"Longxiang Wang,&nbsp;Jiahao Wang,&nbsp;Jun Man,&nbsp;Meiling Dou* and Feng Wang*,&nbsp;","doi":"10.1021/acsaenm.4c0048010.1021/acsaenm.4c00480","DOIUrl":"https://doi.org/10.1021/acsaenm.4c00480https://doi.org/10.1021/acsaenm.4c00480","url":null,"abstract":"<p >Exploring efficient nonpyrolysis conductive metal organic frameworks with high intrinsic reactivity is critical for their application in the electrocatalytic field. Herein, we present electronically conductive π-d-conjugated Co and Fe bimetallic MOF-CoFe-hexahydroxytriphenylene (CoFe-HHTP) nanorods with atomically dispersed Co–O₆ and Fe–O₆ sites for efficient oxygen evolution reaction (OER) catalysis. The introduction of Fe not only increases the electronic conductivity of Co-HHTP with an order of magnitude favoring the electronic transfer during OER catalysis but also tailors the electronic structure of Co, leading to a downshift of Co d-band center that weakens the adsorption of oxygen intermediates on Co sites. As a result, the as-prepared CoFe-HHTP exhibits a significantly improved OER activity showing a lower overpotential (316 mV) at a current density of 10 mA cm^–2 in an alkaline electrolyte compared with pure Co-HHTP (370 mV), outperforming commercial RuO₂ (329 mV). CoFe-HHTP also displays a superior electrochemical durability with only a slight change of potential after a 200 h test at 10 mA cm^–2, outperforming pure Co-HHTP (140 h). The improved durability was due to the hindered dissolution of Co by suppressing structural transformation in the presence of Fe in the alkaline electrolyte. When CoFe-HHTP was used as the anode catalyst, a superior alkaline electrolyzer performance was obtained with a cell voltage of 1.821 V at 500 mA cm^–2 and a stable operation of 50 h. This methodology offers insights into the design and synthesis of conductive MOF-based catalysts for efficient OER catalysis.</p>","PeriodicalId":55639,"journal":{"name":"ACS Applied Engineering Materials","volume":"3 1","pages":"51–63 51–63"},"PeriodicalIF":0.0,"publicationDate":"2024-12-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143084823","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}

{"title":"Alumina-Supported Ternary Palladium–Boron–Phosphorus Mesoporous Alloy Nanospheres as Nitrobenzene Hydrogenation Catalysts","authors":"Chenyan Shi,&nbsp;Qianqian Zhou,&nbsp;Lei Wang,&nbsp;Shuaiwen Xu,&nbsp;Pengfei Tian* and Shenghu Zhou*,&nbsp;","doi":"10.1021/acsaenm.4c0064010.1021/acsaenm.4c00640","DOIUrl":"https://doi.org/10.1021/acsaenm.4c00640https://doi.org/10.1021/acsaenm.4c00640","url":null,"abstract":"<p >In this work, we first report the use of palladium–boron–phosphorus (PdBP) ternary alloys as highly efficient nitrobenzene hydrogenation catalysts, where these alloys feature mesoporous and metal–metalloid–nonmetal ternary alloy nanostructures. The mentioned mesoporous PdBP alloys (m-PdBP) were synthesized by a one-pot aqueous coreduction method followed by loading them on alumina to obtain m-PdBP/Al₂O₃ nanocatalysts. At 45 °C, a nitrobenzene/Pd molar ratio of 2500/1 and atmospheric hydrogen pressure, m-PdBP/Al₂O₃ could achieve 98% conversion of nitrobenzene at the a reaction time of 30 min. m-PdBP/Al₂O₃ is comparable to state-of-the-art Pd-based catalysts for nitrobenzene hydrogenation at atmospheric hydrogen pressure. Characterizations and theoretical calculations indicate that the improvement of catalytic performance can be attributed to the alloying effect of the incorporation of B and P into palladium, which facilitates the desorption of aniline and thus promotes the hydrogenation activity.</p>","PeriodicalId":55639,"journal":{"name":"ACS Applied Engineering Materials","volume":"2 12","pages":"2962–2969 2962–2969"},"PeriodicalIF":0.0,"publicationDate":"2024-12-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143126126","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}