The development of cost-effective and efficient bifunctional electrocatalysts remains a major challenge in coupling biomass-derived platform molecules, such as 5-hydroxymethylfurfural (HMF), with green hydrogen production. In this study, a P-doped Co3S4/NF electrocatalyst with excellent catalytic activity was successfully synthesized using a novel plasma-assisted doping technique. Electrochemical evaluations demonstrated outstanding performance, achieving a low potential of 1.21 V vs. RHE at 100 mA cm−2 in 1 M KOH containing 20 mM HMF. Anion exchange membrane (AEM) simulations under industrial operating conditions confirmed that the catalyst exhibited long-term electrochemical stability at elevated temperatures while effectively coupling the hydrogen evolution reaction (HER) with the HMF oxidation reaction (HMFOR). In situ Raman spectroscopy revealed the dynamic evolution of sulfur and phosphorus species on the surface of the P-Co3S4/NF electrode. These findings indicate that the active species synergistically enhance HMFOR activity through electro-oxidation, dissolution, and re-adsorption processes, contributing to sustained stability. Furthermore, theoretical calculations showed that phosphorus doping optimizes the adsorption of *OOH intermediates, lowering the reaction energy barrier and enabling highly efficient conversion of HMF into 2,5-furandicarboxylic acid (FDCA). This unique plasma-assisted doping strategy offers valuable insights for the rational design of high-performance transition-metal-based electrocatalysts for integrated biomass conversion and hydrogen production.
开发经济高效的双功能电催化剂仍然是将5-羟甲基糠醛（HMF）等生物质衍生平台分子与绿色制氢相结合的主要挑战。本研究采用新型等离子体辅助掺杂技术成功合成了具有优异催化活性的p掺杂Co3S4/NF电催化剂。电化学评价显示了出色的性能，在含有20 mM HMF的1 M KOH中，在100 mA cm - 2条件下，与RHE相比，达到了1.21 V的低电位。工业操作条件下的阴离子交换膜（AEM）模拟证实了该催化剂在高温下具有长期的电化学稳定性，同时有效地耦合了析氢反应（HER）和HMF氧化反应（HMFOR）。原位拉曼光谱揭示了P-Co3S4/NF电极表面硫和磷的动态演化。这些发现表明，活性物质通过电氧化、溶解和再吸附过程协同增强HMFOR活性，有助于维持稳定性。此外，理论计算表明，磷掺杂优化了*OOH中间体的吸附，降低了反应能垒，使HMF高效转化为2,5-呋喃二羧酸（FDCA）。这种独特的等离子体辅助掺杂策略为合理设计用于生物质转化和制氢的高性能过渡金属基电催化剂提供了有价值的见解。
{"title":"Dynamic interfacial reconfiguration of P-Co3S4 nanowire electrocatalysts: Synergistic anion engineering for efficient HMF oxidation and hydrogen evolution coupling","authors":"Taotao Ai, Yanjie Fan, Weiwei Bao, Jie Han, Zhifeng Deng, Peng Jiang, Xueling Wei, Xiangyu Zou, Lizhai Zhang","doi":"10.1016/j.jmst.2025.12.007","DOIUrl":"https://doi.org/10.1016/j.jmst.2025.12.007","url":null,"abstract":"The development of cost-effective and efficient bifunctional electrocatalysts remains a major challenge in coupling biomass-derived platform molecules, such as 5-hydroxymethylfurfural (HMF), with green hydrogen production. In this study, a P-doped Co<sub>3</sub>S<sub>4</sub>/NF electrocatalyst with excellent catalytic activity was successfully synthesized using a novel plasma-assisted doping technique. Electrochemical evaluations demonstrated outstanding performance, achieving a low potential of 1.21 V vs. RHE at 100 mA cm<sup>−2</sup> in 1 M KOH containing 20 mM HMF. Anion exchange membrane (AEM) simulations under industrial operating conditions confirmed that the catalyst exhibited long-term electrochemical stability at elevated temperatures while effectively coupling the hydrogen evolution reaction (HER) with the HMF oxidation reaction (HMFOR). <em>In situ</em> Raman spectroscopy revealed the dynamic evolution of sulfur and phosphorus species on the surface of the P-Co<sub>3</sub>S<sub>4</sub>/NF electrode. These findings indicate that the active species synergistically enhance HMFOR activity through electro-oxidation, dissolution, and re-adsorption processes, contributing to sustained stability. Furthermore, theoretical calculations showed that phosphorus doping optimizes the adsorption of *OOH intermediates, lowering the reaction energy barrier and enabling highly efficient conversion of HMF into 2,5-furandicarboxylic acid (FDCA). This unique plasma-assisted doping strategy offers valuable insights for the rational design of high-performance transition-metal-based electrocatalysts for integrated biomass conversion and hydrogen production.","PeriodicalId":16154,"journal":{"name":"Journal of Materials Science & Technology","volume":"13 1","pages":""},"PeriodicalIF":10.9,"publicationDate":"2025-12-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145717642","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
A novel bond coat composed of γ/γ′ phases that are in equilibrium with the superalloy substrate (equilibrium phase (EQ)) is achieved by microstructure regulation on the basis of traditional MCrAlY coating. The EQ-bonded LC-thermal barrier coating (TBC) outperforms the NiCrAlY-bonded HC-TBC regarding the thermally grown oxide (TGO) growth rate, interfacial toughness, as well as interdiffusion with the substrate, remarkably enhancing the interfacial stability of the multi-layer system. For HC-TBC, the high elastic strain energy in TGO due to the large thickness and the inferior toughness at the TGO/top coat interface due to the formation of spinel leads to the premature failure of the coating. By comparison, the improved performance of LC-TBC benefits from the intermixed zone (IMZ) development atop TGO, which effectively decreases the growth rate of TGO while simultaneously strengthening interfacial bonding. Both the spinel in HC-TBC and the IMZ in LC-TBC are intimately associated with the initial oxidation behavior. Preferential segregation of oxygen at the heterogeneous interface of γ′/α-Cr in the bond coat of HC-TBC initiates the in-situ oxidation of α-Cr and further results in the formation of spinel. On account of the remarkably reduced segregation energy of oxygen at coherent γ/γ′ interface in bond coat of LC-TBC, uniform θ-Al2O3 forms, facilitating the development of IMZ. The findings in this work challenge conventional wisdom on failure behaviors of TBCs and give new insights into the design of the bond coat with superior interfacial stability.
{"title":"Achieving superior interfacial stability of the typical MCrAlY bond coat by microstructural regulation","authors":"Shasha Yang, Yiming Jiang, Minghui Chen, Zebin Bao, Jiemin Wang, Fuhui Wang","doi":"10.1016/j.jmst.2025.12.006","DOIUrl":"https://doi.org/10.1016/j.jmst.2025.12.006","url":null,"abstract":"A novel bond coat composed of γ/γ′ phases that are in equilibrium with the superalloy substrate (equilibrium phase (EQ)) is achieved by microstructure regulation on the basis of traditional MCrAlY coating. The EQ-bonded LC-thermal barrier coating (TBC) outperforms the NiCrAlY-bonded HC-TBC regarding the thermally grown oxide (TGO) growth rate, interfacial toughness, as well as interdiffusion with the substrate, remarkably enhancing the interfacial stability of the multi-layer system. For HC-TBC, the high elastic strain energy in TGO due to the large thickness and the inferior toughness at the TGO/top coat interface due to the formation of spinel leads to the premature failure of the coating. By comparison, the improved performance of LC-TBC benefits from the intermixed zone (IMZ) development atop TGO, which effectively decreases the growth rate of TGO while simultaneously strengthening interfacial bonding. Both the spinel in HC-TBC and the IMZ in LC-TBC are intimately associated with the initial oxidation behavior. Preferential segregation of oxygen at the heterogeneous interface of γ′/α-Cr in the bond coat of HC-TBC initiates the in-situ oxidation of α-Cr and further results in the formation of spinel. On account of the remarkably reduced segregation energy of oxygen at coherent γ/γ′ interface in bond coat of LC-TBC, uniform θ-Al<sub>2</sub>O<sub>3</sub> forms, facilitating the development of IMZ. The findings in this work challenge conventional wisdom on failure behaviors of TBCs and give new insights into the design of the bond coat with superior interfacial stability.","PeriodicalId":16154,"journal":{"name":"Journal of Materials Science & Technology","volume":"150 1","pages":""},"PeriodicalIF":10.9,"publicationDate":"2025-12-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145718288","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
The development of high-performance microwave absorbing materials (MAMs) with broadband operation and temperature-responsive adaptability marks a significant advancement in electromagnetic protection and stealth technologies. Achieving simultaneous broadband absorption and intelligent responsiveness poses challenges in dielectric loss optimization through material selection and structural engineering. This study presents an innovative solution via subwavelength architecture design. We employ a facile electrospray strategy to fabricate reduced graphene oxide microspheres (rGOms) with tunable dimensions, where structural and compositional design further improve microwave absorption. The scale of rGOms correlates with interfacial dipole scales in macroscopic statistics, and their multiscale design results in a broader dielectric relaxation distribution. This synergistically enhances the effective absorption bandwidth (EAB). Furthermore, the discontinuous design of subwavelength units effectively extends the transmission path of electromagnetic waves, leading to additional multiple reflections and scattering within the system. At an equal mass ratio of 700 and 300 μm rGOms, the EAB of rGOms/epoxy (EP) composites reaches 7.2 GHz. Moreover, leveraging dynamic interfacial polarization provided by thermally responsive vanadium dioxide (VO2), the rGOms/VO2/EP composite demonstrates a dynamic adjustment capability that shifts the EAB by 2.6 GHz. This study may serve as a valuable reference for designing intelligent MAMs with broad attenuation frequency ranges based on multi-interface engineering.
{"title":"Multi-Interface engineering in rGO/VO2/EP composites for intelligent and broadband microwave absorption","authors":"Long Ma, Jiangxiao Song, Haoxu Si, Cuiping Li, Chunhong Gong, Jingwei Zhang","doi":"10.1016/j.jmst.2025.12.005","DOIUrl":"https://doi.org/10.1016/j.jmst.2025.12.005","url":null,"abstract":"The development of high-performance microwave absorbing materials (MAMs) with broadband operation and temperature-responsive adaptability marks a significant advancement in electromagnetic protection and stealth technologies. Achieving simultaneous broadband absorption and intelligent responsiveness poses challenges in dielectric loss optimization through material selection and structural engineering. This study presents an innovative solution via subwavelength architecture design. We employ a facile electrospray strategy to fabricate reduced graphene oxide microspheres (rGOms) with tunable dimensions, where structural and compositional design further improve microwave absorption. The scale of rGOms correlates with interfacial dipole scales in macroscopic statistics, and their multiscale design results in a broader dielectric relaxation distribution. This synergistically enhances the effective absorption bandwidth (EAB). Furthermore, the discontinuous design of subwavelength units effectively extends the transmission path of electromagnetic waves, leading to additional multiple reflections and scattering within the system. At an equal mass ratio of 700 and 300 μm rGOms, the EAB of rGOms/epoxy (EP) composites reaches 7.2 GHz. Moreover, leveraging dynamic interfacial polarization provided by thermally responsive vanadium dioxide (VO<sub>2</sub>), the rGOms/VO<sub>2</sub>/EP composite demonstrates a dynamic adjustment capability that shifts the EAB by 2.6 GHz. This study may serve as a valuable reference for designing intelligent MAMs with broad attenuation frequency ranges based on multi-interface engineering.","PeriodicalId":16154,"journal":{"name":"Journal of Materials Science & Technology","volume":"86 1","pages":""},"PeriodicalIF":10.9,"publicationDate":"2025-12-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145718287","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Micro thermoelectric devices (micro-TEDs) have emerged as promising candidates for energy harvesting applications. Despite the development of numerous high-performance thermoelectric materials over the past decades, most micro-TEDs still rely heavily on conventional Bi2Te3-based materials. Effectively integrating advanced thermoelectric materials into micro-TEDs remains a significant challenge. In this work, we theoretically match several recently developed high-performance near-room-temperature thermoelectric materials with micro-TEDs and explore the integration of a manifold microchannel (MMC) heat sink on the cold side to significantly enhance the effective temperature difference across the devices. Upon incorporating the MMC heat sink, the maximum power densities of Bi2Te3-, Mg3Sb2-, and SnSe-based micro-TEDs reach 50.32, 29.68, and 31.07 μW mm−2, respectively, representing increases of 60.63-fold, 56.52-fold, and 57.69-fold compared to devices without heat sinks. These results highlight that coupling micro-TEDs with emerging near-room-temperature thermoelectric materials and a well-engineered MMC heat sink offers a promising route for efficient energy harvesting applications.
{"title":"Manifold microchannel heat sinks enhance the power generation performance of micro-thermoelectric devices","authors":"Jun Pei, Hezhang Li, Hua-Lu Zhuang, Jinfeng Dong, Bowen Cai, Jincheng Yu, Zhihang Shan, Xinyuan Qi, Wenyi Chen, Xiao-Lei Shi, Zhi-Gang Chen, Bo-Ping Zhang","doi":"10.1016/j.jmst.2025.11.053","DOIUrl":"https://doi.org/10.1016/j.jmst.2025.11.053","url":null,"abstract":"Micro thermoelectric devices (micro-TEDs) have emerged as promising candidates for energy harvesting applications. Despite the development of numerous high-performance thermoelectric materials over the past decades, most micro-TEDs still rely heavily on conventional Bi<sub>2</sub>Te<sub>3</sub>-based materials. Effectively integrating advanced thermoelectric materials into micro-TEDs remains a significant challenge. In this work, we theoretically match several recently developed high-performance near-room-temperature thermoelectric materials with micro-TEDs and explore the integration of a manifold microchannel (MMC) heat sink on the cold side to significantly enhance the effective temperature difference across the devices. Upon incorporating the MMC heat sink, the maximum power densities of Bi<sub>2</sub>Te<sub>3</sub>-, Mg<sub>3</sub>Sb<sub>2</sub>-, and SnSe-based micro-TEDs reach 50.32, 29.68, and 31.07 μW mm<sup>−2</sup>, respectively, representing increases of 60.63-fold, 56.52-fold, and 57.69-fold compared to devices without heat sinks. These results highlight that coupling micro-TEDs with emerging near-room-temperature thermoelectric materials and a well-engineered MMC heat sink offers a promising route for efficient energy harvesting applications.","PeriodicalId":16154,"journal":{"name":"Journal of Materials Science & Technology","volume":"15 1","pages":""},"PeriodicalIF":10.9,"publicationDate":"2025-12-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145711033","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-12-09DOI: 10.1016/j.jmst.2025.12.003
Mao Cheng, Yanhui Li, Liliang Pan, Wenjing Zhao, Chi Fan, Tieshan Cao, Li Jiang, Wei Zhang
The design of high-entropy bulk metallic glasses (HE-BMGs) offers a promising strategy to achieve exceptional thermal stability and mechanical robustness of high-temperature structural materials. In this work, novel Fe30Co25Ni15RM5B17.5Si7.5 (RM = Nb, Mo, Ta, W) HE-BMGs with a unique combination of superior thermal stability, high-temperature strength, and wear resistance were developed. Among them, the Ta-bearing alloy (Ta5) exhibits the highest crystallization temperature, the widest supercooled liquid region, and the largest critical diameter for glass formation. The Ta5 HE-BMG demonstrates a sluggish crystallization behavior characterized by delayed nucleation and growth of the complex (Fe, Co, Ni)21Ta2B6 primary phase. It also achieves ultrahigh specific strength even at 823 K and superior wear resistance, outperforming most reported HE-BMGs. Annealing at 833 K for 900 s retains its amorphous structure while further enhancing both the strength and wear resistance. Ab initio molecular dynamics simulations reveal that the Ta addition strengthens interatomic interactions, increases local five-fold atomic symmetry, and suppresses atomic diffusion, which rationalizes the experimental observations. With their exceptional combination of thermal and mechanical properties, the developed HE-BMGs, particularly the Ta5 alloy, emerge as promising candidates for high-temperature structural and wear-resistant applications.
{"title":"Fe–Co–Ni–Ta–B–Si high-entropy bulk metallic glasses with superior thermal stability and high-temperature strength","authors":"Mao Cheng, Yanhui Li, Liliang Pan, Wenjing Zhao, Chi Fan, Tieshan Cao, Li Jiang, Wei Zhang","doi":"10.1016/j.jmst.2025.12.003","DOIUrl":"https://doi.org/10.1016/j.jmst.2025.12.003","url":null,"abstract":"The design of high-entropy bulk metallic glasses (HE-BMGs) offers a promising strategy to achieve exceptional thermal stability and mechanical robustness of high-temperature structural materials. In this work, novel Fe<sub>30</sub>Co<sub>25</sub>Ni<sub>15</sub>RM<sub>5</sub>B<sub>17.5</sub>Si<sub>7.5</sub> (RM = Nb, Mo, Ta, W) HE-BMGs with a unique combination of superior thermal stability, high-temperature strength, and wear resistance were developed. Among them, the Ta-bearing alloy (Ta5) exhibits the highest crystallization temperature, the widest supercooled liquid region, and the largest critical diameter for glass formation. The Ta5 HE-BMG demonstrates a sluggish crystallization behavior characterized by delayed nucleation and growth of the complex (Fe, Co, Ni)<sub>21</sub>Ta<sub>2</sub>B<sub>6</sub> primary phase. It also achieves ultrahigh specific strength even at 823 K and superior wear resistance, outperforming most reported HE-BMGs. Annealing at 833 K for 900 s retains its amorphous structure while further enhancing both the strength and wear resistance. <em>Ab initio</em> molecular dynamics simulations reveal that the Ta addition strengthens interatomic interactions, increases local five-fold atomic symmetry, and suppresses atomic diffusion, which rationalizes the experimental observations. With their exceptional combination of thermal and mechanical properties, the developed HE-BMGs, particularly the Ta5 alloy, emerge as promising candidates for high-temperature structural and wear-resistant applications.","PeriodicalId":16154,"journal":{"name":"Journal of Materials Science & Technology","volume":"143 1","pages":""},"PeriodicalIF":10.9,"publicationDate":"2025-12-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145717644","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
The present study revealed the intrinsic mechanism of post-deformation (relaxation after deformation) ferrite transformation and validated that manipulating grain size and volume fraction of ferrite enhances strength-ductility synergy in a low-carbon martensitic steel. In-situ neutron diffraction and microscopic investigations uncovered that austenite to ferrite transformation preferentially occurs at austenite grain boundaries during relaxation due to localized dislocation concentration. According to the in-situ neutron diffraction measurements, the retained dislocation density was obviously higher than the level before deformation during relaxation at 755°C. Conversely, dislocation density could fully decrease to the level prior to deformation during relaxation at 765°C. Thermodynamic calculations demonstrated that high chemical driving force with sufficient dislocations effectively enhances nucleation and coalescence of similarly oriented grains. Meanwhile, the stored dislocations during relaxation govern the types of transformation behaviors. Therefore, distinct transformation behaviors allow precise tuning of ferrite microstructural features: grain size and volume fraction. This strategy, leveraging the heterogeneity in grain-boundary transformation by holding various relaxation times, increases the mechanical properties of low-carbon martensitic steel. These findings provide valuable microstructure design concepts for overcoming the strength-ductility trade-off in high-strength martensitic steels.
{"title":"Unveiling post-deformation transformation mechanism and ferrite microstructure evolution for tailoring mechanical properties of low-carbon martensitic steels","authors":"Zelin Tong, Chenghui Xia, Wei Li, Wei Ding, Baoqi Guo, Na Min, Wu Gong, Stefanus Harjo, Nobuhiro Tsuji","doi":"10.1016/j.jmst.2025.12.004","DOIUrl":"https://doi.org/10.1016/j.jmst.2025.12.004","url":null,"abstract":"The present study revealed the intrinsic mechanism of post-deformation (relaxation after deformation) ferrite transformation and validated that manipulating grain size and volume fraction of ferrite enhances strength-ductility synergy in a low-carbon martensitic steel. In-situ neutron diffraction and microscopic investigations uncovered that austenite to ferrite transformation preferentially occurs at austenite grain boundaries during relaxation due to localized dislocation concentration. According to the in-situ neutron diffraction measurements, the retained dislocation density was obviously higher than the level before deformation during relaxation at 755°C. Conversely, dislocation density could fully decrease to the level prior to deformation during relaxation at 765°C. Thermodynamic calculations demonstrated that high chemical driving force with sufficient dislocations effectively enhances nucleation and coalescence of similarly oriented grains. Meanwhile, the stored dislocations during relaxation govern the types of transformation behaviors. Therefore, distinct transformation behaviors allow precise tuning of ferrite microstructural features: grain size and volume fraction. This strategy, leveraging the heterogeneity in grain-boundary transformation by holding various relaxation times, increases the mechanical properties of low-carbon martensitic steel. These findings provide valuable microstructure design concepts for overcoming the strength-ductility trade-off in high-strength martensitic steels.","PeriodicalId":16154,"journal":{"name":"Journal of Materials Science & Technology","volume":"39 1","pages":""},"PeriodicalIF":10.9,"publicationDate":"2025-12-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145711032","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Retraction notice to \"Macro to nanoscale deformation of transformation-induced plasticity steels: impact of aluminum on the microstructure and deformation behavior\" [JMST, Volume 34, Issue 5, May 2018, Pages 745-755]","authors":"V.S.Y. Injeti, Z.C. Li, B. Yu, R.D.K. Misra, Z.H. Cai, H. Ding","doi":"10.1016/j.jmst.2025.11.035","DOIUrl":"https://doi.org/10.1016/j.jmst.2025.11.035","url":null,"abstract":"This article has been retracted: please see Elsevier Policy on Article Withdrawal (<span><span>https://www.elsevier.com/about/policies/article-withdrawal</span><svg aria-label=\"Opens in new window\" focusable=\"false\" height=\"20\" viewbox=\"0 0 8 8\"><path d=\"M1.12949 2.1072V1H7V6.85795H5.89111V2.90281L0.784057 8L0 7.21635L5.11902 2.1072H1.12949Z\"></path></svg></span>).","PeriodicalId":16154,"journal":{"name":"Journal of Materials Science & Technology","volume":"26 1","pages":""},"PeriodicalIF":10.9,"publicationDate":"2025-12-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145717645","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
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