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A self-assembling nanoplatform for pyroptosis and ferroptosis enhanced cancer photoimmunotherapy

Light(science & Applications) 2025年第1期14卷 153-166页

作者： Zhichao Wang Yuqi Tang Quan Li Institute of Advanced Materials and School of Chemistry and Chemical Engineering Southeast UniversityNanjing211189China Materials Science Graduate Program Kent State UniversityKentOH44242USA

The microenvironment of immunosuppression and low immunogenicity of tumor cells has led to unsatisfactory therapeutic effects of the currently developed *** cell death,such as pyroptosis and ferroptosis,can efficiently boost antitumor ***,the exploration of nanoplatform for dual function inducers and combined immune activators that simultaneously trigger pyroptosis and ferroptosis remains ***,a multifunctional pH-responsive theranostic nanoplatform(M@P)is designed and constructed by self-assembly of aggregation-induced emission photosensitizer MTCN-3 and immunoadjuvant Poly(l:C),which are further encapsulated in amphiphilic *** nanoplatform is found to have the characteristics of cancer cell targeting,pH response,near-infrared fluorescence imaging,and lysosome ***,after targeting lysosomes,M@P can cause lysosome dysfunction through the generation of reactive oxygen species and heat under light irradiation,triggering pyroptosis and ferroptosis of tumor cells,achieving immunogenic cell death,and further enhancing immunotherapy through the combined effect with the immunoadjuvant Poly(I:C).The anti-tumor immunotherapy effect of M@P has been further demonstrated in in vivo antitumor experiment of 4T1 tumor-bearing mouse model with poor *** research would provide an impetus as well as a novel strategy for dual function inducers and combined immune activators enhanced photoimmunotherapy.

关键词： immunotherapy cancer aggregation

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Texture development and surface reconstruction of BiVO_(4)photoanode via one-pot hydrothermal reaction for enhanced photoelectrochemical water splitting

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Journal of Advanced Ceramics 2025年第3期14卷 133-141页

作者： Sung Won Hwang Yoo Jae Jeong Runfa Tan Indhujasri Saravanan Hyun Soo Han Dong Hoe Kim In Sun Cho Department of Energy Systems Research Ajou UniversitySuwon 16499Republic of Korea Department of Material Science&Engineering Ajou UniversitySuwon 16499Republic of Korea Department of Mechanical Engineering Stanford UniversityStanford 94305USA Department of Material Science&Engineering Korea UniversitySeoul 02841Republic of Korea Materials Science and Engineering Program University of Colorado BoulderBoulder 80303USA

The simultaneous optimization of the bulk and surface characteristics of photoelectrodes is essential to maximize their photoelectrochemical(PEC)*** report a novel one-pot hydrothermal synthesis of textured and surface-reconstructed BiVO_(4)photoanodes(ts-BVO),achieving significant improvements in PEC water *** controlling precursor molarity and ethylene glycol(EG)addition,we developed a stepwise dual reaction(SDR)mechanism,which enables simultaneous bulk texture development and surface *** optimized CoBi/ts-BVO photoanode exhibited a photocurrent density of 4.3 mA∙cm^(−2)at 1.23 V *** hydrogen electrode(RHE)with a high Faradaic efficiency of 98%under one sun *** with nontextured BiVO_(4),the charge transport efficiency increased from 8%to 70%,whereas the surface charge transfer efficiency improved from 9%to 85%.These results underscore the critical role of both bulk and surface engineering in enhancing PEC *** findings offer a streamlined approach for improving the intrinsic properties of photoanodes in solar water splitting.

关键词： BiVO_(4) hydrothermal texture surface reconstruction ethylene glycol(EG) photoelectrochemical water splitting

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Electrocatalysis for sustainable nitrogen management: materials innovation for sensing, removal and upcycling technologies

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science China Chemistry 2025年第6期 2322-2342页

作者： Mei Yi Hongmei Li Minghao Xie Panpan Li Zhaoyu Jin Guihua Yu Institute of Fundamental and Frontier Sciences University of Electronic Science and Technology of China College of Materials Science and Engineering and College of Chemistry Sichuan University Materials Science and Engineering Program and Walker Department of Mechanical Engineering The University of Texas at Austin

The global nitrogen cycle holds immense importance due to its crucial role in supporting life, supplying vital nutrients for plant growth, preserving environmental balance, and enabling the proper functioning of ecosystems. However, human activities frequently disrupt this cycle, leading to the accumulation of nitrates and nitrites in water bodies. This accumulation causes environmental pollution and health risks. Traditional methods for treating nitrogen pollution, including biological, physical, and chemical approaches, have inherent limitations. In recent years, electrocatalysis has emerged as a promising and sustainable approach for nitrogen management. This technology offers superior efficiency, high selectivity, and environmental *** not only enables accurate detection of nitrogen pollutants in the environment but also facilitates their conversion into harmless nitrogen gas. Moreover, recent advancements have focused on the upcycling of nitrogen pollutants into valuable compounds,such as ammonia and urea. In this comprehensive review, we showcase the applications of electrocatalysis in sustainable nitrogen management. Specifically, we highlight its use in the sensing, removal, and upcycling of major nitrogen pollutants,including nitrate（NO3-）, nitrite（NO2-）, and nitric oxide（NO）. We discuss the use of catalysts, such as Pd alloys, Cu-based, and Fe-based materials, in electrochemical sensing and catalysis. Additionally, we explore recent advancements in the conversion of nitrogen pollutants into valuable compounds like ammonia and urea. The review also addresses current challenges and future opportunities in the field, including innovations in sensor and catalyst design, as well as large-scale treatment strategies. We anticipate that these perspectives will provide profound insights for effective nitrogen pollution control and sustainable utilization of nitrogen resources.

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Fe single atom trigger asymmetric In-In polarized site pairs boosting near-infrared N2 photoreduction

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materials Today 2025年 86卷 96-103页

作者： Liang, Huimin Ye, Caichao Wu, Yao Li, Yezi Long, Ran Xiong, Jun Jiang, Wei Di, Jun School of Chemistry and Chemical Engineering National Special Superfine Powder Engineering Research Center Nanjing University of Science and Technology Nanjing210094 China Academy for Advanced Interdisciplinary Studies & Department of Materials Science and Engineering Guangdong Provincial Key Laboratory of Computational Science and Material Design Southern University of Science and Technology Shenzhen518055 China School of Materials Science & Engineering Nanyang Technological University Singapore639798 Singapore National Synchrotron Radiation Laboratory CAS Center for Excellence in Nanoscience School of Chemistry and Materials Science University of Science and Technology of China Hefei230026 China Institute for Energy Research Jiangsu University Zhenjiang212013 China

Building differentiated charge distributed polarized atomic pairs may be an alternative for N2 activation. In this work, CuInS2 atomic layers with asymmetric In-In polarized site pairs are prepared by doping Fe single atoms, as proved by X-ray absorption fine structure spectroscopy, quasi in situ X-ray photoelectron spectra and calculated atomic charge distribution. The engineered Fe single atoms tuned the surface atomic charge distribution, building local polarization center to boost directional surface charge separation. The formed In-In polarized site pairs with asymmetric charge distribution creates distinct interaction with two N atoms in N2 molecule, contributing to the enhanced activation of N2. The alternating pathway is regarded as hydrogenation pathway over Fe-CuInS2 with *NNH formation as rate-determining step. The charge-redistributed surface atomic structure after engineered Fe single atoms strengthens intermediate interaction and lower the rate-determining step energy barrier. Benefiting from these features, Fe-CuInS2 exhibits excellent photocatalytic activity under near-infrared (NIR) irradiation with an ammonia synthesis rate of 94.1 μmol g−1 h−1. In comparison, the N2-NH3 conversion rate of Fe-CuInS2 under ultraviolet–visible (UV–Vis) irradiation could reach 137.4 μmol g−1 h−1, which is about 6.8 times higher than that of CuInS2. The apparent quantum efficiencies of Fe-CuInS2-2 at 380, 400, 450, 500, 550, 650, 700, 800, 850 and 1064 nm were 3.0 %, 3.3 %, 2.7 %, 2.1 %, 2.0 %, 1.5 %, 1.3 %, 0.4 %, 0.7 % and 0.6 %, respectively. © 2025 Elsevier Ltd

关键词： X ray absorption fine structure spectroscopy

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Temperature-dependent microstructural evolution in a compositionally complex solid electrolyte:The role of a grain boundary transition

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Journal of Advanced Ceramics 2025年第3期14卷 163-176页

作者： Shu-Ting Ko Chaojie Du Huiming Guo Hasti Vahidi Jenna L.Wardini Tom Lee Yi Liu Jingjing Yang Francisco Guzman Timothy J.Rupert William J.Bowman Shen J.Dillon Xiaoqing Pan Jian Luo Aiiso Yufeng Li Family Department of Chemical and Nano Engineering University of California San DiegoLa JollaCalifornia 92093USA Program in Materials Science and Engineering University of California San DiegoLa JollaCalifornia 92093USA Department of Materials Science and Engineering University of California IrvineIrvineCalifornia 92697USA Department of Physics and Astronomy University of California IrvineIrvineCalifornia 92697USA Irvine Materials Research Institute University of California IrvineIrvineCalifornia 92697USA

Compositionally complex solid electrolyte(Li_(0.375)Sr_(0.4375))(Ta_(0.375)Nb_(0.375)Zr_(0.125)Hf_(0.125))O_(3)(LSTNZH)samples are synthesized using different sintering temperatures,durations,and cooling conditions(furnace cooling(FC)*** quenching(AQ)).The temperature-dependent grain growth has been examined to investigate the microstructural evolution and the origin of exaggerated(abnormal)grain *** moderate temperatures,the grain growth of LSTNZH follows a cubic root growth model with an Arrhenius temperature *** increasing temperature,bimodal microstructures develop,and the Arrhenius temperature dependence breaks ***,increasing the temperature induces increased Nb segregation at general grain boundaries(GBs),in contrast to classical GB segregation models but suggesting premelting-like GB disordering,which can explain the observed abnormal grain growth(AGG).In addition,the large grains become faceted with increasing temperature,which occurs concurrently with the temperature-induced transitions in GB segregation and grain growth,thereby further supporting the occurrence of a GB phase-like(complexion)*** impacts on the densification,ionic conductivity,and hardness are also *** work provides a new insight into the fundamental understanding of the grain growth mechanisms of the emergent class of medium-and high-entropy compositionally complex ceramics(CCCs),which is essential for tailoring microstructures and material properties.

关键词： compositionally complex ceramics(CCCs) solid electrolytes perovskite grain growth grain boundary(GB) electron backscatter diffraction(EBSD)

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Unassisted photoelectrochemical CO_(2)reduction by employingⅢ-Ⅴphotoelectrode with 15%solar-to-fuel efficiency

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Carbon Energy 2025年第3期7卷 1-10页

作者： Karthik Peramaiah Purushothaman Varadhan Vinoth Ramalingam Bilawal Khan Pradip Kumar Das Hao Huang Hui-Chun Fu Xiulin Yang Vincent Tung Kuo-Wei Huang Jr-Hau He Chemistry Program Center for Renewable Energy and Storage Technologies(CREST)and Division of Physical Science and EngineeringKing Abdullah University of Science and Technology(KAUST)ThuwalSaudi Arabia Institute of Sustainability for Chemicals Energyand Environment(ISCE2)Agency for ScienceTechnologyand Research(A*STAR)Singapore School of Computing Engineering and TechnologyRobert Gordon UniversityAberdeenUK Department of Materials Science and Engineering City University of Hong KongKowloonSARHong KongChina Guangxi Key Laboratory of Low Carbon Energy Materials School of Chemistry and Pharmaceutical SciencesGuangxi Normal UniversityGuilinChina Department of Chemical System and Engineering University of TokyoTokyoJapan

Solar-driven carbon dioxide reduction reaction(CO_(2)RR)provides an oppor tunity to produce value-added chemical feedstocks and ***,achieving efficient and stable photoelectrochemical(PEC)CO_(2)RR into selec tive products is challenging owing to the difficulties associated with the optical and the electrical configuration of PEC devices and electrocatalyst ***,we construct an efficient,concentrated sunlight-driven CO_(2)RR setup consisting of InGaP/GaAs/Ge triple-junction cell as a photoanode and oxide-derived Au(Ox-Au)as a cathode to perform the unassisted PEC CO_(2)*** one-sun illumination,a maximum operating current density of 11.5 mA cm^(-2) with an impressive Faradaic efficiency(FE)of~98%is achieved for carbon monoxide(CO)production,leading to a solar-to-fuel conversion efficiency of~15%.Under concentrated intensity of 10 sun,the photoanode records a maximum current density of~124 mAcm^(-2) and maintains~60%of FE for CO *** results demonstrate crucial advancements in usingⅢ-Ⅴbased photoanodes for concentrated PEC CO_(2)RR.

关键词： photoelectrochemical oxide derived Au concentrated sunlight selec tive products III V photoelectrode pec devices CO reduction solar fuel efficiency

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Achieving high strength and large ductility in a Cr30Co30Ni30Al5Ti5 alloy through intergranular precipitation

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Journal of materials science and Technology 2025年 215卷 167-179页

作者： Zou, Jiawei Chen, Siyu Cheng, Pengming Ding, Jun Zhang, Chongle Zhang, Shengze Zhang, Bozhao Fu, Xiaoqian Chen, Yujie Zhao, Yuping Qi, Xu Gu, Lin Zhang, Ze Sha, Gang Yu, Qian Center of Electron Microscopy and State Key Laboratory of Silicon and Advanced Semiconductor Materials School of Materials Science and Engineering Zhejiang University Hangzhou310027 China School of Materials Science and Engineering Herbert Gleiter Institute of Nanoscience Nanjing University of Science and Technology Nanjing210094 China State Key Laboratory for Mechanical Behavior of Materials School of Materials Science and Engineering Xi'an Jiaotong University Xi'an710049 China Center for Alloy Innovation and Design State Key Laboratory for Mechanical Xi'an Jiaotong University Xi'an710049 China Pico Electron Microscopy Center Innovation Institute for Ocean Materials Characterization Technology Center for Advanced Studies in Precision Instruments Hainan University Haikou570228 China Beijing National Center for Electron Microscopy and Laboratory of Advanced Materials School of Materials Science and Engineering Tsinghua University Beijing100084 China

Precipitation at grain boundaries is typically not regarded as an efficient method for strengthening materials since it can induce grain boundary embrittlement, which detrimentally affects ductility. In this research, we developed a multi-principal element alloy (MPEA) with the composition Cr30Co30Ni30Al5Ti5 (at.%), incorporating both intragranular and intergranular nanoprecipitates. Utilizing multiscale, three-dimensional, and in-situ electron microscopy techniques, coupled with computational simulations, we established that intergranular nanoprecipitation in this material plays a crucial role in enhancing strength and promoting dislocation plasticity. The structure of intergranular nanoprecipitation comprises multiple phases with varying composition and structure. Despite the diversity, the crystal planes conducive to the easy glide of dislocations are well-matched, allowing for the sustained continuity of dislocation slipping across different phase structures. Simultaneously, this structure generates an undulated stress field near grain boundaries, amplifying the strengthening effect and facilitating multiple slip and cross-slip during deformation. Consequently, it promotes the proliferation and storage of dislocations. As a result, our material exhibits a yield strength of approximately 1010 MPa and an ultimate tensile strength of around 1500 MPa, accompanied by a significant fracture elongation of 41 %. Our findings illuminate the potential for harnessing intergranular nanoprecipitation to optimize the strength-ductility trade-off in MPEAs, emphasizing the strategy of leveraging complex compositions for the design of sophisticated functional microstructures. © 2024

关键词： Ductility

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Effect of Sn addition on electrochemical activity of ribbons of Mg-Al-Ca anode material for rechargeable magnesium batteries fabricated by rapid solidification

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Keikinzoku/Journal of Japan Institute of Light Metals 2025年第1期75卷 9-13页

作者： Fukuta, Yoshitaka Kikura, Kensei Tsukeda, Tadayoshi Aida, Tetsuo Tabata, Hironobu Kurihara, Hideki Suzuki, Mayumi Program of Materials Science and Engineering Studies in Science and Engineering Graduate School of Science and Engineering University of Toyama 3190 Gofuku Toyama-shi Toyama930-8555 Japan Graduate School of Science and Engineering University of Toyama Toyama-shi Toyama Japan Faculty of Sustainable Design Academic Assembly University of Toyama Toyama-shi Toyama Japan CHUETSU METAL WORKS CO. LTD. Nakaniikawagun Toyama Japan Saitama Industrial technology Center Kawaguchi-shi Saitama Japan Department of Mechanical Systems Engineering Faculty of Engineering Toyama Prefectural University Imizu-shi Toyama Japan

Magnesium-based batteries are potential candidates for next-generation rechargeable batteries due to the divalent nature of magnesium cations and the natural abundance of magnesium resources. In this study, the electrochemical activity of Mg-6mass%Al-3mass%Ca anodes combined with Sn was investigated. Thin ribbons of the anode specimens were prepared by a single-roll rapid solidification method. The results showed that the electrochemical activity increased upon adding 1 mass% Sn, while it decreased for 3 mass% Sn. Based on the results of an X-ray diffraction analysis, the addition of Sn led to the formation of Mg2Sn and Ca2Sn phases, which increased the lattice distortion. Scanning electron microscopy observations indicated that these secondary phases were homogeneously distributed for 1 mass% Sn addition, while they were coarsely distributed for 3 mass% Sn. © 2025 The Japan Institute of Light Metals.

关键词： X ray diffraction analysis

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Dense carbon nanofiber self-supporting electrode fabricated by orientation/compaction strategy for high volumetric lithium storage capacity

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Progress in Natural science:materials International 2025年第1期35卷 229-237页

作者： Haihui Liu Chaoqun Chen Qiang Xu Yan Song Xiangwu Zhang Chang Ma Tianjin Municipal Key Lab of Advanced Fiber and Energy Storage Technology Tiangong University CAS Key Laboratory of Carbon Materials Institute of Coal Chemistry Chinese Academy of Sciences Fiber and Polymer Science Program Department of Textile Engineering Chemistry and Science Wilson College of Textiles North Carolina State University

Low bulk density greatly restricts the large-scale application of electrospun carbon-based fiber membrane as electrode in energy storage devices. To solve the above challenges, herein an orientation-compaction densification strategy is proposed to enhance the bulk density and volumetric capacity of PAN-based carbon nanofiber membranes as self-supporting electrode used in lithium-ion batteries（LIBs）. Specifically, highly-oriented fibers are achieved by high-speed roller collecting during electrospinning, and compaction densification is conducted by hot-pressing treatment. The effects of collecting speed and hot-pressing pressure on the morphology, conductivity,bulk density, tensile strength, and flexibility of the obtained carbon nanofiber membrane are *** to conventional fiber membranes, of which fibers are disorderly stacked, the oriented fiber membrane is much easier to achieve dense stacking by compaction. The obtained dense carbon nanofiber membrane demonstrates a bulk density of 0.566 g cm-3, and shows a significantly-enhanced volumetric capacity(318.3 mA h cm-3), high-rate performance(86.6 mA h cm-3at 5 A g-1), and satisfactory cycling stability when used as selfsupporting electrode of LIBs.

关键词： Bulk density Densification Electrospinning Orientation-compaction Volumetric capacity

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Titanium nitride nanoparticles as plasmonic nanothermometers

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Optics Express 2025年第4期33卷 6758-6770页

作者： Sarabia-Alonso, Julio Aurelio Pasos, Emmanuel Vidales Belamkar, Aishwarya Wagner, Brandon Mangolini, Lorenzo Department of Mechanical Engineering University of California Riverside 900 University Ave. RiversideCA92521 United States Materials Science and Engineering Program University of California Riverside 900 University Ave. RiversideCA92521 United States

The capability of measuring the temperature at nanometer length scales is highly desirable and useful in numerous fields such as plasmonics, biomedicine, and nanochemistry. Precise and easy-to-implement temperature measurements at these scales would enable the investigation of fundamental processes that occur, for instance, during the synthesis of nanomaterials, or the conversion of electromagnetic energy into thermal one (photothermal conversion). Here, we demonstrate that titanium nitride nanoparticles are effective nanothermometers whose temperature can be measured optically in a reliable and reproducible manner. We leverage the Raman signal from these nanomaterials to measure their temperature, and we do so in two different ways: using the phononic signature induced by the presence of native oxide and using the electronic anti-stoke Raman signal induced by the free electrons in the material. Our findings confirm that titanium nitride nanoparticles, which are already an earth-abundant, low-cost alternative to gold nanoparticles, are also a versatile tool for nanothermometry. © 2025 Optica Publishing Group under the terms of the Optica Open Access Publishing Agreement.

关键词： Titanium nitride

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