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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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Enhanced methanol production from photothermal CO_(2) reduction via multilevel interface design

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Nano Research 2025年第2期18卷 235-241页

作者： Hongmin Wang Bo Shang Chungseok Choi Sungho Jeon Yuanzuo Gao Tyler Wang Nia J.Harmon Mengxia Liu Eric A.Stach Hailiang Wang Department of Chemistry Yale UniversityNew HavenCT 06520USA Energy Sciences Institute Yale UniversityWest HavenCT 06516USA School of Materials Science and Engineering Southeast UniversityNanjing 211189China Current address:SKKU Advanced Institute of Nanotechnology and Department of Nanoengineering Sungkyunkwan UniversitySuwon 16419Republic of Korea Department of Materials Science and Engineering University of PennsylvaniaPhiladelphiaPA 19104USA Department of Physics Yale UniversityNew HavenCT 06511USA Department of Electrical Engineering Yale UniversityNew HavenCT 06511USA

Photothermal CO_(2) hydrogenation is a promising route to produce methanol as a sustainable liquid solar ***,most existing catalysts require a combination of solar irradiation and additional heat input to achieve a satisfactory reaction *** the few that can be driven solely by light,their reaction rates are one order of magnitude *** develop a photothermal catalyst with multilevel interfaces that achieves improvedmethanol production from photothermal CO_(2) hydrogenation without external *** catalyst features a layered structure comprising Cu/ZnO/Al_(2)O_(3)(CZA)covered by oxidized carbon black(oCB),where the oCB/CZA interface promotes efficient heat generation and transfer,and the Cu/oxide interface contributes to high catalytic *** a mild pressure of 8 bar,our oCB/CZA catalyst shows a methanol selectivity of 64.7%with a superior production rate of 4.91 mmol-geza-1-h-1,at least one order of magnitude higher than other photothermal catalysts solely driven by *** work demonstrates a photothermal catalyst design strategy for liquid solar fuel production.

关键词： photothermal catalysis CO_(2)hydrogenation methanol production solar fuel multilevel interface Cu/ZnO/Al_(2)O_(3)(CZA)catalyst

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Low-cost chemical surface smoothing of CO2 laser-etched acrylic using WELD ON 4 acrylic solvent cement

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International Journal of Advanced Manufacturing Technology 2025年第5期138卷 2245-2255页

作者： Moncada, Luis H. Safaripour, Samira Hutter, Tanya Walker Department of Mechanical Engineering The University of Texas at Austin AustinTX78712 United States Materials Science and Engineering Program and Texas Materials Institute The University of Texas at Austin AustinTX78712 United States

With the increasing use of micro-manufactured devices and the demand for low-cost fabrication techniques, this study presents a simple and scalable surface polishing method for laser etched acrylic using WELD-ON 4 acrylic solvent cement, a solvent typically used for bonding thermoplastics. The method’s effectiveness was evaluated by treating acrylic samples up to three times and analyzing changes in transparency, surface roughness average (Ra), luminescence, and wettability. Results show that even a single treatment significantly improved surface smoothness, reduced light scattering, and brought contact angle and optical clarity closer to those of unetched acrylic. After three treatments, the surface became isotropic, with laser-etched lines disappearing. Specifically, a 60% reduction in Ra was observed in the direction perpendicular to the etched lines, while the parallel direction initially showed a similar trend, followed by a slight increase attributed to the formation of surface irregularities caused by the re-solidification of dissolved acrylic. Contact angle measurements indicated that the surface remained hydrophilic, with controllable wettability based on the number of treatments. Overall, this method provides a low-cost, cleanroom-free solution for improving the surface finish of laser-fabricated acrylic components. Its compatibility with complex or recessed geometries makes it particularly suitable for microfluidic devices and other precision applications requiring both optical clarity and controlled surface properties. © The Author(s), under exclusive licence to Springer-Verlag London Ltd., part of Springer Nature 2025.

关键词： Carbon dioxide lasers

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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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Across the Interface: Understanding the Mechanism of Perovskite-Sensitized Triplet-Triplet Annihilation

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ACS Applied Energy materials 2025年第9期8卷 5502-5512页

作者： Sullivan, Colette M. Nienhaus, Lea Department of Chemistry Rice University HoustonTX77005 United States Department of Materials Science and NanoEngineering Rice University HoustonTX77005 United States Department of Physics and Astronomy Rice University HoustonTX77005 United States Department of Chemical and Biomolecular Engineering Rice University HoustonTX77005 United States Rice Advanced Materials Institute Rice University HoustonTX77005 United States

Perovskite-sensitized photon upconversion may provide a viable solution toward developing efficient solid-state upconversion systems due to favorable photophysical properties such as long carrier lifetimes and compositional tunability in the perovskite. This method of photon upconversion differs from the extensively explored solution-based upconversion systems due to free carrier generation within bulk perovskites, which results in triplet generation by charge injection rather than bound triplet exciton transfer. In addition to differing sensitizer charge generation mechanisms, generated triplets must diffuse within the solid state prior to successful upconversion, introducing another layer of complexity. To this end, we outline the current mechanistic understanding of the perovskite-based triplet sensitization process and discuss the future directions of the field and the viability of future technological implementation. © 2025 American Chemical Society.

关键词： charge carriers interface perovskite Triplet−triplet annihilation upconversion

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Recent advances in bio-integrated electrochemical sensors for neuroengineering

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Fundamental Research 2025年第1期5卷 29-47页

作者： Shulin Chen Tzu-Li Liu Yizhen Jia Jinghua Li Department of Materials Science and Engineering The Ohio State UniversityColumbusOH 43210USA Chronic Brain Injury Program The Ohio State UniversityColumbusOH 43210USA

Detecting and diagnosing neurological diseases in modern healthcare presents substantial challenges that directly impact patient *** complex nature of these conditions demands precise and quantitative monitoring of disease-associated biomarkers in a continuous,real-time *** chemical sensing strategies exhibit restricted clinical effectiveness due to labor-intensive laboratory analysis prerequisites,dependence on clinician expertise,and prolonged and recurrent ***-integrated electronics for chemical sensing is an emerging,multidisciplinary field enabled by rapid advances in electrical engineering,biosensing,materials science,analytical chemistry,and biomedical *** review presents an overview of recent progress in bio-integrated electrochemical sensors,with an emphasis on their relevance to neuroengineering and *** traverses vital neurological biomarkers and explores bio-recognition elements,sensing strategies,transducer designs,and wireless signal transmission *** integration of in vivo biochemical sensors is showcased through *** review concludes by outlining future trends and advancements in in vivo electrochemical sensing,and highlighting ongoing research and technological innovation,which aims to provide inspiring and practical instructions for future research.

关键词： Biochemical sensing Neuroengineering Bioimplants Analytical chemistry Bio-integrated electronics

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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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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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Biobased Poly(ester amide)s as Sustainable Coating materials for Vegan Leather with Improved Haptic Sensation

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ACS Sustainable Chemistry and engineering 2025年第20期13卷 7585-7597页

作者： Ryu, Jieun Hao, Lam Tan Kim, Hyeri Lee, Somyong Jeon, Hyeonyeol Hwang, Dong Soo Park, Jeyoung Park, Cheol Hun Oh, Dongyeop X. Koo, Jun Mo Park, Sung Bae Ulsan44429 Korea Republic of Pohang37673 Korea Republic of Ulsan44429 Korea Republic of Pohang37673 Korea Republic of Daejeon34113 Korea Republic of Department of Chemical and Biomolecular Engineering Sogang University Seoul04107 Korea Republic of Department of Polymer Science and Engineering and Program in Environmental and Polymer Engineering Inha University Incheon22212 Korea Republic of Department of Organic Materials Engineering Chungnam National University Daejeon34134 Korea Republic of Department of Materials Science and Engineering Chungnam National University Daejeon34134 Korea Republic of

Increased consumer awareness of animal welfare and environmental sustainability has driven the development of vegan leather alternatives to natural leather. Fossil-derived leather substitutes offer superior strength and thermal stability but often lack biodegradability, carbon neutrality and aesthetics. Biorenewable alternatives are more eco-friendly but typically suffer from insufficient thermal and mechanical properties and poor moisture resistance. This study presents the synthesis of mechanically reinforced, thermally enhanced and biodegradable poly(ester amide)s (PEAs) incorporating hydrogen bonds as vegan leather coating materials. Synthesized from biobased 1,4-butanediol, adipic acid and nylon 46 via a two-step transesterification/polycondensation process, the resulting PEAs exhibit over eight times higher tensile strength, 3-fold greater toughness, and enhanced thermal stability compared to their constituting homopolymers, poly(butylene adipate) and nylon 46. All PEAs disintegrate within 18 weeks and achieve over 60% biodegradation rate relative to cellulose under composting conditions within one month. When applied to mushroom fabrics, the PEA coating provides haptic sensations (slipperiness and softness) comparable to commercially available leather. Life-cycle assessment indicates that PEA-coated leather imposes considerably lower environmental impacts than both bovine and polyurethane-based leather. This novel material holds promise as a sustainable, high-performance vegan leather substitute. © 2025 American Chemical Society.

关键词： Biodegradability

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Quantum Interference in a Molecular Analog of the Crystalline Silicon Unit Cell

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Journal of the American Chemical Society 2025年第19期147卷 16602-16610页

作者： Hight, Matthew O. Pimentel, Ashley E. Siu, Timothy C. Wong, Joshua Y. Nguyen, Jennifer Carta, Veronica Su, Timothy A. Department of Chemistry University of California RiversideCA92506 United States Materials Science & Engineering Program University of California RiversideCA92506 United States

This manuscript describes the emergence of destructive σ-quantum interference (σ-DQI) in sila-adamantane, a molecule whose cluster core is isostructural with the crystalline silicon unit cell. To reveal these σ-DQI effects, we take a bridge-cutting approach where we conceptually pare sila-adamantane down to its bicyclic Si[3.3.1] and linear oligosilane forms. Scanning tunneling microscopy break-junction (STM-BJ) measurements reveal that conductance in single-molecule junctions of the tricyclic sila-adamantane is 2.7-times lower than their bicyclic Si[3.3.1] analog. The only structural difference between their cluster cores is a remote dimethylsilylene bridge that is present in sila-adamantane yet absent in Si[3.3.1]. Density functional theory calculations reveal that this dimethylsilylene enforces C3 symmetry at the sila-diamondoid bridgeheads, allowing each electrode to couple into the three cluster bridge dimensions equally. Though each bridge alignment is sterically equivalent, they have profound electronic differences: when electrodes align with the long branches of sila-adamantane, strong σ-DQI interactions occur between frontier molecular orbitals that suppress electronic transmission across the molecular junction. We exploit these alignment-dependent σ-DQI effects to create new forms of stereoelectronic conductance switches, where a reversible mechanical stimulus controls which pathway through the diamondoid framework the electrodes align through. This represents the first example of dynamic modulation of σ-DQI and enables us to achieve switching ratios (average on/off ∼5.6) higher than previously reported σ-stereoelectronic switches. These studies reveal how the innate dimensionality and symmetry of crystalline silicon influence charge transport at its most fundamental level, and how these principles can be harnessed to control quantum interference in single-molecule electronics. © 2025 The Authors. Published by American Chemical Society.

关键词： Molecular orbitals

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