Fazil T.P, Aparna Krishna, Aneena M.S., Mohammed Mudassir, C. N. Shyam Kumar, Mohamed Ouda, Deepalekshmi Ponnamma, Soney Varghese
{"title":"Ni/Fe-Catalyzed Graphitization of Biomass-Derived Carbon-Based Epoxy Composites for Tunable X-Band EMI Shielding","authors":"Fazil T.P, Aparna Krishna, Aneena M.S., Mohammed Mudassir, C. N. Shyam Kumar, Mohamed Ouda, Deepalekshmi Ponnamma, Soney Varghese","doi":"10.1002/adsu.70679","DOIUrl":"https://doi.org/10.1002/adsu.70679","url":null,"abstract":"<p>Coconut fiber (CF) was impregnated with Ni and Fe precursors and pyrolyzed at 1000°C to obtain the respective transition-metal-modified carbon fillers, Ni-CF and Fe-CF. Such modified carbon fillers were incorporated into an epoxy matrix (0.5–10 wt.%), and the electromagnetic responses of the resulting composites were evaluated in the X-band frequency (8.2–12.4 GHz). Ni-assisted graphitization led to the development of a more ordered carbon framework, as indicated by a shift in the C (002) reflection to a higher angle, a lower I<sub>D</sub>/I<sub>G</sub> ratio (0.65), and the presence of more coherent nanoscale carbon domains (d<sub>002</sub> = 0.339 nm, Lc = 3.5 nm). At 10 wt.% loading, Ni-CF/epoxy achieved a band-averaged SE<sub>T</sub> of 23.4 ± 0.5 dB, with SE<sub>A</sub> = 20.5 ± 0.3 dB and SE<sub>R</sub> = 2.9 ± 0.2 dB. In contrast, Fe-CF exhibited a higher I<sub>D</sub>/I<sub>G</sub> ratio (1.14), together with a more heterogeneous and defect-rich carbon structure (d<sub>002</sub> = 0.356 nm, Lc = 2.1 nm). At 10 wt.% loading, Fe-CF/epoxy reached a band-averaged SE<sub>T</sub> of 19.4 ± 1.6 dB, with SE<sub>A</sub> = 15.5 ± 1.6 dB and SE<sub>R</sub> = 3.9 ± 0.1 dB. Low-frequency broadband dielectric spectroscopy showed stronger polarization and localized charge-transport response for Ni-CF/epoxy and broader interfacial relaxation for Fe-CF/epoxy.</p>","PeriodicalId":7294,"journal":{"name":"Advanced Sustainable Systems","volume":"10 10","pages":""},"PeriodicalIF":5.6,"publicationDate":"2026-10-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/adsu.70679","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"149145892","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Li Li, Wenpeng Wang, Zhenzhen Zhao, Yuelai Li, Li Pan, Hangmin Xu, Yun Chen, Xingwang Zhu
{"title":"Understanding and Steering Nitrogen Fate in Photocatalytic Nitrate Reduction","authors":"Li Li, Wenpeng Wang, Zhenzhen Zhao, Yuelai Li, Li Pan, Hangmin Xu, Yun Chen, Xingwang Zhu","doi":"10.1002/adsu.70676","DOIUrl":"https://doi.org/10.1002/adsu.70676","url":null,"abstract":"<div>\u0000 \u0000 <p>Photocatalytic nitrate reduction is assessed through nitrate conversion, although the reaction can redistribute nitrogen among nitrite, nitric oxide (NO)-derived intermediates, nitrous oxide (N<sub>2</sub>O), dinitrogen (N<sub>2</sub>), ammonia/ammonium (NH<sub>3</sub>/NH<sub>4</sub><sup>+</sup>), and emerging C–N products. The environmental and resource value of the process depends on nitrogen fate rather than nitrate disappearance alone. This review establishes a product-centred framework for understanding and steering that fate. We first consolidate the nitrogen network across surface, liquid, and gas phases, and distinguish primary selectivity from the final product distribution after secondary conversion and phase transfer. We then relate product formation to three coupled levels: nitrate entry, branching of NO-derived intermediates, and branch completion; surface functions governing adsorption, intermediate binding, cooperative sites, and active hydrogen; and the photochemical redox environment, including charge delivery and the oxidation half-reaction. Evidence from model systems, real waters, and time-resolved operation shows why high selectivity under one condition cannot be treated as an intrinsic catalyst property. On this basis, N<sub>2</sub>-oriented treatment requires verified removal without nitrite, ammonium, or N<sub>2</sub>O leakage, whereas NH<sub>3</sub>-oriented conversion requires product preservation, capture, and a favourable process balance. Connecting working-interface chemistry with water-matrix effects, reactor operation, and product recovery provides a route from empirical nitrate removal to deliberate nitrogen management.</p>\u0000 </div>","PeriodicalId":7294,"journal":{"name":"Advanced Sustainable Systems","volume":"10 10","pages":""},"PeriodicalIF":5.6,"publicationDate":"2026-10-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"149145810","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Ambient Silicate Curing Transforms Compacted Recycled Concrete Powder Into a Low-Carbon Construction Material","authors":"Sothyrak Rath, Nami Hasegawa, Phyo Thant Hein, Sabrina Harahap, Yuya Sakai","doi":"10.1002/adsu.70673","DOIUrl":"https://doi.org/10.1002/adsu.70673","url":null,"abstract":"<div>\u0000 \u0000 <p>Recycled concrete powder (RCP) derived from demolition waste is largely underutilized due to its inherently low binding capacity. Here, we investigate a sodium silicate solution curing method that refines the pore structure of compacted RCP at ambient temperature, without thermal treatment or CO<sub>2</sub> exposure. Compacted RCP specimens are cured in sodium silicate solutions at 0, 6, and 12 wt% concentrations. After 28 days, the 6% treatment reduces water absorption rate by 75%, and increases flexural strength by 69% compared to the uncured sample. Microstructural characterization reveals rapid calcium consumption to form calcium silicate hydrate and silica-rich gels, which establish interparticle bridges and refine the capillary pore network. The 6% condition outperformed the 12% condition, suggesting a kinetic threshold at which excessive silicate concentrations trigger rapid surface mineralization that creates a diffusion-limiting barrier, restricting further water and ion transport and hindering the continued hydration of unreacted cement. This study uses an extensive naturally carbonated RCP, indicating that the route does not depend on a high residual portlandite content. A cradle-to-gate assessment indicates 89%–91% lower carbon emissions than conventional autoclaved and carbonation-cured concrete bricks.</p>\u0000 </div>","PeriodicalId":7294,"journal":{"name":"Advanced Sustainable Systems","volume":"10 10","pages":""},"PeriodicalIF":5.6,"publicationDate":"2026-09-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"149146935","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Wood-Based Cellulose Nanocrystals as Reinforcement for Sustainable Concrete Composites","authors":"Ravi Patel, Amin Babaei-Ghazvini, Bishnu Acharya","doi":"10.1002/adsu.70674","DOIUrl":"https://doi.org/10.1002/adsu.70674","url":null,"abstract":"<p>This study evaluates wood-derived cellulose nanocrystals (WCNCs), produced via non-conventional processes, as nano-reinforcement in normal-strength concrete with a fixed mixed design. Physical properties, water absorption, and microstructure were examined for reference and WCNC-modified concretes. Optimal WCNC dosage (0.05 wt.%) improved workability-strength balance and significantly enhanced mechanical performance: compressive strength, splitting tensile strength, and maximum flexural load at failure increased by 16.10%, 13.60%, and 16.70%, respectively. Microstructural analyses indicated that WCNCs refined pore structure, bridge microcracks, and reduced permeability, contributing to greater resistance against corrosive chemicals and improved durability of cured composites. Although the hydrophilic nature of WCNCs slightly delayed initial setting, accelerated later-age hydration was inferred from strength development, suggesting beneficial long-term cementitious reactions. These findings demonstrate that eco-friendly WCNCs can effectively upgrade conventional concrete into more sustainable, high-performance green composites without altering the base mixture proportions. The results support further scale-up and life-cycle assessment to quantify environmental benefits and optimize dosage for diverse exposure conditions.</p>","PeriodicalId":7294,"journal":{"name":"Advanced Sustainable Systems","volume":"10 10","pages":""},"PeriodicalIF":5.6,"publicationDate":"2026-09-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/adsu.70674","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"149146936","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Zichang You, Chujun Zheng, Chengshuai Bao, Yan Lu, Zhaoyin Wen
{"title":"In Situ Lithium Compensation Driven Grain Boundary Engineering for Garnet Based Solid State Electrolytes","authors":"Zichang You, Chujun Zheng, Chengshuai Bao, Yan Lu, Zhaoyin Wen","doi":"10.1002/adsu.70666","DOIUrl":"https://doi.org/10.1002/adsu.70666","url":null,"abstract":"<div>\u0000 \u0000 <p>Solid-state lithium metal batteries (SSLMBs) have attracted significant attention due to their high safety and energy density. Garnet-type electrolytes are among the most promising candidates, yet the poor sinterability of Li<sub>7</sub>La<sub>3</sub>Zr<sub>2</sub>O<sub>12</sub> (LLZO) often leads to internal dendrite growth. Moreover, conventional LLZO fabrication requires expensive sacrificial lithium to compensate for lithium loss during sintering. Here, we introduce lithium-rich Li<sub>4</sub>SiO<sub>4</sub> (LSO) as a sintering additive into Ta-doped LLZO (LLZTO) to enable densification without external sacrificial lithium, reducing cost while enhancing dendrite resistance. During sintering, LSO decomposes into Li<sub>2</sub>O and Li<sub>2</sub>SiO<sub>3</sub>/Li<sub>2</sub>Si<sub>2</sub>O<sub>5</sub>, providing a lithium-rich atmosphere and in situ pinning at grain boundaries to suppress abnormal grain growth. Consequently, the bending strength is doubled, accompanied by an increase in the critical current density (CCD) from 0.4 to 0.9 mA cm<sup>−2</sup>. Symmetric and full cells assembled with this electrolyte also demonstrated excellent long term cycling stability. This strategy offers a cost-effective route to high performance SSLMBs and provides new insights for garnet electrolyte design and dendrite suppression.</p>\u0000 </div>","PeriodicalId":7294,"journal":{"name":"Advanced Sustainable Systems","volume":"10 10","pages":""},"PeriodicalIF":5.6,"publicationDate":"2026-09-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"149146937","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Design Considerations of Photocatalysts for the Simultaneous Degradation of Mixed Pollutants in Wastewater: A Review","authors":"Anupamaraj Kizhakke Purayil, Thi Thong Chuong Nguyen, Chinh Chien Nguyen, Shubhankar Kumar Bose, Sakar Mohan","doi":"10.1002/adsu.70667","DOIUrl":"https://doi.org/10.1002/adsu.70667","url":null,"abstract":"<div>\u0000 \u0000 <p>The growing presence of complex mixtures of pollutants in natural water bodies poses a major challenge to global water quality and environmental safety. Unlike single-pollutant systems, real wastewater contains diverse organic, inorganic, microbial, and emerging contaminants that interact through competitive adsorption, synergistic effects, and inhibitory pathways, making their simultaneous removal highly demanding. Although many photocatalysts have been successfully demonstrated for degrading individual pollutants under isolated conditions, their simultaneous one-pot degradation of coexisting pollutants remains relatively underexplored, largely due to the experimental and analytical complexity involved in evaluating photocatalytic efficiency in mixed systems. This gap is critical, as real-world wastewater typically contains multiple pollutants concurrently, often exhibiting greater toxicity than individual contaminants. Photocatalysis has emerged as a promising advanced oxidation process capable of utilizing solar energy to treat such multifaceted pollutant matrices. This review provides a comprehensive overview of pollutant classes, photocatalytic mechanisms, photocatalyst design, and challenges associated with multi-pollutant systems, including diverse organic-organic, organic-inorganic, and heavy-metal mixtures. Furthermore, key experimental challenges, including spectral overlap and matrix interference that complicate accurate efficiency assessment, are highlighted. By integrating mechanistic insights, material innovations, and analytical limitations, this review outlines future directions for designing robust photocatalytic nanomaterials capable of treating realistic, complex wastewater streams.</p>\u0000 </div>","PeriodicalId":7294,"journal":{"name":"Advanced Sustainable Systems","volume":"10 10","pages":""},"PeriodicalIF":5.6,"publicationDate":"2026-09-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"149146917","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Sn Doping Enhances Light Absorption of Lanthanum Poly(Heptazine Imide) for Efficient Photocatalytic Hydrogen Evolution","authors":"Jinhua Su, Hui Li, Shusheng Pan, Guoqiang Zhang","doi":"10.1002/adsu.70671","DOIUrl":"https://doi.org/10.1002/adsu.70671","url":null,"abstract":"<div>\u0000 \u0000 <p>Lanthanum poly(heptazine imide) (La-PHI) is a novel, highly crystalline PHI material. However, its visible-light absorption remains weak due to the limited contribution of La<sup>3+</sup> to the band structure of PHI. Considering that the ionic radius of Sn<sup>2+</sup> is comparable to that of La<sup>3+</sup>, Sn<sup>2+</sup> can stably occupy the identical sites within the PHI framework. Meanwhile, the 5p orbitals of Sn<sup>2+</sup> can effectively hybridize with the N 2p orbitals, thereby introducing intermediate energy levels. Experimental results demonstrate that Sn<sup>2+</sup> doping generates an intermediate level at approximately 2.30 eV within the forbidden band, effectively broadening the light absorption range. Through optimizing the Sn<sup>2+</sup> doping amount, the photocatalytic activity of the obtained sample under 420 < λ < 780 nm is 5.3 times that of the original La-PHI. This study indicates that Sn<sup>2</sup><sup>+</sup> doping is an effective strategy for extending the light absorption range, and the introduction of intermediate levels provides new insights into the design of highly efficient PHI-based photocatalysts.</p>\u0000 </div>","PeriodicalId":7294,"journal":{"name":"Advanced Sustainable Systems","volume":"10 10","pages":""},"PeriodicalIF":5.6,"publicationDate":"2026-09-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"149146934","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Derangula Venkateswarlu, Andrew Simon George, Nagaraj Sabarinathan, Suraj Soman, Surya Prakash Singh
{"title":"Donor Engineering of D–π–A Organic Sensitizers for Enhanced Indoor Dye-Sensitized Solar Cells Using Copper-Based Electrolytes","authors":"Derangula Venkateswarlu, Andrew Simon George, Nagaraj Sabarinathan, Suraj Soman, Surya Prakash Singh","doi":"10.1002/adsu.70663","DOIUrl":"https://doi.org/10.1002/adsu.70663","url":null,"abstract":"<div>\u0000 \u0000 <p>Herein, we have designed and synthesized two novel metal-free organic D-π-A dyes with 6-methoxy-N-(4-(methylthio)phenyl)-N-phenylnaphthalen-2-amine <b>(SP-3)</b> and N-(4-(methylthio)phenyl)-N-phenylpyren-2-amine <b>(SP-4)</b> as the donor moiety, cyanoacrylic acid as the anchoring unit and thiophene as the π-spacer. Both <b>SP-3</b> and <b>SP-4</b> based DSCs reproduced efficiencies of 4.06% and 3.58% under standard 1 sun illumination, and an in-depth interfacial charge transfer study revealed the influence of oxygen-linked naphthalene donor unit on the electron diffusion within the TiO<sub>2</sub> scaffold, pushing charge collection efficiency (ηcc) above 50% for <b>SP-3</b> based DSC. Further, co-sensitization with XY1b dye enhances the device performance with a PCE of 6.02% under 1 sun illumination. Improved lifetime and faster electron transport/diffusion helped SP-3:XY1b to achieve an efficiency at par with SP-4:XY1b even with a lower fill factor (FF) below 50. However, lower FF, which is an indication of severe recombination within the system, becomes prominent under lower illumination intensities, where SP-4:XY1b superseded SP-3:XY1b with a PCE of 31.37% under standard 1000 lux WW CFL illumination. A complete indoor performance analysis was carried out for the co-sensitized devices, and SP-4:XY1b gives a PCE above 27% under various illumination intensities (1000, 700, 500, 200 lux) and sources (WW CFL, WW LED, DL LED).</p>\u0000 </div>","PeriodicalId":7294,"journal":{"name":"Advanced Sustainable Systems","volume":"10 10","pages":""},"PeriodicalIF":5.6,"publicationDate":"2026-09-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"149146795","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Tianyu Li, Song Wei, Xiaoguang Zhang, Ran Tao, Yan Wang, Junqiao Li, Fanbo Meng
{"title":"A Biomimetic Gill-Cover and Adaptive Magnetic-Switching Coupled Triboelectric–Electromagnetic Hybrid Generator for Self-Powered Environmental Monitoring in Low-Wind-Speed Mining Areas","authors":"Tianyu Li, Song Wei, Xiaoguang Zhang, Ran Tao, Yan Wang, Junqiao Li, Fanbo Meng","doi":"10.1002/adsu.70668","DOIUrl":"https://doi.org/10.1002/adsu.70668","url":null,"abstract":"<div>\u0000 \u0000 <p>Wind energy, as a widely available, abundant, and widely distributed renewable energy source, poses a formidable challenge in reliably capturing its low-speed energy over extended periods. Addressing the specific demand for low startup wind speed in areas with scarce wind resources, such as mining regions, this study proposes a bionic gill-cover and adaptive magnetic-switching-coupled triboelectric-electromagnetic hybrid generator (BM-TENG). This device utilizes a biomimetic gill structure coupled with adaptive magnetic switching to harvest broadband wind energy, thereby enhancing energy collection performance at low wind speeds. The BM-TENG achieves low start-up wind speeds and high rotational speeds through its biomimetic gill-like cover and non-contact operation mode. Compared to conventional scoops of the same size, the BM-TENG operates at a start-up wind speed as low as 1.5 m/s—a 28.57% reduction—while increasing rotational speed by 44.58% at 4 m/s wind speeds. Through a synergistic mechanism of magnetic force and centrifugal force, BM-TENG operates in non-contact mode at low wind speeds and in soft-contact mode at high wind speeds. At 4 m/s wind speed, BM-TENG delivers an output power of 53.4 mW. It demonstrates excellent stability, maintaining 82% output after 150 h of operation. Demonstrations confirm that BM-TENG can reliably power downstream electrical devices.</p>\u0000 </div>","PeriodicalId":7294,"journal":{"name":"Advanced Sustainable Systems","volume":"10 10","pages":""},"PeriodicalIF":5.6,"publicationDate":"2026-09-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"149146804","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Ren Yang, Lu Han, Huifang Liu, Liying Wan, Xian-Yan Xu, Xiao Lin, Xibao Li
{"title":"Zinc Vacancy-Mediated S-Scheme ZCS/ZnS-Vzn Heterojunction for Efficient Photocatalytic Hydrogen Production","authors":"Ren Yang, Lu Han, Huifang Liu, Liying Wan, Xian-Yan Xu, Xiao Lin, Xibao Li","doi":"10.1002/adsu.70628","DOIUrl":"https://doi.org/10.1002/adsu.70628","url":null,"abstract":"<div>\u0000 \u0000 <p>Photocatalytic H<sub>2</sub> generation via water splitting using sulfide semiconductors is hindered by narrow light absorption, rapid charge recombination, and photocorrosion. A core–shell ZCS/ZnS-Vzn heterojunction was constructed with tunable zinc vacancies. These vacancies introduce a mid-gap defect level for two-step visible-light absorption, form an ohmic‑like contact that directs S-scheme charge transfer from ZnS-Vzn to ZCS, and serve as hole traps (Vzn) to reduce the required sacrificial agent concentration from 20 to 10 vol%. The optimal composite achieves 2063.8 µmol h<sup>−1</sup> g<sup>−1</sup> H<sub>2</sub> evolution triggered by visible light, 25-fold and 16-fold higher than pristine ZnS-Vzn and ZCS, respectively. The S-scheme pathway also suppresses photocorrosion, ensuring excellent stability. This work demonstrates that vacancy-mediated S-scheme engineering offers a facile strategy for designing durable, high-performance sulfide photocatalysts for solar fuel production.</p>\u0000 </div>","PeriodicalId":7294,"journal":{"name":"Advanced Sustainable Systems","volume":"10 10","pages":""},"PeriodicalIF":5.6,"publicationDate":"2026-09-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"149146514","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}