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Hollow crystalline red phosphorus for efficient visible-light photocatalytic hydrogen evolution from pure water splitting 中空结晶红磷用于可见光光催化纯水裂解析氢
IF 9.2 2区 工程技术 Q1 ENERGY & FUELS Pub Date : 2026-01-28 DOI: 10.1016/j.susmat.2026.e01897
Danyang Wang , Xuanxuan Zhang , Xinhui Zhai , Zhen Wei , Jiguang Deng , Hongxing Dai , Yun Hau Ng , Lin Jing
Hydrogen production through solar-driven photocatalytic pure-water splitting is a promising strategy for achieving carbon-neutral energy systems, yet the development of simple and single-component semiconductor photocatalysts that operate efficiently under visible-light irradiation remains highly challenging. Herein, we report for the first time the synthesis of hollow crystalline red phosphorus (h-CRP) nanospheres, featuring a well-defined thin-shell architecture, enhanced visible-light absorption, shortened charge-transport pathways, and an optimized band structure favorable for overall water splitting. Benefiting from these structural advantages, h-CRP exhibits a markedly improved photocatalytic hydrogen evolution rate under visible-light irradiation, outperforming conventional rod-like CRP and amorphous RP. This work provides new insights into the structural design of phosphorus-based photocatalysts and highlights the great potential of hollow CRP nanostructures for efficient solar-to‑hydrogen conversion, while circumventing the complexity and material constraints typically associated with heterojunction-based overall water-splitting systems.
通过太阳能驱动的光催化纯水分解制氢是实现碳中和能源系统的一种很有前途的策略,然而,在可见光照射下高效运行的简单单组分半导体光催化剂的开发仍然非常具有挑战性。在此,我们首次报道了空心晶体红磷(h-CRP)纳米球的合成,具有明确的薄壳结构,增强的可见光吸收,缩短的电荷传输途径,以及有利于整体水分解的优化能带结构。得益于这些结构优势,h-CRP在可见光照射下表现出明显提高的光催化析氢速率,优于传统的杆状CRP和无定形RP。这项工作为磷基光催化剂的结构设计提供了新的见解,并强调了空心CRP纳米结构在高效太阳能到氢转化方面的巨大潜力,同时规避了基于异质结的整体水分解系统通常相关的复杂性和材料限制。
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引用次数: 0
Orange peel − derived CoFe₂O₄ spinel: A sustainable nanocatalyst for dye removal, water splitting, and CO₂ reduction 橘子皮衍生的CoFe₂O₄尖晶石:一种可持续的纳米催化剂,用于染料去除,水分解和CO₂还原
IF 9.2 2区 工程技术 Q1 ENERGY & FUELS Pub Date : 2026-01-28 DOI: 10.1016/j.susmat.2026.e01869
Odín Reyes-Vallejo , Francisco J. Cano , Rocío Sánchez-Albores , Edith Luévano-Hipólito , J. Escorcia-García , Leticia M. Torres-Martínez , Pathiyamattom Joseph Sebastian
The pressing need for sustainable and eco−friendly solutions has driven a paradigm shift towards innovative materials to tackle critical environmental and energy challenges. This study pioneers a green, waste−to−resource methodology for synthesizing cobalt ferrite (CoFe₂O₄) spinel nanoparticles, leveraging orange peel powder as a natural reducing and stabilizing agent. By transforming agro−industrial waste into high−performance nanomaterials, this work exemplifies the seamless integration of circular economy principles with cutting−edge nanotechnology. Comprehensive characterization by XRD, SEM−TEM, BET, and UV−Vis spectroscopy revealed a well−defined cubic spinel structure with an optical bandgap of 1.46 eV, optimized for visible−light absorption. Advanced techniques, including Raman, XPS, and FTIR, uncovered a partially inverted spinel configuration, with Co2+ and Fe3+ ions distributed across tetrahedral and octahedral sites. The CoFe₂O₄ nanoparticles demonstrated exceptional multifunctionality, excelling in both environmental remediation and renewable energy applications. In water treatment, the nanoparticles achieved remarkable dye removal efficiencies of 83.49% for malachite green (MG) and 49.73% for methylene blue (MB) through a synergistic adsorption−photocatalysis mechanism under visible light. In visible light−driven energy production, they facilitated hydrogen evolution (480 μmol/g) and formic acid (180 μmol/g) production from H2O and CO2 reduction, respectively. These achievements underscore the superior performance of the material compared to conventional photocatalysts. This approach establishes an efficient and sustainable route for nanomaterial synthesis, positioning orange peel−derived CoFe₂O₄ as a promising candidate for large−scale applications in water purification, renewable energy conversion, and carbon capture. By combining eco−compatibility with high catalytic efficiency, this study provides a scientifically grounded framework for advancing green nanotechnology.
对可持续和生态友好解决方案的迫切需求推动了向创新材料的范式转变,以应对关键的环境和能源挑战。该研究开创了一种绿色,废物到资源的方法来合成钴铁氧体(CoFe₂O₄)尖晶石纳米颗粒,利用橙皮粉作为天然还原剂和稳定剂。通过将农业-工业废物转化为高性能纳米材料,这项工作体现了循环经济原则与尖端纳米技术的无缝结合。通过XRD, SEM - TEM, BET和UV - Vis光谱综合表征,发现具有清晰的立方尖晶石结构,光学带隙为1.46 eV,对可见光吸收进行了优化。包括拉曼、XPS和FTIR在内的先进技术发现了部分倒置的尖晶石结构,Co2+和Fe3+离子分布在四面体和八面体上。CoFe₂O₄纳米颗粒表现出优异的多功能性,在环境修复和可再生能源应用方面都表现出色。在水处理中,纳米颗粒在可见光下通过协同吸附-光催化机制对孔雀石绿(MG)和亚甲基蓝(MB)的染料去除率分别达到83.49%和49.73%。在可见光驱动的能源生产中,它们分别促进了H2O还原氢(480 μmol/g)和CO2还原甲酸(180 μmol/g)的生成。这些成就强调了该材料与传统光催化剂相比的优越性能。该方法建立了一种高效和可持续的纳米材料合成途径,将橘子皮衍生的CoFe₂O₄定位为大规模应用于水净化、可再生能源转换和碳捕获的有希望的候选材料。通过将生态兼容性与高催化效率相结合,本研究为推进绿色纳米技术提供了科学基础框架。
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引用次数: 0
A sustainable strategy of plant-derived nanozyme and polysaccharide microneedles for multifunctional therapy of infected wounds 植物源性纳米酶和多糖微针用于感染性伤口多功能治疗的可持续策略
IF 9.2 2区 工程技术 Q1 ENERGY & FUELS Pub Date : 2026-01-27 DOI: 10.1016/j.susmat.2026.e01893
Peiyuan Li , Wenlin Zhou , Qing Guo , Siyan Liang , Chumei Liang , Wei Su
The development of multifunctional wound dressings from sustainable resources is critical to advancing green biomedical materials for effective wound repair. In this study, we present an eco-friendly microneedle delivery platform (LutCe-QCS-GP MN) with integrated reactive oxygen scavenging and antibacterial functions. The system features a sustainable nanozyme (LutCe), formed by self-assembly of the plant-derived flavonoid luteolin and cerium ions, which exhibits robust superoxide dismutase-like activity. These LutCe nanozymes organic-inorganic hybrids were synthesized through a green assembly process and demonstrate potent scavenging capability against superoxide anions, hydroxyl radicals, and reactive nitrogen species. Incorporated into the tips of the microneedles, they directly alleviate oxidative stress at the wound site. Simultaneously, an antimicrobial polysaccharide-based matrix provides effective defense against wound pathogens, preventing infection and secondary tissue damage. By synergistically combining sustainable antioxidant nanozymes with natural antibacterial components, the LutCe-QCS-GP MN system significantly reduced oxidative stress and bacterial load in wounds, markedly accelerating the healing process. Comprehensive in vitro and in vivo safety evaluations support the biosafety of the platform, underscoring its potential for clinical translation. This work not only introduces a promising therapeutic strategy for wound management but also highlights the valorization of natural, sustainable resources in functional material design, offering a meaningful reference for green technology applications in biomedicine.
利用可持续资源开发多功能创面敷料是推进绿色生物医用材料有效修复创面的关键。在这项研究中,我们提出了一个集活性氧清除和抗菌功能于一体的生态友好型微针输送平台(LutCe-QCS-GP MN)。该系统具有可持续的纳米酶(LutCe),由植物来源的黄酮类木犀草素和铈离子自组装形成,具有强大的超氧化物歧化酶样活性。这些LutCe纳米酶是通过绿色组装工艺合成的,具有清除超氧阴离子、羟基自由基和活性氮的能力。在微针的尖端,它们直接减轻了伤口部位的氧化应激。同时,基于抗菌多糖的基质可有效防御伤口病原体,防止感染和继发性组织损伤。通过将可持续抗氧化纳米酶与天然抗菌成分协同结合,luce - qcs - gp MN系统显著降低了伤口的氧化应激和细菌负荷,显著加快了愈合过程。全面的体外和体内安全性评估支持该平台的生物安全性,强调其临床转化的潜力。本研究不仅介绍了一种有前景的伤口治疗策略,而且强调了功能材料设计中自然、可持续资源的价值,为绿色技术在生物医学中的应用提供了有意义的参考。
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引用次数: 0
Lanthanum-driven carbon capture via oxidative pyrolysis constructs La2O2CO3@biochar for phosphate adsorption and bacteriostasis 镧驱动碳捕获通过氧化热解构建La2O2CO3@biochar的磷酸盐吸附和抑菌
IF 9.2 2区 工程技术 Q1 ENERGY & FUELS Pub Date : 2026-01-27 DOI: 10.1016/j.susmat.2026.e01896
Lijun Yang , Yiyi Shen , Zhixu Du , Xiaotong He , Hong Li , Lichun Dai
The removal of nutrients (phosphate) and pathogen (e.g., E. coli, and S. aureus) are of great importance to the water quality. Lanthanum carbonates possess balanced properties in adsorption performance, chemical stability and biosafety. Herein, a route, lanthanum (La)-enabled carbon capture during oxidative pyrolysis, was developed for the synthesis of biochar-supported La carbonate (La2O2CO3/biochar) as antibacterial phosphate adsorbent. The results showed that the CO2 generated from oxidative pyrolysis could be captured by La, leading to the formation of La2O2CO3 on biochar surface. The resultant La2O2CO3@biochar possessed a high phosphate adsorption capacity of ∼134.66 mg/g at a low dosage of 0.1 g/L. Furthermore, the material exhibited remarkable dual functionality, achieving >99.99% inactivation of S. aureus and E. coli without compromising its adsorption capacity. This synergistic nutrient-capturing and antibacterial capability addresses two critical challenges in water treatment, i.e., eutrophication control and pathogen elimination, within a single-step process. Finally, this study proposed an alternative route for the synthesis of biochar-supported La carbonates as highly efficient antibacterial phosphate adsorbent for advanced water treatment.
去除营养物(磷酸盐)和病原菌(如大肠杆菌和金黄色葡萄球菌)对水质至关重要。碳酸镧具有良好的吸附性能、化学稳定性和生物安全性。本文提出了一种氧化热解过程中镧(La)激活碳捕获的方法,用于合成生物炭负载的碳酸镧(La2O2CO3/生物炭)作为抗菌磷酸盐吸附剂。结果表明,氧化热解产生的CO2可以被La捕获,导致生物炭表面形成La2O2CO3。所得La2O2CO3@biochar在低用量为0.1 g/L的情况下,具有高的磷酸盐吸附量~ 134.66 mg/g。此外,该材料表现出显著的双重功能,在不影响吸附能力的情况下,对金黄色葡萄球菌和大肠杆菌实现了99.99%的失活。这种协同的营养捕获和抗菌能力解决了水处理中的两个关键挑战,即富营养化控制和病原体消除,在单步过程中。最后,本研究提出了一种合成生物炭负载的La carbonates作为深度水处理高效抗菌磷酸盐吸附剂的替代途径。
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引用次数: 0
Lotus pod-inspired self-floating photothermal system based on laser-ablated Ag nanoparticles on macroporous polyvinyl formal sponge for green seawater desalination and oil absorption 基于激光烧蚀银纳米粒子的大孔聚乙烯醇海绵自漂浮光热系统的研究
IF 9.2 2区 工程技术 Q1 ENERGY & FUELS Pub Date : 2026-01-25 DOI: 10.1016/j.susmat.2026.e01895
Mariam El-Adl , S.E. Samra , Amr Awad Ibrahim , Mina Shawky Adly
Pollution and water scarcity have become major global issues that endanger both ecological sustainability and human health. Though traditional evaporator designs have limited efficiency and salt accumulation, solar-driven water purification offers a promising green and eco-friendly solution. In this study, a soft, flexible, and self-floating photoabsorber was prepared by a simple method with a bioinspired cone architecture from the lotus pod. The fabricated device is characterized by excellent photothermal conversion, rapid water transportation through the macrochannels, and exceptional salt rejection. Laser ablation was applied to convert the surface of the polyvinyl formal (poly(vinyl alcohol) formaldehyde, PVF) sponge into a black material-based laser-induced graphene (LIG) decorated with silver nanoparticles (Ag NPs). The generated nanocomposite exhibits remarkable mechanical durability under stress-strain tension and high photothermal efficiency for seawater desalination. This photothermal exhibits remarkable performance, which is attributed to multi-directional solar energy absorption through a porous structure, enhanced thermal localization, and good salt rejection. Furthermore, the photothermal materials adhered to the surface tightly and floated on the water surface without tilting. The designated LIG-Ag-based PVF sponge exhibited an efficiency of 108.7% under one sun irradiation, along with a significant rate of 1.57 kg m−2 h−1. Moreover, it demonstrated good performance in terms of salt resistance, chemical and mechanical stability, recyclability and absorption of organic liquids. The cone-like design can be used as an excellent candidate for different applications related to water desalination and purification due to its simplicity, cost-effective production process, and improved solar photothermal efficiency.
污染和缺水已成为危害生态可持续性和人类健康的重大全球性问题。虽然传统的蒸发器设计效率有限,而且会积累盐分,但太阳能驱动的水净化提供了一个有前途的绿色环保解决方案。本研究以莲荚为原料,采用仿生锥形结构,采用简单的方法制备了一种柔软、灵活、自漂浮的光吸收材料。该装置具有优异的光热转换、快速的水通过大通道输送和优异的排盐性能。采用激光烧蚀的方法将聚乙烯醇甲醛(PVF)海绵表面转化为黑色材料基激光诱导石墨烯(LIG),表面装饰有银纳米粒子(Ag NPs)。所制备的纳米复合材料在应力-应变拉伸下具有良好的力学耐久性和较高的海水淡化光热效率。这种光热材料表现出优异的性能,这归功于多孔结构对太阳能的多向吸收,增强的热局部化和良好的防盐性能。光热材料紧贴水面,漂浮在水面上不倾斜。在所设计的ligg - ag基PVF海绵在一次太阳照射下的效率为108.7%,速率为1.57 kg m−2 h−1。此外,它在耐盐性、化学和机械稳定性、可回收性和吸收有机液体方面表现出良好的性能。由于其简单,具有成本效益的生产过程和提高的太阳能光热效率,锥状设计可以作为与水淡化和净化相关的不同应用的优秀候选者。
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引用次数: 0
Scaling up ceramic recovery from end-of-life solid oxide cells: Process optimization and evaluation of recovered materials 从报废固体氧化物电池中扩大陶瓷回收:工艺优化和回收材料的评估
IF 9.2 2区 工程技术 Q1 ENERGY & FUELS Pub Date : 2026-01-22 DOI: 10.1016/j.susmat.2026.e01878
S. Saffirio , S. Anelli , J.F. Basbus , A. Barbucci , A.G. Sabato , F. Smeacetto , S.L. Fiorilli
This study introduces a scalable and sustainable method for recovering yttria-stabilized zirconia (YSZ) and nickel (as NiO) from end-of-life (EoL) solid oxide cells (SOCs). The process combines hydrothermal disaggregation at 200 °C with acid leaching into a single-step treatment, enabling whole-cell recycling and eliminating the need for complex layer separation. Optimised conditions – 50 g of SOC powder treated with 1 M HNO₃ for 1 h – achieved ≈92 wt% YSZ recovery while minimizing reagent use and processing time. The recovered YSZ showed a particle size distribution (445 ± 140 nm) comparable to virgin 3YSZ (470 ± 90 nm), with minimal Ni contamination (0.1 wt%) and preserved yttria content. When sintered at 1300 °C for 3 h, the material reached 95.5% relative density and an ionic conductivity of 7.9 × 10−3 S cm−1 at 800 °C, closely matching virgin 3YSZ (97.8%, 9.4 × 10−3 S cm−1). A residual monoclinic phase (17.4 wt%), which may slightly reduce transformation toughening, did not significantly affect ionic transport. Reuse pathways for recovered YSZ include closed-loop reintegration into SOC electrolytes or supports, and open-loop valorisation such as thermal barrier coatings or catalytic substrates. Concurrently, ≈99 wt% of Ni has been recovered in the form of NiO, with Co and La contamination below 1 wt%, further supporting circular economy strategies.
本研究介绍了一种可扩展和可持续的方法,用于从报废固体氧化物电池(soc)中回收氧化钇稳定的氧化锆(YSZ)和镍(NiO)。该工艺将200°C的水热分解与酸浸结合为一步处理,实现了全细胞回收,无需复杂的层分离。优化的条件-用1 M HNO₃处理50 g SOC粉末1小时-实现了≈92 wt%的YSZ回收率,同时最大限度地减少了试剂的使用和处理时间。回收的YSZ的粒径分布(445±140 nm)与原始3YSZ的粒径分布(470±90 nm)相当,镍污染最小(0.1 wt%),钇含量保持不变。在1300℃烧结3 h时,该材料的相对密度达到95.5%,800℃时离子电导率为7.9 × 10−3 S cm−1,与未加工的3YSZ (97.8%, 9.4 × 10−3 S cm−1)非常接近。残留的单斜相(17.4 wt%)可能会略微降低相变增韧,但对离子传输没有显著影响。回收YSZ的再利用途径包括闭环重新整合到SOC电解质或载体中,以及开环增值,如热障涂层或催化基质。同时,约99 wt%的Ni以NiO的形式被回收,Co和La污染低于1 wt%,进一步支持循环经济战略。
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引用次数: 0
Injectable biomimetic composite hydrogel containing total flavonoids of rhizoma drynariae for bone regeneration 含干骨总黄酮的可注射仿生复合水凝胶用于骨再生
IF 9.2 2区 工程技术 Q1 ENERGY & FUELS Pub Date : 2026-01-22 DOI: 10.1016/j.susmat.2026.e01894
Yuanbin Zhang , Yueting Sun , Yong Lang , Qi Sun , Quanwei Ding , Kejie Zhang , Lingfeng Pan , Kailong Zhang , Jianhua Zhang , Guohua Jiang
Bone tissue engineering materials exhibit significant potential in the realm of bone defect regeneration owing to their outstanding biocompatibility, appropriate mechanical support, and well-defined osteoinductive activity. Nevertheless, the existing materials commonly encounter the issue of insufficient interfacial adhesion, which renders it arduous to attain long-term stable residence and controlled drug release at complex defect sites. In this study, a strongly adhesive composite hydrogel system loaded with The total flavonoids of Rhizoma Drynariae (TFRD) was developed as a bone tissue engineering material for bone defect regeneration. The composite hydrogel was consisted of dopamine-functionalized hyaluronic acid (HA-DA) and mussel adhesion protein (MAP). This hydrogel system leveraged the interfacial bonding between the dopamine (DA) and 3,4-dihydroxyphenylalanine (DOPA) groups of mussel mucin to realize strong adhesion at the bone defect site. Simultaneously, the stable and sustained release of TFRD was realized through enzyme-responsive degradation. In addition, the obtained hydrogel system not only possessed favorable biocompatibility and biodegradability but can also mimicked the extracellular matrix environment to mitigate the stimulation of surrounding tissues and reduce the risk of inflammatory reactions, thereby providing a suitable milieu for the drugs to exert their effects and promoting the bone defect regeneration process.
骨组织工程材料由于其出色的生物相容性、适当的机械支持和明确的骨诱导活性,在骨缺损再生领域显示出巨大的潜力。然而,现有的材料普遍存在界面粘附不足的问题,这使得在复杂的缺陷部位难以实现长期稳定的停留和药物的可控释放。本研究以黄芩总黄酮(TFRD)为载体,制备了一种强粘接复合水凝胶体系,作为骨缺损再生的骨组织工程材料。复合水凝胶由多巴胺功能化透明质酸(HA-DA)和贻贝粘附蛋白(MAP)组成。该水凝胶系统利用了贻贝黏液中多巴胺(DA)和3,4-二羟基苯丙氨酸(DOPA)基团之间的界面键合,实现了骨缺损部位的强粘附。同时,通过酶反应降解实现TFRD的稳定缓释。此外,所获得的水凝胶体系不仅具有良好的生物相容性和生物降解性,还可以模拟细胞外基质环境,减轻对周围组织的刺激,降低炎症反应的风险,从而为药物发挥作用提供合适的环境,促进骨缺损再生过程。
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引用次数: 0
From medical waste to energy storage: Sulfonation−ball−milling derived porous carbon from waste masks for high−performance supercapacitors 从医疗废物到能源储存:磺化-球磨-从高性能超级电容器的废物掩膜中获得多孔碳
IF 9.2 2区 工程技术 Q1 ENERGY & FUELS Pub Date : 2026-01-22 DOI: 10.1016/j.susmat.2026.e01890
Xinlin Ma , Zengyuan Fan , Meng Liu , Yuhan Cui , Hai Ni , Yunpeng Wu , Qiushi Sun , Bin Fu , Jiawei Wang
The massive disposal of medical masks during the COVID−19 pandemic poses serious environmental challenges, highlighting the need for sustainable recycling strategies. Herein, we report a synergistic sulfonation–ball milling activation–carbonization route, to transform waste polypropylene masks into sulfur−doped hierarchical porous carbons with controllable pore structure and heteroatom incorporation. The optimized sample (SPMM−B0.5−700) delivers a high specific surface area of 601.6 m2 g−1, abundant mesopores, and enriched heteroatom functionalities. Benefiting from the combined effects of enhanced sulfur doping and regulated hierarchical porosity, it achieves a remarkable capacitance of 353 F g−1 at 1 A g−1 in a three−electrode system and 122.6 F g−1 at 1 A g−1 in a symmetric supercapacitor, along with an energy density of 33.4 Wh kg−1 and excellent cycling stability over 10000 cycles. This research not only provides a sustainable solution for medical waste management, but also demonstrates the potential of upcycled carbon materials in energy storage applications.
在COVID - 19大流行期间,医用口罩的大量处置构成了严重的环境挑战,凸显了可持续回收战略的必要性。在此,我们报告了一种协同磺化-球磨活化-碳化路线,将废弃聚丙烯掩膜转化为具有可控孔结构和杂原子掺入的硫掺杂分层多孔碳。优化后的样品(SPMM - B0.5 - 700)具有601.6 m2 g - 1的高比表面积,丰富的介孔和丰富的杂原子功能。得益于增强硫掺杂和调节分层孔隙率的综合效应,该材料在三电极体系中在1ag−1时达到353 F g−1,在对称超级电容器中在1ag−1时达到122.6 F g−1,能量密度为33.4 Wh kg−1,并且在10000次循环中具有出色的循环稳定性。该研究不仅为医疗废物管理提供了可持续的解决方案,而且展示了升级再生碳材料在储能应用中的潜力。
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引用次数: 0
Efficient urea oxidation from strontium ferrite nanostructures synthesized using iron recovered from waste iron ore slime 利用废铁矿泥回收的铁合成铁酸锶纳米结构高效氧化尿素
IF 9.2 2区 工程技术 Q1 ENERGY & FUELS Pub Date : 2026-01-21 DOI: 10.1016/j.susmat.2026.e01889
Sapna Devi , Sunaina , Sushma Kumari , Kritika Sood , Santanu Sarkar , Pratik Swarup Dash , Menaka Jha
SrFeO3 is a perovskite-type mixed oxide with the general formula ABO3, well known for its distinctive structural features, including oxygen vacancies and the unusual oxidation states of iron. These characteristics impart high ionic mobility, tunable electronic conductivity, and excellent redox flexibility, making SrFeO3 highly suitable for diverse catalytic and energy-related applications. In this study, a sustainable approach is demonstrated for the recovery of iron values from iron ore slimes, which are then utilized to synthesize SrFeO3 nanoplates through an eco-friendly method. The resulting SrFeO3 exhibits remarkable electrocatalytic activity towards urea electrolysis, requiring a low overpotential of 1.57 V and showing a small Tafel slope of 29 mV dec−1, indicative of fast reaction kinetics. In addition, the catalyst displays excellent durability for up to 18 h, confirming its robustness under prolonged electrochemical operation. Such performance parameters highlight the material's potential to significantly reduce the energy demand of urea oxidation, thereby enhancing the overall efficiency of urea-assisted electrolysis systems. The development of this waste-derived catalytic material aligns with global efforts to promote sustainable and environmentally responsible technologies. By converting low-value waste into high-value functional oxides, the work supports waste-to-wealth strategies while contributing to cleaner chemical synthesis and greener energy production. Overall, the study not only establishes a practical route for utilizing industrial waste but also demonstrates the potential of SrFeO3 nanostructures as efficient electrocatalysts, advancing the broader goals of pollution reduction, resource circularity, and sustainable energy development.
SrFeO3是一种钙钛矿型混合氧化物,通式为ABO3,以其独特的结构特征而闻名,包括氧空位和铁的不同寻常的氧化态。这些特性赋予SrFeO3高离子迁移率、可调电子导电性和优异的氧化还原灵活性,使其非常适合各种催化和能源相关应用。在本研究中,我们展示了一种从铁矿石泥中回收铁值的可持续方法,然后通过一种环保的方法将其用于合成SrFeO3纳米板。所得SrFeO3对尿素电解表现出显著的电催化活性,需要1.57 V的低过电位和29 mV dec−1的小Tafel斜率,表明反应动力学快速。此外,该催化剂表现出长达18小时的优异耐久性,证实了其在长时间电化学操作下的稳健性。这些性能参数突出了该材料在显著降低尿素氧化能量需求方面的潜力,从而提高了尿素辅助电解系统的整体效率。这种源自废物的催化材料的开发符合促进可持续和对环境负责的技术的全球努力。通过将低价值废物转化为高价值的功能性氧化物,这项工作支持废物转化财富战略,同时有助于更清洁的化学合成和更绿色的能源生产。总的来说,该研究不仅为工业废弃物的利用开辟了一条实用的途径,而且展示了SrFeO3纳米结构作为高效电催化剂的潜力,推动了减少污染、资源循环和可持续能源发展的更广泛目标。
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引用次数: 0
MXene-based catalysts for electrochemical nitrate and nitrogen reduction: A review toward sustainable nitrogenous fuels 基于mxene的电化学还原硝酸盐和氮催化剂:可持续含氮燃料的研究进展
IF 9.2 2区 工程技术 Q1 ENERGY & FUELS Pub Date : 2026-01-21 DOI: 10.1016/j.susmat.2026.e01892
Ubaid Ullah Jan , Kiruthika Mariappan , Subramanian Sakthinathan , Te-Wei Chiu , Yu-Han Tsai , Muhammad Sheraz Ahmad , Arshid Numan , Chao-Lin Liu , Ching-Lung Chen
In recent years, MXenes have emerged as promising materials for eco-friendly electrochemical nitrate reduction and nitrogen fixation in nitrogen reduction reactions (NRR). MXene possesses high hydrophilicity, large specific surface area, excellent electrical conductivity, and numerous active sites, making it a suitable candidate for catalytic applications. These features support functionalization and enhancement methods, including the integration of co-catalysts and the formation of MXene-based composites and hybrids. Notably, MXene–metal composite catalysts have been reported to achieve Faradaic efficiencies exceeding 95%, underscoring their strong industrial potential for efficient electrochemical nitrate reduction. MXene-based nitrate reduction presents challenges related to scalability, stability, and industrial integration, as well as an unclear structure-activity relationship that affects catalytic performance. Improving selectivity, faradaic efficiency, and nitrate conversion rates remains crucial, while deeper insights into reaction mechanisms and active sites are needed for optimized performance. This review provides a comprehensive overview of the properties, synthesis methods, and applications of MXene-based materials in electrochemical nitrate reduction and nitrogen reduction reactions, focusing on their roles as catalysts. Additionally, current challenges and future directions for sustainable nitrogen-based fuel production are discussed in detail. This work aims to offer valuable insights into the strategic design of MXene catalyst for ENR and NRR. The review also examines the impact of MXene structure, including layer spacing, surface termination, and edge chemistry, on enhancing electrocatalytic efficiency. A particular emphasis is placed on the synthesis of 2D and 3D Mxene metal composite, as well as single-atom catalysts (SACs), which enhance performance by creating highly active and selective sites for ENR. These advances have improved conversion rates and selectivity for desired products, such as NH₃ and N₂. The review examines NO₃ reduction, particularly ENR, using MXene catalysts, analyzing important reaction pathways, intermediates, and reaction rate parameters. Furthermore, the review also discusses how various experimental conditions, such as pH, applied potential, and nitrate concentration, influence the reaction rate and desired product distribution. The final section identifies the challenges and future directions for the ENR, particularly in scaling up the synthesis of MXene-based materials and achieving greater control over product selectivity for industrial applications. Improving the efficiency and selectivity of NO3 to clean nitrogenous fuel conversion will be critical for realizing the potential of MXenes in sustainable energy technologies.
近年来,MXenes作为生态友好型电化学硝酸还原和氮还原反应(NRR)中固氮的重要材料。MXene具有高亲水性,大比表面积,优异的导电性和众多的活性位点,使其成为催化应用的合适候选者。这些特性支持功能化和增强方法,包括整合共催化剂和形成基于mxene的复合材料和杂化材料。值得注意的是,据报道,MXene-metal复合催化剂的法拉第效率超过95%,强调了它们在高效电化学还原硝酸盐方面的强大工业潜力。基于mxene的硝酸盐还原存在着与可扩展性、稳定性和工业集成相关的挑战,以及影响催化性能的不明确的构效关系。提高选择性、法拉第效率和硝酸盐转化率仍然至关重要,而更深入地了解反应机制和活性位点则需要优化性能。本文综述了mxene基材料的性质、合成方法及其在电化学硝酸还原和氮还原反应中的应用,重点介绍了其催化剂的作用。此外,还详细讨论了可持续氮基燃料生产的当前挑战和未来方向。本研究旨在为ENR和NRR的MXene催化剂的战略设计提供有价值的见解。本文还研究了MXene结构(包括层间距、表面终止和边缘化学)对提高电催化效率的影响。特别强调的是2D和3D Mxene金属复合材料的合成,以及单原子催化剂(SACs),它们通过为ENR创造高活性和选择性位点来提高性能。这些进步提高了转化率和所需产品的选择性,如NH₃和N₂。该综述研究了使用MXene催化剂的NO₃−还原,特别是ENR,分析了重要的反应途径、中间体和反应速率参数。此外,本文还讨论了不同的实验条件,如pH、应用电位和硝酸盐浓度对反应速率和期望产物分布的影响。最后一节确定了ENR的挑战和未来方向,特别是在扩大mxene基材料的合成和实现对工业应用产品选择性的更好控制方面。提高NO3在清洁含氮燃料转化中的效率和选择性对于实现MXenes在可持续能源技术中的潜力至关重要。
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Sustainable Materials and Technologies
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