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Easy Preparation of Carbon Nano Onion—Poly Ionic Liquid-Like Hybrids Through the Deep Eutectic Monomer (DEM) Approach and Their Use in Heterogeneous Catalysis 用深度共晶单体法制备碳纳米洋葱-聚离子类液体杂化物及其在多相催化中的应用
IF 6.1 3区 材料科学 Q2 GREEN & SUSTAINABLE SCIENCE & TECHNOLOGY Pub Date : 2026-02-05 DOI: 10.1002/adsu.202501449
Rossella Infantino, Gabriele Maria Gargano, Aravind Kannoth Anilkumar, Michał Bartkowski, Benedetto Taormina, Carmela Aprile, Michelangelo Gruttadauria, Vincenzo Campisciano, Silvia Giordani, Francesco Giacalone

Carbon nano-onions (CNOs) are efficiently functionalized using a sustainable approach based on polymerizable deep eutectic solvents (PDESs), or deep eutectic monomers (DEMs). These systems replace conventional organic solvents, acting simultaneously as dispersing media and functionalization reagents. The method enables the rapid introduction of functional groups such as –OH, –NH3⁺Br, and –SO3 onto CNO surfaces. The resulting materials are comprehensively characterized by TGA, 13C-CPMAS-TOSS NMR, FT-IR spectroscopy, TEM, AFM, DLS, and XPS. Notably, sulfonate-functionalized CNOs support the Keggin-type polyoxometalate H3PW12O40 (PW12), which acts as a recyclable heterogeneous catalyst for the oxidation of alcohols to carbonyl compounds.

{"title":"Easy Preparation of Carbon Nano Onion—Poly Ionic Liquid-Like Hybrids Through the Deep Eutectic Monomer (DEM) Approach and Their Use in Heterogeneous Catalysis","authors":"Rossella Infantino,&nbsp;Gabriele Maria Gargano,&nbsp;Aravind Kannoth Anilkumar,&nbsp;Michał Bartkowski,&nbsp;Benedetto Taormina,&nbsp;Carmela Aprile,&nbsp;Michelangelo Gruttadauria,&nbsp;Vincenzo Campisciano,&nbsp;Silvia Giordani,&nbsp;Francesco Giacalone","doi":"10.1002/adsu.202501449","DOIUrl":"https://doi.org/10.1002/adsu.202501449","url":null,"abstract":"<div>\u0000 \u0000 <p>Carbon nano-onions (CNOs) are efficiently functionalized using a sustainable approach based on polymerizable deep eutectic solvents (PDESs), or deep eutectic monomers (DEMs). These systems replace conventional organic solvents, acting simultaneously as dispersing media and functionalization reagents. The method enables the rapid introduction of functional groups such as –OH, –NH<sub>3</sub>⁺Br<sup>−</sup>, and –SO<sub>3</sub><sup>−</sup> onto CNO surfaces. The resulting materials are comprehensively characterized by TGA, <sup>13</sup>C-CPMAS-TOSS NMR, FT-IR spectroscopy, TEM, AFM, DLS, and XPS. Notably, sulfonate-functionalized CNOs support the Keggin-type polyoxometalate H<sub>3</sub>PW<sub>12</sub>O<sub>40</sub> (PW<sub>12</sub>), which acts as a recyclable heterogeneous catalyst for the oxidation of alcohols to carbonyl compounds.</p>\u0000 </div>","PeriodicalId":7294,"journal":{"name":"Advanced Sustainable Systems","volume":"10 2","pages":""},"PeriodicalIF":6.1,"publicationDate":"2026-02-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146129937","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}
引用次数: 0
Eco-Intelligent Photothermal Systems at the Water- Energy Nexus Forge a New Era of Freshwater Generation 生态智能光热系统在水-能源的纽带打造淡水发电的新时代
IF 6.1 3区 材料科学 Q2 GREEN & SUSTAINABLE SCIENCE & TECHNOLOGY Pub Date : 2026-02-05 DOI: 10.1002/adsu.202501681
Geetika Jain, Shuvayoo Das, Keshav Kumar Chaudhary, Siddhartha Pahari, Monalisa Mukherjee, Sandip Chakrabarti

The escalating global water crisis necessitates the development of sustainable and energy-efficient freshwater generation technologies that reduce reliance on fossil fuels. The burgeoning field of photothermal desalination offers a promising paradigm shift within the water–energy nexus, utilizing solar energy for water purification. This review systematically examines the multifaceted advancements in photothermal desalination, emphasizing the pivotal role of interfacial heating over bulk heating in enhancing energy efficiency. We delineate the relevance of osmoregulatory strategies observed in mangrove ecosystems, presenting them as bio-inspired paradigms for augmenting freshwater production under hypersaline conditions. Additionally, it offers a comprehensive overview of diverse photothermal materials and evaporator architectures that influence overall performance, including light absorption, heat localization, and water transport. Furthermore, we discussed the current strategies to mitigate salt blockage or fouling, a critical issue that can degrade system performance and longevity. Finally, the review connects photothermal desalination research to the United Nations Sustainable Development Goals and highlights current global efforts and governmental investments driving this technology forward. Herein, we aim to foster the future innovation and development efforts toward more robust, efficient, and scalable photothermal desalination solutions for sustainable freshwater production.

{"title":"Eco-Intelligent Photothermal Systems at the Water- Energy Nexus Forge a New Era of Freshwater Generation","authors":"Geetika Jain,&nbsp;Shuvayoo Das,&nbsp;Keshav Kumar Chaudhary,&nbsp;Siddhartha Pahari,&nbsp;Monalisa Mukherjee,&nbsp;Sandip Chakrabarti","doi":"10.1002/adsu.202501681","DOIUrl":"https://doi.org/10.1002/adsu.202501681","url":null,"abstract":"<div>\u0000 \u0000 <p>The escalating global water crisis necessitates the development of sustainable and energy-efficient freshwater generation technologies that reduce reliance on fossil fuels. The burgeoning field of photothermal desalination offers a promising paradigm shift within the water–energy nexus, utilizing solar energy for water purification. This review systematically examines the multifaceted advancements in photothermal desalination, emphasizing the pivotal role of interfacial heating over bulk heating in enhancing energy efficiency. We delineate the relevance of osmoregulatory strategies observed in mangrove ecosystems, presenting them as bio-inspired paradigms for augmenting freshwater production under hypersaline conditions. Additionally, it offers a comprehensive overview of diverse photothermal materials and evaporator architectures that influence overall performance, including light absorption, heat localization, and water transport. Furthermore, we discussed the current strategies to mitigate salt blockage or fouling, a critical issue that can degrade system performance and longevity. Finally, the review connects photothermal desalination research to the United Nations Sustainable Development Goals and highlights current global efforts and governmental investments driving this technology forward. Herein, we aim to foster the future innovation and development efforts toward more robust, efficient, and scalable photothermal desalination solutions for sustainable freshwater production.</p>\u0000 </div>","PeriodicalId":7294,"journal":{"name":"Advanced Sustainable Systems","volume":"10 2","pages":""},"PeriodicalIF":6.1,"publicationDate":"2026-02-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146135797","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}
引用次数: 0
Surface and Interface Engineered Hydrated Nickel Hydroxide on Nickel Enables Rapid Active Species Shuffling in Alkaline Hydrogen Electrocatalysis 表面和界面工程水合氢氧化镍在镍上实现了碱氢电催化中的快速活性物质洗牌
IF 6.1 3区 材料科学 Q2 GREEN & SUSTAINABLE SCIENCE & TECHNOLOGY Pub Date : 2026-02-04 DOI: 10.1002/adsu.202501510
Krishnamoorthy Silambarasan, Gopinathan M Anilkumar, Sasikala Devi Assa Aravindh, Hidenori Kuroki, Takeo Yamaguchi

Achieving acid-like hydrogen oxidation reaction (HOR) and hydrogen evolution reaction (HER) activity in alkaline media using low-cost, non-precious metal catalysts is essential for energy conversion technologies. Here, we demonstrate the indispensable role of water within the catalyst layer in enhancing HOR/HER kinetics, mediated by hydrated and dehydrated oxophilic sites on nickel (Ni) catalysts coated with nickel hydroxide (Ni(OH)2). Electrochemical measurements combined with density functional theory (DFT) calculations show that an acid-like environment creates at the electrified interface through water molecules that bridge active hydrogen and oxygen species within the catalyst surface layer. This interfacial behavior differs from that described in conventional bulk and interface models. Our findings highlight the importance of interfacial hydrogen bonding network across the interface in hydrogen electrocatalysis and provide guidance for the design of efficient catalysts for alkaline fuel cell and electrolyzer applications.

{"title":"Surface and Interface Engineered Hydrated Nickel Hydroxide on Nickel Enables Rapid Active Species Shuffling in Alkaline Hydrogen Electrocatalysis","authors":"Krishnamoorthy Silambarasan,&nbsp;Gopinathan M Anilkumar,&nbsp;Sasikala Devi Assa Aravindh,&nbsp;Hidenori Kuroki,&nbsp;Takeo Yamaguchi","doi":"10.1002/adsu.202501510","DOIUrl":"https://doi.org/10.1002/adsu.202501510","url":null,"abstract":"<p>Achieving acid-like hydrogen oxidation reaction (HOR) and hydrogen evolution reaction (HER) activity in alkaline media using low-cost, non-precious metal catalysts is essential for energy conversion technologies. Here, we demonstrate the indispensable role of water within the catalyst layer in enhancing HOR/HER kinetics, mediated by hydrated and dehydrated oxophilic sites on nickel (Ni) catalysts coated with nickel hydroxide (Ni(OH)<sub>2</sub>). Electrochemical measurements combined with density functional theory (DFT) calculations show that an acid-like environment creates at the electrified interface through water molecules that bridge active hydrogen and oxygen species within the catalyst surface layer. This interfacial behavior differs from that described in conventional bulk and interface models. Our findings highlight the importance of interfacial hydrogen bonding network across the interface in hydrogen electrocatalysis and provide guidance for the design of efficient catalysts for alkaline fuel cell and electrolyzer applications.</p>","PeriodicalId":7294,"journal":{"name":"Advanced Sustainable Systems","volume":"10 2","pages":""},"PeriodicalIF":6.1,"publicationDate":"2026-02-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://advanced.onlinelibrary.wiley.com/doi/epdf/10.1002/adsu.202501510","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146129985","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}
引用次数: 0
A Deep Learning Enabled Sustainable Self-Powered Wearable Tactile Sensor toward Gesture Recognition 面向手势识别的深度学习可持续自供电可穿戴触觉传感器
IF 6.1 3区 材料科学 Q2 GREEN & SUSTAINABLE SCIENCE & TECHNOLOGY Pub Date : 2026-02-04 DOI: 10.1002/adsu.202501208
Siddabattula Geetha Sri Priyanka, Vemuru Srikanth, Kaliyannan Manojkumar, Dhara Sateesh, Venkateswaran Vivekananthan

Flexible and wearable piezoelectric sensors have gained attention for applications in human-machine interfacing (HMI) and the artificial intelligence of things (AIoT). In this study, antimony-doped barium titanate (Ba0.3Sb₀.₇TiO3) was used to fabricate a piezoelectric nanogenerator (PENG) for finger movement sensing and gesture recognition. The polymer-to-particle ratio was optimized, with 20 wt.% yielding the best performance. The optimized PENG generated a maximum output of 50 V and 1.5 µA under applied force, validated by charging commercial capacitors and powering LEDs. For real-time applications, the device was scaled to finger size and integrated into a wearable glove capable of detecting finger motion. The generated electrical signals were processed using convolutional neural networks (CNNs), converting the signals into readable text through deep learning. Using this approach, the glove successfully recognized the words “SOS” and “HELLO,” demonstrating the potential of the PENG for smart wearable applications. This work highlights the integration of piezoelectric sensing with AI-enabled gesture recognition, offering a promising route for advanced wearable healthcare devices and interactive technologies.

{"title":"A Deep Learning Enabled Sustainable Self-Powered Wearable Tactile Sensor toward Gesture Recognition","authors":"Siddabattula Geetha Sri Priyanka,&nbsp;Vemuru Srikanth,&nbsp;Kaliyannan Manojkumar,&nbsp;Dhara Sateesh,&nbsp;Venkateswaran Vivekananthan","doi":"10.1002/adsu.202501208","DOIUrl":"https://doi.org/10.1002/adsu.202501208","url":null,"abstract":"<div>\u0000 \u0000 <p>Flexible and wearable piezoelectric sensors have gained attention for applications in human-machine interfacing (HMI) and the artificial intelligence of things (AIoT). In this study, antimony-doped barium titanate (Ba<sub>0.3</sub>Sb₀.₇TiO<sub>3</sub>) was used to fabricate a piezoelectric nanogenerator (PENG) for finger movement sensing and gesture recognition. The polymer-to-particle ratio was optimized, with 20 wt.% yielding the best performance. The optimized PENG generated a maximum output of 50 V and 1.5 µA under applied force, validated by charging commercial capacitors and powering LEDs. For real-time applications, the device was scaled to finger size and integrated into a wearable glove capable of detecting finger motion. The generated electrical signals were processed using convolutional neural networks (CNNs), converting the signals into readable text through deep learning. Using this approach, the glove successfully recognized the words “SOS” and “HELLO,” demonstrating the potential of the PENG for smart wearable applications. This work highlights the integration of piezoelectric sensing with AI-enabled gesture recognition, offering a promising route for advanced wearable healthcare devices and interactive technologies.</p>\u0000 </div>","PeriodicalId":7294,"journal":{"name":"Advanced Sustainable Systems","volume":"10 2","pages":""},"PeriodicalIF":6.1,"publicationDate":"2026-02-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146129986","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}
引用次数: 0
Recycling of Spent Lithium-Ion Batteries into Fluorinated Binder-Enabled Electrocatalysts for Efficient Hydrogen Generation Systems 废锂离子电池回收成高效制氢系统的氟化粘合剂电催化剂
IF 6.1 3区 材料科学 Q2 GREEN & SUSTAINABLE SCIENCE & TECHNOLOGY Pub Date : 2026-02-03 DOI: 10.1002/adsu.202501679
Jing-Xian Chen, Mengyao Gao, Dessie AshagrieTafere, Xiang-Mao Huang

The rapid expansion of lithium-ion battery (LIB) applications in electric vehicles and electronics has led to growing volumes of spent cathodes, highlighting the urgent need for sustainable recycling and upcycling strategies. In this study, we develop a binder-engineering approach to upcycle spent LiFePO4 (LFP) cathodes into efficient electrocatalysts for the hydrogen evolution reaction (HER) in alkaline media. By incorporating fluorine-rich Nafion as a functional binder and acetylene black (AB) as a conductive additive, the resulting catalyst-M12 N-AB(0.3)/NF-exhibits significantly enhanced HER activity. It delivers a low overpotential of 205.3 mV at current density of 10 mA cm−2 and a Tafel slope of 102 mV dec−1, outperforming gelatin-based analogs (overpotential: 256.1 mV) and most reported waste-derived HER catalysts. Electrochemical impedance spectroscopy reveals reduced charge transfer resistance and improved ion-electron transport. The catalyst demonstrates excellent durability over 96 h of continuous operation and 3000 cyclic voltammetry cycles, with performance even improving post-cycling. Driven by the solar energy, substituting the values, the theoretical energy efficiency was determined to be 𝜂𝑡ℎ𝑒𝑜𝑟𝑒𝑡𝑖𝑐𝑎𝑙 with 80.7% which highlights the capability of the recycled LFP-based electrode to enable sustainable approach for solar-to-hydrogen energy conversion from converting spent LIBs.

{"title":"Recycling of Spent Lithium-Ion Batteries into Fluorinated Binder-Enabled Electrocatalysts for Efficient Hydrogen Generation Systems","authors":"Jing-Xian Chen,&nbsp;Mengyao Gao,&nbsp;Dessie AshagrieTafere,&nbsp;Xiang-Mao Huang","doi":"10.1002/adsu.202501679","DOIUrl":"https://doi.org/10.1002/adsu.202501679","url":null,"abstract":"<div>\u0000 \u0000 <p>The rapid expansion of lithium-ion battery (LIB) applications in electric vehicles and electronics has led to growing volumes of spent cathodes, highlighting the urgent need for sustainable recycling and upcycling strategies. In this study, we develop a binder-engineering approach to upcycle spent LiFePO<sub>4</sub> (LFP) cathodes into efficient electrocatalysts for the hydrogen evolution reaction (HER) in alkaline media. By incorporating fluorine-rich Nafion as a functional binder and acetylene black (AB) as a conductive additive, the resulting catalyst-M12 N-AB(0.3)/NF-exhibits significantly enhanced HER activity. It delivers a low overpotential of 205.3 mV at current density of 10 mA cm<sup>−2</sup> and a Tafel slope of 102 mV dec<sup>−1</sup>, outperforming gelatin-based analogs (overpotential: 256.1 mV) and most reported waste-derived HER catalysts. Electrochemical impedance spectroscopy reveals reduced charge transfer resistance and improved ion-electron transport. The catalyst demonstrates excellent durability over 96 h of continuous operation and 3000 cyclic voltammetry cycles, with performance even improving post-cycling. Driven by the solar energy, substituting the values, the theoretical energy efficiency was determined to be 𝜂<sub>𝑡ℎ𝑒𝑜𝑟𝑒𝑡𝑖𝑐𝑎𝑙</sub> with 80.7% which highlights the capability of the recycled LFP-based electrode to enable sustainable approach for solar-to-hydrogen energy conversion from converting spent LIBs.</p>\u0000 </div>","PeriodicalId":7294,"journal":{"name":"Advanced Sustainable Systems","volume":"10 2","pages":""},"PeriodicalIF":6.1,"publicationDate":"2026-02-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146129877","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}
引用次数: 0
Tailoring Cobalt Phthalocyanine-Based Anodes: Unveiling the Superiority of Cross-Linked Polymer Architectures over Monomers for Lithium-Ion Storage 裁剪钴酞菁基阳极:揭示交联聚合物结构优于锂离子存储单体的优势
IF 6.1 3区 材料科学 Q2 GREEN & SUSTAINABLE SCIENCE & TECHNOLOGY Pub Date : 2026-02-03 DOI: 10.1002/adsu.202501667
Keshavananda Prabhu Channabasavana Hundi Puttaningaiah, Shambhulinga Aralekallu

The development of high-capacity and stable anode materials beyond graphite remains a critical challenge for advancing lithium-ion battery (LIB) technology. Organometallic materials such as metallophthalocyanines (MPcs) offer reversible redox activity, tunability, and high theoretical capacity, yet their practical use is constrained by low conductivity, electrolyte solubility, and limited cycling stability. In this study, we address these limitations through a molecular engineering strategy by synthesizing and directly comparing monomeric cobalt phthalocyanine (CoPc) with a novel cross-linked polymeric cobalt phthalocyanine (pCoPc) as anode materials for LIBs. The pCoPc is prepared via a one-pot cyclotetramerization of pyromellitic dianhydride with a cobalt source, forming an extended conjugated network. FTIR, Raman, XRD, and electron microscopy confirm the successful construction of the polymeric framework, which exhibits reduced particle size and a porous, interconnected morphology relative to monomeric CoPc. As a LIB anode, pCoPc delivers a high specific capacity of 1087 mAh g−1 at 100 mA g−1 over 100 cycles, along with excellent rate capability and long-term stability. These improvements arise from enhanced structural integrity, increased accessible redox sites, improved conductivity, and suppressed dissolution. This work highlights polymeric MPcs as promising anode materials and presents a rational design strategy for high-energy organometallic electrodes.

{"title":"Tailoring Cobalt Phthalocyanine-Based Anodes: Unveiling the Superiority of Cross-Linked Polymer Architectures over Monomers for Lithium-Ion Storage","authors":"Keshavananda Prabhu Channabasavana Hundi Puttaningaiah,&nbsp;Shambhulinga Aralekallu","doi":"10.1002/adsu.202501667","DOIUrl":"https://doi.org/10.1002/adsu.202501667","url":null,"abstract":"<div>\u0000 \u0000 <p>The development of high-capacity and stable anode materials beyond graphite remains a critical challenge for advancing lithium-ion battery (LIB) technology. Organometallic materials such as metallophthalocyanines (MPcs) offer reversible redox activity, tunability, and high theoretical capacity, yet their practical use is constrained by low conductivity, electrolyte solubility, and limited cycling stability. In this study, we address these limitations through a molecular engineering strategy by synthesizing and directly comparing monomeric cobalt phthalocyanine (CoPc) with a novel cross-linked polymeric cobalt phthalocyanine (pCoPc) as anode materials for LIBs. The pCoPc is prepared via a one-pot cyclotetramerization of pyromellitic dianhydride with a cobalt source, forming an extended conjugated network. FTIR, Raman, XRD, and electron microscopy confirm the successful construction of the polymeric framework, which exhibits reduced particle size and a porous, interconnected morphology relative to monomeric CoPc. As a LIB anode, pCoPc delivers a high specific capacity of 1087 mAh g<sup>−1</sup> at 100 mA g<sup>−1</sup> over 100 cycles, along with excellent rate capability and long-term stability. These improvements arise from enhanced structural integrity, increased accessible redox sites, improved conductivity, and suppressed dissolution. This work highlights polymeric MPcs as promising anode materials and presents a rational design strategy for high-energy organometallic electrodes.</p>\u0000 </div>","PeriodicalId":7294,"journal":{"name":"Advanced Sustainable Systems","volume":"10 2","pages":""},"PeriodicalIF":6.1,"publicationDate":"2026-02-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146129917","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}
引用次数: 0
Sustainable Development of Iron–Air Batteries as Long-Duration Energy Storage Systems: The Key to Improving the Redox Kinetics of Iron-Based Anode 铁-空气电池作为长寿命储能系统的可持续发展:提高铁基阳极氧化还原动力学的关键
IF 6.1 3区 材料科学 Q2 GREEN & SUSTAINABLE SCIENCE & TECHNOLOGY Pub Date : 2026-02-03 DOI: 10.1002/adsu.202501101
Zirui Zhao, Zunhao Fan, Zhaoxia Yang, Nan Meng, Fang Lian

The long-duration energy storage (LDES) technologies are being developed to cope with the inherent intermittency of solar and wind power as renewable sources. Iron–air batteries (IABs), which leverage earth-abundant iron and oxygen, have emerged as a transformative LDES solution due to their ultralow projected cost, inherent non-flammability, exceptional theoretical energy density, and minimal environmental footprint. This review begins with an overview of the fundamental principles and technical development history of IABs, followed by a comprehensive analysis of their current research landscape. In particular, ongoing challenges and advances in critical components including metal electrodes, electrolytes, and cell structures have been focused on to provide insights into redox kinetics-improving the mechanism of iron-based anode. These advances facilitate the scaling up of IABs and their integration with renewable infrastructure, thereby advancing the sustainable development of renewable energy.

{"title":"Sustainable Development of Iron–Air Batteries as Long-Duration Energy Storage Systems: The Key to Improving the Redox Kinetics of Iron-Based Anode","authors":"Zirui Zhao,&nbsp;Zunhao Fan,&nbsp;Zhaoxia Yang,&nbsp;Nan Meng,&nbsp;Fang Lian","doi":"10.1002/adsu.202501101","DOIUrl":"https://doi.org/10.1002/adsu.202501101","url":null,"abstract":"<div>\u0000 \u0000 <p>The long-duration energy storage (LDES) technologies are being developed to cope with the inherent intermittency of solar and wind power as renewable sources. Iron–air batteries (IABs), which leverage earth-abundant iron and oxygen, have emerged as a transformative LDES solution due to their ultralow projected cost, inherent non-flammability, exceptional theoretical energy density, and minimal environmental footprint. This review begins with an overview of the fundamental principles and technical development history of IABs, followed by a comprehensive analysis of their current research landscape. In particular, ongoing challenges and advances in critical components including metal electrodes, electrolytes, and cell structures have been focused on to provide insights into redox kinetics-improving the mechanism of iron-based anode. These advances facilitate the scaling up of IABs and their integration with renewable infrastructure, thereby advancing the sustainable development of renewable energy.</p>\u0000 </div>","PeriodicalId":7294,"journal":{"name":"Advanced Sustainable Systems","volume":"10 2","pages":""},"PeriodicalIF":6.1,"publicationDate":"2026-02-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146135969","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}
引用次数: 0
Strategies and Advances in Interfacial Engineering for Electrochemical Nitrate Reduction to Ammonia Catalysts 硝酸电化学还原制氨催化剂界面工程策略与进展
IF 6.1 3区 材料科学 Q2 GREEN & SUSTAINABLE SCIENCE & TECHNOLOGY Pub Date : 2026-02-03 DOI: 10.1002/adsu.202501234
Peiyuan Zheng, Haoran Jin, Mingming Zhang, Cui Lai

Electrochemical conversion of nitrate into ammonia represents a sustainable strategy for mitigating nitrogen-related environmental burdens while enabling green ammonia production. Electrochemical nitrate reduction to ammonia (eNitRR) involves a sequence of electron transfer steps and reaction intermediates that are difficult to stabilize and control under ambient conditions. This review focuses on recent progress in interfacial engineering approaches that enhance the catalytic activity, improve product selectivity, and maintain structural and operational stability throughout the reaction process. Four main ideas are summarized: i) designing active sites from single atoms to larger structures; ii) adjusting the electronic structure by changing coordination and d-band properties; iii) controlling surface atoms and crystal faces to guide reaction phases; iv) using defects and stress to change charge movement during the reaction. It is further demonstrated how these strategies have been applied across representative material systems, including metal oxides, MOF-based frameworks, and π-conjugated carbon materials. These designs help improve the reaction process and the final performance. Finally, some new directions are discussed, including vacancy control, combining multiple catalysts, and using light to help the reaction, which may lead to better and scalable eNitRR systems.

{"title":"Strategies and Advances in Interfacial Engineering for Electrochemical Nitrate Reduction to Ammonia Catalysts","authors":"Peiyuan Zheng,&nbsp;Haoran Jin,&nbsp;Mingming Zhang,&nbsp;Cui Lai","doi":"10.1002/adsu.202501234","DOIUrl":"https://doi.org/10.1002/adsu.202501234","url":null,"abstract":"<p>Electrochemical conversion of nitrate into ammonia represents a sustainable strategy for mitigating nitrogen-related environmental burdens while enabling green ammonia production. Electrochemical nitrate reduction to ammonia (eNitRR) involves a sequence of electron transfer steps and reaction intermediates that are difficult to stabilize and control under ambient conditions. This review focuses on recent progress in interfacial engineering approaches that enhance the catalytic activity, improve product selectivity, and maintain structural and operational stability throughout the reaction process. Four main ideas are summarized: i) designing active sites from single atoms to larger structures; ii) adjusting the electronic structure by changing coordination and d-band properties; iii) controlling surface atoms and crystal faces to guide reaction phases; iv) using defects and stress to change charge movement during the reaction. It is further demonstrated how these strategies have been applied across representative material systems, including metal oxides, MOF-based frameworks, and π-conjugated carbon materials. These designs help improve the reaction process and the final performance. Finally, some new directions are discussed, including vacancy control, combining multiple catalysts, and using light to help the reaction, which may lead to better and scalable eNitRR systems.</p>","PeriodicalId":7294,"journal":{"name":"Advanced Sustainable Systems","volume":"10 2","pages":""},"PeriodicalIF":6.1,"publicationDate":"2026-02-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146135926","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}
引用次数: 0
Synergistic Solar-Powered Water−Electricity Cogeneration from Diverse Saline Water Enabled by a Multistage Solar Still Based on Zwitterion-Modified Janus Membranes 基于两性离子修饰Janus膜的多级太阳能蒸馏器实现了多种盐水的协同太阳能水-电热电联产
IF 6.1 3区 材料科学 Q2 GREEN & SUSTAINABLE SCIENCE & TECHNOLOGY Pub Date : 2026-02-03 DOI: 10.1002/adsu.202501728
Mingxing Ye, Jingjing Li, Jun Zhao, Yuke Sun, Zhihang Wang, Xiaofeng Xu

The global pursuit of sustainable development is increasingly constrained by freshwater scarcity and the growing energy crisis. Integrating solar-powered hybrid systems that couple photovoltaic electricity generation with passive steam-based desalination offers a promising solution. Although thermally localized multi-stage solar stills have been explored, stable water production in saline environments remains challenging. Herein, a photovoltaic (PV) cell integrated with a nine-stage membrane distillation (MD) device are developed, enabling simultaneous electricity and clean water generation from diverse saline water (3.5%–20%). Zwitterion-modified Janus membranes, together with the multi-stage architecture, synergistically cool down the PV cell, suppress salt crystallization, recycle vaporization enthalpy, and repurpose waste heat. As a result, the integrated device achieves a high water production rate of 3.89 kg m−2 h−1, while simultaneously maintaining a stable electricity generation efficiency of 15.3% under 1 sun, maximizing the total solar energy conversion. Under natural sunlight, a daily clean water yield of 10.8 kg m−2 day−1 is achieved, placing this system among the best-performing solar stills reported to date. This study highlights a low-carbon cogeneration of clean water and electricity, extending the applicability of solar conversion technologies to saline environments.

{"title":"Synergistic Solar-Powered Water−Electricity Cogeneration from Diverse Saline Water Enabled by a Multistage Solar Still Based on Zwitterion-Modified Janus Membranes","authors":"Mingxing Ye,&nbsp;Jingjing Li,&nbsp;Jun Zhao,&nbsp;Yuke Sun,&nbsp;Zhihang Wang,&nbsp;Xiaofeng Xu","doi":"10.1002/adsu.202501728","DOIUrl":"https://doi.org/10.1002/adsu.202501728","url":null,"abstract":"<div>\u0000 \u0000 <p>The global pursuit of sustainable development is increasingly constrained by freshwater scarcity and the growing energy crisis. Integrating solar-powered hybrid systems that couple photovoltaic electricity generation with passive steam-based desalination offers a promising solution. Although thermally localized multi-stage solar stills have been explored, stable water production in saline environments remains challenging. Herein, a photovoltaic (PV) cell integrated with a nine-stage membrane distillation (MD) device are developed, enabling simultaneous electricity and clean water generation from diverse saline water (3.5%–20%). Zwitterion-modified Janus membranes, together with the multi-stage architecture, synergistically cool down the PV cell, suppress salt crystallization, recycle vaporization enthalpy, and repurpose waste heat. As a result, the integrated device achieves a high water production rate of 3.89 kg m<sup>−2</sup> h<sup>−1</sup>, while simultaneously maintaining a stable electricity generation efficiency of 15.3% under 1 sun, maximizing the total solar energy conversion. Under natural sunlight, a daily clean water yield of 10.8 kg m<sup>−2</sup> day<sup>−1</sup> is achieved, placing this system among the best-performing solar stills reported to date. This study highlights a low-carbon cogeneration of clean water and electricity, extending the applicability of solar conversion technologies to saline environments.</p>\u0000 </div>","PeriodicalId":7294,"journal":{"name":"Advanced Sustainable Systems","volume":"10 2","pages":""},"PeriodicalIF":6.1,"publicationDate":"2026-02-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146129879","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}
引用次数: 0
Harnessing Interfacial Synergies in Carbon-Polymer Nanocomposites for Efficient Energy Storage and Conversion 利用碳-聚合物纳米复合材料的界面协同作用实现高效的能量存储和转换
IF 6.1 3区 材料科学 Q2 GREEN & SUSTAINABLE SCIENCE & TECHNOLOGY Pub Date : 2026-02-03 DOI: 10.1002/adsu.202501406
Ghulam Mooin Ud Din, Abid Ali, Sheza Muqaddas, Zafar Iqbal, Munawar Iqbal, Habib Elhouichet, Arif Nazir, Norah Alwadai, Hafiz Muhammad Yasir

Energy storage and conversion technologies are crucial in the global shift toward renewable energy sources, addressing the intermittent nature of solar and wind energy and enhancing the stability and reliability of power grids. Polymer/carbon composites have emerged as pivotal materials in this realm, due to their unique ability to combine the electrical conductivity and mechanical strength of carbon materials with the versatility and chemical stability of conductive polymers. This review delves into how these methods affect conductivity, capacitance, and stability, thereby enhancing the efficiency and durability of devices such as supercapacitors and batteries. The discussion extends to the characterization of these materials using advanced techniques that elucidate their structural integrity and functional capabilities, providing insights into their performance enhancements. The applications of polymer/carbon composites in energy storage systems are highlighted by their use in supercapacitors and batteries, where they contribute to increased energy density, faster charge–discharge cycles, and improved longevity. As the demand for more efficient and sustainable energy storage solutions continues to grow, the insights provided by this review into the properties and applications of polymer/carbon composites pave the way for future innovations in energy technologies, ultimately guiding researchers and technologists in developing next-generation materials for advanced energy systems.

{"title":"Harnessing Interfacial Synergies in Carbon-Polymer Nanocomposites for Efficient Energy Storage and Conversion","authors":"Ghulam Mooin Ud Din,&nbsp;Abid Ali,&nbsp;Sheza Muqaddas,&nbsp;Zafar Iqbal,&nbsp;Munawar Iqbal,&nbsp;Habib Elhouichet,&nbsp;Arif Nazir,&nbsp;Norah Alwadai,&nbsp;Hafiz Muhammad Yasir","doi":"10.1002/adsu.202501406","DOIUrl":"https://doi.org/10.1002/adsu.202501406","url":null,"abstract":"<div>\u0000 \u0000 <p>Energy storage and conversion technologies are crucial in the global shift toward renewable energy sources, addressing the intermittent nature of solar and wind energy and enhancing the stability and reliability of power grids. Polymer/carbon composites have emerged as pivotal materials in this realm, due to their unique ability to combine the electrical conductivity and mechanical strength of carbon materials with the versatility and chemical stability of conductive polymers. This review delves into how these methods affect conductivity, capacitance, and stability, thereby enhancing the efficiency and durability of devices such as supercapacitors and batteries. The discussion extends to the characterization of these materials using advanced techniques that elucidate their structural integrity and functional capabilities, providing insights into their performance enhancements. The applications of polymer/carbon composites in energy storage systems are highlighted by their use in supercapacitors and batteries, where they contribute to increased energy density, faster charge–discharge cycles, and improved longevity. As the demand for more efficient and sustainable energy storage solutions continues to grow, the insights provided by this review into the properties and applications of polymer/carbon composites pave the way for future innovations in energy technologies, ultimately guiding researchers and technologists in developing next-generation materials for advanced energy systems.</p>\u0000 </div>","PeriodicalId":7294,"journal":{"name":"Advanced Sustainable Systems","volume":"10 2","pages":""},"PeriodicalIF":6.1,"publicationDate":"2026-02-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146129919","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}
引用次数: 0
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Advanced Sustainable Systems
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