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Bio-based materials for sustainable energy harvesting: Applications in TENGs, PENGs, and solar-powered seawater desalination systems

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Chemical Engineering Journal 2025年 516卷

作者： Ding, Yutong Deng, Linbing Liu, Xiao-Xiao Wang, Lili Meng, Yanrong Ouyang, Mi Chen, Feng Huang, Zhao-Xia Kuang, Tairong Lab State Key Laboratory of Advanced Separation Membrane Materials Zhejiang Key Laboratory of Advanced Polymer Materials Modification and Application Technology College of Materials Science and Engineering Zhejiang University of Technology Hangzhou310014 China National Engineering Research Center of Novel Equipment for Polymer Processing Key Laboratory of Polymer Processing Engineering Ministry of Education Guangdong Provincial Key Laboratory of Technique and Equipment for Macromolecular Advanced Manufacturing Department of Mechanical and Automotive Engineering South China University of Technology Guangzhou510641 China School of Advanced Manufacturing Technology Guangdong Mechanical & Electrical Polytechnic Guangzhou510550 China Department of General Medicine First Medical Center of Chinese PLA General Hospital Beijing100039 China

The global energy crisis has intensified the need for sustainable energy solutions, yet conventional energy production still relies on non-renewable, environmentally damaging materials. Although significant advances have been made in green energy technologies, a critical gap remains in the development of materials that are both renewable and environmentally friendly. Bio-based materials, derived from renewable resources, offer a timely and sustainable alternative that can significantly improve the efficiency, functionality, and environmental compatibility of energy conversion devices. This review highlights the role of bio-based materials in addressing these challenges, focusing on their applications in emerging green energy technologies, particularly triboelectric nanogenerators (TENGs), piezoelectric nanogenerators (PENGs), and solar-powered seawater desalination systems. It provides a comprehensive overview of the latest advances in preparation methods, material properties, and their practical applications in energy conversion systems. By discussing the unique advantages and material selection challenges, this review underscores the importance of bio-based materials in the continued development of sustainable, high-performance energy harvesting devices. Furthermore, it emphasizes their potential to contribute to global sustainability goals, offering a critical pathway to more eco-friendly and cost-effective energy solutions. © 2025 Elsevier B.V.

关键词： Solar power generation

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Tungsten Phosphide on Nitrogen and Phosphorus-Doped Carbon as a Functional Membrane Coating Enabling Robust Lithium-Sulfur Batteries

SSRN

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SSRN 2024年

作者： Li, Canhuang Yu, Jing Zhang, Chaoqi Wang, Jian Yang, Dawei Xiao, Ke Li, Hao Huang, Chen Cheng, Yapeng Ren, Yuchuan Qi, Xuede Yang, Tianxiang Li, Junshan Wang, Jiaao Henkelman, Graeme Arbiol, Jordi Nan, Junmin Cabot, Andreu Catalonia Institute for Energy Research-IREC Sant Adrià de Besòs Barcelona08930 Spain Department of Chemistry Universitat de Barcelona Barcelona08028 Spain College of Materials Science and Engineering Fuzhou University No.2 Xueyuan Road Minhou County Fujian Province Fuzhou City350108 China Department of Electronic and Biomedical Engineering Universitat de Barcelona Barcelona08028 Spain UlmD89081 Germany Henan Province Key Laboratory of Photovoltaic Materials School of Future Technology Henan University Kaifeng475004 China State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of Technology China Chongqing University of Technology China CSIC and BIST Campus UAB Bellaterra Barcelona Catalonia08193 Spain School of Environmental Engineering and Chemistry Luoyang Institute of Science and Technology Henan Luoyang471023 China Institute for Advanced Study Chengdu University Chengdu610106 China Department of Chemistry The Oden Institute for Computational Engineering and Sciences The University of Texas at Austin AustinTX78712-0165 United States School of Chemistry South China Normal University Guangzhou510006 China ICREA Pg. Lluis Companys Barcelona Catalonia08010 Spain

Lithium-sulfur batteries (LSBs) hold great potential as future energy storage technology, but their widespread application is hampered by the slow polysulfide conversion kinetics and the sulfur loss during cycling. In this study, we detail a one-step approach to growing tungsten phosphide (WP) nanoparticles on the surface of nitrogen and phosphorus co-doped carbon nanosheets (WP@NPC). We further demonstrate that this material provides outstanding performance as a multifunctional separator in LSBs, enabling higher sulfur utilization and exceptional rate performance. These excellent properties are associated with the abundance of lithium polysulfide (LiPS) adsorption and catalytic conversion sites and rapid ion transport capabilities. Experimental data and density functional theory calculations demonstrate tungsten to have a sulfophilic character while nitrogen and phosphorus provide lithiophilic sites that prevent the loss of LiPSs. Furthermore, WP regulates the LiPS catalytic conversion, accelerating the Li-S redox kinetics. As a result, LSBs containing a polypropylene separator coated with a WP@NPC layer show capacities close to 1500 mAh g-1 at 0.1C and coulombic efficiencies above 99.5% at 3C. Batteries with high sulfur loading, 4.9 mg cm−2, are further produced to validate their superior cycling stability. This work demonstrates the use of multifunctional separators as an effective strategy to promote LSB performance. © 2024, The Authors. All rights reserved.

关键词： Polysulfides

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Ultrafast Carrier Dynamics and Terahertz Photoconductivity of Mixed-Cation and Lead Mixed-Halide Hybrid Perovskites

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Chinese Physics Letters 2019年第2期36卷 83-91页

作者： Wan-Ying Zhao Zhi-Liang Ku Li-Ping Lv Xian Lin Yong Peng Zuan-Ming Jin Guo-Hong Ma Jian-Quan Yao Department of Physics Shanghai University State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of Technology Department of Chemical Engineering School of Environmental and Chemical EngineeringShanghai University STU & SIOM Joint Laboratory for Superintense Lasers and Applications College of Precision Instrument and Opto-electronics Engineering Institute of Laser and Opto-electronicsTianjin University

Using time-dependent terahertz spectroscopy, we investigate the role of mixed-cation and mixed-halide on the ultrafast photoconductivity dynamics of two different methylammonium(MA) lead-iodide perovskite thin films. It is found that the dynamics of conductivity after photoexcitation reveals significant correlation on the microscopy crystalline features of the samples. Our results show that mixed-cation and lead mixed-halide affect the charge carrier dynamics of the lead-iodide perovskites. In the(5-AVA)_(0.05)(MA)_(0.95) PbI_(2.95) Cl_(0.05)/spiro thin film, we observe a much weaker saturation trend of the initial photoconductivity with high excitation fluence, which is attributed to the combined effect of sequential charge carrier generation, transfer, cooling and polaron formation.

关键词： Ultrafast Carrier Dynamics Terahertz Photoconductivity Mixed-Cation Lead Mixed-Halide Hybrid Perovskites

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A Highly Stable and Non-Flammable Deep Eutectic Electrolyte for High-Performance Lithium Metal Batteries

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Angewandte Chemie 2024年第43期136卷

作者： Li Zhao Ao Xu Yu Cheng Hantao Xu Prof. Lin Xu Prof. Liqiang Mai State Key Laboratory of Advanced Technology for Materials Synthesis and Processing School of Materials Science and Engineering Wuhan University of Technology Wuhan 430070 P.R. China Hubei Longzhong Laboratory Wuhan University of Technology (Xiangyang Demonstration Zone) Xiangyang 441000 Hubei P.R. China Hainan Institute Wuhan University of Technology Sanya 572000 P.R. China

Deep eutectic electrolytes (DEEs) are regarded as one of the next-generation electrolytes to promote the development of lithium metal batteries (LMBs) due to their unparalleled advantages compared to both liquid electrolytes and solid electrolytes. However, its application in LMBs is limited by electrode interface compatibility. Here, we introduce a novel solid dimethylmalononitrile (DMMN)-based DEE induced by N coordination to dissociate LiTFSI. We confirmed that the DMMN molecule can promote the dissociation of LiTFSI by the interaction between the N atom and Li + , and form the hydrogen bond with TFSI − anion, which can promote the dissociation of LiTFSI to form DEE. More importantly, due to the absence of active α-hydrogen, DMMN exhibits greatly enhanced reduction stability with Li metal, resulting in favorable electrode/electrolyte interface compatibility. Polymer electrolytes based on this DEE exhibit high ionic conductivity (0.67 mS cm −1 at 25 °C), high oxidation voltage (5.0 V vs. Li + /Li), favorable interfacial stability, and nonflammability. Li‖LFP and Li‖NCM811 full batteries utilizing this DEE polymer electrolyte exhibit excellent long-term cycling stability and excellent rate performance at high rates. Therefore, the new DMMN-based DEE overcomes the limitations of traditional electrolytes in electrode interface compatibility and opens new possibilities for improving the performance of LMBs.

关键词： dimethylmalononitrile nitrile group deep eutectic electrolytes stable interfacial compatibility lithium metal batteries

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The effect of Y3+ on microstructure and scintillation properties of hot-pressed Eu2+ doped CaF2 transparent ceramics

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Journal of Luminescence 2025年 286卷

作者： Zhou, Zhiwei Zhang, Pengshuai Chen, Guanyu Yuan, Dan Jing, Wentao Yang, Yu Jin, Qianqian Lan, Yuangang Mei, Bingchu School of Electronic Engineering Guangxi University of Science and Technology Liuzhou545006 China Guangxi Key Laboratory of Multidimensional Information Fusion for Intelligent Vehicles Guangxi University of Science and Technology Liuzhou545006 China Guangxi Colleges and Universities Key Laboratory of Microwave Communication and Micro–Nano Photoelectric Technology Guangxi University of Science and Technology Liuzhou545006 China State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of Technology Wuhan430070 China

CaF2:Eu2+ transparent ceramics with and without Y3+ doping were fabricated by the hot-pressed sintering method under the inert atmosphere via the co-precipitation-synthesized nanoparticles. After the co-doping of Y3+, there was no significant change in the particle size of the nanoparticles, but the grain size of the ceramics was markedly reduced. The optical transmission of CaF2: Eu2+, Y3+ ceramics at 425 nm achieved approximately 46.3 %, surpassing that of CaF2:Eu2+ ceramics. With Y3+ ions co-doping, the photoluminescence (PL) and X-ray induced emission spectra displayed stronger emission bands at 422 nm ascribed to 5d-4f transitions of Eu2+ ions and weaker emission peaks at 550–650 nm range originating from 4f-4f transitions of Eu3+ ions in Eu2+:CaF2 ceramic. Furthermore, the effect of co-doped Y3+ ions on the scintillation decay lifetime, pulse height spectra, and thermoluminescence of the samples were investigated. © 2025

关键词： Scintillation

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Ultrahigh-temperature film capacitors via homo/heterogeneous interfaces

Research Square

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Research Square 2021年

作者： Liu, Ming Lu, Rui Shen, Zhonghui Ma, Chunrui Duan, Tingzhi Lu, Lu Hu, Guangliang Hu, Tian-Yi You, Caiyin Mi, Shaobo Jia, Chun-Lin Chen, Long-Qing School of Microelectronics Xi’an Jiaotong University Xi'an China State Key Laboratory for Mechanical Behavior of Materials Xi’an Jiaotong University Xi’an China State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Center of Smart Materials and Devices Wuhan University of Technology Wuhan China International School of Materials Science and Engineering Wuhan University of Technology Wuhan China School of Materials Science and Engineering Xían University of Technology Xi'an China Ernst Ruska Centre for Microscopy and Spectroscopy with Electrons ForschungszentrumJülich JülichD-52425 Germany Department of Materials Science and Engineering The Pennsylvania State University University ParkPA United States

High-performance dielectric capacitors are in high demand for advanced electronics and electric power systems. They possess high power density (on the order of Megawatt) and exhibit ultrafast charge/discharge capability (on a microsecond scale) and long-term storage lifetime1-5, and thus they are particularly demanded in pulse power systems such as high-power microwaves, hybrid electric vehicles, and high-frequency inverters. However, their relatively low operating temperature limits their widespread applications6-9Here, guided by phase-field simulations, we synthesized capacitors with an energy storage density of 55.4 joules per cubic centimeter, energy efficiency of over 82%, and superior thermal stability and fatigue properties at record high operating temperature of 400°C. These ultrahigh-temperature performances are achieved through a relatively simple method of introduction and engineering of interfaces within the capacitors, which greatly improve their high-temperature stability, relaxation behavior, and breakdown strength. Our work not only successfully fabricated capacitors with potential applications in high-temperature electric power systems and electronic technologies but also opens up a promising and general route for designing high-performance electrostatic capacitors through interface engineering. © 2021, CC BY.

关键词： Energy storage

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Alloying effect enhanced bimetallic Ni-Fe/TiO 2 catalysts for selective hydrogenation of 1,3-butadiene in the presence of an excess of propylene

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Molecular Catalysis 2023年 550卷

作者： Wei-Hao Wang Bo Jiang Zhao Wang Ya Chen Yao Li Ting-Ting Luo Feng Cheng Bao-Lian Su The State Key Laboratory of Advanced Technology for Material Synthesis and processing Wuhan University of Technology Wuhan 430070 China Center for Materials Research and Analysis Wuhan University of Technology Wuhan 430070 China Laboratory of Inorganic Materials Chemistry (CMI) University of Namur 61 Rue de Bruxelles B-5000 Namur Belgium

Nickel is a promising Pd alternative candidate for selective alkynes/alkadienes hydrogenation owing to its high catalytic activity and cheap price, however, with fatal restrictions of low alkenes selectivity and inferior stability caused by its strong olefin adsorption and the cleavage of carbon-carbon bond. Herein, controlled amounts of iron were introduced into nickel as catalytic assistant by deposition-precipitation with urea on TiO 2 support. Using 1,3-butadiene in an excess of propylene to simulate the industrial process, the additional Fe shows a significant enhancement to the catalytic performance of Ni, i.e., Ni-Fe/TiO 2 with Ni/Fe atomic ratio 1:0.33 shows >94% of 1,3-butadiene conversion and >95% of alkenes selectivity after above 200 h of time on stream, superior to that of commercial Pd/Al 2 O 3 catalyst. Further in-situ analysis reveals that the alloying effect from the formation of Ni-rich Ni-Fe intermetallic compound (e.g., Ni 3 Fe alloy) enlarges the distance between two Ni active sites and enriches the electronic density of Ni sites, resulting in a weak adsorption of butenes products for offering such excellent catalytic performance. To the best of our knowledge, this is the first in-depth exploration on supported Ni-Fe bimetallic catalyst for selective hydrogenation of light alkynes/alkadienes. It shows a high potential for replacing the commercial Pd-based catalysts.

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Research on the stability of organic/inorganic hybrid perovskite materials for IEC61215 purpose

Research on the stability of organic/inorganic hybrid perovs...

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第六届新型太阳能电池材料科学与技术学术研讨会

作者： Jiang He Zhiliang Ku Yong Peng State key lab of advanced technology for materials synthesis and processing Wuhan University of Technology

Organi/Inorganic perovskite materials behavior differently under a testing condition of IEC61215. In this research, the behavior of series of perovskite materials with varied A cations under the thermal cycling testing standards were studied. We analyzed the defeating mechanisms of those materials through temperature depended XRD, SEM and AFM ***. Finally, we draw a conclusion that FACsPb（I/Br） perovskite materials could the most stable one under thermal cycling testing condition. This perovskite materials can be stable because the phase change related materials decomposition under frequent temperature change does not happen in this material, however other perovskite materials will decompose. A device with an architecture of FTO/TiO/FACsPbI/graphite electrode was then encapsulated and tested under a condition of -30℃-85℃ for 200 times. After testing, the device finally kept about 83% of its initial power conversion efficiency.

关键词： Standard stability tests Perovskite solar cells thermal cycling tests

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Synergistic effects of carbon doping and coating of TiO2 with exceptional photocurrent enhancement for high performance H2 production from water splitting

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能源化学 2021年第5期56卷 141-151页

作者： Yingying Wang Yan-Xin Chen Tarek Barakat Tian-Ming Wang Alain Krief Yu-Jia Zeng Marvin laboureur Luca Fusaro Hong-Gang Liao Bao-Lian Su Laboratory of Inorganic Materials Chemistry (CMI) University of Namur B-5000 Namur Belgium Namur Institute of Structured Matter (NISM) University of Namur B-5000 Namur Belgium Laboratory of Inorganic Materials Chemistry (CMI) University of Namur B-5000 Namur Belgium Xiamen Institute of Rare Earth Materials Haixi Institutes Chinese Academy of Sciences Xiamen 361021 Fujian China Xiamen Institute of Rare Earth Materials Haixi Institutes Chinese Academy of Sciences Xiamen 361021 Fujian China College of Physics and Optoelectronic Engineering Shenzhen University Shenzhen 518060 Guangdong China State Key Laboratory of Physical Chemistry of Solid Surfaces College of Chemistry and Chemical Engineering Xiamen University Xiamen 361005 Fujian China Laboratory of Inorganic Materials Chemistry (CMI) University of Namur B-5000 Namur Belgium Namur Institute of Structured Matter (NISM) University of Namur B-5000 Namur Belgium State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of Technology Wuhan 430074 Hubei China

The 'one pot' simultaneous carbon coating and doping of TiO2 materials by the hydrolysis of TiCl4 in fructose is *** synergistic effect of carbon doping and coating of TiO2 to significantly boost textural,optical and electronic properties and photocurrent of TiO2 for high performance visible light H2 production from water splitting has been comprehensively *** doping can significantly increase the thermal stability,thus inhibiting the phase transformation of the Titania material from anatase to rutile while carbon coating can suppress the grain aggregation of *** synergy of carbon doping and coating can not only ensure an enhanced narrowing effect of the electronic band gap of TiO2 thus extending the absorption of photocatalysts to the visible regions,but also promote dramatically the separation of electron-hole *** to these synergistic effects,the carbon coated and doped TiO2 shows much superior photocatalytic activity for both degradation of organics and photocatalytic/photoelectro chemical (PEC) water splitting under simulated sunlight *** photocatalytic activity of obtained materials can reach 5,4 and 2 times higher than that of pristine TiO2,carbon doped TiO2 and carbon coated TiO2,respectively in the degradation of organic *** carbon coated and doped TiO2 materials exhibited more than 37 times and hundreds of times photocurrent enhancement under simulated sunlight and visible light,respectively compared to that of pristine *** present work providing new comprehensive understanding on carbon coating and doping effect could be very helpful for the development of advanced TiO2 materials for a large series of applications.

关键词： Carbon coating and doping TiO2 One-pot PEC water splitting Solar light photocatalysis

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Appending Coronene Diimide with Carbon Nanohoops Allows for Rapid Intersystem Crossing in Neat Film

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Angewandte Chemie 2024年第18期136卷

作者： Jingjing Zhao Jingwen Xu Dr. Huaxi Huang Kangwei Wang Prof. Dr. Di Wu Prof. Dr. Ramesh Jasti Prof. Dr. Jianlong Xia State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Center of Smart Materials and Devices Wuhan University of Technology 430070 Wuhan China These authors contributed equally International School of Materials Science and Engineering Wuhan University of Technology 430070 Wuhan China School of Chemistry Chemical Engineering and Life Science Wuhan University of Technology 430070 Wuhan China Department of Chemistry and Biochemistry Materials Science Institute University of Oregon 97403 Eugene Oregon USA

The development of innovative triplet materials plays a significant role in various applications. Although effective tuning of triplet formation by intersystem crossing (ISC) has been well established in solution, the modulation of ISC processes in the solid state remains a challenge due to the presence of other exciton decay channels through intermolecular interactions. The cyclic structure of cycloparaphenylenes (CPPs) offers a unique platform to tune the intermolecular packing, which leads to controllable exciton dynamics in the solid state. Herein, by integrating an electron deficient coronene diimide (CDI) unit into the CPP framework, a donor-acceptor type of conjugated macrocycle ( CDI-CPP ) featuring intramolecular charge-transfer (CT) interaction was designed and synthesized. Effective intermolecular CT interaction resulting from a slipped herringbone packing was confirmed by X-ray crystallography. Transient spectroscopy studies showed that CDI-CPP undergoes ISC in both solution and the film state, with triplet generation time constants of 4.5 ns and 238 ps, respectively. The rapid triplet formation through ISC in the film state can be ascribed to the cooperation between intra- and intermolecular charge-transfer interactions. Our results highlight that intermolecular CT interaction has a pronounced effect on the ISC process in the solid state, and shed light on the use of the characteristic structure of CPPs to manipulate intermolecular CT interactions.

关键词： cycloparaphenylenes rylene diimides triplet materials intersystem crossing

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