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<title cf:type="text"><![CDATA[ -->Cellulose Intelligent Materials and Energy Devices]]></title>
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<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[Preparation and Performance Study of Paper-based Electrode Materials Modulated by Zirconium-Tannin Supramolecular Coordination of Polyaniline]]></title>
<link><![CDATA[http://zgzz.ijournals.cn/zgzzen/ch/reader/view_abstract.aspx?file_no=202510011&flag=1]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[To address the problems of easy agglomeration and low loading of polyaniline on the surface of cellulose fibers， this study used a zirconium-tannin supramolecular coordination polymer to modify the fibers， thereby regulating the <i>in-situ</i> polymerization of aniline monomers and successfully preparing a high-loading nano-network structure of polyaniline on the fiber surface. The results showed that through modification with the zirconium-tannin supramolecular coordination polymer， the deposition rate of polyaniline on the cellulose fibers reached as high as 34.45%， and the electrical conductivity of the composite material reached 22.73 S/m. Electrochemical test results revealed that the prepared composite paper-based electrode achieved an area-specific capacitance of up to 2 947 mF/cm² at a current density of 2 mA/cm². When this electrode material was assembled into a symmetric supercapacitor， it could achieve an energy density of 33.55 mWh/cm³ at a power density of 95.47 mW/cm³.]]></description>
<pubDate>2025/10/28 19:45:45</pubDate>
<category><![CDATA[Cellulose Intelligent Materials and Energy Devices]]></category>
<author><![CDATA[SUN Kexin,ZHENG Shuo,CHEN Xiaohong,CHANG Ziyang,JIA Zhixin,GUO Daliang,ZHAO Huifang,SHA Lizheng]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name>SUN Kexin,ZHENG Shuo,CHEN Xiaohong,CHANG Ziyang,JIA Zhixin,GUO Daliang,ZHAO Huifang,SHA Lizheng</atom:name>
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<guid><![CDATA[http://zgzz.ijournals.cn/zgzzen/ch/reader/view_abstract.aspx?file_no=202510011&flag=1]]></guid><cfi:id>6</cfi:id><cfi:read>true</cfi:read></item>
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<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[Preparation and Capacitive Performance Study of the Lignin-containing Cellulose Nanofibril/Polypyrrole Composite Film]]></title>
<link><![CDATA[http://zgzz.ijournals.cn/zgzzen/ch/reader/view_abstract.aspx?file_no=202510012&flag=1]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[In this study， lignin-containing cellulose nanofibril (LCNF) was prepared using poplar chemi-mechanical pulp as the raw material， which was sequentially subjected to 2，2，6，6-tetramethylpiperidine-N-oxide (TEMPO) radical oxidation， high-shear treatment and high-pressure homogenization. The LCNF was then used as a flexible substrate to prepare LCNF/polypyrrole (LNP) composite film electrodes. Furthermore， the effects of TEMPO oxidation degree on the residual lignin content， yield and morphology of LCNF， as well as on the microstructure of LNP composite film were investigated， and the structure-activity relationship between LNP structure and capacitance performance was analyzed. The results showed that as the degree of TEMPO oxidation increased， the lignin content and size of the LCNF decreased gradually. The morphology of LCNF and LNP composite film could be altered by the lignin through the regulation of fibrillation. This could further affect the microstructure of LNP composite film through adhesion， thereby improving its capacitance performance. In addition， lignin could also provide pseudocapacitance of LNP composite film via the reversible conversion of the quinone/hydroquinone structure. Moreover， the supercapacitor assembled with the LNP-13.8% composite film exhibited a power density of 499.9 μW/cm² and an energy density of 88.6 μWh/cm²， demonstrating excellent energy storage capability.]]></description>
<pubDate>2025/10/28 19:45:46</pubDate>
<category><![CDATA[Cellulose Intelligent Materials and Energy Devices]]></category>
<author><![CDATA[XU Feng,WANG Dongxing,CI Xiaolei,SHAO Xuejun,WANG Yuebin,LIU Chunlan,TIAN Baonong,GE Yinkai]]></author>
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<atom:name>XU Feng,WANG Dongxing,CI Xiaolei,SHAO Xuejun,WANG Yuebin,LIU Chunlan,TIAN Baonong,GE Yinkai</atom:name>
</atom:author>
<guid><![CDATA[http://zgzz.ijournals.cn/zgzzen/ch/reader/view_abstract.aspx?file_no=202510012&flag=1]]></guid><cfi:id>5</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[Preparation of Cellulose Nanofiber-based Antifreeze Double Network Gel and Its Strain Sensing Properties]]></title>
<link><![CDATA[http://zgzz.ijournals.cn/zgzzen/ch/reader/view_abstract.aspx?file_no=202510013&flag=1]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[In this study， a deep eutectic solvent (DES) was prepared by ethylene glycol (EG) and zinc chloride (ZnCl₂), and it was used as solvent replacing water. Acrylamide (AM) was used as a monomer， and polyacrylamide (PAM) was polymerized under UV irradiation. Then， the cellulose nanofiber (CNF) and polyvinyl alcohol (PVA) were introduced to enhance mechanical properties， resulting in a DES-PVA/PAM/CNF antifreeze double network gel. The results showed that the prepared DES-PVA/PAM/CNF antifreeze double network gels exhibited the best antifreeze performance with freezing point as low as -73.03 ℃ when the molar ratio of ZnCl<sub>2</sub> to EG was 1∶5. Further investigation of the effects of CNF content on the gel properties revealed that the best overall performances were achieved when the CNF content was 0.4% (based on the mass of EG). At normal temperature， the fracture strength of the gel was up to 0.94 MPa， and the strain at break was 844.5%， at low temperature， the fracture strength was still maintained at 0.92 MPa， exhibiting excellent adaptability at low temperatures. In addition， after assembling the gel as a strain sensor， the monitoring of human skin-attached motion was successfully realized.]]></description>
<pubDate>2025/10/28 19:45:47</pubDate>
<category><![CDATA[Cellulose Intelligent Materials and Energy Devices]]></category>
<author><![CDATA[HE Xin,HU Jianquan,LIU Yuxin]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name>HE Xin,HU Jianquan,LIU Yuxin</atom:name>
</atom:author>
<guid><![CDATA[http://zgzz.ijournals.cn/zgzzen/ch/reader/view_abstract.aspx?file_no=202510013&flag=1]]></guid><cfi:id>4</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[Preparation and Properties of Iridescent Films with Cellulose Nanocrystals and Deep Eutectic Solvents]]></title>
<link><![CDATA[http://zgzz.ijournals.cn/zgzzen/ch/reader/view_abstract.aspx?file_no=202510014&flag=1]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[This study successfully fabricated flexible cellulose nanocrystal (CNC) structurally colored films by integrating a deep eutectic solvent (DES) into the CNC system through evaporation-induced self-assembly method and vacuum-assisted self-assembly method. The interaction mechanism between DES and CNC， along with the effects of both assembly techniques on the film’s microstructure， structural color， mechanical properties， and humidity-responsive behavior， were systematically investigated. The results showed that both methods enhanced the flexibility of CNC films. The vacuum-assisted assembly approach endowed the CNC-V and CNC/DES-V films with uniform structural colors (pearl-blue and cyan-blue)， smaller polydomain structures and pitches (132 and 160 nm)， higher tensile strengths ((58.4±2.1) MPa and (27.9±1.7） MPa)， and a narrower humidity-responsive color range (from blue to light yellow). In contrast， the evaporation-induced self-assembly method provided the CNC-E and CNC/DES-E films with brighter structural colors (blue and cyan)， larger pitches (136 and 175 nm)， and a broader humidity-induced color-shifting range (from cyan to orange).]]></description>
<pubDate>2025/10/28 19:45:48</pubDate>
<category><![CDATA[Cellulose Intelligent Materials and Energy Devices]]></category>
<author><![CDATA[MENG Yahui,XU Qingliang,ZHAO Huifang,SHA Lizheng,HE Zhiyang]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name>MENG Yahui,XU Qingliang,ZHAO Huifang,SHA Lizheng,HE Zhiyang</atom:name>
</atom:author>
<guid><![CDATA[http://zgzz.ijournals.cn/zgzzen/ch/reader/view_abstract.aspx?file_no=202510014&flag=1]]></guid><cfi:id>3</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[Research Progress and Future Prospects of High-performance Battery Separators]]></title>
<link><![CDATA[http://zgzz.ijournals.cn/zgzzen/ch/reader/view_abstract.aspx?file_no=202510015&flag=1]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[As an essential component of batteries， separators physically isolate the anode and cathode to prevent short circuits. Their microstructural properties critically influence battery cycling efficiency and capacity retention. With the rapid adoption of new energy vehicles in recent years， the demand for high-performance battery separators has intensified. Conventional polyolefin-based separators face limitations such as poor thermal resistance causing shrinkage， inadequate electrolyte wettability， and other drawbacks that hinder their application in next-generation high-efficiency battery systems. Consequently， modification of traditional separators or adoption of novel separator materials has become imperative. This paper systematically summarized recent global advances in both modified conventional separators and emerging separator materials. It further analyzed existing technological bottlenecks， challenges in developing high-performance separators， and future research directions. This work provided valuable insights for advancing separator technology and enhancing overall battery charge-discharge performance.]]></description>
<pubDate>2025/10/28 19:45:49</pubDate>
<category><![CDATA[Cellulose Intelligent Materials and Energy Devices]]></category>
<author><![CDATA[BI Xinyu,LI Weiwei,ZHANG Hongman,TIAN Hui,WANG Wenkang,CAO Qingting,YANG Chenhao,ZHANG Meiyun]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name>BI Xinyu,LI Weiwei,ZHANG Hongman,TIAN Hui,WANG Wenkang,CAO Qingting,YANG Chenhao,ZHANG Meiyun</atom:name>
</atom:author>
<guid><![CDATA[http://zgzz.ijournals.cn/zgzzen/ch/reader/view_abstract.aspx?file_no=202510015&flag=1]]></guid><cfi:id>2</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[Research Progress of Cellulose-based Carbon Materials as Oxygen Reduction Reaction Catalysts]]></title>
<link><![CDATA[http://zgzz.ijournals.cn/zgzzen/ch/reader/view_abstract.aspx?file_no=202510016&flag=1]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[In recent years， as the demand for clean-energy technologies continues to rise， conventional Pt-based catalysts are constrained by high cost， resource scarcity， and limited stability， which in turn propels the development of non-precious-metal catalysts. Using abundant， renewable cellulose to prepare porous carbon catalysts offers advantages of low cost， high specific surface area， orderly and tunable porosity， and good chemical stability and conductivity. This review systematically summarized the preparation methods and formation mechanisms of cellulose-based carbon materials， mainly discussed the effects of different approaches including hydrothermal carbonization， chemical/physical activation， hard templating， and aerogel carbonization on structures and properties of cellulose-based carbon materials， reviewed progress in their application to the oxygen reduction reaction (ORR)， compared the performances of cellulose-derived carbons with different architectures， and outlined prospects for their research and application in ORR catalysis.]]></description>
<pubDate>2025/10/28 19:45:50</pubDate>
<category><![CDATA[Cellulose Intelligent Materials and Energy Devices]]></category>
<author><![CDATA[SUN Aoran,ZHANG Zhenzhong,JIANG Chengshan,ZHANG Lei,YANG Guihua,CHEN Jiachuan]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name>SUN Aoran,ZHANG Zhenzhong,JIANG Chengshan,ZHANG Lei,YANG Guihua,CHEN Jiachuan</atom:name>
</atom:author>
<guid><![CDATA[http://zgzz.ijournals.cn/zgzzen/ch/reader/view_abstract.aspx?file_no=202510016&flag=1]]></guid><cfi:id>1</cfi:id><cfi:read>true</cfi:read></item>
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