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CARBOHYDRATE POLYMERS · 2020 · IF 7.182

Metal complexed-enzymatic hydrolyzed chitosan improves moisture retention of fiber papers by migrating immobilized water to bound state

Huijuan Wang,Heping Cui,Xuejiao Wang,Chao Lin,Shuqin Xia,Khizar Hayat,Shahzad Hussain,Muhammad Usman Tahir,Xiaoming Zhang

To obtain chitosan (CTS) with narrower molecular weight distribution, CTS with weight-average molecular weight ( M W ) of 197.30 kDa was first metal complexed and then degraded into five CTSs with M W of 107.90, 56.48, 10.40, 5.67 (CTS-4) and 3.66 kDa. Decrease of M W did not cause a significant change in chemical structure of the residue CTS, but the crystal structure was transformed significantly. The moisture retention increased firstly and then decreased as the M W of CTS decreased. CTS-4 was superior to CTSs with other M W and propylene glycol in terms of the moisture retention. The lower water activity and increase of net isosteric heat were observed in CTS-4, which was due to the migration of immobilized water to a bound-state caused by mounting newly formed chain-end hydrophilic groups per unit weight. CTS-4 could effectively improve moisture retention, showing a potential to substitute commonly used humectant such as propylene glycol.

研究领域: 材料科学 · 生物化学
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JOURNAL OF CATALYSIS · 2017 · IF 6.844

Peroxymonosulfate enhanced photoelectrocatalytic degradation of phenol activated by Co3O4 loaded carbon fiber cathode

Shanshan Liu,Xu Zhao,Yanbin Wang,Huixin Shao,Meng Qiao,Yan Wang,Shen Zhao

In this paper, a photoelectrocatalytic (PEC) system consisting of γ-Bi 2 MoO 6 anode and Co 3 O 4 loaded carbon fiber paper (Co 3 O 4 /CFP) cathode prepared by a hydrothermal method was established and used to degrade phenol . In order to enhance the PEC degradation efficiency of phenol, peroxymonosulfate (PMS) was introduced into this system. At an applied bias of 1.5   V, the removal efficiency of 10   mg/L phenol was increased from 6% to 100% with 2   mM   PMS addition into the PEC process. The degradation rate constant of phenol was also increased to be 0.0496   min −1 . Effects of PMS concentration, applied bias and initial pH were investigated. Based on the ESR analysis, sulfate radicals (SO 4 − ) and hydroxyl radicals (HO ) were proved to be the dominant oxidizing species for phenol degradation in the combined system. The PMS was activated to generate SO 4 − by loaded Co 3 O 4 , in which photogenerated-electrons accelerated the cobalt cycle process on the cathode. As a result, Co leaching was largely inhibited. The stability of the PEC system for organics degradation was exhibited.

CAS / MDL: 70693-62-8 7601-89-0
研究领域: 环境科学 · 化学工程
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INTERNATIONAL JOURNAL OF HYDROGEN ENERGY · 2019 · IF 4.084

One-step electrodeposition of cauliflower-like CozNiySx@polypyrrole electrocatalysts on carbon fiber paper for hydrogen evolution reaction

Qing Li,Wenjun Yan,Ye Liu,Haiyan Du,Zhongde Wang,Xiaogang Hao,Guoqing Guan

Transition-metal chalcogenides as the promising alternatives to noble-metal-based electrocatalysts for hydrogen evolution reaction (HER) with high activity and durability in water splitting have attracted extensive attention in recent years. Herein, Co z Ni y S x @PPy composites with three-dimensional (3D) cauliflower-like were firstly prepared on carbon fiber paper (CFP) via a simple and efficient electrochemical reduction of elemental sulfur in the precursor of S@PPy composite coated on CFP to react with Co and Ni ions in the electrolyte. The optimum electrode, i.e., Co z Ni y S x @PPy/CFP-6 (A-6) prepared by using an electrolyte with a Co/Ni molar ratio of 0/6, showed excellent catalytic activity (with an overpotential of 185 mV@10 mA cm −2 and a small Tafel slope of 78.13 mV dec −1 ) as well as long-term stability (at least 100 h) in 1 M KOH solutions. This work provides a novel way to fabricate effective and non-noble-metal electrodes for HER in water splitting.

研究领域: 材料科学 · 电化学
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ELECTROCHIMICA ACTA · 2015 · IF 4.504

NiCoO2 nanowires grown on carbon fiber paper for highly efficient water oxidation

Yang Yang,Ming Zhou,Wenlong Guo,Xun Cui,Yanhong Li,Feila Liu,Peng Xiao,Yunhuai Zhang

Water oxidation is a critical step in water splitting to make hydrogen fuel. We report a hybrid material consisting of NiCoO 2 nanowires grown on carbon fiber paper (denoted as NiCoO 2 @CFP) as a highly efficient oxygen evolution reaction (OER) electrocatalyst. In 0.1   M KOH, the highly nanostructured NiCoO 2 catalyst presents a small overpotential of ∼0.303   V at a current density of 10   mA   cm −2 and a low Tafel slope of ∼57   mV   dec −1 , comparable to the commercial precious RuO 2 catalyst. Such a good performance for OER may be attributed to the NaCl-type structure of the NiCoO 2 nanowires and CFP substrate, which can boost the formation of active Ni-Co layered hydroxide/oxyhydroxide species during the catalysis process. Additionally, the aligned 3D structure of NiCoO 2 @CFP plays an important role in the high catalytic activity for OER. These merits combined with the satisfactory stability of the hybrid material indicate that it is a promising material for water oxidation.

CAS / MDL: 12036-10-1
研究领域: 材料科学 · 能源化学 · 催化化学
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JOURNAL OF MATERIALS SCIENCE-MATERIALS IN ELECTRONICS · 2018 ·Vol. 29 ·期 10 ·8636-8648 · IF 2.324

CuCo2S4 nanotubes on carbon fiber papers for high-performance all-solid-state asymmetric supercapacitors

Yuan Xiaofang,Tang Bin,Sui Yanwei,Huang Saifang,Qi Jiqiu,Pu Yuguang,Wei Fuxiang,He Yezeng,Meng Qingkun,Cao Peng

In this study, CuCo 2 S 4 directly grown on carbon fiber papers (CFP) were prepared by a low-cost hydrothermal method. We also studied the influence of two different sulfur sources on the morphology and performance of CuCo 2 S 4 . Compared to TAA as sulfur source, the performance and morphology of CuCo 2 S 4 by Na 2 S·9H 2 O are better. The CuCo 2 S 4 –Na 2 S nanotubes possess irregular diameters from 100 to 200 nm. An electrode made of the synthesized CuCo 2 S 4 –Na 2 S nanotubes/CFP composite exhibits a maximum specific capacitance of 456 F g −1 at 1 A g −1 and 83% of capacitance retention after 5000 cycles at 5 A g −1 . The synthesized CuCo 2 S 4 –Na 2 S/CFP is used to construct an all-solid-state asymmetric supercapacitor (ASC) as the positive electrode, while and the negative electrode is made of a Fe 2 O 3 /reduced graphene oxide (rGO) composite on Ni foam. This asymmetric device has delivered an energy density of 50 W h kg −1 and a power density of 700 W kg −1 at an operating voltage of 1.5 V. It retains a long cycling life—78.2% capacity retention ratio after 5000 cycles. This work demonstrates the feasibility of the CuCo 2 S 4 –Na 2 S nanotubes in the applications of high-performance supercapacitors.

研究领域: 材料科学 · 能源存储技术
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Cell Reports Physical Science · 2023 · IF 8.9

Point-of-care nucleic acid testing with a one-step branched-DNA-based functional carbon biosensor

Xueqi Wang,Kai Sun,Han Wang

Nucleic acid biomarkers play important roles in early diagnosis, routine management, and prognosis of diseases. However, current nucleic acid testing (NAT) approaches either require cumbersome instruments or lack sensitivity for short detection time, making point-of-care (POC) NAT challenging. Here, we report an ultrasensitive carbon fiber paper (CFP)-based electrochemical biosensor with one-step branched DNA (bDNA)-based molecular signal amplification system for rapid, sensitive, and low-cost replication-free NAT. For nucleic acid quantification, the proposed biosensor exhibits a wide linear range of 10 aM–1 μM and a low limit of detection (LOD) of 1.4 aM. For fast semi-quantitative detection, the biosensor can evaluate the concentration of nucleic acids within 10 min with a threshold as low as 1 fM. Furthermore, the biosensor demonstrates negligible batch-to-batch variation with a relative standard deviation (RSD) of 4.25% at the cost of less than $1/device. The present one-step bDNA-based electrochemical biosensor serves as a promising and universal method for rapid, sensitive, and portable NAT.

研究领域: 生物医学工程 · 分子诊断学
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CERAMICS INTERNATIONAL · 2024 · IF 5.1

Multifunctional Ti3C2Tx/Fe3O4/glass fiber paper composites for flexible microwave absorption materials with ultralow filling ratio

Ao Zhang,Wei Wang,Ruopeng Cui,An Du,Jinsheng Jia,Yonggang Huang,Chunlei Wan,Ruina Ma

The preparation of multifunctional microwave absorbing materials with the characteristics of stronger absorption, wider bandwidth, lighter weight, higher strength and thinner thickness is an urgent research direction. Due to the difficulty of controllable distribution of absorbers, excellent microwave absorption performance is usually accompanied by large absorber amount and thickness, which can result in microwave absorption composite materials lack flexibility, mechanical properties, and adaptability to the environment. In this study, Ti 3 C 2 T x /Fe 3 O 4 /glass fiber paper composite was prepared by vacuum-assisted filtration. The controllable pore structure constructed by glass fiber enables uniform distribution of MXene/Fe 3 O 4 and effectively spreading of MXene monolayer film, enhancing conductivity loss and interface loss. By controlling the diameter of glass fiber, the pore size and the distribution of absorber can be regulated, thereby achieving a minimum reflection loss of up to −57.2 dB at an ultra-low filling ratio of 1.66 wt%. With the addition amount of 1.90 wt%, the effective absorption bandwidth can cover the whole X-band. The ultra-low specific reflection loss exceeds most of fabric materials and MXene-based absorbers. Meanwhile, the composite material exhibited excellent mechanical properties with a tensile strength of 3.054 kN/m and a burst resistance of 290 kPa. In addition, the adhesion between the filler and the glass fiber was increased by adding acrylic resin-based aqueous adhesive, and the surface grafting functional group (-F) made the composite material superhydrophobic. This work provides a new strategy to synthesize multifunctional absorbing material with low filling ratio and strong environmental practicality.

研究领域: 材料科学 · 电磁学
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ACS Sustainable Chemistry & Engineering · 2018 · IF 6.14

Self-Supported NiSe2 Nanowire Arrays on Carbon Fiber Paper as Efficient and Stable Electrode for Hydrogen Evolution Reaction

Yajie Guo,Dong Guo,Feng Ye,Ke Wang,Zhongqi Shi,Xianjue Chen,Chuan Zhao

NiSe2 nanowire (NW) arrays grown on flexible carbon fiber paper (CFP) were synthesized, for the first time, through a novel thermal selenization method in vacuum instead of flowing inert gas. The ultrathin NiSe2 NWs uniformly cover the CFP, contributing to the large surface area and fast charge transportation. Desirably, this binder-free and hierarchical electrode shows favorable activity for hydrogen evolution reaction (HER). It only requires an overpotential of 172 mV to afford the current density of 100 mA cm–2 in 0.5 M H2SO4, corresponding to a low Tafel slope of 32.44 mV dec–1. After 1000 continuous cycles, the HER activity of NiSe2 NWs is well-maintained. Moreover, the current density remains unchanged in prolonged electrolysis, indicating an excellent durability of NiSe2 NWs. The novel preparation method described in this study could inspire future work on the synthesis of transition-metal dichalcogenides with high purity and ultrasmall nanostructure toward improved electrocatalytic activity.

研究领域: 材料科学 · 电化学
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ELECTROCHIMICA ACTA · 2016 · IF 4.803

Self-grown MnO2 nanosheets on carbon fiber paper as high-performance supercapacitors electrodes

Wenhui Dang,Chengjun Dong,Zhifang Zhang,Gang Chen,Yude Wang,Hongtao Guan

MnO 2 was self-grown on carbon fiber paper (CFP) via a facile redox reaction , which is constructed by interconnected ultrathin nanosheets array. The CFP acts as both a supporting scaffold and a reducing agent for MnO 2 growth. The obtained MnO 2 /CFP composite was directly used as electrodes for supercapacitors , delivering a high specific capacitance of 713.7   F/g (0.5   A/g). Cyclic stability testing of the MnO 2 /CFP electrode reveals 86.8% retention in specific capacitance after 1200 cycles at 5.0   A/g. The nanosheet morphology of the MnO 2 on CFP brings about more efficient electroactive sites and facilitates the electrolyte penetration, allowing greater access for ions to active reaction sites. Hence, the attractive electrochemical performances exhibited by this MnO 2 /CFP electrode endow them potentially promising candidates for supercapacitors.

研究领域: 材料科学 · 能源存储
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ACS Sensors · 2019 · IF 6.944

Surface Engineering of Carbon Fiber Paper toward Exceptionally High-Performance and Stable Electrochemical Nitrite Sensing

Wenxin Zhu,Yi Zhang,Jiandong Gong,Yiyue Ma,Jing Sun,Tao Li,Jianlong Wang

In this work, we introduce our recent finding that the carbon fiber paper (CFP) treated by simple air annealing (OCFP) could be used for exceptionally high-performance electrochemical nitrite sensing. The air-annealing process endows the pristine CFP with higher defective edge/plane sites, more oxygen-containing functional groups, higher roughness, and improved wettability. The electrochemical studies show that the OCFP exhibits excellent sensing performance for nitrite, with an ultralow determination limit of 0.1 μM and a detection limit of 0.07 μM, an ultrawide linear determination range of 0.1–3838.5 μM, a fast current response of 1 s, and a high sensitivity of 930.4 μA mM–1 cm–2. These performance values are comparable or even superior to those for most reported noble- or transition-metal-based advanced nitrite sensors. Besides, this electrode also presents satisfactory stability, reproducibility, and feasibility of nitrite sensing in food samples. As an ideal monolithic and metal-free catalyst with ultrahigh and stable detection performance, the OCFP has a high potential to be integrated into next-generation electrochemical sensing devices.

研究领域: 材料科学 · 分析化学 · 环境科学
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JOURNAL OF POWER SOURCES · 2017 · IF 6.395

Mace-like hierarchical MoS2/NiCo2S4 composites supported by carbon fiber paper: An efficient electrocatalyst for the hydrogen evolution reaction

Lan Sun,Tao Wang,Long Zhang,Yunjin Sun,Kewei Xu,Zhengfei Dai,Fei Ma

The rational design and preparation of earth-abundant, stable and efficient electrocatalysts for hydrogen production is currently the subject in extensive scientific and technological researches toward the future of a clean-energy society. Herein, a mace-like MoS 2 /NiCo 2 S 4 hierarchical structure is designed and synthesized on carbon fiber paper via a facile hydrothermal method , and evaluated as electrocatalyst for hydrogen evolution reaction . In the MoS 2 /NiCo 2 S 4 /carbon fiber paper hierarchical structures, MoS 2 nanosheets are dispersively distributed on the surface of NiCo 2 S 4 nanowires, which provides an enlarged surface area , abundant interfaces and catalytic active sites. As for hydrogen evolution reaction , such MoS 2 /NiCo 2 S 4 /carbon fiber paper heterostructures give rise to a hydrogen evolution reaction catalytic current density of 10 mA cm −2 with a lower overpotential of 139 mV and a smaller Tafel slope of 37 mV·dec −1 than those of MoS 2 /carbon fiber paper and NiCo 2 S 4 /carbon fiber paper counterparts, exhibiting a prominent electrocatalytic performance. Moreover, the electrocatalytic properties change little after 5000 CV cycles and continual electrolysis for 12 h without obvious decay, respectively, demonstrating high durability and stability. The excellent hydrogen evolution reaction performances endow the hierarchical configuration MoS 2 /NiCo 2 S 4 /carbon fiber paper with promising alternative in HER and other related renewable energy fields.

研究领域: 材料科学 · 能源化学
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CATALYSIS LETTERS · 2025 ·Vol. 155 ·期 2 ·1-12 · IF 2.4

Ceramic Fiber Paper-Based Manganese Oxides Catalyst for Room Temperature Formaldehyde Oxidation

Wang Xiuxiu,Zhao Jiawei,Zhao Chuanjun,Zhang Yexin,Mahmud Sakil,Zhang Jian

The catalytic removal of trace formaldehyde (HCHO) at ambient temperatures is crucial for improving indoor air quality, necessitating the use of monolithic catalysts over traditional powder forms for real-world applications. In this study, an aluminosilicate fiber-woven ceramic filter paper (CFP) was selected as the substrate, onto which a Mn 2 O 3 catalyst was in situ coated via a combustion method utilizing Mn(NO 3 ) 2 as the oxidant and glycine as the fuel. The resulting monolithic Mn 2 O 3 /CFP catalyst was compared to a MnO 2 /CFP catalyst, prepared by direct decomposition of Mn(NO 3 ) 2 on the same substrate. The Mn 2 O 3 /CFP catalyst exhibited superior characteristics for HCHO oxidation, including a more porous architecture, higher redox capability, and an abundance of surface-active oxygen species with enhanced mobility of surface lattice oxygen. These features enabled the Mn 2 O 3 /CFP catalyst to achieve significantly higher HCHO conversion at room temperature (90%) compared to the MnO 2 /CFP catalyst (21%). Additionally, in a durability test carried out in a mode of dynamic flow at room temperature, the Mn 2 O 3 /CFP catalyst maintained a high HCHO conversion rate of 66% over 11 days, demonstrating its potential for practical indoor air purification applications. Graphical abstract

CAS / MDL: 10377-66-9
研究领域: 环境科学 · 材料科学
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