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ChemistrySelect · 2024 ·Vol. 9 ·期 17 ·e202401101 · IF 1.9

Mining Metal-Biomolecular Framework/PANI Composite CO Sensor: Material Synthesis, Gas Sensing Performance and Mechanism

Xiangming Hu,Zhenyu Yang,Mingyue Wu,Yuntao Liang,Wei Wang,Fusheng Wang,Qian Zhang,Jingran Mao,Ning Yang,Xuwei Wang

Graphical This paper selectes MBioFs with copper ions as the metal center to design an MBioFs/PANI composite suitable for CO gas sensors. The morphology and nanostructure of the prepared materials were thoroughly analyzed, followed by testing their gas-sensing properties. Subsequently, the gas sensing mechanism of composite materials was proposed and discussed in detail. In addressing the issue of poor gas sensitivity in semiconductor CO sensor materials used in mining, such as pure PANI. This study utilized an ice-water bath in combination with an in-situ polymerization method to synthesize a new composite material consisting of Cu(II)-racemic glutamate nanofibers and PANI. The morphology, structure, and chemical bonds of the composite material were analyzed using scanning electron microscopy-energy dispersive spectroscopy (SEM-EDS) and spectral analysis. The material's ability to detect CO (100–500 ppm) at room temperature was investigated, revealing a response value of up to 6.8 % for 400 ppm CO detection when the composite material was deposited on a ceramic interdigital electrode. The material exhibited good selectivity and responsiveness to CO detection at room temperature, attributed to the heterojunction formed between Cu(II)-racemic glutamate nanofibers and PANI, which enhanced carrier migration. Consequently, the Cu(II)-racemic glutamate nanofiber/PANI composite(Cu(II)-RGlu/PANI) material shows promise as a high-performance sensing material for CO detection at room temperature and as a low-power, integrable sensor material for underground coal mines. This research contributes to the development of a theoretical framework for such applications.

研究领域: 材料科学 · 传感技术
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CHEMICAL PHYSICS LETTERS · 2025 · IF 3.1

Quartz sand@PDA/Co-Mn-ZIF as efficient peroxymonosulfate activator for enhanced degradation of tetracycline hydrochloride in aqueous solutions

Simin Li,Ziran Chang,Fengbing Tang,Tianshuo Sui,Lemin Li,Jingbo Mu,Zhennan Shi

The QS@PDA/Co-Mn-ZIF catalyst, synthesized using quartz sand as a base material, effectively degrades TCH through the activation of PMS. The Co-Mn-ZIF component activates PMS, while PDA ensures the adhesion of ZIF to quartz, facilitating catalyst recovery. This design enhances electron transport and metal ion redox reactions, generating reactive species that degrade TCH. It achieves a 94 % TCH removal rate from a 100 mg/L solution within 40 min, demonstrating stability under various pH and water conditions. The catalytic mechanism was elucidated·through radical trapping experiments and electron paramagnetic resonance analysis. QS@PDA/Co-Mn-ZIF shows great potential for treating recalcitrant and high-concentration organic wastewater.

CAS / MDL: 299-11-6 64-75-5
研究领域: 环境科学 · 催化化学
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INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES · 2024 · IF 7.7

Synergy of metallic Co and oxygen vacancy sites in Co/Ce-MOF catalysts for efficiently promoting lignin derived phenols and macromolecular lignin hydrodeoxygenation

Changzhou Chen,Jie Jiang,Yajun Liu,Xialin Ji,Mengqing Zhou,Jun Zhao,Jianchun Jiang

The enhanced utilization of biomass-derived chemicals for the generation of high value aromatics through an advanced catalytic strategy has captured considerable attention within the realm of eco-friendly manufacturing. This work presented four innovative three-dimensional rod-shaped mesoporous Ce-based MOF materials, which were coupled with a H-donor solvent to facilitate vanillin hydrodeoxygenation and macromolecular lignin. Under the optimized conditions (30 mg CoCe@C catalyst, 2 MPa N 2 pressure, 15 mL isopropanol, 190 °C, and 5 h), the CoCe@C catalyst achieved nearly complete conversion of vanillin and demonstrated 87.8 % selectivity in the hydrogen-donor solvent. The characterization findings suggested that the synergy between metallic Co and oxygen vacancy sites enabled the effective activation of CHO group in vanillin, leading to formation of reactive product MMP . In addition, the optimal CoCe@C catalyst could also achieve macromolecular lignin hydrodeoxygenation to obtain high yield of lignin oil products with narrower molecular weight distribution . This study presented a viable approach for the concurrent utilization of lignin derivatives in the generation of high value fuels and chemicals.

研究领域: 化学工程 · 生物质能利用 · 催化科学
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ACS Omega · 2019 · IF 2.584

Ambient Temperature NO Adsorber Derived from Pyrolysis of Co-MOF(ZIF-67)

Bo Lin,Aiyong Wang,Yanglong Guo,Yuanqing Ding,Yun Guo,Li Wang,Wangcheng Zhan,Feng Gao

Co-, Ni-, and Zn-containing MOFs are prepared and then pyrolyzed to generate materials for ambient temperature NO adsorption. Materials containing Co are much more efficient for NO adsorption than those containing Ni and Zn; therefore, Co is identified as the active phase. The best performing material studied here achieves 100% low concentration (10 ppm) NO adsorption for more than 15 h under a weight hourly space velocity of 120 000 mL g–1 h–1. Powder X-ray diffraction, X-ray photoelectron spectroscopy, Fourier transform infrared, and Raman spectroscopies, along with scanning electron microscopy and TEM, are used to probe the physicochemical properties of the materials, particularly the Co active phase, and chemistries involved in NO adsorption–desorption. NO adsorbs on oxygen-covered Co nanoparticle surfaces in the form of nitrates and desorbs as NO at higher temperatures as a result of surface nitrate decomposition. NO storage capacity decreases gradually upon repeated NO adsorption–desorption cycles, likely because of Co3O4 formation during these processes.

研究领域: 材料科学 · 环境科学 · 化学工程
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NEW JOURNAL OF CHEMISTRY · 2025 · IF 2.5

Degradation of methylene blue by ozone oxidation activated by N and S co-doped biochar supported Co–Al layered double hydroxides

Danli Tang,Dengjie Zhong,Yongxian Zhou,Yunlan Xu,Tanxia Xiang,Wantao Li,Yuanfang Yang,Chunmiao Fan,Jisai Chen

Dye pollution has caused great harm to the ecological environment. In this paper, N and S co-doped biochar (K-NSBC) was obtained by a calcination–alkali activation method, then Co/Al layered double hydroxide (Co/Al-LDH) was anchored on it by a co-precipitation method to activate ozone (O3) to degrade methylene blue (MB). When the O3 concentration was 3.12 mg L−1, catalyst dosage was 0.6 g L−1, the MB concentration was 25 mg L−1, and pH was 6.8, the degradation efficiency of MB reached 99.65%. The degradation efficiency still remained at 92.75% even after Co/Al-LDH@K-NSBC was recycled five times. The results of material characterization and quenching experiments show that the presence of oxygen vacancies (Ov) on the metal surface not only accelerates the exchange of oxygen and the generation of active free radicals, but also promotes the conversion of Co3+/Co2+ and the activation of O3. Pyridine N, graphite N and thiophene S provide electron-rich groups, which promote the activation of O3 to produce reactive oxygen species (ROS). Among them, 1O2 is the main ROS leading to the degradation of MB, and its intermediates ˙OH and ˙O2− also participate in the oxidation of MB. This study is expected to provide new ideas and directions for the design of highly efficient and stable ozonation activators and industrialization of non-phase catalytic ozonation degradation of dye wastewater.

CAS / MDL: 75-65-0
研究领域: 环境科学 · 催化材料
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COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS · 2024 · IF 4.9

Polypyrrole nanoclips-coated Co/C nanostructures with enhanced microwave absorption

Huihuang Shen,Changdong Ju,Junjun Wang,Huabo Huang,Jiayou Ji,Liang Li

There is a challenge to boost the electromagnetic wave absorption performance of magnetic carbon-based materials by rationally adjusting the structure of MOF. In this paper, nanoclip-shaped polypyrrole (PPy) was wrapped on the surface of the Co/C nanoparticle derived from Co-MOF via in-situ polymerization of pyrrole with the help of cetylammonium bromide. The electromagnetic parameters of prepared Co/C@PPy can be easily tuned by adjusting the feed ratio of PPy to Co/C. The optimum value of reflection loss (RL) for Co/C@PPy is −45.49 dB at 2.4 mm and 15.12 GHz when the feed ratio of pyrrole to Co/C is 200 μL to 80 mg, and the effective absorption bandwidth (EAB, RL ≤ −10 dB) reaches 5.97 GHz (11.76–17.73 GHz) at the matching thickness of 2.5 mm. This study paves the way for further design and preparation of the nanocomposites based on MOF-derived nanostructures with excellent EMW absorption performance.

研究领域: 材料科学 · 电磁学
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RSC Advances · 2014 ·Vol. 5 ·期 12 ·9130-9137 · IF 3.708

Au/CuO nanosheets composite for glucose sensor and CO oxidation

Jiahuan Lei,Yu Liu,Xinyu Wang,Pan Hu,Xinsheng Peng

Au nanoparticles/mesoporous CuO nanosheets were successfully synthesized by the assembly of negatively charged AuCl4−1 and positively charged CuO nanosheets using sodium citrate and thermal reduction, respectively. The structure and morphology were characterized in detail. Both the loading amount of Au nanoparticles and the performance were controlled by the reduction process. The resulting Au/CuO NSs exhibited good catalytic activity for CO oxidation and good non-enzymatic sensitivity for glucose.

CAS / MDL: 38260-01-4
研究领域: 材料科学 · 化学 · 生物传感 · 催化反应
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JOURNAL OF ELECTROANALYTICAL CHEMISTRY · 2023 · IF 4.5

Modificationally doped Se element and in-situ doped V element to elevate the supercapacitor performance of Co-MOF

Guiquan Liu,Shiyu Li,Rumisa Baikeri,Guorong Wang,Zhiliang Jin

Metal-organic skeleton (MOF) with adjustable pore skeleton and finely reaction sites has been widely accepted in the application of high-performance supercapacitors. Here, the Se-Co-MOF-1 nano-particles obtained by modified doped Se element to Co-MOF and the CoV 3 -MOF nano-sheets obtained by in-situ doped V element in Co-MOF. As a result, Se-Co-MOF-1 and CoV 3 -MOF electrode materials have more electrochemical reactivity, better conductivity and better stability. At a certain current density, Se-Co-MOF-1 and CoV 3 -MOF electrode materials have better mass-specific capacitance and better rate performance than Co-MOF. Furthermore, the Se-Co-MOF-1//AC ASC and CoV 3 -MOF//AC ASC are also assembled, which show relatively excellent power density and energy density compared to similar work reported. The Se-Co-MOF-1//AC ASC and CoV 3 -MOF//AC ASC after 10,000 cycles, their mass-specific capacitance retention rate are still 70.00 %, which further shows the reliable stability of Se-Co-MOF-1 and CoV 3 -MOF electrode materials. This result proves that the synthetic schemes of MOF nano-sheets/nano-particles can be selected as the source of the strategy for preparing excellent electrode materials.

研究领域: 材料科学 · 电化学
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CHEMICAL ENGINEERING JOURNAL · 2023 · IF 15.1

Converting commercial MnO2 into Co-doped LiNi0.5Mn1.5O4 with adjustable disordered/ordered phase ratio by a quaternary molten salt

Yinyin Zhang,Fangzhong Liu,Ting Song,Yong Pei,Xianyou Wang,Xiongwei Wu,Manjun Xiao,Qi Deng,Bei Long

The electrochemical performances of LiNi 0.5 Mn 1.5 O 4 (LNMO) materials are strongly correlated with the ratio of disordered to ordered phases. Nevertheless, there are few reports on the adjustment of ordered and disordered phase ratio. In this paper, the ratio of ordered to disordered phases in LNMO is successfully adjusted by using a quaternary molten salt, which is proven by XRD refinement, FT-IR, and XPS. Reductive quaternary molten salt and Co doping are favorable for Ni/Mn cation disorder, leading to the increased disordered phase. LNMO with an appropriate ratio of ordered to disordered phases can exhibit enhanced electronic/ionic transfer rate and structural stability, revealed by electrochemical tests and ex situ characterizations. Therefore, the optimized material delivers a reversible capacity of 121 mA h g −1 at 20 mA g −1 and a long cyclic life with 61 mA h g −1 at 1000 mA g −1 over 1200 cycles. The present work offers a new idea for achieving a regulated ratio of ordered to disordered phases in LNMO.

研究领域: 材料科学 · 电化学
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NEW JOURNAL OF CHEMISTRY · 2024 · IF 2.7

Design of Fe/Co-N doped porous carbon sheets by hard template strategy as an oxygen reduction catalyst for Mg-air batteries

Kun Liu,Yujing Ling,Xianglong Guan,Ke Hu,Angli Zhang,Kaiqi Liu,Haoyi Li,Guangnian Xu,Xu-Cheng Fu

The commercialization of magnesia-air batteries (Mg-air) necessitates the development of highly efficient, cost-effective, and durable electrocatalysts for oxygen reduction reaction (ORR), replacing expensive and unstable precious metal electrocatalysts. A hard template-assisted synthesis of FeCo nanoparticles immobilized on N-doped porous carbon (Fe-Co-C-N) for the ORR is reported. The half-wave potential of Fe-Co-C-N for ORR (E1/2=0.88 V vs. RHE) is elevated by 40 mV compared to that of 20 wt% Pt/C (E1/2=0.84 vs. RHE). The catalyst exhibits exceptional catalytic performance and remarkable stability. The discharge voltage of the Mg-air battery, utilizing Fe-Co-C-N as the cathode catalyst (1.29 V), surpasses that of the battery employing 20 wt% Pt/C as the cathode catalyst (1.28 V). The Mg-air battery with Fe-Co-C-N as the cathode catalyst exhibited excellent discharge stability and maintained a stable discharge for over 200 hours. The present study offers valuable insights into the structural design and regulatory mechanisms governing the performance of M-N-C catalysts in Mg-air batteries.

CAS / MDL: 7647-14-5
研究领域: 材料科学 · 电化学 · 能源存储
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CHEMICAL ENGINEERING JOURNAL · 2025 · IF 13.2

Co(II) sites embedded within Beta zeolite as efficient catalyst for propane dehydrogenation

Zhikang Xu,Yunxing Zhang,Xing Wu,Haibo Zhu

Co-based catalysts are emerging as one of the most promising catalysts for propane dehydrogenation (PDH) due to their abundant availability, environmental friendliness, and efficient activation of the C–H bond. Isolated Co(II) is recognized as the active site for activating the C–H bond in PDH; however, the controllable synthesis of Co catalysts with well-defined isolated Co(II) remains a challenge. In this study, a direct and straightforward route was developed for the synthesis of Co-Beta using a fluorine-assisted hydrothermal crystallization method. The structure of Co-Beta was studied using various characterization tools, including XRD, STEM, H 2 -TPR, UV–vis, XPS, solid-state 29 Si MAS NMR and EXAFS techniques. It was confirmed that the Co species are incorporated into the structure of Beta zeolite, existing as isolated Co(II) sites embedded within the framework of Beta zeolite. The optimized catalyst, 1.0Co-Beta, exhibits excellent performance in PDH, achieving a propane conversion of approximately 50 % and propylene selectivity of around 96 % at 600 °C. This performance surpasses that of previously reported non-noble metal catalysts. This study provides fundamental insights on the design and synthesis of highly dispersed metal oxide catalysts for PDH.

研究领域: 催化化学 · 材料科学
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JOURNAL OF APPLIED ELECTROCHEMISTRY · 2016 ·Vol. 47 ·期 3 ·361-367 · IF 2.223

Co–Fe–Se ultrathin nanosheet-fabricated microspheres for efficient electrocatalysis of hydrogen evolution

Xiao Mingshu,Zhang Zhonghui,Tian Yanping,Miao Yuqing,Wang Jiahai

Abstract In this work, the synthesis of Co–Fe–Se ultrathin nanosheet-fabricated microspheres was reported for the first time as electrocatalysts toward hydrogen evolution reaction (HER). The Co–Fe–Se ternary compounds exhibited high electrocatalytic activity of HER with low onset potential in acid media due to the high specific surface area of Co–Fe–Se ultrathin nanosheet-fabricated microspheres. The presence of multiwall carbon nanotubes improved the immobilization effect of Co–Fe–Se catalysts and electron transfer between catalysts and electrode surface, leading to the improved stability and HER electrocatalysis. The non-noble metal-based ternary compounds of Co–Fe–Se obtained from earth-abundant elements may enlighten a new way of exploring cost-effective catalysts for HER to develop hydrogen energy. Graphical Abstract

研究领域: 材料科学 · 电化学
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