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Co(OH)F
CHEMICAL ENGINEERING JOURNAL · 2024 · IF 13.3

Highly sensitive toluene sensor based on silver Ear-Like F-doped Co3O4 templated from Co(OH)F Guided by SiO2 nanospheres

Zhijia Liao,Ninghao Chu,Zhenyu Yuan,Yanbai Shen,Fanli Meng

This study successfully synthesized “silver ear-like” Co(OH)F using 15 nm SiO 2 spheres as seeds. Gas sensitivity of Co(OH)F with and without SiO 2 spheres to toluene was compared at different annealing temperatures. The results demonstrate that the Co(OH)F-Si-350 sensor exhibits optimal gas sensitivity to toluene, with a response of 35 (R g /R a ) to 100 ppm of toluene at 220℃, with response and recovery times of 50 s and 80 s, respectively. Notably, the sensor detected toluene concentrations as low as 50 ppb, indicating good sensitivity to low concentrations. These findings suggest that the structural transformation resulting from the introduction of SiO 2 nanospheres, forming ultra-thin nanosheet clusters (∼12 nm), provides abundant active sites, effectively promoting substance diffusion and adsorption/desorption processes. Additionally, the incorporation of fluorine enhances the Lewis acidity of the material, facilitating the formation of stable adsorption states for gas molecules on the surface. These results reveal the significant impact of the structural transformation caused by the introduction of SiO 2 nanospheres on gas sensitivity, providing a strong theoretical foundation for further optimizing gas sensor design.

CAS / MDL: 10026-22-9
研究领域: 材料科学 · 传感器技术 · 化学工程
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CHEMICAL ENGINEERING JOURNAL · 2022 · IF 16.744

Highly-ordered arrangement of Co(OH)F filaments: Planting flower-like Co(OH)F in conductive membrane substrate accelerating Li+ transfer and redox reaction in Li–S batteries

Guocui Cai,Helong Jiang,Fangyi Chu,Xiangcun Li,Xiaobin Jiang,Xiao Wu,Gaohong He,Yan Dai

Here, the conventionally disordered Co(OH)F filaments are rearranged to form highly-ordered flower-like Co(OH)F architectures in a conductive membrane substrate. The important findings contribute to designing delicate nanostructures and improving the catalytic activity of advanced materials for energy applications. The hierarchically porous CNT@NC membrane with CNT as the core and N -doped carbon as the crosslinking shell is scalably designed firstly for strengthening the transport of Li + and electrons in the electrode, providing an ultrahigh porosity for growing flower-like Co(OH)F on both surfaces and interior of the membrane, as well as offering electrons for the redox reactions through the roots of the Co(OH)F flowers. Furthermore, the ordered Co(OH)F bundles with divergent and open-ended structures provide the catalyst with the broad reaction interface and active sites for polysulfides (LiPSs) anchoring and catalytic conversion at a low energy barrier, significantly facilitating the diffusion of ions and electrolyte in the catalyst, and thus effectively alleviating the shuttle effect. Owing to the synergistic effect between the conductive membrane substrate and the grown Co(OH)F catalyst, the Co(OH)F-CNT@NC cathode generates a high reversible capacity and excellent long-term cycling performance (622 mAh·g −1 at 1C after 600 cycles). Conclusively, the proposed facile strategy provides insights regarding the design of novel cathode materials for high-areal-capacity Li–S batteries.

研究领域: 材料科学 · 储能 · 纳米技术 · 电化学 · 电池技术
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CRYSTENGCOMM · 2022 ·Vol. 24 ·期 34 ·6018-6030 · IF 3.756

Hierarchical Co(OH)F/CoFe-LDH heterojunction enabling high-performance overall water-splitting

Mingliang Qin,Yamei Wang,Huaming Zhang,Muhammad Humayun,Xuefei Xu,Yanjun Fu,Marsil K. Kadirov,Chundong Wang

Due to the serious energy and environmental issues, hydrogen generation via water splitting has been regarded as a green and promising alternative strategy to the use of fossil fuels. Developing highly efficient and non-noble metal based dual-functional electrocatalysts for overall water splitting to generate hydrogen and oxygen has become more critical. In order to fulfill the requirements of efficient hydrogen evolution reaction (HER) and oxygen evolution reaction (OER), herein, we report novel hierarchical Co(OH)F@CoFe-LDH heterostructured nanorod arrays fabricated via a facile two-step approach. The resultant Co(OH)F@CoFe-LDH displays exceptional electrocatalytic OER and HER activity with a small overpotential of 240 mV and 130 mV at 10 mA cm−2, respectively. Further, the electrocatalyst revealed excellent long-term stability during a recyclability test for 37 h. The superior performance of Co(OH)F@CoFe-LDH can be attributed to the synergistic effect at the interface of the Co(OH)F nanorods and the covered CoFe-LDH nanosheets. Meanwhile, Co(OH)F@CoFe-LDH as a water electrolyzer to produce a current density of 10 mA cm−2 requires a small voltage of 1.58 V. This work paves the way for the design and construction of low cost and highly efficient 3D hierarchical electrodes for practical applications in electrocatalysis.

CAS / MDL: 12036-10-1
研究领域: 材料科学 · 能源化学
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CHEMICAL ENGINEERING JOURNAL · 2023 · IF 15.1

Synthesis of Co(OH)F@Al nanobelt array on various substrates for pyro-MEMS

Yuxiang Li,Xi Chen,Lei Zhang,Ruishan Han,Iftikhar Hussain,Xiaoxia Ma,Kaili Zhang

Metastable intermolecular composites (MICs) composed by solid fuel and oxidizer can undergo violent redox reaction with release of huge amount of energy. Integration of MIC with microelectromechanical-system (MEMS) is of particular interest to meet the demand of miniaturization in modern pyrotechnic devices. Meanwhile, fluorine-containing oxidizers are favored in MIC owing to their potential to fluorinate the oxide passivation layer in common elemental fuels. Herein, Co(OH)F was employed for the first time as a novel fluorine-containing oxidizer in Al-based MIC. Vertically aligned Co(OH)F@Al nanobelt arrays (NAs) with tunable morphology were successfully fabricated on a variety of substrates (Si, glass, Ni, Cu, Ti) via a facile hydrothermal synthesis followed by electron beam evaporation. The whole fabrication process is highly compatible with modern MEMS technology. The thermal behavior of pure Co(OH)F and Co(OH)F@Al composites was comprehensively investigated by TG-DSC and a series of ex-situ and in-situ characterization. It was found that, Co(OH)F@Al composites achieved main exothermal reaction before melting of Al regardless of morphology and equivalence ratio. This feature is attributed to the etching of Al 2 O 3 shell by HF released from Co(OH)F which is termed as pre-ignition reaction. To elucidate the effect of micro-structure on the actual specific heat release, we proposed a phenomenological model which can be a reference for future micro-structure design of MIC.

CAS / MDL: 12125-01-8 10026-22-9
研究领域: 材料科学 · 化学工程
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MOLECULES · 2025 ·Vol. 30 ·期 17 ·3529 · IF 4.6

Fluoride-Mediated Synthesis of Co(OH)F and Electronic Structure Optimization for Enhanced Water Oxidation Performance

Qianqian Dong,Yuhao Li,Jihao Liu,Yaru Wen,Junjie Wang,Haining Mo,Qianqian Jin,Shaohui Zhang,Xiong He

This study deciphers the anionic modulation mechanism of halide ions (F−/Cl−) in cobalt-based hydroxides for oxygen evolution reaction (OER). Phase-pure Co(OH)2, Co(OH)F, and Co2(OH)3Cl were fabricated via substrate-independent hydrothermal synthesis to eliminate conductive support interference. Electrocatalytic evaluation on glassy carbon electrodes demonstrates fluoride’s superior regulatory capability over chloride. X-ray photoelectron spectroscopy (XPS) analyses revealed that F−incorporation induces charge redistribution through Co → F electron transfer, optimizing the electronic configuration via ligand effects. F−incorporation simultaneously guided the anisotropic growth of 1D nanorods and reduced surface energy, thereby enhancing the wettability of Co(OH)F. The engineered Co(OH)F catalyst delivers exceptional OER performance: 318 mV overpotential at 10 mA/cm2in 1 M KOH with 94% current retention over 20 h operation. This study provides a synthetic strategy for preparing pure-phase Co(OH)F and compares halide ions’ effects on enhancing OER activity through electronic structure modulation and morphological control of basic cobalt salts.

CAS / MDL: 1310-58-3 7447-40-7
研究领域: 材料科学 · 电化学 · 催化 · 无机化学 · 纳米技术
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Nanomaterials · 2024 ·Vol. 14 ·期 7 ·573 · IF 4.4

MOF-Mediated Construction of NiCoMn-LDH Nanoflakes Assembled Co(OH)F Nanorods for Improved Supercapacitive Performance

Zhou Wang,Yijie Lian,Xinde Zhu,Qi Wang

The application of transition metal hydroxides has long been plagued by its poor conductivity and stability as well as severe aggregation tendency. In this paper, a novel hierarchical core–shell architecture, using an F-doped Co(OH)2nanorod array (Co(OH)F) as the core and Mn/Ni co-doped Co(OH)2nanosheets (NiCoMn-LDH) as the shell, was constructed via an MOF-mediated in situ generation method. The obtained Co(OH)F@ NiCoMn-LDH composites exhibited excellent supercapacitive performance with large specific capacitance as well as improved rate capability and long-term stability. The effect of the Ni/Mn ratio on the supercapacitive performance and energy storage kinetics was systematically investigated and the related mechanism was revealed.

研究领域: 材料科学 · 能源存储与转换
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Journal of Energy Storage · 2025 · IF 9.8

A self-supporting Co(OH)F nanosquares with ion and electron conductive structure for high performance electrochemical energy storage

Shakeel Ahmad,Muhammad Tariq,Umar Farooq,Henmei Ni,Afaq Ullah Khan,Zainab M. Almarhoon,Abdulaziz A. Alanazi,Talal M. Althagafi,Kamran Tahir,Sameerah I. Al-Saeedi

The integration of Cobalt hydroxide fluoride Co( OH )F-based materials is expected to significantly enhance the electrochemical performance of supercapacitor electrodes. In this work, Co( OH )F with various morphologies was synthesized using a simple hydrothermal method and evaluated as an electrode material for supercapacitors. The porous nano square-like morphology exhibited excellent durability in electrochemical reactions, providing abundant active sites. Furthermore, the highly electronegative fluorine atom contributes to fast ion diffusion to electrode surface and reduces intrinsic resistance during the reaction, leading to remarkable electrochemical performance. Remarkably, the optimized Co( OH )F 450 exhibited an ultrahigh specific capacitance of 558 F g −1 at a current density of 1 A g −1 , which is greater than that of Co( OH )F 300 , and Co( OH )F 150 electrodes. Furthermore, the device delivered outstanding cyclic performance, maintaining 80 % capacitance retention after 10,000 charge-discharge cycles. Finally, the Co( OH )F 450 electrode demonstrates a promising energy density of 27 Wh kg −1 at a power density of 2571 W kg −1 . Above results suggest that Co( OH )F 450 electrode could pave way for the development of high-performance electrodes in the field of energy storage.

研究领域: 材料科学 · 能源存储
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COMBUSTION AND FLAME · 2023 · IF 4.4

Fabrication and reaction mechanism study of Co(OH)F@Al nanowire arrays: A functional fluorine-containing metastable intermolecular composite

Yuxiang Li,Kaili Zhang

Metastable intermolecular composites (MICs) comprising solid fuels and oxidizers at nano-scale exhibit high energy densities and fast reaction speeds. As most metal and metalloid fuels are passivated by the natural oxide layer on the surface which acts as a reaction barrier, fluorine-containing oxidizers are of particular interest to promote the reactivity through interfacial fluoridation. In this work, cobalt hydroxy fluoride (Co(OH)F) was introduced as a functional fluorine-containing oxidizer, and core-shell structured Co(OH)F@Al nanoarray was fabricated onto a glass substrate . The thermal behavior and reaction mechanism of pure Co(OH)F and Co(OH)F@Al composites were thoroughly investigated, and Co(OH)F@Al was compared with CoO@Al and Co 3 O 4 @Al with identical morphology. In the Co(OH)F@Al composite, a pre-ignition reaction was observed which was attributed to the etching of Al 2 O 3 shell by HF and the fluoridation of Al core by HF and CoF 2 . With the assistance of pre-ignition reaction, Co(OH)F@Al can complete main exothermal reaction before Al melting in a solid-state mechanism, and its peak temperature is around 200 ℃ lower than those of MICs employing CoO and Co 3 O 4 as oxidizers.

CAS / MDL: 12125-01-8
研究领域: 材料科学 · 化学工程
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ChemNanoMat · 2022 ·Vol. 8 ·期 6 ·e202200085 · IF 3.82

Electrodeposition of Amorphous Fe−P Shell on Co(OH)F Nanowire Arrays for Boosting Oxygen Evolution Electrocatalysis in Alkaline Media

Yang Gu,Chuqian Meng,Shuyue Dong,Hexin Zhu,Qian Liu,Yonglan Luo,Qingquan Kong,Tingshuai Li

High-performance earth-abundant electrocatalysts for oxygen evolution reaction (OER) are highly desirable. In this report, we successfully synthesized amorphous Fe−P shell electrodeposited on Co(OH)F nanowire arrays supported on titanium mesh (Fe−P@Co(OH)F/TM) as an efficient catalyst for OER. Such catalyst exhibits excellent OER activity with a low overpotential of 267 mV to reach the geometrical current density of 10 mA cm −2 in 1.0 M KOH. In addition, it has good electrochemical durability to maintain its activity for at least 20 h.

研究领域: 材料科学 · 电化学
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SENSORS AND ACTUATORS B-CHEMICAL · 2023 · IF 8.4

Porous rod-like Co(OH)F/Co3O4 heterojunction-based acetic anhydride gas sensor with high response and low operating temperature

Zhijia Liao,Zhenyu Yuan,Hongliang Gao,Fanli Meng

In response to the pressing demand for acetic anhydride gas detection, this study introduces a novel gas sensor for precisely detecting acetic anhydride concentrations. The optimum conditions for the synthesis of cobalt hydroxyfluoride/cobalt oxide (CHFCO) heterojunctions with good acetic anhydride gas sensitivity were determined by carefully adjusting the calcination time, hydrothermal time and ammonium fluoride content. The best performing composite CHFCO sensor with porous rod particles was tested at 180 ℃ and achieved a response rate of 260 for 100 ppm acetic anhydride gas, with response and recovery times of 60 and 40 s, respectively. In comparison to other prepared sensors, the detection response for acetic anhydride was improved by a factor of 4.30–23.63. Moreover, the CHFCO sensor reliably detected acetic anhydride at a concentration of 500 ppb, exhibiting a response value of 1.56. Notably, the sensor demonstrated great selectivity, moisture resistance , and stability. The findings highlight the significant enhancements in gas-sensitive performance to acetic anhydride achieved by the abundant hydroxyl bonds on the surface of CHFCO heterojunction, the presence of fluorine ions , and the modulation of the band gap. These results provide valuable insights for the advancement of acetic anhydride gas sensors based on CHFCO heterojunction.

CAS / MDL: 10026-22-9
研究领域: 材料科学 · 化学工程
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