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Journal of Energy Storage · 2024 · IF 8.9

High-performance biomass tar-based nanofibers with CoNi nanosheets prepared by electrospinning for supercapacitor electrode material

Haifeng Jiang,Mingfu Yao,Jiaxin Wang,Wenpeng Hong

Biomass-based nanofibers prepared by electrospinning have broad prospects in the field of supercapacitors. In this work, biomass tar-based carbon nanofibers (CNFs) are prepared by electrospinning technology, and the CoNi nanosheets are grown on the surface of CNFs. The obtained electrode materials have a three-dimensional open petal-like nanofiber structure, and the results of the electrochemical performances show that the CoNi@CNF-1 has a specific capacitance of 474.4F g −1 at 0.5 A g −1 , an energy density of 65.9 Wh kg −1 and a power density of 250 W kg −1 . After 5000 charge-discharge cycles, the CoNi@CNF-1 still maintains 95.4 % of its original capacitance in the three-electrode system. This work provides an important reference for the effective treatment of biomass tar and its application in the field of electrochemical energy storage.

研究领域: 材料科学 · 能源存储 · 环境工程
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JOURNAL OF ALLOYS AND COMPOUNDS · 2019 · IF 4.175

Enhanced microwave absorption performance of porous and hollow CoNi@C microspheres with controlled component and morphology

Yang Liu,Zhuo Chen,Wenhan Xie,Feng Qiu,Yang Zhang,Shaokun Song,Chuanxi Xiong,Lijie Dong

Microwave absorbers with broadband absorption and lightweight features are highly desirable in electromagnetic interference and pollution treatment. Here, porous and hollow CoNi@C (CNC) microspheres derived from metal-organic frameworks (MOFs) are fabricated by a facile solvothermal route and subsequent annealing process. The morphology, structure, microwave absorption properties and their internal relationship are systematically investigated. For the porous and hollow CNC microspheres, the minimum RL can reach −44.8 dB at 10.7 GHz and the ultra-wide effective absorption bandwidth can reach up to 13.3 GHz (4.7–18.0 GHz) within the thickness of 1.6–4.0 mm. The CNC microspheres exhibit superior microwave absorption performance, attributing to the improved impedance matching and attenuation ability. The hollow structure, interfacial polarization, the synergistic effect between CoNi alloy and graphitized carbon simultaneously account for the microwave absorption mechanisms. Therefore, the present work provides the promising options on the design and preparation of lightweight and high-efficient microwave absorber with tunable component and specific morphology.

研究领域: 材料科学 · 电磁学
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DALTON TRANSACTIONS · 2019 ·Vol. 48 ·期 47 ·17499-17506 · IF 4.052

Superfine CoNi alloy embedded in Al2O3 nanosheets for efficient tandem catalytic reduction of nitroaromatic compounds by ammonia borane

Sihang Cheng,Yanchun Liu,Yingnan Zhao,Xinyu Zhao,Zhongling Lang,Huaqiao Tan,Tianyu Qiu,Yonghui Wang

Aromatic amino compounds are important and universally used chemical intermediates in a wide range of industrial fields. Thus, their production with high efficiency and selectivity under ambient conditions is expected and demanded in modern industry. Herein, a series of superfine CoNi alloy nanoparticles embedded in Al2O3 nanosheet (CoxNi1−x/Al2O3, where x represents the content of Co in the precursor) catalysts was fabricated from CoNiAl-LDH and used to catalyze the tandem dehydrogenation of ammonia borane (AB) and hydrogenation of nitroaromatics to the corresponding amines. Systematic experiments indicate that the composition, size, morphology and catalytic performance of the CoxNi1−x/Al2O3 catalysts can be easily controlled by changing the content of Ni in the CoNiAl-LDH precursor. Particularly, Co0.67Ni0.33/Al2O3 exhibited the best tandem catalytic performance among the six samples. This as-prepared catalyst not only showed a moderate turn-over-frequency value (TOF: 34.5 molH2 molCo0.67Ni0.33−1 min−1 at 298 K without base or additives) and relatively low activation energy (32.4 kJ mol−1) for the dehydrogenation of AB, but also superior catalytic activity (conversion yield reaching up to 100%) and selectivity (>99%) for the tandem reductive transformation of in excess of sixteen types of nitroaromatics to aromatic amines. Density functional theory (DFT) calculations suggest that the construction of the CoNi alloy optimized the electronic structure with respect to the pure component, promoting its activity for AB hydrolysis and nitroaromatics hydrogenation. Finally, the catalyst could be easily recycled using a magnet due to the magnetic properties of the Co0.67Ni0.33 alloy.

研究领域: 材料科学 · 催化化学
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ACS Applied Materials & Interfaces · 2024 · IF 8.3

Spatial Confinement of Lithium Borohydride in Bimetallic CoNi-Doped Hollow Carbon Frameworks for Stable Hydrogen Storage

Ying Ding,Chaoqun Li,Xiaoyue Zhang,Wei Chen,Xuebin Yu,Guanglin Xia

While lithium borohydride is one of the most promising hydrogen storage materials due to its ultrahigh hydrogen storage density, high thermodynamic stability, kinetic barriers, and poor reversibility, it is far from being used in practical applications. Herein, we prepare a cubic hollow carbon dodecahedron uniformly modified with a bimetallic CoNi alloy (CoNi/NC) for preserving the stable catalytic effect of CoNi alloys toward reversible hydrogen storage. It is theoretically confirmed that bimetallic CoNi alloys effectively weaken the B–H bonds of LiBH4 by extending their average length to 1.33, 0.09 and 0.04 Å longer than that of LiBH4 and LiBH4 under metallic Co, respectively. More importantly, the alloying of Co with Ni avoids the reattachment of H from LiBH4 to the Co surface, which prevents LiBH4 from dehydrogenation for the formation of H2 on the Co surface, thus resulting in an ultralow hydrogen desorption energy of 0.1, 1.85 and 0.52 eV lower than that of LiBH4 and LiBH4 under metallic Co. Therefore, the onset and peak hydrogen desorption temperatures decrease to 130 and 355 °C, respectively, 170 and 97 °C lower than that of bulk LiBH4. More importantly, a reversible H2 capacity of 9.4 wt % is achieved even after 10 cycles.

CAS / MDL: 10026-22-9 13478-00-7
研究领域: 材料科学 · 化学工程 · 能源科学
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ACS Omega · 2022 · IF 4.132

Waste PET Plastic-Derived CoNi-Based Metal–Organic Framework as an Anode for Lithium-Ion Batteries

Yaxin Wang,Huimin Wang,Shuyuan Li,Shaorui Sun

Recycling waste PET plastics into metal–organic frameworks is conducive to both pollution alleviation and sustainable economic development. Herein, we have utilized waste PET plastic to synthesize CoNi-MOF applied to lithium battery anode materials via a low-temperature solvothermal method for the first time. The preparation process is effortless, and the sources’ conversion rate can reach almost 100%. In addition, the anode performance of MOFs with various Co/Ni mole ratios was investigated. The as-synthesized Co0.8Ni-MOF exhibits excellent crystallinity, purity, and electrochemical performance. The initial discharge and charge capacities are 2496 and 1729 mAh g–1, respectively. Even after 200 cycles, the Co0.8Ni-MOF electrode can exhibit a high Coulombic efficiency of over 99%. Consequently, given the environmental and economic benefits, the Co0.8Ni-MOF derived from waste PET plastic is thought to be an appealing anode material for lithium-ion batteries.

CAS / MDL: 64-17-5 68-12-2 107-21-1
研究领域: 材料科学 · 环境科学 · 能源存储
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JOURNAL OF MEMBRANE SCIENCE · 2022 · IF 10.53

3D hollow CoNi-LDH nanocages based MMMs with low resistance and CO2-philic transport channel to boost CO2 capture

Wenji Zheng,Jingbang Yu,Zhongyue Hu,Xuehua Ruan,Xiangcun Li,Yan Dai,Gaohong He

Layered double hydroxide (LDH) bearing numerous hydroxyl groups shows high affinity with CO 2 and is promising in mixed matrix membranes (MMMs) based CO 2 capture. However, its non-porous structure limits the further improvement of CO 2 permeability. In this work, 3D hollow CoNi-LDH nanocages were developed to construct low-resistance and CO 2 -philic transport channel in MMM by in-situ etching of ZIF-67 template. The resultant material exhibits hollow structure with cavity size of about 500 nm, mesopores and micropores from LDH stacking and ZIF-67 template. The outer layered CoNi-LDH nanosheets can attract more CO 2 molecules by their abundant hydroxyl groups, resulting in an improvement in dissolution selectivity of CO 2 over N 2 . Meanwhile, the tortuous gas diffusion paths originated from 2D nanosheet stacking can further enhance the CO 2 selectivity over N 2 . Moreover, the hollow nanocages provide CO 2 molecules with fast transport path, resulting in high CO 2 permeability. As a result, compared with pure Pebax membrane and 2D LDH/Pebax MMM, all the 3D hollow CoNi-LDH/Pebax MMMs present enhanced CO 2 permeability. The 3D hollow CoNi-LDH-2h/Pebax MMM performs the highest CO 2 permeability of 135.49 Barrer, which are increased by 141.95% and 71.50% than those of the above two membranes, respectively. The selectivity of 3D hollow CoNi-LDH-2h/Pebax MMM is about 26.30% higher than that of the pure Pebax membrane. The present membrane presents comparable CO 2 capture capacity in contrast with most reported Pebax based MMMs and surpasses the Robeson upper bond. Together with the good long-term stability, the 3D hollow CoNi-LDH nanocages are believed to be a promising candidate for MMMs to improve CO 2 capture.

CAS / MDL: 10026-22-9 693-98-1
研究领域: 材料科学 · 环境科学
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Journal of Materials Chemistry A · 2022 ·Vol. 10 ·期 31 ·16439-16447 · IF 14.511

CdS nanocages@defective-CoNi-LDH with bilayer porous hollow frameworks toward optimized sono-photocatalytic performance

Bin Fang,Zipeng Xing,Fan Du,Weifeng Kong,Zhenzi Li,Wei Zhou

Sono-photocatalysis is considered a promising strategy for water decontamination and hydrolysis, and it is crucial to improve the sensitivity of the catalyst to mechanical forces to obtain more energy. In a single photocatalyst, the hollow structure refracts sunlight many times to improve light utilization, but with a sono-photocatalyst, can the hollow structure refract sound waves to enhance the sound field energy? This paper reports formation of CdS with different structures by controlling the etching rate and wrapping with hollow defective CoNi-LDH (HD-CoNi-LDH) to form a bilayer porous hollow framework structure. Characterization confirmed that evolution of CdS from the solid gave the bilayer a hollow framework state and improved the degree of sound field energy absorption. It was further shown that the honeycomb-like porous structure of HD-CoNi-LDH enhanced sound field energy absorption, which then acted on CdS to enable piezoelectric photocatalysis. Specifically, strong sound field absorption by hollow CdS@HD-CoNi-LDH increased the hydrogen precipitation rate by 3.5 times and the degree of bisphenol A degradation by approximately 30% compared to solid CdS. This work provides a new perspective for sono-photocatalysis.

研究领域: 材料科学 · 环境科学 · 化学工程
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JOURNAL OF COLLOID AND INTERFACE SCIENCE · 2024 · IF 9.4

CoNi-layered double hydroxide derived CoS2/NiS2 dodecahedron decorated with ReS2 Z-scheme heterojunction for efficient hydrogen evolution

Changdi Wang,Tingting Ji,Wenqian Luan,Dong Yao,Ruiyang Zhao,Jishu Han,Lei Wang

The high efficient utilization of light absorption and the effective separation of photogenerated carriers are critical factors in enhancing the performance of photocatalysts. In this study, CoNi-layered double hydroxide was synthesized using zeolitic imidazolate frameworks-67 as a template, followed by calcination to form CoS 2 /NiS 2 . Subsequently, ReS 2 was deposited onto the surface of CoS 2 /NiS 2 , resulting in the ReS 2 /CoS 2 /NiS 2 photocatalyst demonstrated notable hydrogen evolution activity under visible light, achieving a maximum hydrogen production rate of 40111.8 μmol/g. The construction of the Z-scheme heterojunction was found to facilitate the transfer and separation of photogenerated carriers while extending the lifetime of photogenerated electrons, thereby contributing to the enhancement of photocatalytic activity. This study provides a new approach for the development of sulfide heterojunctions aimed at improving photocatalytic hydrogen production efficiency.

研究领域: 材料科学 · 能源化学
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APPLIED CATALYSIS B-ENVIRONMENTAL · 2020 · IF 16.683

One-step efficient non-hydrogen conversion of cellulose into γ-valerolactone over AgPW/CoNi@NG composite

Shanhui Zhu,Huan Liu,Sen Wang,Xiaoqing Gao,Pengfei Wang,Jianguo Wang,Weibin Fan

One-step efficient conversion of cellulose into value-added γ-valerolactone (GVL) is of great interest because it not only integrates complex tandem reactions in one-step, but also does not need additional hydrogen sources. To achieve this goal, it is crucial to fabricate high-performance catalyst that can accelerate both hydrolysis of cellulose and further transformation of generated stoichiometric levulinic acid (LA) and formic acid (FA) into GVL. CoNi nanoparticles encapsulated in N-doped thin graphene shell gave GVL yield as high as 55.9 % at 200 °C combined with Ag + -exchanged heteropolyacid (AgPW). This composite catalyst is highly resistant to the corrosion of LA and FA, and hence shows high catalytic stability. LA-adsorption FTIR spectra and DFT calculations indicate that LA and FA can penetrate through shell graphene layers into core CoNi sites via cracks. Compared to H 2 , FA can much more rapidly reduce LA because of its low dissociation energy barrier and high dissociation rate.

CAS / MDL: 25249-54-1 9003-39-8
研究领域: 化学工程 · 催化 · 材料科学 · 生物化工
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Catalysis Science & Technology · 2021 ·Vol. 11 ·期 16 ·5579-5589 · IF 6.119

The synergy of photodeposited CoNi co-catalysts for the photocatalytic performance of C3N4/CdS nanosheets: optimized Gibbs free energy and Co–S bridging bonds

Qixiao Gai,Shoutian Ren,Xiaochun Zheng,Wenjun Liu,Quanli Dong

Transition metal co-catalysts exhibit considerable potential in the photocatalytic water splitting process, but their limited activity and poor stability inhibit their extensive application, and therefore effective schemes are required to further enhance their co-catalytic performance. In this article, 2D/2D C3N4/CdS heterogeneous photocatalysts are first synthesized, and then CoNi alloyed NPs are selectively loaded on their CdS nanosheets by a convenient photodeposition method. The CoNi loading amount and Co/Ni ratio are adjusted by the photodeposition time and precursor Co2+/Ni2+ ratio, respectively. Meanwhile, Co–S bonds are formed between CdS and CoNi NPs. Their optimal hydrogen evolution rate can reach up to 2936.65 μmol g−1 h−1, which is higher than that of C3N4/CdS with Co, Ni or Pt as co-catalysts (i.e. 844.59, 2385.96 and 2486.66 μmol g−1 h−1), respectively. The enhanced photocatalytic performance should be due to the following three points: (1) the formation of the 2D/2D C3N4/CdS heterojunction; (2) the optimized Gibbs free energy of the CoNi co-catalysts; (3) the formation of Co–S bonds between CoNi and CdS. Our work provides a cost-effective scheme to exploit stable and efficient photocatalysts.

研究领域: 材料科学 · 能源化学
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RSC Advances · 2021 ·Vol. 11 ·期 39 ·24065-24071 · IF 3.361

Sweetsop-like α-Fe2O3@CoNi catalyst with superior peroxidase-like activity for sensitive and selective detection of hydroquinone

Min Feng,Shaohua Wen,Xiaofang Chen,Die Deng,Xiupei Yang,Run Zhang

Hydroquinone (HQ) is poorly degradable in the ecological environment and is highly toxic to human health even at a low concentration. The colorimetric method has the advantages of low cost and fast analysis, which provides the possibility for simple and rapid detection of HQ. In this work, a new colorimetric method has been developed for HQ detection based on a peroxidase-like catalyst, α-Fe2O3@CoNi. This sweetsop-like α-Fe2O3@CoNi catalyst enables H2O2 to produce hydroxyl (˙OH), leading to the oxidization of colorless 3,3′,5,5′-tetramethylbenzidine (TMB) to blue oxTMB. In the presence of HQ, the blue oxTMB is reduced to colorless, which allows for colorimetric detection of HQ in water samples. This method has been validated by detecting HQ in water samples with high selectivity, rapid response, broad detection range (0.50 to 30 μM), and low detection limit (0.16 μM).

研究领域: 环境科学 · 分析化学
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CHEMOSPHERE · 2022 · IF 8.943

CoNi alloy anchored onto N-doped porous carbon for the removal of sulfamethoxazole: Catalyst, mechanism, toxicity analysis, and application

Zhibin Liu,Xiuping Sun,Zhirong Sun

Developing highly efficient, stable, recyclable, and application value heterogeneous catalysts in advanced oxidation processes has essential application value in the degradation of refractory pollutants. In this paper, the CoNi alloy anchored onto N-doped porous carbon (CoNi-600@NC) catalyst was prepared using bimetallic doped metal-organic frameworks as precursors. The magnetic CoNi-600@NC can activate peroxymonosulfate (PMS) to degrade sulfamethoxazole (SMX). Therefore, SMX can be removed 100% within 25 min. CoNi-600@NC/PMS has a broad pH (3–9) application range, good applicability, and repeatability. Radical quenching, quantitative and electrochemical experiments proved that the degradation of SMX was dominated by free radical (Superoxide anions) and non-free radical pathways (surface-bound radicals). Mechanistic analysis showed that the interaction between Co-N x /pyridine N-sites and graphitized carbon with PMS induced the formation of surface-bound active species. Moreover, CoNi nanoparticles promoted the redox cycle of metals. The synergistic catalytic mechanisms between the CoNi alloy and the abundant functional groups gave CoNi-600@NC excellent catalytic properties and applicability. Using density functional theory predicted the reaction sites of SMX and proposed four degradation pathways. The toxicity of intermediates was comprehensively evaluated. In addition, a CoNi-600@NC continuous flow reactor was constructed with a daily treatment capacity of 45 L and 100% SMX removal. This study expands the application of persulfate advanced oxidation technology by synthesizing recyclable magnetic catalysts and provides new synergistic degradation mechanisms for removing refractory organics.

研究领域: 环境科学 · 催化材料 · 污染治理
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