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Ni MOF衍生
COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS · 2021 · IF 4.539

Synthesis of Ni-MOF derived NiO/rGO composites as novel electrode materials for high performance supercapacitors

X. Li,J. Li,Y. Zhang,P. Zhao

Ni-MOF derived NiO nanosheets growing on rGO have been successfully synthesized by a hydrothermal method following by a series of calcination procedures (300 °C, 400 °C, and 450 °C). The influence of the introduction of rGO and the calcination temperature on electrochemical performance of Ni - MOF derived NiO nanosheets as the electrode material were highlighted in detail. For the three-electrode test system, Ni-MOF derived NiO/rGO composites subjected to calcination at 300 °C demonstrated the highest specific capacitance (435.25 F·g −1 at 1 A·g −1 ), and maintained 68.00% of its initial value at 8 A·g −1 . Its specific capacitance was increased by 49.34% when compared with the initial value after 25,000 cycles at 50 mV·s −1 . With the increase in calcination temperature, the specific capacitance presented the downward tendency (400 °C: 171.50 F·g −1 at 1 A·g −1 , 450 °C: 116.00 F·g −1 at 1 A·g −1 ) due to the reduction in specific surface area originating from the agglomeration of NiO nanosheets. The introduction of rGO greatly enhanced the electrochemical performance of the composites treated at 300 °C (increased by 40.40% at 1 A·g −1 and 47.30% in specific capacitance at 8 A·g −1 ). The assembled hybrid supercapacitors (HSC) with Ni-MOF derived NiO/rGO composites (300 °C) and active carbon as the cathode and anode also displayed the outstanding electrochemical performance. The value of energy density reached to 76.96 Wh·kg −1 at the power density of 400 W·kg −1 . All these results confirm that the MOF-derived NiO/ rGO composite should be a potential electrode material for supercapacitors .

研究领域: 材料科学 · 电化学
✓ 已验证 DOI 高影响因子
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Small · 2024 · IF 13

Simultaneous Efficient Photocatalytic Hydrogen Evolution and Degradation of Dye Wastewater without Cocatalysts and Sacrificial Agents Based on g-C3N5 and Hybridized Ni-MOF Derivative-CdS-DETA

Yongzhuo Yu,Wei Li,Yuxin Huang,Huixing Yang,Chaoyu Lv,Hui xiang Yan,Di Lin,Shichao Jiao,Linlin Hou,Zhiliang Wu

Inspired by energy conversion and waste reuse, hybridized Ni-MOF derivative-CdS-DETA/g-C 3 N 5 , a type-II heterojunction photocatalyst, is synthesized by a hydrothermal method for simultaneous and highly efficient photocatalytic degradation and hydrogen evolution in dye wastewater. Without the addition of cocatalysts and sacrificial agents, the optimal MOF-CD(2)/CN5 (i.e. Ni-MOF derivative-CdS-DETA (20 wt.%)/g-C 3 N 5 ) exhibit good bifunctional catalytic activity, with a H 2 evolution rate of 2974.4 µmol g −1 h −1 during the degradation of rhodamine B (RhB), and a removal rate of 99.97% for RhB. In the process of H 2 -evolution-only, triethanolamine is used as a sacrificial agent, exhibiting a high H 2 evolution rate (19663.1 µmol g −1 h −1 ) in the absence of a cocatalyst, and outperforming most similar related materials (such as MOF/g-C 3 N 5 , MOF-CdS, CdS/g-C 3 N 5 ). With the help of type-II heterojunction, holes are scavenged for the oxidative degradation of RhB, and electrons are used in the decomposition of water for H 2 evolution during illumination. This work opens a new path for photocatalysts with dual functions of simultaneous efficient degradation and hydrogen evolution.

研究领域: 材料科学 · 环境科学 · 化学
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SEPARATION AND PURIFICATION TECHNOLOGY · 2021 · IF 7.312

An electrochemically induced dual-site adsorption composite film of Ni-MOF derivative/NiCo LDH for selective bromide-ion extraction

Mengfang Jiang,Xuefeng Zhang,Xiao Du,Xiaowei An,Fengfeng Gao,Xiaogang Hao,Guoqing Guan,Zhong Liu,Jun Li,Abuliti Abudula

An electrochemically induced electrode with bromide ion (Br - ) dual adsorption sites was obtained by in-situ growing of Ni-MOF derivative/NiCo layered double hydroxide (Ni-MOF(D)/NiCo LDH) composite film on the stainless-steel wire mesh via an electrodeposition-assisted solvothermal method, which exhibited excellent Br - selectivity from ionic mixture solutions of Br - , NO 3 – and I - in an electrochemically switched ion exchange (ESIX) system. The Br - extraction capacity was as high as 126.30 mg·g −1 and the separation factors of Br - /NO 3 – and Br - /I - were 8.29 and 4.83 respectively. Combining the simulation and experimental results, it was confirmed that the highly efficient selective extraction of Br - in neutral solution should be derived from the dual-site (i.e., electrochemically induced laminate metal coordination sites and interlayer anion exchange sites of NiCo LDH) adsorption. Furthermore, the electrode demonstrated superior adsorption–desorption performance and electrochemical stability because of the in-situ growth strategy, which enhanced the binding force between NiCo LDH and substrate and improved the electrical conductivity of NiCo LDH, and provided a storage space for Br - . This study served deep understanding of ions selective extraction mechanism of LDH-based materials in the ESIX process, which could be a novel reaction concept for the design of those electrodes with specific recognition sites in the applications of them in other fields such as supercapacitors, sensors and batteries.

研究领域: 材料科学 · 环境科学 · 电化学
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JOURNAL OF MOLECULAR CATALYSIS A-CHEMICAL · 2016 · IF 3.958

Highly efficient and recyclable Ni MOF-derived N-doped magnetic mesoporous carbon-supported palladium catalysts for the hydrodechlorination of chlorophenols

Xueliang Cui,Wei Zuo,Meng Tian,Zhengping Dong,Jiantai Ma

Ni MOF-derived N-doped magnetic mesoporous carbon-supported Pd nanoparticles (Pd/Ni-mCN) were prepared and used in the hydrodechlorination (HDC) of chlorophenols (CPs) water pollutants with H 2 at mild reaction conditions. The Pd/Ni-mCN catalyst was characterized in detail by transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS), X-ray diffraction (XRD), N 2 adsorption/desorption, and vibrating sample magnetometry (VSM). The Pd/Ni-mCN nanocatalyst showed high activity and complete HDC conversion of a target pollutant such as 4-CP after 90   min at ambient conditions. Other CPs compounds such as 2-CP, 3-CP, 2,4-dichlorophenol (2,4-DCP), and 2,4,6-trichlorophenol (2,4,6-TCP) were also tested in the HDC reaction. 2-CP was the only intermediate product in the HDC of 2,4-DCP, with phenol being the final product. The HDC of 2,4,6-TCP proceeded with the intermediate formation of 2-CP and 2,4-DCP, this being potentially originated from the steric hindrance of the ortho-substituted Cl atom. Additionally, Pd/Ni-mCN exhibited high catalytic stability and recyclability. Thus, Pd/Ni-mCN was successfully recycled owing to its superparamagnetic properties and reused for at least five times showing stable conversions (above 99% at 90   min) the HDC of 4-CP.

研究领域: 催化 · 环境化学 · 材料科学
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