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JOURNAL OF ALLOYS AND COMPOUNDS · 2022 · IF 6.371

An isopropanol sensor based on MOF-derived NiO/NiCoxFe2−xO4 porous nanocube with improved response and selectivity

Wei Wang,Jing Han,Caixia Liu,Jingran Zhou,Yan Ma,Xin Li,Shengping Ruan

Semiconductor oxides with porous structure have good gas permeability and large reaction surface, which is an important advantage as gas sensing materials. Here, an isopropanol sensor based on PBA-derived spinel NiO/NiCo x Fe 2−x O 4 (x = 0, 0.02, 0.06, 0.10) porous nanocubes were successfully prepared. A series of techniques were used to characterize the crystal structure, morphology and element properties of the products. Gas-sensing measurements show that the doping of Co element can significantly improve the isopropanol-detecting ability of NiO/NiFe 2 O 4 . The reason for the improved sensitivity is that cobalt as a dopant can provide more active adsorption sites and the catalytic effect to enhance the gas response. The test results show that NiO/NiCo 0.06 Fe 1.94 O 4 composite exhibits high response (R g /R a =11.2 at 183.5 °C) and selectivity to 100 ppm isopropanol, which is promising for the detection of isopropanol gas. Also, the isopropanol-sensing mechanism of the Co-doped NiO/NiFe 2 O 4 porous nanocubes was discussed.

CAS / MDL: 13963-58-1
研究领域: 材料科学 · 传感器技术
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SENSORS AND ACTUATORS B-CHEMICAL · 2020 · IF 7.1

Aliovalent Sc and Li co-doping boosts the performance of p-type NiO sensor

Junqing Chang,Mati Horprathum,Dianhui Wang,Gang Meng,Zanhong Deng,Bin Tong,Pinit Kidkhunthod,Tiantian Dai,Meng Li,Hongyu Liu,Wei Tong,Shimao Wang,Xiaodong Fang

Though p-type NiO possesses excellent catalytic oxidation property toward volatile organic compounds (VOCs), intrinsic low sensitivity of NiO (arising from the hole accumulation layer configuration in ambient air atmosphere sensor) restricts its promising applications in VOCs detection. In this study, Sc and Li were proposed to modulate the (surface) properties of NiO nanosheet-flowers based sensors. At the optimal 2 at.% Sc and 5 at.% Li doping ratio (Ni 0.93 Sc 0.02 Li 0.05 O), the sensitivity to 100 ppm ethanol is 118.4 (105 times higher than that of pure NiO), which is comparable to or even higher than most of reported NiO based sensors. Moreover, Ni 0.93 Sc 0.02 Li 0.05 O sensor exhibits a low detection limit of 10 ppb, excellent repeatability and long-term stability (∼30 % decline of response after 7 months). Apart from regulating the carrier concentration, defect characterizations indicate a noticeable increase of stabilized surface oxygen vacancy (O V ) defects and Ni 3+ cations by Sc 3+ and Li + co-doping, which greatly facilitate the adsorption of VOCs molecule (revealed by density functional theory calculation) as well as the subsequent VOCs/NiO interfacial charge interaction, thus contribute to the superior sensing performances. This work demonstrates that co-doping offers an effective avenue for boosting the performances of (p-type) oxide sensors.

CAS / MDL: 6108-17-4
研究领域: 材料科学 · 传感器技术
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CHINESE JOURNAL OF CHEMICAL ENGINEERING · 2025 · IF 3.7

Dielectric barrier discharge coupled with oxygen-vacancy-rich NiO-CeO2 for efficient and low-energy degradation of SF6

Runze Dong,Wenhao Li,Qiyu Yang,Ping Li,Pan Zhang,Lemeng Wang,Dong Fu

How to achieve low energy consumption and high degradation efficiency (DRE) under mild conditions is an important issue in the field of sulfur hexafluoride (SF 6 ) treatment. In this work, a new route of SF 6 degradation promoted by Ni-doped ceria (NiO-CeO 2 ) in a packed bed dielectric barrier discharge (PB-DBD) was proposed. The effects of Ni/Ce molar ratio, input power, SF 6 concentration and flow rate on the DRE of SF 6 were investigated. Compared with DBD or CeO 2 -DBD alone, the combination of DBD and NiO-CeO 2 can significantly promote the SF 6 degradation at lower input power. The Experimental results show that when the dosage of catalyst 1.5NiO-CeO 2 (Ni/Ce mole ratio is 1.5%) is 5 g, DBD input power is 50 W and SF 6 (1.5% SF 6 /98.5% Ar) flow rate is 100 ml·min −1 , the highest DRE can reach 97.7% and the energy yield can reach 11.5 gSF 6 ·(kWh) −1 . Adjusting the catalyst dosage according to the flux of SF 6 ( e.g., using 10 g catalyst to degrade SF 6 with a concentration of 1.5% and a flow rate of 80 ml·min -1 ), the DRE of nearly 99% can be achieved for a long time, which is crucial for industrial application. The mechanism deduction shows that the rich surface and mesopores of the catalyst are beneficial to the adsorption of SF 6 and intermediates, while the doping of Ni can significantly increase the content of oxygen vacancies to improve the degradation. Meanwhile, when NiO-CeO 2 is activated by DBD, the free O· can further promote the degradation. It is this coupling effect that leads to the high efficiency and low energy consumption of SF 6 degradation under mild conditions. It can be expected that this coupling technology route will have a good application prospect in the field of SF 6 treatment.

CAS / MDL: 1306-38-3 13478-00-7
研究领域: 环境科学 · 材料科学
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JOURNAL OF COLLOID AND INTERFACE SCIENCE · 2024 · IF 9.4

Morphology engineering of hollow core@shell structured Co3O4@CuO-NiO for fast hydrogen release from ammonia borane methanolysis

Jinyun Liao,Yuanzhong Li,Jingjing Tian,Yufa Feng,Quanbing Liu,Hao Li

Catalytic methanolysis of ammonia borane is an integrated hydrogen production/storage technology with bright prospects, while its wide application is impeded by the high-cost of catalysts. In this work, hollow core@shell structured (HCSS) Co 3 O 4 @CuO-NiO with a size of 300–500 nm and a shell thickness of ca. 100 nm has been designed for ammonia borane (NH 3 BH 3 ) methanolysis for rapid hydrogen release. The possible formation mechanism of HCSS-Co 3 O 4 @CuO-NiO is proposed based on a series of characterization results, which is crucial for the design and preparation of nanocatalysts with similar architectures. Benefiting from the optimized compositions and electronic structures, the best HCSS-Co 3 O 4 @CuO-NiO sample exhibits high catalytic activity in NH 3 BH 3 methanolysis with a turnover frequency of 67.1 min −1 , surpassing that of all the noble-metal-free catalysts in previous reports. A possible reaction mechanism of NH 3 BH 3 methanolysis is put forward based on the in-situ Fourier transform infrared spectrometer (FTIR) characterization and kinetic isotope effect (KIE) experimental results. This work supplies a novel avenue for developing cheap and robust catalysts towards NH 3 BH 3 methanolysis by tailoring the catalysts’ morphology to hollow core@shell structures.

研究领域: 材料科学 · 催化化学
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INTERNATIONAL JOURNAL OF HYDROGEN ENERGY · 2025 · IF 8.3

Mo-doped Ni/NiO as a highly efficient and stable electrocatalyst for the hydrogen evolution reaction

Zhong Wang,Xinjia Tan,Chuhan Wang,Guojian Li,Shuang Yuan

Ni/NiO is regarded as an ideal candidate material to replace noble metal catalysts due to its good corrosion resistance and excellent hydrogen evolution activity. However, the poor stability of Ni/NiO catalyst in the process of long-term water electrolysis limits its large-scale application. In this study, a facile hydrothermal method was used to successfully synthesize highly active and stable nanoparticulate Mo–Ni/NiO catalysts. Density functional theory (DFT) shows that Mo doping can optimize the charge transfer of Ni/NiO, reduce the d-band center and accelerate the H* dissociation from the catalyst surface. COMSOL numerical simulation further confirmed that the granular structure can enhance the ion concentration and promote H 2 generation. Electrochemical tests showed that the overpotential of Mo–Ni/NiO was only 45 mV when the current density was 10 mA cm −2 in 1 M KOH solution, which was much lower than 158 mV of Ni/NiO. Furthermore, Mo–Ni/NiO exhibited superior stability when operated at a current density of 10 mA cm −2 for 150 h with a reduction of overpotential of only 2 mV. This work provides a simple method for improving the HER activity of catalysts with Mo doping, which provides a new idea for designing catalysts with high activity, excellent stability and low cost.

研究领域: 电化学 · 材料科学 · 催化 · 理论化学
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SENSORS AND ACTUATORS B-CHEMICAL · 2021 · IF 7.46

Design and preparation of hollow NiO sphere- polyaniline composite for NH3 gas sensing at room temperature

Qi Hu,Zhenming Wang,Junyu Chang,Peng Wan,Jiahui Huang,Liang Feng

The accurate and rapid sensing of NH 3 at room temperature is a challenging conundrum for daily life and environment protection. In this work, we have explored an intriguing material, hollow NiO sphere composited with polyaniline (labelled as h-NiO-PANI) for NH 3 gas sensing, fabricated by growing PANI on the hollow NiO sphere derived from solvothermal synthesis and calcination. Ni-Cu glycerate is obtained via solvothermal synthesis, which is a universal way to produce uniform glycerate microspheres. During calcination, the hollow sphere is ingeniously designed by taking advantage of the outward adhesion from CuO to the inner core. Polymerization of aniline on the hollow spheres is beneficial for large specific surface area and gas adsorption. Impressively, the sensor based on h-NiO-PANI exhibits favorable response to NH 3 (ΔR/R 0 =43 % for 10 ppm, 149 s in response and 257 s in recovery), which is greatly better than the counterparts (NiO-PANI and PANI). Moreover, the sensor has also shown superb anti-interference against common volatile organic compounds (VOCs), water and humidity, along with the superior repeatability in 5 cycles and long-term stability in a week, manifesting the sensor a promising candidate in daily application. The enhanced gas sensing performance is attributed to the hollow structure and construction of p-p heterojunctions between NiO and PANI.

CAS / MDL: 62-53-3 13478-00-7
研究领域: 材料科学 · 环境科学 · 化学传感器
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Scientific Reports · 2016 ·Vol. 6 ·期 1 ·1-10 · IF 5.228

Multishelled NiO Hollow Microspheres for High-performance Supercapacitors with Ultrahigh Energy Density and Robust Cycle Life

Qi Xinhong,Zheng Wenji,Li Xiangcun,He Gaohong

Multishelled NiO hollow microspheres for high-performance supercapacitors have been prepared and the formation mechanism has been investigated. By using resin microspheres to absorb Ni 2+ and subsequent proper calcinations, the shell numbers, shell spacing and exterior shell structure were facilely controlled via varying synthetic parameters. Particularly, the exterior shell structure that accurately associated with the ion transfer is finely controlled by forming a single shell or closed exterior double-shells. Among multishelled NiO hollow microspheres, the triple-shelled NiO with an outer single-shelled microspheres show a remarkable capacity of 1280 F g −1 at 1 A g −1 , and still keep a high value of 704 F g −1 even at 20 A g −1 . The outstanding performances are attributed to its fast ion/electron transfer, high specific surface area and large shell space. The specific capacitance gradually increases to 108% of its initial value after 2500 cycles, demonstrating its high stability. Importantly, the 3S-NiO-HMS//RGO@Fe 3 O 4 asymmetric supercapacitor shows an ultrahigh energy density of 51.0 Wh kg −1 at a power density of 800 W kg −1 , and 78.8% capacitance retention after 10,000 cycles. Furthermore, multishelled NiO can be transferred into multishelled Ni microspheres with high-efficient H 2 generation rate of 598.5 mL H 2 min −1 g −1 Ni for catalytic hydrolysis of NH 3 BH 3 (AB).

CAS / MDL: 89-86-1
研究领域: 材料科学 · 电化学
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INORGANIC CHEMISTRY COMMUNICATIONS · 2025 · IF 5.4

Synthesis of Ni-Fe PBA derived NiO/Fe3O4 nanocomposites for chemocatalytic water oxidation and photocatalytic degradation of organic dyes

Naeem Akram,Wenlan Ma,Shehla Riaz,Jia Guo,Ali Ahmad,Jide Wang

In this study, Ni-Fe-based Prussian Blue Analogues (Ni-Fe PBA) served as precursors, giving rise to a NiO/Fe 3 O 4 -based bimetallic catalyst that underwent comprehensive examination for both chemocatalytic water oxidation and photocatalytic degradation of organic dyes. The morphologies and chemical compositions of the precursor and resultant bimetallic catalysts were thoroughly characterized using XRD, SEM, XPS, mapping, and FTIR techniques. The results indicated that the catalytically active center is the NiO/Fe 3 O 4 -based bimetallic nanocomposite. The in-situ-synthesized bimetallic catalyst demonstrated remarkable catalytic oxidation activity when evaluated with Sodium Persulfate (PS) as an oxidant. Oxygen evolution results revealed an impressive catalytic water oxidation activity, with an O 2 production rate of approximately 1594.3 µmol·g −1 ·h −1 . Moreover, the NiO/Fe 3 O 4 catalyst was utilized as a heterogeneous photocatalyst to activate photosensitizer (PS) for the two azo dye’s deterioration caused by the exposure to visible light. Both organic dyes were photocatalytically degraded with great efficiency when Fe 3 O 4 and NiO were combined because they increased the catalyst’s capacity to absorb light. Electron Spin Resonance (ESR) and radical trapping studies revealed that sulfate (SO4· - ) and hydroxyl (OH·) radicals played pivotal roles. The degradation mechanism and pathway for Rhodamine B (RhB) were also elucidated. The exceptional recyclability and stability of the NiO/Fe 3 O 4 catalyst make it particularly promising for potential applications in water treatment, addressing challenges related to energy sustainability and environmental toxicity.

CAS / MDL: 13478-00-7
研究领域: 材料科学 · 环境科学
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JOURNAL OF MATERIALS SCIENCE & TECHNOLOGY · 2023 · IF 10.9

Interface engineering and impedance matching strategy to develop core@shell urchin-like NiO/Ni@carbon nanotubes nanocomposites for microwave absorption

Tianming Jia,Yanling Hao,Xiaosi Qi,Yongchao Rao,Lei Wang,Junfei Ding,Yunpeng Qu,Wei Zhong

It is well recognized that interfacial effect and/or impedance matching play a great impact on microwave absorption. Herein, we proposed a facile strategy to take full advantage of interface engineering and impedance matching for boosting microwave absorption performance (MAPs). Three-dimensional (3D) hierarchical urchin-like core@shell structured NiO/Ni@CNTs multicomponent nanocomposites (MCNCs) were elaborately constructed and produced in high efficiency through a facile continuous chemical bath deposition, thermal treatment, and catalytic chemical vapor decomposition process. By controlling the pyrolysis time, the NiO/Ni@CNTs urchin-like MCNCs with different lengths and aggregation degrees of CNTs could be selectively synthesized. The obtained results revealed that the enhanced CNT contents provided abundant interfaces and effectively aggrandized their interfacial effects, which resulted in improved polarization loss, conductivity loss, and comprehensive MAPs. Impressively, the interfaces and impedance matching in the designed NiO/Ni@CNTs urchin-like MCNCs could be optimized by regulating the pyrolysis temperature, which further improved the comprehensive MAPs. And the designed NiO/Ni@CNTs urchin-like MCNCs could simultaneously display strong absorption capabilities, broad absorption bandwidths, and thin matching thicknesses. Therefore, our findings not only provided a simple and universal approach to produce core@shell structured magnetic carbon-based urchin-like MCNCs but also presented an interface engineering and impedance matching strategy to develop the tunable, strong absorption, broadband, lightweight high-efficiency microwave absorbers.

研究领域: 材料科学 · 电磁学
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SENSORS AND ACTUATORS A-PHYSICAL · 2024 · IF 4.1

A NiO@Ti based linear photoelectrochemical type ultraviolet photodetector

Xiaojun Pan,Xinmiao Zhang,Gang Wang,Hongye Li,Jiang Li,Jianqiao Song,Shimin Wang,Mengjing Jin,Jinyuan Zhou,Lian Zhou

Omnidirectional detection is widely used in optical tracking systems, omni-directional cameras and optical field measurements and so on. However, the planar structures of ultraviolet (UV) photodetectors (PDs) limit their application in omnidirectional detection. In this work, the NiO nanosheets were fabricated on a titanium (Ti) wire substrate by hydrothermal method and then assembled a photoelectrochemical (PEC) type UV photodetector (PD). Under ultraviolet (UV) irradiation of 35 mW cm −2 @ 365 nm, the PD exhibits a stable photocurrent of 1.53 μA cm −2 and repeatable switching cycles. Also, the PD presents fast response and recovery times of 0.074 s and 0.130 s, respectively. Particularly, the PD based on NiO@Ti possesses excellent response for rotation angles in the range from 0° to 360° under UV light irradiation .

研究领域: 光电子学 · 材料科学 · 光子学 · 纳米技术
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CHEMICAL ENGINEERING JOURNAL · 2021 · IF 13.273

Hierarchically porous structure of two-dimensional nano-flakes assembled flower-like NiO promotes the formation of surface-activated complex during persulfate activation

Lu-Lu Zhou,Peng-Xi Liu,Ying Ding,Jia-Rui Xi,Li-Juan Liu,Wei-Kang Wang,Juan Xu

Heterogeneous catalysts with hierarchically porous structure are highly efficient to catalyze chemical reactions. In this work, two-dimensional (2D) nano-flakes assembled flower-like NiO is fabricated and utilized for activating peroxydisulfate (PDS) to degrade organic pollutants bisphenol A (BPA). The results demonstrate that the prepared catalyst exhibits well organized flower structure composed of uniform 2D nano-flakes. PDS combines with the catalyst to form surface-activated NiO-PDS complex, subsequently depriving electrons from BPA. For the optimized NiO-12 catalyst, large specific surface area and hierarchically porous structure benefit to exposes abundant active sites while low resistance promotes electrons transfer, bringing the high BPA degradation rate constant of 0.28 min −1 under the condition of 20 mg/L initial concentration. NiO-12 exerts a capability of catalyzing PDS to mineralize 34% of practical packaging wastewater. This study provides a new strategy to fabricate hierarchical 2D porous catalysts for persulfate activation, with application potential in practical wastewater treatment.

研究领域: 环境科学 · 催化材料
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JOURNAL OF ELECTROANALYTICAL CHEMISTRY · 2022 · IF 4.598

Well-matched core–shell NiO@LaMnO3/MWCNTs p-p homotype heterojunction for ascorbic acid detection

Zhiyang Zhong,Aijuan Xie,Jie Pan,Menglu Li,Jiaojie Wang,Shixin Jiang,Jiaqi Lin,Shichao Zhu,Shiping Luo

A novel core–shell p-p homotype heterojunction based on NiO@LaMnO 3 and multi-walled carbon nanotubes (NiO@LaMnO 3 /MWCNTs) has been designed and synthesized via electrostatic self-assembly method. The phase compositions and morphology were verified by X-ray diffraction (XRD), scanning electron microscope (SEM), transmission electron microscope (TEM). A series of electrochemical tests showed that NiO@LaMnO 3 /MWCNTs modified electrode had a magnifying effect on the electrochemical response signal of ascorbic acid (AA) detection. The current response is linearly increased in the range of 2.60–36.44 μmol/L with the linear regression equation being I (μA)  = 0.5902 C (μmol/L) + 1.4407 (R 2  = 0.9909), and the detection limit (S/N = 3) being 2.41 μmol/L. Moreover, NiO@LaMnO 3 /MWCNTs/GCE electrochemical sensor presented satisfying selectivity, stability, repeatability, and can be used to analyze the AA concentration in real daily drinks. The relatively excellent electrocatalytic activity should be attributed to high electroactive surface area, well-matched core–shell structure and synergetic effect of p-p homotype heterojunction. This work offer applicable guidelines for the design of core–shell p-p heterojunction electrode materials for the application of electrochemical sensor.

CAS / MDL: 308068-56-6
研究领域: 材料科学 · 分析化学 · 生物医学工程
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