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NiGa2O4
SENSORS AND ACTUATORS B-CHEMICAL · 2019 · IF 6.393

Synthesis of NiGa2O4 nanosheets for non-enzymatic glucose electrochemical sensor

Longhua Ding,Jiahui Yan,Zhongyao Zhao,Dongjun Li

Construction of non-enzymatic sensors for glucose is highly attractive and important. In this work, NiGa 2 O 4 nanosheets were employed as an enzyme-free catalyst for glucose electrooxidation. NiGa 2 O 4 nanosheets grown directly onto porous nickel foam (NF) through hydrothermal method. And its morphology and structure was characterized by various techniques. As an electrochemical catalyst, it need not extra bonding or modification with electrode and it has strong adhesion with substrate after annealing process. As a binder-free electrode material, NiGa 2 O 4 @NF exhibits excellent performance for glucose sensing in alkaline media. It has a rapid response time less than 5 s for glucose. And it can distinguish glucose in a wide concentration range of 0.03–2.5 mM, with a detection limit of 5.0 □M. In addition, it displays a high selectivity for glucose. Our study broadens the application area of NiGa 2 O 4 spinel materials and it may have potential in electrochemical analysis of small biomolecules.

研究领域: 材料科学 · 生物医学工程 · 分析化学
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ACS Applied Materials & Interfaces · 2019 · IF 8.456

NiGa2O4/rGO Composite as Long-Cycle-Life Anode Material for Lithium-Ion Batteries

Yongmin Huang,Jiaxing Ouyang,Xun Tang,Yao Yang,Jiangfeng Qian,Juntao Lu,Li Xiao,Lin Zhuang

This work reports a novel Ga-based material, NiGa2O4, which is typically used as a photocatalyst for water splitting, as an anode for Li-ion battery with a long cycle life. High-surface-area reduced graphene oxide (rGO) has been used as the conductive substrate to avoid the aggregation of NiGa2O4 nanoparticles (NPs). Because the size and shape of NiGa2O4 are very sensitive to the pH of the precursor, ethylene glycol has been employed as the solvent, as well as the reduction agent to reduce GO, to avoid using extra surfactants and also to avoid the variation of pH of the precursor. The obtained NiGa2O4/rGO composite possesses high capacity and long cycle life (2000 cycles, 2 A/g), with NiGa2O4 NPs around 3–4 nm that are uniformly distributed on the rGO surface. Full cell performance with LiCoO2 as cathode has also been studied, with the average loss of 0.04% per cycle after 100 cycles (C/2 of LiCoO2). The long cycle life of the composite was ascribed to the self-healing feature of Ga0 formed during charging.

研究领域: 材料科学 · 能源存储
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NEW JOURNAL OF CHEMISTRY · 2023 ·Vol. 47 ·期 16 ·7922-7929 · IF 3.3

Synthesis of NiGa2O4 ultra-thin nanosheets for improved xylene sensing properties and selectivity

Xinhua Tian,Jiayu Li,Qiuju Li,Mingcheng Zhang,Xiaoxin Zou,Jiaqi Jia,Guo-Dong Li

Ultra-thin two-dimensional nanomaterials are ideal candidates for fabricating gas sensors due to their large specific surface area, high carrier mobility and atomic-level thickness; however, the development of ultra-thin two-dimensional nanomaterials still remains a challenge. In this work, NiGa2O4 nanosheets with a thickness of about 3 nm are successfully prepared by calcining the NiGa LDH template. Moreover, the gas sensor fabricated using NiGa2O4 nanosheets shows a high response to xylene (Rg/Ra ≈ 7.7, 10 ppm), remarkable selectivity, a low detection limit (0.3 ppm) and excellent stability at low optimum working temperature (190 °C). This work has promoted the development of high-performance gas sensors based on two-dimensional and wide band gap metal oxide semiconductor materials.

CAS / MDL: 13450-90-3
研究领域: 材料科学 · 传感器技术
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INORGANIC CHEMISTRY COMMUNICATIONS · 2024 · IF 4.4

Hierarchical NiGa2O4@C@CeO2 microstructure for sensitive and selective triethylamine gas sensing

Diwei Deng,Ping Ma,Xianliang Li,Xiaoyu Chen,Yan Xu

Metal oxide heterostructures have been demonstrated excellent candidates acting as novel gas sensors with outstanding sensitivity and selectivity . In this work, a hierarchical NiGa 2 O 4 @C@CeO 2 heterostructure with corn-like NiGa 2 O 4 microcrystals covered by a thin carbon layer and then anchored with numerous amounts of external CeO 2 nanoparticles was prepared through the combination of hydrothermal and a subsequent calcination method. The NiGa 2 O 4 @C@CeO 2 composite demonstrates an excellent selective triethylamine (TEA) detection performance with a response of 11.1 towards 20 ppm TEA and a fast response/recovery time of 81 s/38 s. It also shows terrific selectivity for TEA when mixed with else interfering substances, along with prolonged reusability for at least 15 days. The enhanced TEA sensing performance can be ascribed to the significant improvement of conductivity and effective carrier transfer at the interface. This work provides a feasible method to fabricate metal oxide sensors with improved gas sensing performance.

研究领域: 材料科学 · 化学传感器 · 纳米技术
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SCIENCE OF THE TOTAL ENVIRONMENT · 2020 · IF 6.551

Design and performance of a novel direct Z-scheme NiGa2O4/CeO2 nanocomposite with enhanced sonocatalytic activity

Guowei Wang,Xue Ma,Jue Liu,Lifan Qin,Bing Li,Yuanan Hu,Hefa Cheng

A novel direct Z-scheme NiGa 2 O 4 /CeO 2 nanocomposite was designed and prepared via simple sol-hydrothermal and calcination methods, and its sonocatalytic activity was tested by studying the degradation of a model antimicrobial agent, malachite green (MG), under ultrasonic irradiation. Near complete (96.2%) degradation of MG (at 10 mg/L) could be achieved by the NiGa 2 O 4 /CeO 2 nanocomposite (at 1.0 g/L) after ultrasonic irradiation (40 kHz, 300 W) for 60 min at 25 °C. Under the same conditions, only 51.2 and 72.0% of the MG degraded in the presence of NiGa 2 O 4 and CeO 2 (at 1.0 g/L), respectively. These results demonstrate that the direct Z-scheme NiGa 2 O 4 /CeO 2 nanocomposite has excellent sonocatalytic activity, which is attributed to the matching band-gaps between NiGa 2 O 4 and CeO 2 . The sonocatalytic activity of NiGa 2 O 4 /CeO 2 nanocomposite decreased by 17% after four cycles of reuse, which is indicative of relatively good reusability. Scavenging experiments revealed that sonocatalytic degradation of MG results from the combined action of hydroxyl radicals ( OH) and holes (h + ), with the latter having a greater contribution. The pathways and mechanism of MG degradation were proposed based on the degradation intermediates detected. The results demonstrate that the prepared direct Z-scheme NiGa 2 O 4 /CeO 2 nanocomposite worked as designed and exhibited high and stable sonocatalytic activity during MG degradation, and could thus serve as a promising candidate in sonocatalytic treatment of other organic pollutants in wastewaters. The findings also provide new insights on the mechanism of sonocatalytic degradation and the design of efficient Z-scheme sonocatalysts.

CAS / MDL: 10101-89-0
研究领域: 环境科学 · 材料科学
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Molecular Catalysis · 2017 · IF 0

A new visible-light-induced Z-scheme photocatalytic system: Er3+:Y3Al5O12/(MoS2/NiGa2O4)-(BiVO4/PdS) for refractory pollutant degradation with simultaneous hydrogen evolution

Zepeng Qu,Yang Rong,Liang Tang,Xiaoqing Shu,Xudong Liu,Zhaohong Zhang,Jun Wang

A new visible-light-induced Z-scheme photocatalytic system, Er 3+ :Y 3 Al 5 O 12 /(MoS 2 /NiGa 2 O 4 )-(BiVO 4 /PdS), is designed and prepared by using hydrothermal and mixed-calcination methods And the prepared samples are characterized by X-ray diffractometer (XRD), energy dispersive X-ray spectroscopy (EDX), scanning electron microscopy (SEM), transmission electron microscopy (TEM), Fourier-transform infrared (FTIR) and UV–vis absorption spectra. The photocatalytic activity is evaluated towards Orange G degradation with simultaneous hydrogen evolution under visible-light irradiation. The photocatalytic experiments indicate that the Er 3+ :Y 3 Al 5 O 12 /(MoS 2 /NiGa 2 O 4 )-(BiVO 4 /PdS) as photocatalyst displays very high photocatalytic activity. It can be ascribed to two sides. One is the use of Er 3+ :Y 3 Al 5 O 12 offering ultraviolet-light to activate the wide-band gap NiGa 2 O 4 . Another is the construction of Z-scheme system between NiGa 2 O 4 and BiVO 4 which can result in a more efficient separation of photoexicited charge carriers, thus endowing it with much powerful oxidation and reduction capabilities. Moreover, the reusability study shows that the prepared photocatalyst can be effectively recycled for three repetitive cycles without an apparent deactivation. In addition, the possible Z-scheme mechanism of Er 3+ :Y 3 Al 5 O 12 /(MoS 2 /NiGa 2 O 4 )-(BiVO 4 /PdS) is also proposed, and further evidenced by photoluminescence (PL) spectra. The present work not only designs a new photocatalytic system but also well applies in photocatalytic degradation of refractory pollutant with simultaneous hydrogen evolution.

CAS / MDL: 1313-84-4
研究领域: 环境科学 · 材料科学 · 光催化技术
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