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NiTiO3
Catalysts · 2019 ·Vol. 9 ·期 6 ·561 · IF 3.444

Photocatalytic Performance of NiO/NiTiO3 Composite Nanofiber Films

Bozhi Yang,Xuefeng Bai,Jiaxuan Wang,Minghao Fang,Xiaowen Wu,Yan’gai Liu,Zhaohui Huang,Cheng-Yen Lao,Xin Min

Photocatalytic degradation of pollutants is one of the cleanest technologies for environmental remediation. Herein, we prepared NiO/NiTiO3heterostructure nanofiber (200 nm) films by electrospinning and high temperature heat treatment, using nickel acetate and tetrabutyltitanate as nickel and titanium sources, respectively. The NiO/NiTiO3heterostructure has advantages of good photodegradation rate constant and stability. By controlling the temperature, we can optimize the phase composition of these nanofibers for better photocatalytic performance. Based on our findings of the Rhodamine B degradation results, the best performance was obtained with 10% NiO and 90% NiTiO3; 92.9% of the Rhodamine B (5 mg/L) was degraded after reaction under full spectrum irradiation for 60 min. More importantly, the repeating test showed that these nanofiber films can remain active and stable after multiple cycles. The mechanisms of the photocatalysis reactions were also discussed. This demonstration provides a guideline in designing a new photocatalyst that we hope will serve the environmental needs for this and the coming century.Keywords:NiO/NiTiO3;nanofiber;electrospinning;photocatalyst

CAS / MDL: 6018-89-9
研究领域: 环境科学 · 材料科学
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Royal Society Open Science · 2018 ·Vol. 5 ·期 2 · IF 2.504

Fabrication and electromagnetic performance of talc/NiTiO3 composite

Wen-Li Qin,Tian Xia,Ying Ye,Ping-Ping Zhang

In this study, the electromagnetic (EM) performance of talc/NiTiO3 composite was evaluated. The morphology of talc displayed a lamella structure; there were many nanoparticles of NiTiO3 coated on the talc lamella. Thermal destruction occurred, which increased the surface area from 2.51 m2 g−1 to 79.09 m2 g−1 at the calcined stage at 650°C. The presence of NiTiO3 increased dielectric loss and magnetic loss of talc. The calculation of EM wave absorption of talc/NiTiO3 obtained a maximum reflection loss of −11.94 dB at the thickness of 6.85 mm; the optimum thickness for microwave absorption is 6.3–7.3 mm. This study revealed a new approach for fabricating an EM absorber and broadening applications of both talc and NiTiO3 in EM absorption.

研究领域: 材料科学 · 电磁学
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JOURNAL OF ALLOYS AND COMPOUNDS · 2023 · IF 6.2

Tailoring reversible hydrogen storage performance of NaAlH4 through NiTiO3 nanorods

Jingjing Chen,Chaoqun Li,Wei Chen,Xiaoyue Zhang,Xuebin Yu,Guanglin Xia

Despite of the moderate working temperature and relatively high hydrogen capacity of NaAlH 4 , the slow H 2 absorption and desorption kinetics and poor reversibility pose a major bottleneck hindering its practical application. Herein, porous NiTiO 3 nanorods is constructed to tailor reversible hydrogen storage performance of NaAlH 4 . It is theoretically and experimentally demonstrated that the building of NiTiO 3 nanorods effectively promotes the uniform distribution of catalytic Ni-based species and Ti-based species inside of NaAlH 4 matrix that are capable of synergistically weakening Al-H bonds of NaAlH 4 . As a result, under the catalysis of porous NiTiO 3 nanorods, the onset temperature for H 2 desorption from NaAlH 4 is decreased down to 89 °C, 91 °C lower than that of pure NaAlH 4 . In addition, NaAlH 4 under the catalysis of porous NiTiO 3 nanorods is capable of releasing 4.5 wt% H 2 within 60 min, 3.8 and 0.9 wt% higher than that of NaAlH 4 catalyzed by NiO and TiO 2 , respectively. More importantly, a reversible capacity of 4.6 wt% could be obtained for NaAlH 4 under the catalysis of porous NiTiO 3 nanorods after 5 cycles, corresponding to a capacity retention of 95%, while this value is significantly decreased to 42% for NaAlH 4 without the addition of NiTiO 3 nanorods. This work provides a new perspective for the development and design of high-performance catalysts for realizing reversible hydrogen storage of NaAlH 4 under moderate condition.

研究领域: 材料科学 · 氢储存技术 · 催化剂开发
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MATERIALS SCIENCE IN SEMICONDUCTOR PROCESSING · 2025 · IF 4.6

Hierarchical CaIn2S4/NiTiO3 heterojunction enhanced removal of hexavalent chromium powered by visible irradiation

Yuanyuan Wang,Zhanlin Ma,Jian Wang,Jiaqi Ben,Hangmin Guan,Ping Gu,Yingfei Hu

Given the significance of the visible-light-driven reduction of heavy metal chromium (Cr(VI)), it is promising and challenging to investigate photocatalysts that exhibit strong responsiveness to visible light and possess high carrier separation efficiency. In this research, a CaIn 2 S 4 /NiTiO 3 Z-scheme heterojunction has been successfully constructed through the in-situ growth of CaIn 2 S 4 nanosheets on NiTiO 3 nanorods. The energy band alignment between CaIn 2 S 4 and NiTiO 3 in the hierarchical framework facilitated the formation of the heterojunction, which significantly enhanced visible light absorption, promoted the separation of photogenerated carriers, and maintained the high reducing capability of the CaIn 2 S 4 conduction band electrons. These synergies enabled superior Cr(VI) removal efficiency. At an optimized CaIn 2 S 4 to NiTiO 3 ratio of 1:1, about 95 % removal rate of Cr(VI) was achieved within 80 min of visible-light exposure, accompanied by a reaction rate of 0.036 min −1 that is nearly four times faster than that over CaIn 2 S 4 . Furthermore, the charge transfer driving force and reaction mechanisms were comprehensively investigated by optoelectronic measurements, emphasizing the crucial roles of electrons (e − ) in Cr(VI) reduction. This investigation showcases the potential of the CaIn 2 S 4 /NiTiO 3 Z-scheme heterojunction for photocatalytic applications in Cr(VI)-containing wastewater treatment.

CAS / MDL: 22519-64-8 62-55-5
研究领域: 环境科学 · 材料科学
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CHEMICAL ENGINEERING JOURNAL · 2024 · IF 13.3

Construction of hollow NiTiO3/CuCo2S4 double-shell nanospheres for efficient photocatalytic hydrogen evolution

Yuchen Han,Yue Han,Yuye Yan,Yingxia Zong,Ruiyang Zhao,Jishu Han,Lei Wang

Hydrogen is a secondary fuel with various characteristics that include high safety, environmental protection, high energy and cleanliness. In recent years, the use of solar energy to produce hydrogen has received extensive attention. In this paper, NiTiO 3 nanoparticles were used to modify CuCo 2 S 4 to construct hollow NiTiO 3 /CuCo 2 S 4 double-shell photocatalyst. Under the light irradiation, the optimal hydrogen evolution rate of the synthesized NiTiO 3 /CuCo 2 S 4 photocatalyst was 6.24 mmol g −1 h −1 . The experimental results indicated that the NiTiO 3 /CuCo 2 S 4 composite, featuring a hollow double-shell structure, significantly augmented the capacity for visible light absorption and further suppressed the recombination of photogenerated electrons and holes. Additionally, the formation of a Z-scheme heterojunction within the photocatalyst effectively enhanced the redox capability. The research introduced a promising Z-scheme heterojunction photocatalyst, offered innovative insights into the field of photocatalytic hydrogen evolution, thereby contributing to the conversion of solar energy into chemical fuels.

CAS / MDL: 10026-22-9 6018-89-9
研究领域: 材料科学 · 能源化学 · 光催化
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Catalysis Science & Technology · 2020 ·Vol. 10 ·期 9 ·2931-2947 · IF 5.721

Phosphating 2D CoAl LDH anchored on 3D self-assembled NiTiO3 hollow rods for efficient hydrogen evolution

Yanbing Li,Guorong Wang,Yanbin Wang,Zhiliang Jin

Two photo-active materials with opposite surface potentials, NiTiO3 with a negative potential and CoAl LDH with a positive potential, have been rationally integrated into two-dimensional (2D) active plane phosphated-CoAl LDH with rich active sites and three-dimensional (3D) hollow NiTiO3 rods with more negative zeta potential. The delicate architecture can efficiently accelerate the separation and migration of photo-excited electrons, make the surface potential more negative, enhance thermodynamic H2 evolution reaction, and offer rich active planes for photo-catalytic redox reactions. Based on these highlighted photo-catalytic benefits, the optimal composite exhibits more prominent photo-catalytic hydrogen evolution performance compared with NiTiO3 or CoAl LDH materials alone under visible irradiation. In detail, the stereoscopic catalyst, constructed by phosphating CoAl LDH layers anchored on NiTiO3 hollow rods, exhibits a hydrogen evolution activity of about 594 μmol 5 h−1, which is 11.6 times and 14.8 times that of CoAl LDH (51 μmol 5 h−1) and NiTiO3 (40 μmol 5 h−1) alone, respectively. Also, the density functional theory results reveal the good conductivity, which is beneficial for charge migration in the hybrid sample. The results from the thoroughly conducted characterization studies such as TEM, SEM, XPS, XRD, UV-vis DRS, transient photocurrent, and FTIR spectroscopy have been well researched and they are in good agreement with each other.

研究领域: 材料科学 · 能源化学 · 表面科学
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JOURNAL OF ALLOYS AND COMPOUNDS · 2022 · IF 6.371

Structural, magnetic, and microwave absorbing properties of NiTiO3/CoFe2O4 composites

Rabigul Tursun,Yuchang Su,Jing Zhang,Reyimuaji Yakefu

In this study, different volume ratios (NiTiO 3 : CoFe 2 O 4 = 1:3, 2:3, 1:1) of NiTiO 3 /CoFe 2 O 4 composites were synthesized using the sol-gel method. The effects of different NiTiO 3 volume ratios on the structural, morphological, magnetic, and microwave properties were systematically investigated by X-ray diffraction spectroscopy (XRD), field-emission scanning electron microscopy (FE-SEM), Raman spectroscopy (RAMAN), vibrating-sample magnetometery (VSM), and vector network analysis. Electromagnetic wave absorption analysis indicated that 1:3 composite sample showed the greatest reflection loss (−21.7 dB at 17.1 GHz frequency) at a thickness of 10.0 mm. The microwave absorbing properties decrease with the increasing NiTiO 3 volume ratio. The observed improvement can be attributed to the low degree crystallization of NiTiO 3 that increases magnetic losses through increased exchange resonance.

CAS / MDL: 12052-28-7
研究领域: 材料科学 · 电磁学 · 物理学
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JOURNAL OF SOLID STATE CHEMISTRY · 2024 · IF 3.2

Construction of NiTiO3/g-C3N4 heterojunction with preferable photocatalytic performance for tetracycline degradation

Congtian Liu,Xiaoya Zhu,Ling Wang,Chujun Feng,Jian Rong,Zhongyu Li,Song Xu

Tetracycline antibiotics as one of the most widely used antibiotics at present, are difficult to degrade in the environment, which poses a serious threat to the ecosystem and human health. In this work, NiTiO 3 /g-C 3 N 4 composites were successfully constructed by calcination method using nickel acetate tetrahydrate as nickel source and tetrabutyl titanate as titanium source. The photocatalytic degradation efficiency of the 5 wt% NiTiO 3 /g-C 3 N 4 composite of TC can reach 88.2 % within 150 min, which was 1.4 and 2.2 times higher than that of pure g-C 3 N 4 (63 %) and NiTiO 3 (40 %), respectively. The 5 wt% NiTiO 3 /g-C 3 N 4 composite can still maintain good stability after four cycles. The experimental results showed that the construction of Z-scheme heterojunction can effectively improve the photocatalytic activity of the catalysts and maintain good redox properties at the same time. Furthermore, a possible mechanism of photocatalytic degradation of NiTiO 3 /g-C 3 N 4 heterojunction has been suggested.

研究领域: 环境科学 · 材料科学
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Surfaces and Interfaces · 2025 · IF 6.3

NiTiO3/Co3S4 nanoflowers: Solar-driven Z-scheme photocatalysts for efficient water purification

Ziyi Jiang,Guoyu Wei,Changhong Guo,Huiming Lin

The growing issue of environmental pollution, particularly water contamination by the spread of bacteria and organic dyes, eagerly demands to be resolved. Given its advantages of being efficient, convenient, and eco-friendly, photocatalysis stands out as a promising strategy for water purification. To harness solar energy effectively, Co 3 S 4 nanodots with a narrow band gap were integrated onto the surface of NiTiO 3 nanoflowers to construct heterostructure (NC-x). Detailed characterization revealed that the charge transfer mechanism belonged to a novel Z-scheme, which not only facilitated efficient electron-hole separation into different components but also maintained a high redox potential, leading to the generation of plenty of reactive oxygen species (ROS: . O 2 - and . OH). These ROS were instrumental in damaging bacteria and the degradation of organic dyes. Furthermore, the NC-x nanocomposite exhibited excellent photothermal property and the local hyperthermia further enhanced the photocatalytic reaction. Optimized for composition, NC-2 shows the effective inactivation to E. coli, achieving a lethality rate of 99.50±0.22 % under simulated sunlight irradiation. It has also been successfully applied to treat complex lake water samples, demonstrating significant antibacterial (99.82±1.28 %) and methylene blue (90.60±1.78 %) degradation efficiency, simultaneously. With the novel biocompatibility and decontamination capabilities, NC-2 holds substantial potential for water purification applications.

CAS / MDL: 5593-70-4 62-55-5
研究领域: 环境科学 · 材料科学 · 光催化技术
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Small · 2024 · IF 13

All-Inorganic Perovskite NiTiO3/Cs3Sb2I9 Heterostructure for Photocatalytic CO2 Reduction to CH4 with High Selectivity

Shuhan Fan,Qu Yang,Guilin Yin,Xiaosi Qi,Yuyu Feng,Junfei Ding,Qiong Peng,Yunpeng Qu,Qinglong Wang,Yan Shen,Mingkui Wang,Xiu Gong

Developing efficient and stable halide perovskite-based photocatalysts for highly selectivity reduction CO 2 to valuable fuels remains a significant challenge due to their intrinsic instability. Herein, a novel heterostructure featuring 2D Cs 3 Sb 2 I 9 nanosheets on a 3D flower-like mesoporous NiTiO 3 framework using a top-down stepwise membrane fabrication technique is constructed. The unique bilayer heterostructure formed on the 3D mesoporous framework endowed NiTiO 3 /Cs 3 Sb 2 I 9 with sufficient and close interface contact, minimizing charge transport distance, and effectively promoting the charge transfer at the interface, thus improving the reaction efficiency of the catalyst surface. As revealed by characterization and calculation, the coupling of Cs 3 Sb 2 I 9 with NiTiO 3 facilitates the hydrogenation process during catalytic, directing reaction intermediates toward highly selective CH 4 production. Furthermore, the van der Waals forces inherent in the 3D/2D heterostructure with face-to-face contact provide superior stability, ensuring the efficient realization of photocatalytic CO 2 reduction to CH 4 . Consequently, the optimized 3D/2D NiTiO 3 /Cs 3 Sb 2 I 9 heterostructure demonstrates an impressive CH 4 yield of 43.4 µmol g −1 h −1 with a selectivity of up to 88.6%, surpassing most reported perovskite-based photocatalysts to date. This investigation contributes to overcoming the challenges of commercializing perovskite-based photocatalysts and paves the way for the development of sustainable and efficient CO 2 conversion technologies.

研究领域: 材料科学 · 环境科学 · 化学工程
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JOURNAL OF ELECTRONIC MATERIALS · 2025 · IF 2.5

Synthesis of NiTiO3/TiO2 Composite Nanoparticles by a Green Approach: Application as Sonocatalyst for Dye Degradation

Khoa Vu Dang,Bac Luong Huu

A novel NiTiO 3 /TiO 2 heterostructure was synthesized via a green sol–gel method using lemon juice as a natural precursor. The phase formation, structural, morphological, and optical properties of the synthesized composite were investigated using x-ray diffraction (XRD), Raman scattering, field-emission scanning electron microscopy (FESEM), and diffuse reflectance spectroscopy. XRD and Raman scattering results confirm the coexistence of both ilmenite NiTiO 3 and TiO 2 phases in the composite. The TiO 2 phase in the composite undergoes temperature-dependent phase transformation: it exists as anatase when calcined at 600°C, a mixture of anatase and rutile at 700°C, and pure rutile at 800°C. FESEM reveals that the synthesized NiTiO 3 particles exhibit spherical nanostructures. The NiTiO 3 /TiO 2 composites were investigated for their sonocatalytic activity in the degradation of rhodamine B under ultrasonic irradiation. The composite exhibited significantly enhanced sonocatalytic performance compared to pure NiTiO 3 , which can be attributed to the improved interfacial charge transfer and the synergistic effects between NiTiO 3 and TiO 2 . These results highlight the potential of green-processed composites in advanced oxidation processes for wastewater treatment. Graphic abstract

CAS / MDL: 7550-45-0
研究领域: 材料科学 · 环境工程 · 纳米技术 · 催化 · 绿色化学
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APPLIED SURFACE SCIENCE · 2023 · IF 6.7

NiTiO3/Bi2O3/MoS2 double Z-type heterojunction catalysts realize dual-function applications of photocatalytic fuel cells and lactic acid sensing

Jie Zhou,Nan Zhou,Mingjie Liu,Haokun Tan,Zhichao Wang,Xiaoyuan Zhang,Zhiqiang Su

Sensors in intelligent monitoring and personal healthcare generally face power supply problems, such as cycle charging, regular maintenance, and battery replacement, which greatly limit the applications of sensing devices. Self-powered sensing system with a visible-light-driven photo-fuel cell (PFC) exhibits the advantage of not requiring any external power source for the chemical sensing of analytes. In this work, an enzyme-free PFC self-powered sensing platform was established for sensing sweat lactate using photoelectric conversion technology. A NiTiO 3 /Bi 2 O 3 /MoS 2 double Z-type heterojunction system was prepared by electrostatic interaction and self-assembly as the anode of the PFC. NiTiO 3 , Bi 2 O 3 and MoS 2 formed a double Z-type heterojunction system accelerated the electron transfer and improved the light absorption and photocatalytic efficiency, which in turn improved the perception of LA. In addition. lactic acid sensing experiments showed that the prepared non-enzymatic photoelectrochemical sensors had good detection performance. The assay results showed that the prepared biosensor has a wide detection range (30 μM-5 mM), low detection limit (6 μM), high selectivity(8μA μM −1 cm −2 ) and long-term stability. These assay results demonstrate its potential for applications in fields such as biomedicine and drug analysis.

研究领域: 材料科学 · 生物医学工程 · 光电化学传感器
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