ELECTROCHIMICA ACTA
·
2018
·
IF 5.116
Cao Cui,Jingyun Wang,Zhenguo Luo,Jin Wang,Chunxia Li,Zhengquan Li
Cobalt hydroxide in α-form (α-Co(OH) 2 ) is an attractive electrocatalyst for oxygen evolution reaction (OER). Traditional preparation of α-Co(OH) 2 nanosheets often leads to a packing morphology after synthesis or post electrode fabrication, which severely limits the exposure of surface active sites. In this work, we report the synthesis of a self-supported 3D flower-like structure consisting of 2D α-Co(OH) 2 nanosheets through a metal-organic-framework (MOF)-mediated synthetic method. We found that the formation of MOF intermediates can produce dispersive α-Co(OH) 2 nanosheets with a stable 3D hierarchical structure which can effectively avoid the packing of individual nanosheets. The developed α-Co(OH) 2 nanosheets exhibit an obviously enhanced OER activity in comparison with the nanosheets prepared with traditional method. The prepared α-Co(OH) 2 nanosheets have been well characterized and their formation mechanism is proposed.
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DOI
高影响因子
SCIENCE OF THE TOTAL ENVIRONMENT
·
2022
·
IF 10.753
Yingdong Chen,Rongze Sun,Wentao Yan,Mengyao Wu,Yong Zhou,CongJie Gao
In many important industries, such as the textile printing industry, a large amount of dye/salt wastewater is often discharged, which can destroy the ecological environment of the water body. Membrane technology has a great potential in the treatment of environmental problems caused by dye/salt wastewater. Polyvinyl alcohol (PVA) nanofiltration (NF) membrane has a bright future in dye/salt wastewater treatment , however, works on this are rare. Herein, antibacterial PVA NF membrane incorporated with Cu(OH) 2 nanowires for the dye/salt wastewater treatment is reported. The membrane was prepared via coating the solutions containing PVA, glutaraldehyde and Cu(OH) 2 nanowires on the polyethersulfone ultrafiltration membrane. Cu(OH) 2 nanowires has a diameter of 60 nm and was successfully introduced into the membrane. The introduction of nanowires improved the membrane hydrophilicity and roughness, which is conducive to the improvement of membrane flux. Membrane separation performance for one component solution and dye/salt solution were investigated. The introduction of Cu(OH) 2 increases the flux of the membrane obviously (the highest increase is 178.78% (from 21.49 to 38.42 L·m −2 ·h −1 ·bar −1 , for NaCl solution as the feed). Besides, the membrane doped with nanowires also possessed a high dye/salt selectivity . For one component solution, the dye removal rate was over 97.00% while the salt rejection was low (the lowest was 13.18% (NaCl)). For the dye/salt solution, the dye (Congo Red) rejection kept at a high level (98.91%) and the salt (NaCl) rejection was still low (13.71%), while the flux was also high (37.56 L·m −2 ·h −1 ·bar −1 ). The performance is superior to that of many membranes reported in previous works. Moreover, the Cu(OH) 2 nanowires endowed the membrane with an improved and high antibacterial property. The sterilization rate of Escherichia coli and Staphylococcus aureus reached more than 99.99%.
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DOI
PubMed
高影响因子
APPLIED SURFACE SCIENCE
·
2025
·
IF 6.9
Bingchen Li,Zexiong Cui,Yufeng Tao,Jin Xiong,Jinbo Gao,Lihua Liu,Shiwei Song,Pengfei Tian
The slow kinetics of the cathodic hydrogen evolution reaction (HER) present a significant obstacle for alkaline water electrolysis. Consequently, developing non-precious metal HER catalysts with high activity and stability remains a challenge. This study reports a heterostructure catalyst composed of Mo-doped amorphous Ni(OH) 2 nanosheets modified Fe 3 O 4 crystal nanoparticles (Mo-NiOH@Fe 3 O 4 ). This unique structure exhibits a three-dimensional, coral-like structure, which significantly increases the electrochemically active surface area and exposes more active sites to the electrolyte. The incorporation of Mo-doped amorphous Ni(OH) 2 enriches electron density around Fe atoms, modulating their electronic state and optimizing intrinsic activity. As an alkaline hydrogen evolution catalyst, Mo-NiOH@Fe 3 O 4 requires overpotentials of only 23.7 and 140.6 mV to achieve 10 and 100 mA cm −2 , respectively, demonstrating exceptional catalytic activity. Furthermore, it shows negligible performance degradation at 100 mA cm −2 and maintains stability for over 120 h. This work demonstrates that a heterostructure strategy, integrating Mo-doped amorphous Ni(OH) 2 with Fe 3 O 4 , provides a reasonable route for developing low-cost, high-performance HER catalysts.
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产品关联
DOI
高影响因子
JOURNAL OF PHYSICS D-APPLIED PHYSICS
·
2025
·Vol. 58
·期 38
·385502
·
IF 3.2
Qixiong Zhang,Jiujun Zhu,Yafei Hou,Qi Yang,Hai Jiang,Jing Cuan,Weiping Li
Dielectric capacitors offer fast charge/discharge rates and high-power density but are limited by low energy density, requiring bulky stacking. Although single-layer composites attempt to combine both high dielectric constant and breakdown strength, a trade-off often limits their effectiveness. To resolve this conflict, sandwich-structured composites spatially separate polarization and insulation functions into different layers. However, the abrupt dielectric contrast at interlayer interfaces often results in localized electric field distortion, undermining breakdown reliability. In this work, we develop filler-gradient composites by varying the loading of Ni(OH)2 nanosheets to construct transitional interlayers. This design mitigates electric field imbalance in conventional sandwich structures, enhancing dielectric constant, breakdown strength, and energy density. The results demonstrate that the filler-gradient structure facilitates uniform electric field distribution and enhanced interfacial polarization, resulting in a high energy density of 21.1J cm−3 at 685.5MV m−1, and discharge efficiency of 70.1%.
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产品关联
DOI
高影响因子
JOURNAL OF ALLOYS AND COMPOUNDS
·
2025
·
IF 6.3
Peirong Chen,Chengguang Lang,Jianshan Ye,Wenfeng Zhan,Guangquan Wu,Liang Chen,Jianzheng Li,Lin Xu,Mingxi Liang,Kunpeng Xu,Liuzhang Ouyang
Developing an efficient and scalable approach to fabricate catalysts with high activity and long-term stability remains a critical challenge in electrochemical hydrogen production. In this study, we present a straightforward method utilizing mechanochemical ball milling to synthesize nickel oxide and molybdenum carbide composites. The incorporation of nickel oxide into molybdenum carbide was observed to induce a synergistic effect, leading to improved electrochemical oxygen evolution reaction (OER) activity and long-term stability. Moreover, a two-electrode alkaline electrolyzer incorporating these materials demonstrated superior overall water-splitting efficiency. This approach presents a viable and scalable method for the large-scale synthesis of advanced water-splitting catalysts with commercial potential.
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产品关联
DOI
高影响因子
APPLIED SURFACE SCIENCE
·
2018
·
IF 4.439
Shuaipeng Wang,Li Xu,Weixin Lu
Non-noble metal catalysts with high-performance are intensively exploited toward water electrolysis. Herein, we fabricate a novel Ni 3 S 2 @Co(OH) 2 heterostructure with a tentative method combining hydrothermal method with electrodeposition, in which the Ni 3 S 2 nanosheets are evenly integrated with Co(OH) 2 nanoparticles. Electrochemical tests reveal preeminent catalytic activities and durability on this heterostructure for both hydrogen evolution reaction (HER) and oxygen evolution reaction (OER). It presents high catalytic activities of 110 and 257 mV at 10 mA cm −2 for HER and OER, respectively, in 1.0 M KOH solution. Moreover this bifunctional electrode requires only 1.61 V to reach 10 mA cm −2 and shows excellent durability when assembled as an electrolyzer, superior than that of Pt-C||IrO 2 . The promoted activities are benefited from the interfacial cooperation and synergistic effect between Ni 3 S 2 and Co(OH) 2 , because of which the charge-transfer ability is enhanced and surface reactivity is of furtherance. This work is of very profound significance on electrocatalysts for water splitting, specific performances: (1) This heterostructure is synthesized based on interface engineering. (2) The promoted performance is due to the synergistic effect of two onefold-components. (3) The catalysis activities for HER and OER can synchronously reach ideal states when it is used as bifunctional catalyst.
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高影响因子
ACS Applied Materials & Interfaces
·
2021
·
IF 9.229
De Zhao,Zhihua Wu,Wei Zhang,Jian Yu,He Li,Wen Di,Yourong Duan
To date, ZnO array-based microfluidic fluorescence assays have been widely investigated and have exhibited excellent performance in the detection of cancer biomarkers. However, the requirements of highly sensitive detection necessitate further improvement of current Zn-based fluorescence detection devices. Here, a rhombus-like Zn(OH)F array-based microfluidic fluorescence detection device is proposed. Construction of Zn(OH)F arrays on the inner wall of a microchannel is carried out via a microfluidic chemical method. A substrate-induced growth strategy for Zn(OH)F arrays is proposed, and various micro/nanostructured Zn(OH)F arrays are successfully obtained. Zn(OH)F nanorod arrays with a high aspect ratio can be constructed on the columnar ZnO nanorod arrays, and the results indicate that the fluorescence enhancement factor (EF) of the Zn(OH)F arrays toward Cy3 is approximately 4-fold that of the ZnO nanorod arrays, which can be attributed to the higher excitation light absorption and evanescent electric field. In human epididymis-specific protein 4 (HE4) detection, the limit of detection (LOD) reaches 9.3 fM, and the dynamic linear range is 10 fM to 100 pM. It has been demonstrated that Zn(OH)F nanorod array-based microfluidic devices are excellent fluorescence assay platforms that also provide a new design and construction strategy for fluorescence enhancement substrates for the detection of biomarkers.
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DOI
高影响因子
JOURNAL OF SOLID STATE CHEMISTRY
·
2021
·
IF 3.498
Qiao Zhao,Hanbo Li,Yaan Cao
A series of the In(OH) 3 species modified ZnS (ZnS–In(OH) 3 X% (X = 2, 5, 7, 10)) photocatalysts were synthesized by a hydrothermal method . ZnS–In(OH) 3 X% (X = 2, 5, 7, 10) exhibited the improvement of photocatalytic activity for the photoreduction of CO 2 into CO compared with ZnS. Characterized by X-ray diffraction (XRD), fourier transforms infrared spectra (FT-IR), high resolution transmission electron microscope (HRTEM), X-ray photoelectron spectroscopy (XPS) valence band spectra, UV–vis diffuse reflectance spectra, photoluminescence (PL) and time-resolved PL decay curves, the crystal structure, band structure and behaviors of photogenerated charge carriers for photocatalyst were explored up. It was revealed that the modification of In(OH) 3 surface species on surface of ZnS can prolong the fluorescence lifetimes of photogenerated charge carriers, enhance the separate of photoinduced charge carriers efficiently and promote better matching between the band structure and the redox potential of the CO 2 /CO, resulting in improvement of photocatalytic activity efficiently for ZnS–In(OH) 3 X% (X = 2, 5, 7, 10) photocatalysts . This work may offer a new understanding to study the effect of surface species modification on photocatalytic performance of photocatalyst.
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高影响因子
International Journal of Electrochemical Science
·
2023
·
IF 1.5
Jiao Chen,Hongye Qin,Yaping Pan,Jinli Wu,Jianan Liu,Wanying Lin,Jun Jiang,Enzuo Liu,Junwei Sha,Fang He,Liying Ma,Naiqin Zhao
It is necessary and challenging to develop platinum-based electrocatalysts with low Pt content and high performance for industrial development in a suitable strategy. Herein, ultralow Pt (0.35 wt%) loading Ni(OH) 2 nanosheets (named as 2-Pt/Ni(OH) 2 ) with cataphracted structure is synthesized on nickel foam by one-step hydrothermal process. It only needs an overpotential of 34 mV to achieve a current density of 10 mA cm -2 without any significant decrease for 40 hours. This excellent performance of hydrogen evolution reaction (HER) is attributed to the fact that the cataphracted structure not only has a larger active area and more active sites, but also effectively limits the size of Pt nanoparticles to 2~3 nm, which results in a higher active quality. In addition, the relatively simple and easily operational one-step method can reduce the Pt content to 0.35 wt% significantly. This facile strategy opens up new approaches in the rational design and synthesis of low loading Pt electrocatalysts with eminent electrocatalytic activity for industrial production.
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高影响因子
Materials Research Express
·
2021
·Vol. 8
·期 10
·105002
·
IF 1.62
Wenchang Xi,Pan Jian,Xisong Mao,Deyang Ning,Xuewen Xia,Guohua Liu,Dongyang Shi,Yuanpei Lan
In this work, aiming to evaluate and compare the luminescent property of Eu3+ doped La(OH)3 nanorods and its decomposed compounds of LaOOH and La2O3, La(OH)3: Eu3+ nanorods were synthesized and the decomposition behaviors in air and hydrogen were revealed. Then the luminescent property of 0%–8% Eu3+ doped La(OH)3 nanorods and the 300 °C–800 °C calcined La(OH)3: Eu3+- 4% were studied. Results show that LaOOH is intermediate product during the degradation of La(OH)3 in air or H2, which can be formed at a temperature range in 372.3 °C–592.9 °C in air. Intensity of emission spectra of La(OH)3: Eu3+ nanorods increases with the rising of Eu3+ dopant concentration, and the emission property of Eu3+ doped LaOOH and La2O3 is varied and strengthened with that of La(OH)3: Eu3+. Luminescent matrixes of LaOOH and La2O3 show similar emission spectrum and intensity, and the transitions of the D0 → 7F1 and D0 → 7F2 of Eu3+ each bifurcate into two peaks for both europium (III) doped La2O3 and LaOOH. The revealed results suggest that LaOOH is a relative thermal-stable compound and should be an appropriate matrix as similar as La2O3 for luminescent applications.
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高影响因子
Carbon Letters
·
2023
·Vol. 33
·期 5
·1395-1406
·
IF 4.5
Chen Zhangjing,Li Liangliang,Cheng Gang
Photocatalytic CO 2 reduction is a promising approach for reducing CO 2 emissions and achieving the goal of carbon neutrality. In this work, selectively coupling Cu(OH) 2 and CuO with amine-modified brookite TiO 2 (NH 2 –B–TiO 2 ) has been achieved by a simple precipitation method. The results show that CuO is better than Cu(OH) 2 as a co-catalyst to enhance the CO 2 photoreduction capability of NH 2 –B–TiO 2 . The highest rates of CO 2 conversion to CH 4 and CO of NH 2 –B–TiO 2 –CuO composite reach 6.05 and 3.25 μmol h −1 g −1 , respectively, which is higher than 8 times the yield of CH 4 of NH 2 –B–TiO 2 . It is proposed that the NH 2 –B–TiO 2 –CuO composite offers an effective charge transfer through the formation of a p–n junction between NH 2 –B–TiO 2 and CuO interfaces, while in the NH 2 –B–TiO 2 –Cu(OH) 2 composite, the Cu(OH) 2 dominantly serves as an electron sink to capture photo-induced electrons, promoting photo-induced carrier separation. This work provides an ingenious synthetic method for selectively anchoring Cu(OH) 2 and CuO on semiconductors with different charge transfer routes for an efficient CO 2 photoreduction. Graphical abstract
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高影响因子
JOURNAL OF NANOPARTICLE RESEARCH
·
2013
·Vol. 15
·期 8
·1-8
·
IF 2.175
Wang Minmin,Ren Wanzhong,Zhao Yunan,Liu Yan,Cui Hongtao
In this work, β-Ni(OH) 2 monolayer nanosheets, which had been thought to be unachievable, were successfully prepared for the first time by a one-pot strategy using epoxide as precipitation agent and sodium dodecyl sulfate (SDS) as surfactant. The characterization results indicate that the formation of monolayer morphology depends on the mediation of SDS molecules. The XRD patterns demonstrate the loose and defective packing of Ni(OH) 2 layers in the SDS intercalated samples. The disappearing of vibration band of free hydroxyl groups in the FTIR spectra suggests the interlayer separation resulted by SDS. The TEM and AFM images further confirm the formation of monolayer nanosheets. It is proposed that the in situ modification of the secondary growth unit of β-Ni(OH) 2 by SDS allows its two-dimensional anisotropic growth through steric hindrance of SDS molecules. In addition, this effect allows isolation of β-Ni(OH) 2 from solvent with keeping of monolayer nanosheet state in dry powder. The electrochemical measurement results indicate that β-Ni(OH) 2 monolayer nanosheets own much higher urea electrolysis performance than their corresponding multilayer structure.
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高影响因子
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