JOURNAL OF COLLOID AND INTERFACE SCIENCE
·
2023
·
IF 9.9
Pengfei Zhou,Songbo Chen,Haoyun Bai,Chunfa Liu,Jinxian Feng,Di Liu,Lulu Qiao,Shuangpeng Wang,Hui Pan
Electrochemical water splitting is the primary method to produce green hydrogen, which is considered an efficient alternative to fossil fuels for achieving carbon neutrality. For meeting the increasing market demand for green hydrogen, high-efficiency, low-cost, and large-scale electrocatalysts are crucial. In this study, we report a simple spontaneous corrosion and cyclic voltammetry (CV) activation method to fabricate Zn-incorporated NiFe layered double hydroxide (LDH) on commercial NiFe foam, which shows excellent oxygen evolution reaction (OER) performance. The electrocatalyst achieves an overpotential of 565 mV and outstanding stability of up to 112 h at 400 mA cm −2 . The active layer for OER is shown to be β-NiFeOOH according to the results of in-situ Raman. Our findings suggest that the NiFe foam treated by simple spontaneous corrosion has promising industrial applications as a highly efficient OER catalyst.
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高影响因子
IONICS
·
2023
·Vol. 29
·期 7
·2853-2864
·
IF 2.8
Wang Wenping,Zhao Zhiyi,Deng Jiayao,Lang Wei,Zhen Lipeng,Lu Huimin
The oxygen reduction reaction of the cathode in an Al-air battery plays a key role in the performance of the entire battery. Generally, Pt and its alloys are recognized as catalysts with high oxygen reduction catalytic performance, but their application is limited by the rare earth content and high cost. In this paper, α-MnO 2 nanotubes are prepared using a hydrothermal method and used as a template. Nano-Ni–Mn bimetallic oxides with different compositions are prepared with different NiO and α-MnO 2 ratios by calcination. The effects of morphology, phase, and Mn 3+ /Mn 4+ and Ni 3+ /Ni 2+ ratios on electrochemical performance and battery discharge performance are analyzed. The results show that the contents of α-MnO 2 and Ni 6 MnO 8 in NM-12 catalyst are low, and the molar ratio of Mn 3+ /Mn 4+ and Ni 3+ /Ni 2+ is high. Also, the specific surface area of NM-12 is relatively high. Finally, the catalyst prepared with a NiO to α-MnO 2 ratio of 1:2 shows better electrochemical catalytic performance and battery discharge performance that is comparable to that obtained for a commercial 20 wt% Pt/C catalyst.
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JOURNAL OF COLLOID AND INTERFACE SCIENCE
·
2023
·
IF 9.9
Wen-Chao Geng,Jing-Jing Li,Ji-Long Sang,Yu-Xin Xia,Yong-Jun Li
Pt-based multi-metallic electrocatalysts containing hetero-junctions are found to have superior catalytic performance to composition-equivalent counterparts. However, in bulk solution, controllable preparation of Pt-based hetero-junction electrocatalyst is an extremely random work owing to the complexity of solution reactions. Herein, we develop an interface-confined transformation strategy, subtly achieving Au/PtTe hetero-junction-abundant nanostructures by employing interfacial Te nanowires as sacrificing templates. By controlling the reaction conditions, composition-varied Au/PtTe can be easily obtained, such as Au 75 /Pt 20 Te 5 , Au 55 /Pt 34 Te 11 , and Au 5 /Pt 69 Te 26 . Moreover, each Au/PtTe hetero-junction nanostructure appears to be an array consisting of side-by-side Au/PtTe nanotrough units and can be directly used as a catalyst layer without further post-treatment. All Au/PtTe hetero-junction nanostructures show better catalytic activity towards ethanol electrooxidation than commercial Pt/C because of the combining contributions of Au/Pt hetero-junctions and the collective effects of multi-metallic elements, where Au 75 /Pt 20 Te 5 exhibits the best electrocatalytic performance among three Au/PtTe nanostructures owing to its optimal composition. This study may provide technically feasible guidance for further maximizing the catalytic activity of Pt-based hybrid catalysts.
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INTERNATIONAL JOURNAL OF HYDROGEN ENERGY
·
2023
·
IF 7.2
Lingxuan Meng,Lingye Zhang,Suyi Liu,Feng Wang,Huimin Wu
Pollution-free and low-cost bifunctional catalysts are important part for hydrogen production . In this paper, composite catalysts Ni 0.2 Mo 0.8 N/CeO 2 -x/NF (x = n(Ce)/n(Ni)- 0.1, 0.3, 0.5) were synthesized via hydrothermal and calcination methods on foam nickel (NF). Experimental results show that the composites have better properties than CeO 2 /NF, Ni 0.2 Mo 0.8 N/NF and MoN/CeO 2 /NF. The electrochemical properties of the composites depend on the ratio of nickel and cerium . A proper proportion of nickel leads to a larger specific surface area, increased electron capacity, more active sites, and better overall performance. Among the tested composites, Ni 0.2 Mo 0.8 N/CeO 2 -0.3/NF exhibits the best electrochemical performance and is well-suited for catalyzing the hydrogen evolution reaction (HER) and urea oxidation reaction (UOR). For HER, the potential is −120 mV @ 100 mA cm −2 . And for UOR, the UOR potential is only 1.462 V @ 100 mA cm −2 . A two-electrode electrolyzer of Ni 0.2 Mo 0.8 N/CeO 2 -0.3/NF|| Ni 0.2 Mo 0.8 N/CeO 2 -0.3/NF was also built. Overall urea splitting (OUS) is 1.672 V @ 100 mA cm −2 , which is 187 mV smaller than overall water splitting (OWS, 1.859 V). Therefore, Ni 0.2 Mo 0.8 N/CeO 2 has potential application in hydrogen production from urea-rich wastewater electrolysis.
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高影响因子
MOLECULES
·
2023
·Vol. 28
·期 13
·5029
·
IF 4.6
Wei Wang,Ling An,Chi Qian,Yanqing Li,Meiping Li,Xianzhao Shao,Xiaohui Ji,Zhizhou Li
1,3-bis(cyclohexylmethyl)cyclopentane, a renewable high-density fuel, was first produced in a high overall carbon yield (79.5%) with vanillin and cyclopentanone, which can be derived from biomass. The synthetic route used in this work contains two steps. In the first step, 2,5-bis(4-hydroxy-3-methoxybenzylidene)cyclopentanone was synthesized by aldol condensation of vanillin and cyclopentanone under the catalysis of sulphuric acid. Over the optimized condensation, a high carbon yield (82.6%) of 2,5-bis(4-hydroxy-3-methoxybenzylidene) cyclopentanone was achieved at 80 ºC. In the second step, 2,5-bis(4-hydroxy-3-methoxybenzylidene) cyclopentanone was hydrodeoxygenated over the Pd/HY catalyst in cyclohexane as solvent. High carbon yields of 1,3-bis(cyclohexylmethyl)cyclopentane (96.2%) was obtained. The polycycloalkane mixture as obtained has a density of 0.943 g mL−1and a freezing point of −35 °C. It can be blended into conventional high-density fuels (e.g., JP-10) for rockets and missile propulsion as a potential application.Keywords:high-density fuel;vanillin;cyclopentanone;aldol condensation;hydrodeoxygenation
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International Journal of Electrochemical Science
·
2023
·
IF 1.5
Haiyan Wang,Yanan Chen,Wenfu Xie,Xiaoxue Han,Qian Feng,Rong Jiang,Hu Shang,Feifei Zhang,Linna Gao,Zonghua Wang
A novel Pt/Ni-Fe layered double hydroxide (Pt/Ni-Fe LDH) electrocatalyst was fabricated by a two-step facile process for oxidation of methanol in alkaline medium. It is found that Pt/Ni-Fe LDH electrocatalyst exhibits higher electrocatalytic activity, better anti-poisoning ability and stability for methanol oxidation comparing to pure Pt black and commercial Pt/C catalyst. Such an enhancement is probably attributed to the synergistic effect of Ni-Fe LDH and the uniform loading of Pt nanoparticles on the LDH layers. When ionic liquid (IL) was introduced to the composites, the prepared Pt/IL/Ni-Fe LDH exhibits even better electrocatalytic behaviors (205.6 mA mg -1 Pt, I f /I b=5.67) than the Pt/Ni-Fe LDH. Moreover, the morphology and structure of composites were characterized using scanning electron microscope equipped with an energy dispersive X-ray spectrometry, transmission electron microscope, X-ray diffraction, and FT-IR spectra. It is found that the Ni-Fe LDH have a flake-like morphology, the mean diameter of Pt nanoparticles in Pt/Ni-Fe LDH and Pt/IL/Ni-Fe LDH electrocatalyst is 4.36 nm and 3.09 nm, smaller than that in pure Pt black and commercial Pt/C electrocatalyst (8.70 nm and 6.48 nm).
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JOURNAL OF MATERIALS SCIENCE-MATERIALS IN ELECTRONICS
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2023
·Vol. 34
·期 18
·1-15
·
IF 2.8
Shi Haofan,Li Jinping,Zhang Gaoming,Meng Songhe
SiCN ceramic is a candidate material for high-temperature sensors because of its stability and semiconductor characteristics at high temperatures. The free carbon content within the SiCN ceramics is a main factor that affects its conductivity. This study adjusted the free carbon content inside amorphous SiCN by adding divinylbenzene into the precursor. The electrical properties of SiCN ceramics with different free carbon contents were explored using ultraviolet fluorescence spectrum and temperature-resistant experiments. The results showed that with the increase of divinylbenzene from 0 to 20%, the conductivity of SiCN ceramics at room temperature increases from 2.77 × 10 −9 to 3.66 × 10 −4 S/cm, and the forbidden bandwidth decreases from 3.81 to 2.25 eV. At the same time, the increase of divinylbenzene content would promote the hybridization extent of free carbon from sp 3 to sp 2 and improve the degree of order. This work could pave the way for applying amorphous SiCN serving as temperature sensors.
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International Journal of Electrochemical Science
·
2023
·
IF 1.5
Lu Qin,Xiaochun Yu,Jun Li,Shuangyan Li,Yiyan Liu,Pengcheng Qian,Jichang Wang,Shun Wang,Huile Jin
Among existed oxygen reduction electrocatalysts, iron-based catalysts have shown great advantages of low cost and extraordinary reactivity, which are even comparable to commercialized platinum based catalysts. However, the propensity of iron catalysts to aggregate and passivate has emerged as a fundamental barrier to high-power fuel cell applications. In this study, biomass egg yolk derived carbon nanotubes were designed as an armor to host iron complexes, offering multiple active sites such as Fe-N x , Fe 3 C, Fe 2 P for efficient oxygen reduction reaction (ORR). Although the true active sites of iron-based catalysts on the enhanced ORR activities is still under debates, a consensus on the contributions of Fe-N x active center has been reached via a smart material design in this work, which enables ORR onset potential at 0.9 V vs. RHE with excellent four-electron selectivity in alkaline media. Meanwhile, the state-of-the-art carbon shells promote the performance stability remarkably (retaining above 96% of its activity after 27 hours).
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Energy Technology
·
2023
·Vol. 11
·期 8
·2300118
·
IF 3.8
Peiyao Pan,Qingle Zeng,Xiaoxiao Li,Chao Liu,Jinming Zeng,Tongxiang Liang,Xiaopeng Qi
Electrocatalytic water splitting provides an effective way to store electrical energy (i.e., solar and wind energy) intermittently. It is believed that developing electrocatalysts with excellent stability, high catalytic efficiency, and abundant natural reserves is the key to the industrialization of electrochemical water splitting. Herein, nickel–molybdenum electrocatalyst formed on the surface of a low-cost etched stainless-steel mesh via a one-step electrodeposition method exhibits a low hydrogen evolution overpotential of 53 mV and oxygen evolution overpotential of 261 mV at a current density of 10 mA cm −2 due to the synergistic effect of nickel and molybdenum. Moreover, the as-prepared catalyst demonstrates superior hydrogen evolution reaction (HER) catalytic performance than commercial Pt/C at current density exceed 200 mA cm −2 . The electrocatalyst also shows excellent HER and oxygen evolution reaction stabilities at high current density attribute to the tightly bond between electrocatalyst and the etched stainless-steel mesh, as well as the surface reconstruction of catalyst during the cycle test. The facile electrodeposition method has lower requirements on production equipment, using stainless steel mesh as the basement reduces the production cost, the nickel–molybdenum alloy possesses excellent electrolytic water splitting performance and stability. These results indicate that this work can provide an idea for the industrialization of electrochemical water splitting.
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高影响因子
Small
·
2023
·Vol. 19
·期 34
·2301640
·
IF 13.3
Fan Zhang,Renjie Ji,Xiaoyang Zhu,Hongke Li,Yating Wang,Jingpeng Wang,Fei Wang,Hongbo Lan
Highly active bifunctional electrocatalysts for oxygen evolution reaction (OER) and oxygen reduction reaction (ORR) have always been the key factors to affect the performance of zinc–air batteries. However, integrating the independent reaction sites of ORR and OER in a catalyst remains a major challenge. Herein, a collaborative strategy based on defect induction and doping is proposed to prepare the strain-regulated Pt–NiO@Ni sub-micron particles (Pt–NiO@Ni SP). Benefiting from the synergistic effect of tensile strain and Pt-doped, the metallic Ni-based sub-micron particles with tensile strain as the catalyst carriers can effectively optimize the electronic distribution of atomic structures in Pt and NiO on the surface of particles, leading to reduce the energy barrier of intermediates for ORR and OER. Consequently, the Pt–NiO@Ni SP exhibits outstanding bifunctional catalytic activity with the ΔE index of 0.65 V under a low Pt loading, outperforming that of the benchmark Pt/C+IrO 2 catalysts (0.76 V). Impressively, the Pt–NiO@Ni SP-based liquid zinc–air battery develops a high open-circuit potential (1.47 V), excellent energy density (188.2 mW cm −2 ), and favorable cyclic charge–discharge cycling durability (200 h at 20 mA cm −2 ). This work provides an innovative avenue for the rational construction of highly active bifunctional electrocatalysts for practical applications.
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JOURNAL OF PHARMACEUTICAL SCIENCES
·
2023
·
IF 3.8
Wenxuan Cao,Jingbao Chen,Long Wu,Yu hang Xu,Yun Meng,Xiang Li,Zhiyun Zheng,Xiaoqin Chu
Purpose The aim of this study was to develop liquid crystal (LC) precursors to obtain novel long-acting analgesics for injection based on depot systems and compare the difference between the cubic and hexagonal precursors in delivering Diclofenac sodium (DS). Methods Diclofenac sodium liquid crystal precursor injections were prepared and characterized, followed by in vitro release, pharmacodynamic , and pharmacokinetic studies. Results The optimal formulations were prepared with a ratio of Phytantriol/ethanol/water as 76:19:5 for cubic LC precursors, and a ratio of Phytantriol/ethanol/water/Vitamine-E acetate as 72:18:5:5 for hexagonal, both loading various drug dosages (2.5%, 3.75% and 5%), respectively. Polarized light microscopy and small angle diffraction confirmed that the precursors were isotropic fluids and transformed into gels with Pn3m or HII framework in water. Rheological studies have shown that precursors belong to Newtonian fluids and gels to pseudoplastic fluids. The release showed that the DS in the commercial injection (DS-inj) was completely liberated within 6 h, whereas only 46.55% and 49.73% of the DS in 2.5% cubic precursors and 2.5% hexagonal precursors were freed, respectively. Pharmacodynamic studies have shown that cubic, hexagonal and DS-inj raised the pain threshold in mice by 169.4%, 157.3% and 113.79%, respectively. The mean retention times of DS in cubic and hexagonal were 3.16 and 2.67 times longer than DS-inj, respectively, according to pharmacokinetic results. Conclusion In conclusion, cubic and hexagonal are both promising analgesic sustained release formulations. In addition, based only on the current comparison, cubic seems to have a better long-acting effect.
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高影响因子
Advanced Energy Materials
·
2023
·Vol. 13
·期 22
·2300325
·
IF 27.8
Zhen Zhang,Tianping Wang,Weiwen Wang,Xiangnan Wang,Xianglin Luo,Chong Cheng,Xikui Liu
Metallophthalocyanines (MPcs) hold great promise in the electrochemical reduction of oxygen; however, their practical applications in energy storage and conversion are still limited by their low stability and poor water oxidation activity. Herein, a novel stable 2D imide-linked metalphthalocyanine framework (denoted as FePc-PI) is reported, that has atomically dispersed Fe-N 4 sites deposited on the KB substrate via in situ growth, followed by incorporation of ultrafine nickel oxide nanoparticles (NiO x @FePc-PI/KB) to induce bifunctional electrocatalytic activities for the oxygen reduction reaction and oxygen evolution reaction. Benefitting from the robust aromatic backbone, the engineered catalytic centers, and the unique electronic structures owing to the interaction between the Fe-N 4 sites and NiO x species, the newly developed NiO x @FePc-PI/KB catalyst exhibits excellent reversible oxygen bifunctional activity ( E 1/2 = 0.926 V, η 10 = 285 mV), delivering a record-low overpotential difference (Δ E ) of 0.59 V, which far exceeds the noble-metal-based Pt/C+RuO 2 benchmark (Δ E = 0.77 V) and represents the highest level for reported bifunctional electrocatalysts. Furthermore, the rechargeable aqueous Zn-air batteries assembled with the NiO x @FePc-PI/KB catalyst deliver a high peak power density of 232.9 mW cm −2 and long-term cycling durability over 1400 cycles. Flexible all-solid-state Zn-air batteries exhibit stable cycling at various flat/bent/flat states, thus demonstrating their excellent prospects in realistic implementations.
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