INTERNATIONAL JOURNAL OF ENERGY RESEARCH
·
2020
·Vol. 45
·期 4
·5841-5851
·
IF 3.741
Zhi Ming Wang,Peng Liu,Yan Peng Cao,Feng Ye,Chao Xu,Xiao Ze Du
Summary In this study, novel Pt-IrO 2 nanofiber catalysts for oxygen evolution reaction (OER) were successfully prepared using the electrospinning method with a high-concentration precursor solution. The composition and structure of catalysts were characterized, and the electrocatalytic performance of the nanofiber catalysts in water electrolysis was investigated from various aspects such as overpotential, charge transfer resistance, and exchange current density. Special attention was paid on the effect of Pt/Ir ratio on the electrocatalytic activity of the electrospun nanofibers. The results showed that the Pt-IrO 2 nanofiber catalysts with average fiber diameters ranging from 10 to 100 nm can be successfully obtained by the electrospinning method, and the average diameter decreased with the increase of Pt content. Since a bigger amount of IrO 2 content and a thinner fiber structure are all beneficial to the electrocatalytic performance, the Pt-IrO 2 catalysts with Pt:Ir = 1:9 and Pt:Ir = 9:1 both showed better catalytic performance for OER than the commercial IrO 2 , which was also demonstrated by the lower charge transfer resistance and higher exchange current density. As a result, the overpotentials of Pt-IrO 2 catalysts with Pt:Ir = 1:9 and Pt:Ir = 9:1 are 50 mV and 32 mV lower than the overpotential of the commercial IrO 2 at 30 mA cm −2 in 0.5 M H 2 SO 4 , respectively. The electrospun Pt-IrO 2 nanofiber catalyst with proper Pt content seems to be very promising since it can not only improve the catalytic performance and the safety of PEM electrolysis cells, but also reduce the amount of more expensive Ir in catalysts.
研究领域:
材料科学
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电化学
·
纳米材料
·
能源化学
·
催化化学
✓ 已验证
DOI
高影响因子
JOURNAL OF COLLOID AND INTERFACE SCIENCE
·
2023
·
IF 9.9
Xin Guan,Huijie Pei,Xiaoyu Chen,Chen Chang,Siyuan Shao,Yu-Mo Zhang,Xingping Zhou,Hui Nie,Xiaolin Xie
The adsorption-catalysis synergy for accelerated conversion of polysulfides is critical toward the electrochemical stability of lithium-sulfur battery (LSB). Herein, a non-metallic polymer network with anion receptor units, trifluoromethanesulfonyl (CF 3 SO 2 -) substituted aza-ether, was in-situ integrated on PE separator, working as an efficient host for anchoring lithium thiophosphates (LPS) as redox mediators and polysulfides through Lewis acid-base interaction. The anchored LPS on the modified PE separator displayed a robust chemical adsorption ability towards polysulfides through the formation of S S bond. Meanwhile, LPS decreased the energy barrier of Li 2 S nucleation and promoted redox reaction kinetics. The battery with LPS decorated separator revealed a long cycling lifespan with a per cycle decay of 0.056 % after 600 cycles, and a competitive initial capacity of 889.1 mAh/g when the of sulfur cathode increased to 3 mg cm −2 . This work developed a new design strategy to promote the utilization of lithium phosphorus sulfide compounds in LSB.
研究领域:
电化学
·
能源材料
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纳米材料
·
界面化学
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储能技术
✓ 已验证
DOI
高影响因子
Small
·
2024
·Vol. 21
·期 4
·2410657
·
IF 13
Jia Wang,De Wang,Zelin Zhao,Ganggang Chang,Wei Guo,Jun Xu,Yinyu Xiang,Junrui Li,Junsheng Li
Developing cost-effective ruthenium (Ru)-based HER electrocatalysts as alternatives to commercial Pt/C is crucial for the advancement of proton exchange membrane water electrolysis (PEMWE). However, the strong hydrogen adsorption of Ru-based catalysts restricts its activity. Herein, a strategy is reported to tune the electronic structure and improve mass transfer by implanting Ru atoms onto the (002) facet of two-dimensional zeolitic imidazolate framework-67 (Ru@ L ZIF (002) ) to optimize the d -band center ( ε d ) of Ru and the hydrogen spillover behavior. Benefiting from the ultrathin nanosheet structure and optimized ε d of Ru, the over-strong H adsorption energy is weakened and the electron/mass transfer is facilitated. Ru@ L ZIF (002) exhibits an overpotential of 9.2 mV at 10 mA cm −2 and a long-lasting stability of 35 days at 100 mA cm −2 . The mass activity and price activity of Ru@ L ZIF (002) is 2.9 and 14.7 times higher than Pt/C, respectively. More impressively, Ru@ L ZIF (002) delivers a cell voltage of 2.01 V at a high current density of 4 A cm −2 in PEMWE. The excellent long-term durability of 1200 hours operating at 4 A cm −2 with an ultralow decay rate of 7.5 × 10 −3 mV h −1 has been achieved, making it promising as a cost-effective alternative to Pt/C catalyst for PEMWE applications.
研究领域:
电催化
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材料科学
·
能源化学
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纳米材料
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电化学工程
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可持续能源技术
✓ 已验证
DOI
高影响因子
Physica Status Solidi-Rapid Research Letters
·
2019
·Vol. 13
·期 7
·1900063
·
IF 3.729
Di Wu,Jiao Shi,Xiaoming Zheng,Jinxin Liu,Weidong Dou,Yongli Gao,Xiaoming Yuan,Fangping Ouyang,Han Huang
One-dimensional (1D) atomically thin crystals have attracted considerable interest due to their unique properties and potential applications. Herein, the chemical vapor deposition (CVD) growth of molybdenum disulfide (MoS 2 ) nanoribbons on sapphire(0001) supported monolayer MoS 2 flakes without catalysts as well as the characterizations by means of Raman and photoluminescence (PL) spectroscopy, optical microscopy (OM), atomic force microscopy (AFM), and scanning transmission electron microscopy (STEM). The Raman and PL results is reported, as well as OM images reveal that such MoS 2 nanoribbons grow on monolayer MoS 2 flakes. STEM and selected area electron diffraction (SAED) results reveal that they are grown along the 〈 10 1 ¯ 0 〉 direction with atomically sharp edges. Controlled experiments show that the deficiency of sulfur vapor at the beginning of growth induced 1D MoO x S 2− x crystals as precursors. The subsequent sulfurization changes them into MoS 2 nanoribbons. These findings provide a facile approach to MoS 2 nanoribbons and enrich the horizon of the preparation of nanostructured transition metal dichalcogenides.
研究领域:
材料科学
·
纳米科技
·
表面科学
·
凝聚态物理
·
低维材料
✓ 已验证
DOI
高影响因子
TETRAHEDRON-ASYMMETRY
·
2010
·
IF 2.625
Zhen-Wei Zhang,Gui Lu,Miao-Miao Chen,Ning Lin,Yong-Bo Li,Tamio Hayashi,Albert S.C. Chan
The first asymmetric Mannich-type reaction of methyl isocyanoacetate with N -sulfonylimines catalyzed by cinchona alkaloid derivatives yielded 2-imidazolines with high diastereoselectivities and good enantioselectivities (up to >99:1 dr and 70% ee). This reaction provided a convenient route to access various substituted 2-imidazoline-4-carboxylates and related α,β-diamino acids in high enantiomeric purities.
研究领域:
有机化学
·
药物化学
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不对称合成
·
催化化学
·
生物有机化学
✓ 已验证
DOI
高影响因子
JOURNAL OF POLYMER SCIENCE PART A-POLYMER CHEMISTRY
·
2012
·Vol. 50
·期 24
·5177-5184
·
IF 3.919
Yonggang Gao,Lin Gu,Yusheng Qin,Xianhong Wang,Fosong Wang
Low-molecular weight oligo(carbonate-ether) diols are important raw materials for polyurethane formation, which with tunable carbonate unit content (CU) may endow new thermal and mechanical performances to polyurethane. Herein, facile synthesis of oligo(carbonate-ether) diols with number average molecular weight ( M n ) below 2000 g mol −1 and CU tunable between 40% and 75% are realized in high activity by immortal copolymerization of CO 2 /propylene oxide (PO) using zinc-cobalt double metal cyanide complex (Zn-Co-DMCC) in the presence of sebacic acid (SA). M n of the oligomer is in good linear relationship to the mole ratio of PO and SA (PO/SA) and hence can be precisely controlled by adjusting PO/SA. Besides, the molecular weight distribution is quite narrow due to the rapid reversible chain transfer in the immortal copolymerization. High pressure and low temperature are favorable for raising CU. In all the reactions, the weight fraction of propylene carbonate ( W PC ) can even be controlled as low as 2.0 wt %, and the catalytic activity of Zn-Co-DMCC is above 1.0 kgg −1 cat. © 2012 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2012
研究领域:
高分子化学
·
催化化学
·
绿色化学
·
功能材料
·
聚合物合成
·
二氧化碳利用
✓ 已验证
DOI
高影响因子
JOURNAL OF HAZARDOUS MATERIALS
·
2011
·
IF 3.723
Hui Wang,Yuming Huang
Prussian-blue (PB)-modified γ-Fe 2 O 3 magnetic nanoparticles (PBMNPs) were successfully synthesized based on electric interactions between negatively charged [Fe(CN) 6 ] 4− and positively charged γ-Fe 2 O 3 nanoparticles. The in situ PB coating was generated by the coordinating reaction between the adsorbed [Fe(CN) 6 ] 4− and the ferric ions on the surface of γ-Fe 2 O 3 NPs. The as-prepared PBMNPs were characterized by FT-IR, XRD, TEM, and used to remove organic pollutants from aqueous solution, namely, using methylene blue (MB) as model compound. The experimental results showed that the target compound could be removed efficiently from solution over a wide pH range from 3 to 10 in the presence of PBMNPs as peroxidase-like catalyst and H 2 O 2 as oxidant. Under optimal conditions, MB could be removed completely after 120 min of reaction at 298 K; the chemical oxygen demand (COD) removal efficiency and the total organic carbon (TOC) abatement efficiency were 53.6% and 35%, respectively. Furthermore, the PBMNPs catalysts showed high magnetization, temperature tolerance, long-term storage and operational stability, and they could be readily separated from solution by applying an external magnetic field. Finally, a possible reaction mechanism for MB degradation was also discussed.
研究领域:
环境科学
·
纳米材料学
·
催化化学
·
水处理技术
·
环境功能材料
✓ 已验证
DOI
高影响因子
Small
·
2019
·Vol. 15
·期 48
·1901527
·
IF 10.856
Zhaofeng Zhai,Bing Leng,Nianjun Yang,Bing Yang,Lusheng Liu,Nan Huang,Xin Jiang
Tremendous demands for highly sensitive and selective nonenzymatic electrochemical biosensors have motivated intensive research on advanced electrode materials with high electrocatalytic activity. Herein, the 3D-networked CuO@carbon nanowalls/diamond (C/D) architecture is rationally designed, and it demonstrates wide linear range (0.5 × 10 −6 –4 × 10 −3 m ), high sensitivity (1650 µA cm −2 m m −1 ), and low detection limit (0.5 × 10 −6 m ), together with high selectivity, great long-term stability, and good reproducibility in glucose determination. The outstanding performance of the CuO@C/D electrode can be ascribed to the synergistic effect coming from high-electrocatalytic-activity CuO nanoparticles and 3D-networked conductive C/D film. The C/D film is composed of carbon nanowalls and diamond nanoplatelets; and owing to the large surface area, accessible open surfaces, and high electrical conduction, it works as an excellent transducer, greatly accelerating the mass- and charge-transport kinetics of electrocatalytic reaction on the CuO biorecognition element. Besides, the vertical aligned diamond nanoplatelet scaffolds could improve structural and mechanical stability of the designed electrode in long-term performance. The excellent CuO@C/D electrode promises potential application in practical glucose detection, and the strategy proposed here can also be extended to construct other biorecognition elements on the 3D-networked conductive C/D transducer for various high-performance nonenzymatic electrochemical biosensors.
研究领域:
生物医学工程
·
纳米医学
·
电化学传感
·
生物传感器
·
材料科学
·
分子诊断
·
转化医学
✓ 已验证
DOI
高影响因子
JOURNAL OF CLUSTER SCIENCE
·
2017
·Vol. 28
·期 6
·3059-3066
·
IF 1.471
Liang Hua,Yang Zhen-Yuan,Yan Min-Hao,Xie Su-Yuan
The fullerenes that violate isolated pentagon rule (IPR) have unusual electronic properties resulting from their fused-pentagon structures. Numerous non-IPR fullerenes have now been captured by chlorination, affording opportunity to go insight into the properties involved in non-IPR fullerenes in the forms of chlorofullerenes (CFs). Here cyclic voltammetry (CV) is employed to probe the electrochemical properties of non-IPR #1809 C 60 Cl 8 in comparison with those of #271 C 50 Cl 10 . Differing from IPR-satisfying CFs such as C 60 Cl 8 and C 60 Cl 10 (referring to I
h -symmetric C 60 ), the two non-IPR CFs exhibit divergent electroactive polymerization characters. In addition, the electrocatalytic effect of ferrocene that is otherwise employed as internal reference has been shown in the CV process of CFs.
研究领域:
材料化学
·
物理化学
·
纳米材料
·
电化学
·
富勒烯化学
✓ 已验证
DOI
高影响因子
Physica Status Solidi-Rapid Research Letters
·
2023
·Vol. 18
·期 7
·2300102
·
IF 2.8
Wenlong Chu,Ruifeng Xin,Luwei Zou,Xiulian Fan,Xilong Zhou,Cheng Li,Yu Zhou
2D nonlayered materials have attracted more and more attention due to their novel properties and special surface structures. However, due to isotropic chemical bonds within the crystal, the synthesis of ultrathin 2D nonlayered materials is an urgent challenge. Herein, α -Fe 2 O 3 2D nanosheets as thin as ≈8.2 nm on different substrates using self-designed ultralow concentration precursors combined with Gibbs free energy and Se catalysts design are successfully synthesized. The thickness-dependent growth mechanism is systematically studied, demonstrating the thermodynamic and kinetic controlling factors. The as-grown α -Fe 2 O 3 nanosheets are demonstrated with single-crystal structures without any other elements doping. The α -Fe 2 O 3 nanosheets photodetectors show the reasonable response performance with the positive photoconductive mechanism. This improved chemical vapor deposition method provides a promising idea for the synthesis of ultrathin 2D nonlayered materials.
研究领域:
材料科学
·
纳米科技
·
表面科学
·
凝聚态物理
·
光电子学
✓ 已验证
DOI
高影响因子
RSC Advances
·
2017
·Vol. 7
·期 12
·6972-6980
·
IF 3.108
Xiaohui Liu,Qian Zhu,Qiuyan Zhang,Yanguang Zhang,Chen Ding
Over the past few years, ionic liquids (ILs) have been widely reported as reaction media for reverse atom transfer radical polymerization (ATRP). In particular, almost all the ILs with the structure [Hmim][RCOO] (R represents an alkyl group) have been used as ligands for a reverse ATRP system. However, the facile, simple and low-cost ILs, 1-alkyl-3-methylimidazole chloride ([Rmim][Cl]), have rarely been employed as ligands for reverse ATRP. In this article, a [Rmim][Cl] was successfully employed as a ligand for the reverse ATRP of methyl methacrylate with Fe(III) as catalyst and 2,2′-azobisisobutyronitrile as initiator. The key to success is to adjust the FeCl3/[Rmim][Cl] molar ratio value to 1 : 1. The results indicated that the polymerization with [Rmim][Cl] as a ligand proceeded in a controlled/“living” fashion, as evidenced by the first-order kinetic plot, low polydispersity index values, and increase in polymer molecular weight with monomer conversion. The effects of various experimental parameters, including different catalysts, reaction temperatures, solvents, and molar ratios of FeCl3/[Rmim][Cl], on the polymerization were investigated in detail. Furthermore, 1H NMR and gel permeation chromatography analyses confirmed the halogen-containing chain-end functionality of the resultant polymer.
研究领域:
高分子化学
·
有机合成
·
催化化学
·
功能材料
·
可控自由基聚合
✓ 已验证
DOI
高影响因子
INTERNATIONAL JOURNAL OF HYDROGEN ENERGY
·
2023
·
IF 7.2
Xingxing Li,Yan Zhu,Nan Zhang,Yansheng Gong,Rui Wang,Huanwen Wang,Jun Jin,Ling Zhao,Beibei He
The development of symmetrical solid oxide fuel cells (SSOFCs) faces a significant challenge in designing electrode materials that exhibit both high activity and stability. In this work, a novel layered perovskite oxide symmetric electrode material PrBaFe 1.8 Hf 0.2 O 5+δ (PBFH) for SSOFCs is proposed and synthesized. Doping Hf at the B-site of PrBaFe 2 O 5+δ (PBF) improves the stability in reducing atmosphere and increases the concentration of oxygen vacancies . Furthermore, a small amount of RuO x is deposited by atomic layer deposition (ALD) onto PrBaFe 1.8 Hf 0.2 O 5+δ scaffold as symmetric electrodes. The surface modification of ALD-RuO x significantly boosts the catalytic activity for both fuel oxidation and oxygen reduction, simultaneously. Compared to PBF electrodes, the interfacial polarization resistances of RuO x -PBFH decrease to 0.77 Ω cm 2 under H 2 /Ar and 0.021 Ω cm 2 under air atmosphere at 800 °C, respectively. At 800 °C, SSOFCs equipped with RuO x -PBFH symmetric electrodes exhibit a high peak power density of 0.85 W cm −2 and 0.41 W cm −2 using humidified hydrogen and propane as fuels, respectively. Moreover, the RuO x -PBFH electrode demonstrates long-lasting performance, displaying high resistance against coking. These findings reveal a facile ALD approach for tailoring symmetric perovskite electrodes, offering robust and efficient electrocatalysis with efficient noble metal utilization.
研究领域:
材料科学
·
电化学
·
能源材料
·
固体离子学
·
催化化学
·
功能陶瓷
✓ 已验证
DOI
高影响因子
危险品化学品经营许可证（带存储）