RSC Advances
·
2016
·Vol. 6
·期 100
·97783-97790
·
IF 3.289
Ying Sun,Qizan Huang,Xueqin Zhang,Xiaojing Ding,Pei Han,Baoping Lin,Hong Yang,Lingxiang Guo
In recent years, side chain engineering has been proven to play a critical role in the development of high performance conjugated polymers for organic electronics. Here, we report a new strategy to improve charge transport property through side chain functionalization. A series of carbazole–diketopyrrolopyrrole based conjugated polymers P1, P2 and P3 with different side chains have been designed and synthesized. For P2 and P3, a pyrene and carbazole unit were incorporated into the terminal of the alkyl side chain, respectively. Thermal properties, crystallinities, UV-vis absorptions, electrochemical properties as well as charge transport properties of the polymers were investigated in detail. Interestingly, results showed that incorporation of the fused aromatic ring into the side chain terminal not only changed the absorption and electrochemical properties, but also affected the charge transport properties. The pyrene and carbazole group in the side chain terminal significantly promoted aggregation of the polymer chains, which would provide short-range order for improved charge carrier mobility. Compared to the hole mobility (0.019 cm2 V−1 s−1) for polymer P1 with the whole alkyl chains, increased hole mobilities of 0.081 cm2 V−1 s−1 and 0.052 cm2 V−1 s−1 were achieved for polymer P2 and polymer P3, respectively. It is worthy to note that our strategy gives rise to no increment of the crystallinity of the polymer, being beneficial for the practical application of soft electronics since high crystallinity of the material usually leads to poor thin film uniformity and weak mechanical resilience. In this respect, we offer a promising tool to aid rational polymer design for enhanced charge transport property.
研究领域:
高分子化学
·
有机电子学
·
材料科学
·
半导体材料
·
光电功能材料
✓ 已验证
DOI
高影响因子
LANGMUIR
·
2019
·
IF 3.683
Yanru Yin,Ning Ma,Jing Xue,Guoqiang Wang,Shuibo Liu,Hongliang Li,Peizhi Guo
Four types of palladium (Pd) nanoparticles were prepared from the systems containing PdCl2 or Na2PdCl4 with or without the assistance of poly(vinylpyrrolidone) (PVP). Two types of Pd nanoparticles obtained in the absence of PVP were obviously larger than those synthesized with the assistance of PVP. The former large Pd particles showed typical features in cyclic voltammetry in H2SO4 solution, whereas two types of small Pd nanoparticles did not. However, small nanoparticles treated first in an electrochemical way in 0.5 M KOH solution displayed the adsorption and desorption peaks similar to those of typical Pd-modified electrodes in H2SO4 solution. Large Pd nanoparticles from the PdCl2 synthesis system showed a catalytic specific current of 629 mA/mg in the electrocatalysis of ethanol, whereas large particles from the Na2PdCl4 system showed a current of 262 mA/mg. The maximum catalytic currents of small Pd nanoparticles without surface cleaning treatment were 1382 and 1019 mA/mg for samples from the Na2PdCl4 and PdCl2 systems, respectively, higher than those being treated in KOH solution first, and the electrocatalytic stability of the two untreated samples was better. However, small nanoparticles after the electrochemical treatment can reach the maximum catalytic current faster. The synthesis and structure–property relation of four types of Pd nanoparticles have been discussed and analyzed on the basis of systematically experimental data.
研究领域:
材料科学
·
电化学
✓ 已验证
DOI
PubMed
高影响因子
ANALYTICA CHIMICA ACTA
·
2019
·
IF 5.256
Mengxiao Zhong,Maoqiang Chi,Yun Zhu,Ce Wang,Xiaofeng Lu
Controllable fabrication of novel and uniform noble metal nanoparticles on a specific support with a superior catalytic or electrocatalytic performance is of significantly importance for practical applications. In this report, we demonstrated an effective way to fabricate uniform thin-walled Pd/polypyrrole (PPy) hollow nanotubes . The prepared Pd/PPy hybrid nanotubes exhibited an excellent peroxidase-like activity to oxidize a typical peroxidase substrate such as 3,3′,5,5′-tetramethylbenzidine in comparison with traditional Pd/C and Pd black catalysts. The outstanding catalytic activity of the Pd/PPy hybrid nanotubes for peroxidase mimicking could be resulting from their unique hollow characteristic and an interfacial effect between PPy and Pd components. Based on the favorable catalytic property of the Pd/PPy hybrid nanotubes, a convenient and rapid colorimetric way to sensitively determine ascorbic acid has been presented. The detection limit was around 0.062 μM and an excellent selectivity was also achieved. The developed detection system in this study could be extended to the fields of bioscience and biotechnology with promising prospects.
研究领域:
生物化学
·
材料科学
·
分析化学
✓ 已验证
产品关联
DOI
PubMed
高影响因子
JOURNAL OF ELECTROANALYTICAL CHEMISTRY
·
2016
·
IF 2.822
Yanmeng Cai,Yue Wang,Xinyu Han,Liwen Zhang,Shichang Xu,Jixiao Wang
The composites of carbon nanotube (CNT) and the conducting polymer polypyrrole (PPy) doped with dodecyl benzene sulfonate (DBS − ) and Cl − were prepared respectively by chemical oxidation method and made into two types of composite electrode (PPy-DBS/CNT and PPy-Cl/CNT) for capacitive deionization (CDI) cell. Enhanced electrochemical performance of the composite electrodes was confirmed by cyclic voltammetry (CV) and electrochemical impedance spectroscopy (EIS) test. The results of CV showed that the specific capacitance of PPy/CNT doped with either DBS − or Cl − was about 2.3–2.5 times that of the CNT electrode. And EIS test demonstrated that the charging resistance for both the PPy-DBS/CNT and PPy-Cl/CNT electrodes was dramatically reduced and only about 10% that of the CNT electrode. By pairing the two composite electrodes with CNT electrodes, four cells were assembled to study the effects of electrode assembling patterns on the desalination performance of the CDI process. The results indicated that the CDI cells involving either the PPy-DBS/CNT electrode or the PPy-Cl/CNT electrode, or both of them exhibited much higher electrosorption capacity (from 40.8 to 72.36 mg/g) than that of the CDI cell assembled with two CNT electrodes (about 12.6 mg/g). And the composite electrodes kept good stability and fast regeneration rate after several desalting cycles. Thus, it is believed that the enhanced performance and optimized electrode assembly of the CDI cell should be with the composite electrodes that have the good ability of ion selective adsorption for cations or anions.
研究领域:
材料科学
·
环境工程
·
电化学
·
水处理技术
·
功能高分子材料
✓ 已验证
DOI
高影响因子
JOURNAL OF APPLIED POLYMER SCIENCE
·
2022
·Vol. 139
·期 21
·52199
·
IF 3.057
Wenjiao Wang,Mingming Zheng,Jiajia Ren,Mingliang Ma,Xunqian Yin,Tingxi Li,Yong Ma
Magnetic Fe 3 O 4 /MnO 2 /TiO 2 /polypyrrole (PPy) heterostructure as adsorbent for adsorbing Mn 7+ was synthesized by combining hydrothermal method and chemical oxidation method. The heterostructure was characterized by field-emission scanning electron microscope, Fourier transform infrared spectroscopy, X-ray diffraction, and vibrating sample magnetometer. Its saturation magnetization is 18.88 emu/g, so it is easy to separate it from the solution. The feasibility of Fe 3 O 4 /MnO 2 /TiO 2 /PPy heterostructure to remove Mn 7+ was researched in detail. It is found that the optimal pH is 2. The initial adsorption rate can reach 4.60 mg/g min. At 288.15 K, the maximum equilibrium adsorption capacity is 202.8 mg/g. Adsorption kinetics follows a pseudo second order model, as well as is determined by through membrane diffusion processes. The Langmuir isotherm model is used to describe the adsorption isotherm behavior. Besides, thermodynamic parameters indicate spontaneous adsorption behavior, and entropy of the endothermic reaction increases. Finally, the cycle test results show that the adsorbent has better cycle performance, displaying broad application prospects.
研究领域:
环境科学
·
材料科学
·
化学工程
·
纳米技术
·
污染控制
✓ 已验证
DOI
高影响因子
Bioactive Materials
·
2017
·Vol. 3
·期 1
·74-79
·
IF 0
Zhengao Wang,Jinquan Zeng,Guoxin Tan,Jingwen Liao,Lei Zhou,Junqi Chen,Peng Yu,Qiyou Wang,Chengyun Ning
To improve the osteointegration property of biomedical titanium, nano-architectured electroactive coating was synthesized through the electrochemical polymerization of dopamine and pyrrole. The highly binding affinity of Ca 2+ to the catechol moiety of doped dopamine enabled efficient interaction between polypyrrole/polydopamine nanowires and mineral ions. The results indicate that the PPy/PDA nanowires preserved its efficient electro-activity and accelerated the hydroxyapatite deposition in a simulated body fluid. The PPy/PDA nanowires coating could be applied to promote the osteointegration of titanium implant.
研究领域:
生物材料学
·
骨科学
·
表面工程
·
组织工程
·
生物医学工程
·
纳米医学
✓ 已验证
DOI
JOURNAL OF HETEROCYCLIC CHEMISTRY
·
2022
·Vol. 59
·期 9
·1561-1572
·
IF 2.035
Ling Jiang,Si-Yu Yan,Jing-Wen Dong,Li-Dan Ye,Yue Cheng,Xiao-He Chu
A series of polysubstituted pyrroles were rapidly synthesized in moderate to good yields via catalyst-free one-pot three-component reaction of 1,3-dicarbonyl compounds with primary amines and nitrostyrenes by using liquid-assisted grinding. This protocol provides several advantages over the conventional chemical synthesis, such as simple work-up procedure, wide substrate scope, short reaction time, and environmental friendliness. Structures of polysubstituted pyrroles were confirmed by 1 H NMR, 13 C NMR, and ESI-MS studies.
研究领域:
有机化学
·
药物化学
·
绿色化学
·
合成方法学
·
杂环化学
✓ 已验证
DOI
高影响因子
MATERIALS LETTERS
·
2016
·
IF 2.437
Yan Fang,Xiaohong Jiang,Lihong Niu,Shujie Wang
Polypyrrole/aligned carbon nanotubes (PPy/ACNTs) core-shell nanotube arrays on metal foil have been fabricated through an electrochemical method. The as-prepared PPy/ACNTs electrode materials with novel nanostructure , which is very conducive to the transmission of electrons and ions, possess greatly improved electrochemical performance. The specific capacitances of PPy/ACNTs electrode materials can reach 505 F/g ( vs. the both mass of PPy and ACNTs) in three-electrode system. In two-electrode system, the specific capacitances of the PPy/ACNTs electrode materials can reach 456 F/g ( vs. the both mass of PPy and ACNTs). The PPy/ACNTs electrode materials also exhibit greatly improved rate capability and superior cycling performance.
研究领域:
材料科学
·
电化学
·
纳米科技
·
能源存储
·
功能材料
✓ 已验证
DOI
高影响因子
JOURNAL OF ELECTROANALYTICAL CHEMISTRY
·
2016
·
IF 2.822
Xinhe Zhang,Bo Jin,Linlin Li,Tuo Cheng,Huanhuan Wang,Peiming Xin,Xingyou Lang,Chuncheng Yang,Wang Gao,Yongfu Zhu,Qing Jiang
Non-graphitizable carbon (NGC) has been obtained by carbonizing tubular polypyrrole (T-PPy) synthesized through a self-degraded template method . K-NGC/S composite has been prepared by mixing S with K-NGC via melt-diffusion method where NGC has been activated by potassium hydroxide (denoted as K-NGC) and is used as a conductive additive. The as-prepared K-NGC/S composite shows good specific discharge capacity and rate capability with an initial specific discharge capacity of 1121.9 mAh g − 1 and a specific discharge capacity of 729.7 mAh g − 1 after 50 cycles at a current density of 335 mA g − 1 , which is better than pure S. This improvement in the specific discharge capacity and the rate capability of the cell with K-NGC/S composite as a cathode material is realized by the existence of K-NGC, which can offers a superb conductive environment for S, effectively encapsulate S, restrain the outward diffusion of polysulfides , buffer volume change upon cycling and reduce the dissolution of lithium polysulfides into the electrolyte. The good electrochemical performance of K-NGC/S composite would make it become a promising cathode material for lithium-sulfur batteries.
研究领域:
材料科学
·
电化学
·
能源存储
·
纳米材料
·
电池技术
✓ 已验证
DOI
高影响因子
Journal of Materials Chemistry A
·
2013
·Vol. 1
·期 47
·14943-14950
·
IF 0
Hai Fu,Zhong-jie Du,Wei Zou,Hang-quan Li,Chen Zhang
A carbon nanotube reinforced polypyrrole nanowire network was constructed by in situ polymerization of pyrrole in the presence of carbon nanotubes using cetyltrimethylammonium bromide micelles as a soft template. Carbon nanotubes as a reinforcer were embedded into a network of polypyrrole nanowires, thus retaining in the latter a complete network. The resulting network possessed a specific surface area of 112.1 m2 g−1 and a rough porous structure. The embedding of carbon nanotubes decreased the charge transfer resistance in the polypyrrole nanowires and allowed easy access and rapid diffusion of ions/electrons. When applied as a capacitive electrode, a specific capacitance of 183.2 F g−1 was observed at a current density of 8 A g−1. The specific capacitance retention was 85% after 1000 cycles at 1 A g−1. An asymmetric supercapacitor was fabricated using the network as a positive electrode and active carbon as a negative electrode, and when operated at a maximum voltage of 1.5 V, had a high energy density (15.1 W h kg−1 at 3000 W kg−1). A long-term cycling test of the asymmetric supercapacitor at a current density of 1 A g−1 displayed a capacitance retention of 72% even after 3000 cycles of charge and discharge.
研究领域:
材料科学
·
纳米科技
·
电化学
·
能源存储
·
高分子科学
✓ 已验证
DOI
Journal of Materials Chemistry A
·
2014
·Vol. 2
·期 19
·6740-6746
·
IF 0
Weining Sun,Xiaofeng Lu,Yan Tong,Junyu Lei,Guangdi Nie,Ce Wang
In this report, a palladium/polypyrrole/polyacrylonitrile (Pd/PPy/PAN) composite nanofiber membranes was synthesized by a one-pot redox polymerization process between pyrrole monomers and Na2PdCl4 in the presence of electrospun PAN nanofibers, without the introduction of any other surfactants or reductants. The as-prepared Pd/PPy/PAN nanofiber membrane exhibited good catalytic performance towards hydrogen generation from the hydrolysis of ammonia borane (AB). The apparent activation energy (Ea) was calculated to be about 33.5 kJ mol−1. In addition, the Pd nanoparticles (Pd NPs) were encapsulated in PPy layers on the surface of the PAN nanofibers, enabling the catalyst to be stable against poisoning and easily separated from the suspension system. The catalytic activity does not weaken after five cycles. This study indicated that the obtained Pd/PPy/PAN composite nanofiber membrane could be applied as an alternative in exploring new catalysts for hydrogen generation, as hydrogen is an important fuel as a clean power source.
研究领域:
材料化学
·
纳米催化
·
能源材料
·
高分子科学
·
氢能源
✓ 已验证
DOI
JOURNAL OF COLLOID AND INTERFACE SCIENCE
·
2023
·
IF 9.9
Zecheng Yang,Liluo Shi,Hao Wang,Jianzhen Xiong,Xuena Xu,Limei Sun,Jiangmin Jiang,Quanchao Zhuang,Yaxin Chen,Zhicheng Ju
Carbon nanosheets (CNS) have garnered significant interest as anode materials for potassium-ion batteries (PIBs) due to the excellent potassium storage kinetics and rate performance. Moreover, tuning the thickness of CNS can enhance the potassium storage performance by exposing abundant surface active sites and shortening the K + migration path. Herein, crystallization-induced thickness tuning of carbon nanosheets in polyvinyl pyrrolidone-potassium chloride (PVP-KCl) solution is reported to enhance the fast potassium storage. PVP with varying molecular weights is employed to induce the crystallization behavior of KCl, leading to the formation of KCl grains with controllable sizes. Concurrently, these KCl grains act as hard templates for dispersing the PVP molecules to fabricate carbon nanosheets on the surface during annealing. PVP with high molecular weight is beneficial for hindering ion migration to reduce crystal sizes, which can decrease the thickness of carbon nanosheets. The ultrathin structure exposes abundant potassium storage sites, endowing CNS with high reversible capacity (359.0 mAh/g at 100 mA/g). The reduction in the migration path of K + ions facilitate rapid ion and electron transport kinetics, resulting in rate performance with a capacity of 181.9 mAh/g at 1 A/g. Our work extends the application of the crystallization-induced strategy for controllable designing carbon nanosheets, and puts forward some conceptions on improving the potassium storage performance of carbon anode materials.
研究领域:
材料科学
·
电化学
·
纳米能源
·
储能技术
·
碳材料
·
电池材料
✓ 已验证
DOI
高影响因子
危险品化学品经营许可证（带存储）