ORGANIC ELECTRONICS
·
2019
·
IF 3.495
Xin Qi,Ganghong Liu,Duo Wang,Ning Zhu,Yuqing Zhang,Zehao Zhang,Cuncun Wu,Xiangdong Li,Wei Luo,Yingqiang Li,Haozhe Hu,Zhijian Chen,Lixin Xiao,Shufeng Wang,Bo Qu
Interfacial modification as a feasible strategy to improve the properties of perovskite solar cells (PSCs) has been widely studied in recent years. In this work, PbCl 2 modification at the interface of SnO 2 /CH 3 NH 3 PbI 3 was used for CH 3 NH 3 PbI 3 -based planar PSCs. The introduction of PbCl 2 between SnO 2 and CH 3 NH 3 PbI 3 layers boosted the crystallization of perovskite film, which promoted the photovoltaic properties of corresponding PSCs. The open circuit voltage ( V OC ) and fill factor (FF) of the PbCl 2 -modified devices (1 mg/mL) were 1.11 V and 0.79, respectively, which were both higher than those of the reference devices without PbCl 2 (1.04 V and 0.76). Moreover, a steady-state power output efficiency exceeding 19% was obtained for the PbCl 2 -modified devices (1 mg/mL), which implied that PbCl 2 modification was an effective and low cost strategy for efficient PSCs.
研究领域:
材料科学
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光伏技术
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纳米科技
·
表面与界面工程
·
能源材料
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半导体器件
·
功能材料
✓ 已验证
DOI
高影响因子
JOURNAL OF MEMBRANE SCIENCE
·
2019
·
IF 7.015
Ziqiang Tong,Xiufeng Liu,Baoquan Zhang
A series of sphere-like polyelectrolyte complexes (PECs) and their homogeneous polyelectrolyte complex membranes (HPECMs) were synthesized by using sodium carboxymethyl cellulose (CMCNa) and poly(diallyldimethylammonium chloride) (PDDA). Different compositions or ionic complexation degrees (ICD) of PECs could be characterized by FT-IR spectra. The circular dichroism spectrum (CD) and field emission scanning electron microscopy (FESEM) were employed to examine the conformation and morphology of PECs, respectively. Zeta (ζ) potential was utilized to investigate the charge density of PEC particles while the surface hydrophilicity of HPECMs was studied by using contact angle (CA) meter. When subjected to ethanol dehydration, HPECMs revealed a satisfactory pervaporation performance and desired anti-trade-off phenomenon. For HPECM 0.31 and HPECM 0.57, the permeation fluxes were 2.25 kg m −2 h −1 and 2.93 kg m −2 h −1 , and the water content in permeate reached up to 99.35 wt% and 99.38 wt%, with respect to 10 wt% water in feed under 70 °C. All the results indicated that small-sized and sphere-like PECs were truly in favor of enhancing the pervaporation performance in ethanol dehydration.
研究领域:
高分子科学
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膜分离技术
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化学工程
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材料科学
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物理化学
✓ 已验证
DOI
高影响因子
JOURNAL OF POWER SOURCES
·
2014
·
IF 5.211
Q.Q. Xiong,J.P. Tu,X. Ge,X.L. Wang,C.D. Gu
Fe 2 O 3 nanospindles assembled with nanoparticles as primary building blocks are directly synthesized by a versatile ionothermal strategy in the choline chloride/urea mixture-based deep eutectic solvent system. The proposed ionothermal protocol is attractive and environmental friendly because choline chloride and urea are both naturally biocompatible compounds. As an anode material for lithium-ion batteries, the resultant Fe 2 O 3 nanospindles show high capacity and good cycle stability (921.7 mAh g −1 at a current density of 200 mA g −1 up to 50 cycles), as well as the excellent rate capability. The good electrochemical performance can be attributed to the nanospindle structure with high sufficient interfacial contact area between the active material and electrolyte, the short diffusion distance of Li ions . The environmentally benign strategy proposed in this study is expected to offer an attractive technique for the ionothermal synthesis of electrochemical energy storage materials .
研究领域:
材料科学
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电化学
·
纳米科技
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能源存储
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无机合成
✓ 已验证
DOI
高影响因子
IONICS
·
2016
·Vol. 22
·期 11
·2225-2233
·
IF 2.119
Lu Juanjuan,Liu Yuelin,Liu Xinhe,Lu Xiaoquan,Liu Xiuhui
In this article, we constructed an electrochemical sensor for highly sensitive determination of β-nicotinamide adenine dinucleotide (NADH) using the poly(diallyldimethylammonium chloride)-functionalized reduced graphene oxide nanocomposite modified electrode (PDDA-rGO/GCE). The nanocomposite was characterized by transmission electron microscopy, Fourier transform-infrared spectrometry, ultraviolet-visible absorption spectrometry, cyclic voltammetry, and electrochemical impedance spectroscopy. The experimental results demonstrated that the fabricated sensor exhibited excellent electrocatalytic activity on the oxidation of NADH with a decreased about 200 mV in overpotential and 5.0-fold increment in the oxidation peak current compared to a bare GCE. Applying cyclic voltammetry, a wide linear range from 1.0 × 10 −7 to 2.9 × 10 −3 M with low limit of detection (LOD) of 3.4 × 10 −8 M and high sensitivity of 463.3 μA mM −1 cm −2 were obtained, which was superior to other NADH electrochemical sensors reported previously. Furthermore, the fabricated NADH sensor possessed excellent selectivity, reproducibility, and stability. The oxidation mechanism of NADH at the PDDA-rGO/GCE was also discussed in detail.
A simple NADH sensing platform based on PDDA-rGO composite is constructed, which exhibits an ultra-low detection limit ( 3.4×10-8 M) towards the oxidation of NADH, and the electrochemical reaction mechanism of NADH is discussed in detail.
研究领域:
生物电化学
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生物传感器
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纳米生物技术
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分子诊断
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转化医学
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电分析化学
✓ 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
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