Energy Technology
·
2021
·Vol. 9
·期 12
·2100743
·
IF 3.631
Xin Hou,Penggang Ren,Zhong Dai,Zhengzheng Guo,Zengping Zhang,Aiyue Sun,Wenwei He,Fang Ren,Yanling Jin
Herein, nitrogen, oxygen codoped porous carbon nanofibers (CNFs) from corn residue-derived lignin are fabricated via the electrospinning method, followed by introduction of graphenes (GNs) via a simple “brush-coating and drying” process. The obtained GN-coated carbon nanofibers (CNFs@GNs) exhibit a 3D network architecture, abundance of heteroatoms, excellent electrical conductivity, high specific surface area (700.92 m 2 g −1 ), thus boosting the electrochemical performances. The CNFs@GNs electrode delivers a higher specific capacitance of 271.1 F g −1 than CNFs (200.3 F g −1 ) at 1 A g −1 . Furthermore, the assembled CNFs@GNs symmetric supercapacitor exhibits an energy density of 20.3 Wh kg −1 at the power density of 199.97 W kg −1 together with a high charge/discharge reversibility of 97.3% and Coulombic efficiency of 99.81% after 10 000 cycles. This “brush-coating and drying” strategy utilized here provides a convenient and efficient route for designing CNFs and GN composites and can be utilized in other active materials.
研究领域:
材料科学
·
纳米科技
·
电化学
·
能源存储
·
功能材料
✓ 已验证
DOI
高影响因子
MATERIALS & DESIGN
·
2016
·
IF 3.997
XinRong Liu,Ming Zhang,TingTing Yang,LiNa Wang,Han Zhu,ShunLi Wang,MingLiang Du
Carbon nanofibers served as nanoreactors for the design and construction of PtCo alloy carbon core-shell nanostructures with nitrogen doping (PtCo/NCNF) through a combination of electrospinning and nitrogen doping treatments. The PtCo/NCNF hybrid consists of PtCo alloy nanoparticles surrounded by a few of N-doped carbon layers , demonstrating a typical core-shell structures. The PtCo/NCNF hybrid can both served as electrode materials for electrocatalytic water splitting including hydrogen evolution reaction (HER) and oxygen evolution reaction (OER). For the HER performance, the PtCo/NCNF exhibits very small onset potential of 20 mV, an overpotential of 50 mV at a j (vs RHE) = 10 mA cm − 2 and Tafel slope of 30 mV dec − 1 . The PtCo/NCNF hybrid also exhibits high OER activity with an onset potential of 310 mV, an overpotential of 400 mV at a j of 10 mA cm − 2 and a small Tafel slope of 76 mV dec − 1 . The high catalytic activities of PtCo alloy for HER and OER originate from the 3D hierarchical structures, well-dispersed PtCo alloy, high conductivity of NCNF, protection from the carbon-encapsulated structure, and the introduction of nitrogen.
研究领域:
材料科学
·
纳米技术
·
电化学
·
能源化学
·
催化化学
·
功能材料
✓ 已验证
DOI
高影响因子
CHEMICAL ENGINEERING JOURNAL
·
2016
·
IF 5.31
Shunhang Wei,Rong Wu,Xiaoxiang Xu,Jikang Jian,Haixia Wang,Yanfei Sun
Black core-shelled anatase titania were successfully prepared using a simple one-step synthetic method by calcining colloid titania precursor in N 2 flow under atmospheric pressure. The physicochemical properties of the as-prepared samples were characterized by various techniques such as X-ray diffraction, high resolution transmission electron microcopy, etc. The samples demonstrate a unique core-shelled structure and electron paramagnetic resonance spectra reveal the presence of high concentration of Ti 3+ and oxygen vacancies at the surface, which accounts for their black appearance. A possible mechanism for the formation of such core–shell structure is proposed based on the results (X-ray photoelectron spectra, etc) of products prepared under different ration between urea and hydrochloric acid. Ethanol absolute is found to have critical effect in preventing phase transition of titania (from anatase to rutile) upon elevated temperatures. The black appearance of the sample powder (high visible light absorption) as well as slow electron/hole recombination rate after introducing oxygen vacancies/N species signify the core-shelled anatase titania as an efficient visible light active photocatalyst.
研究领域:
材料科学
·
光催化
·
纳米材料
·
表面化学
·
无机合成
✓ 已验证
DOI
高影响因子
CERAMICS INTERNATIONAL
·
2020
·Vol. 46
·期 13
·21560-21568
·
IF 3.83
Mingcai Li,Xuejie Zhang,Yinjian Zheng,Yaliang Xu,Haoran Zhang,Yingliang Liu,Bingfu Lei
The discovery of light converter excited by near-ultraviolet (UV) superior broadband blue-emitting lighting source is a main challenge in plant growth LEDs. In this study, SrLu 2 O 4 :Ce 3+ , Li + , F − blue phosphor has been synthesized via a solid-state reaction. Benefitting from doping of F − ions, SrLu 2 O 4 :Ce 3+ , Li + , F − phosphor (λ ex = 405 nm, λ em = 460 nm) shows a strong broadband (FWHM = 90 nm) blue-emitting with lower critical concentration of Ce 3+ ions and an increasing 6.9% thermal quenching performance (92.1% @ 423 K of the peak intensity at room temperature). Moreover, a blue light converter composed of SrLu 2 O 4 :Ce 3+ , Li + , F − phosphor and glass matrix is obtained based on phosphor-in-glass (PiG) technology, exhibiting excellent thermal stability and outstanding moisture resistance . A red light converter with commercial red phosphor is obtained by the same method. Furthermore, by combining of two light converters with near-UV chip, a proof-of-concept plant growth high power LED is achieved and applied in indoor Italian lettuce growing in comparison with commercial plant lamps.
研究领域:
材料科学
·
光学工程
·
农业光电子学
·
固体发光
·
无机非金属材料
✓ 已验证
DOI
高影响因子
Advanced Electronic Materials
·
2023
·Vol. 9
·期 11
·2300392
·
IF 6.2
Guangliang Li,Lingxian Kong,Qi Su,Xianhua Tan,Xuning Zhang,Zhiyong Liu,Tielin Shi,Guanglan Liao,Bo Sun
Few-layer black phosphorus (FL-BP) shows great potential in infrared polarization-sensitive photodetection due to its narrow bandgap and strong in-plane anisotropy. However, FL-BP is easy to be oxidized and degraded, which severely restricts its applications. Herein, a simple and scalable in situ interfacial passivation method based on pentacene film is reported to enhance the ambient stability of FL-BP as well as achieve n-type doping for improved polarization-sensitive photoimaging. High crystal quality FL-BP flakes with intrinsic anisotropy are prepared by electrochemical exfoliation. The morphology and Raman spectra of FL-BP/pentacene exhibit excellent stability 28 days after passivation. In addition, the hole mobility is significantly enhanced and dark current is substantially suppressed due to the interfacial passivation and n-type doping effect. The FL-BP/Pentacene based photodetector shows a broadband response from visible to near-infrared with good stability. The photoresponsivity under 915 nm illumination is calculated as 2.2 mA W −1 with an anisotropy ratio of 1.29. Furthermore, the polarization imaging under the irradiation at zigzag and armchair directions directly reveals the strong infrared polarization-sensitive imaging capability of FL-BP/pentacene. This work also opens up new avenues to enhance the photoresponse and stability of various optoelectronics based on similarly unstable 2D materials.
研究领域:
纳米材料学
·
光电子学
·
二维材料
·
半导体物理
·
红外成像
·
表面科学
✓ 已验证
DOI
高影响因子
JOURNAL OF ALLOYS AND COMPOUNDS
·
2016
·
IF 3.014
Dong Zhang,Xuanxuan Ma,Qi Zhang,Yanru Xie,Qiang Shi,Qiangru Wang,Wenjun Wang
Zn x Al 2 O 4 :Cr 3+ (0.8 ≤ x ≤ 4) phosphors with spinel structure were prepared by using sol-gel method. The structure, morphology and photoluminescence properties were analyzed by using X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), electron paramagnetic resonance (EPR) and photoluminescence (PL). The spinel structure of ZnAl 2 O 4 was formed for all samples, and hexagonal structure of ZnO appeared in the powders with x ≥ 1.1. The results of XRD, SEM and TEM showed that the crystallinity of Zn x Al 2 O 4 :Cr 3+ phosphors was improved with increasing the value of x . The PL spectra showed a series of sharp emission peaks ranging from 650 nm to 730 nm assigned to spin-forbidden 2 E g → 4 A 2 g transition of Cr 3+ ions in spinel lattices. The most intense emission was observed in Zn 1.2 Al 2 O 4 :Cr 3+ powders, and the results of EPR showed that this enhancement resulted from the best dispersity of Cr 3+ ions in Zn x Al 2 O 4 lattices.
研究领域:
材料科学
·
无机化学
·
固体物理
·
发光材料
·
纳米材料
✓ 已验证
DOI
高影响因子
INTERNATIONAL JOURNAL OF ENERGY RESEARCH
·
2022
·Vol. 46
·期 12
·17056-17067
·
IF 4.672
Tao Lyu,Shiying Lin,Lanlan Mo,Feijun Wang,Ziqiang Shao
Summary Natural polyelectrolyte complex has designable structure, unique advantages of composite and strong intermolecular or intramolecular force without chemical cross-linking agents, showing the advantages of good biodegradability and low toxicity. This work reports an application research of natural polyelectrolyte in energy storage device. A multi-doped hierarchically porous carbon is fabricated from polyelectrolyte of sodium lignosulfonate and chitosan and used as electrode material of supercapacitor. The material characterization reveals its large specific surface area of 1768 m 2 g −1 , pore volume of 0.94 cm 3 g −1 with optimum 3D porous structure, and high heteroatom (oxygen, nitrogen, and sulfur) concentration. Benefit from these, the electrodes it made exhibit 354 F g −1 specific capacitance at 1 A g −1 current density, outstanding rate retention of 82.9% at a testing environment of 20 A g −1 , and 97.8% capacitance retention in 3 M KOH electrolyte after 10 000 cycles. Using this material, all-solid symmetric supercapacitor devices show 30.11 Wh kg −1 energy density at 520.88 W kg −1 power density and retains 20.90 Wh kg −1 at 1.03 kW kg −1 . These remarkable electrochemical performances prove the promising porous carbon in this work as electrode material with excellent performance for supercapacitors.
研究领域:
材料科学
·
电化学
·
能源存储
·
纳米材料
·
功能材料
·
碳材料
✓ 已验证
DOI
高影响因子
SOLID STATE IONICS
·
2020
·
IF 3.107
Yayu Guo,Huilan Guan,Wenxiu Peng,Xuelei Li,Yue Ma,Dawei Song,Hongzhou Zhang,Chunliang Li,Lianqi Zhang
Li 7 P 3 S 11 (70Li 2 S·30P 2 S 5 ) sulfide is a promising electrolyte candidate for all-solid-state lithium batteries (ASSLBs) owing to its high ionic conducivity and wide electrochemical stability window. However, the sensitivity to moisture and the poor interfacial compatibility with electrodes limit the conventional application of Li 7 P 3 S 11 . Herein, we present a substitution strategy to produce a O-incorporated 70Li 2 S·(30-x)P 2 S 5 ·xP 2 O 5 (mol%) sulfide electrolyte to address above issues. The elaborately designed electrolyte is prepared via wet vibration ball milling technique with P 2 O 5 substitution content of 1, 3 and 5. As a result, the 70Li 2 S·27P 2 S 5 ·3P 2 O 5 electrolyte displays the highest ionic conductivity of 2.61× 10 −3 S cm −1 which outperforms than that of pristine Li 7 P 3 S 11 (ionic conductivity of 1.35 × 10 −3 S cm −1 ) and the assembled LiCoO 2 @LiNbO 3 /70Li 2 S·27P 2 S 5 ·3P 2 O 5 /Li-In ASSLB exhibits the superior capacity retention of 93.2% after 100 cycles at 0.5C. The reason for the developed electrochemical performance lies in the substitution of the non-bridging sulfur atom with bridging oxygen atom, from which the interaction between electrolyte and lithium ions is weakened, thereby the rapid transfer of lithium ions is facilitated. Furthermore, Raman and XRD results indicate that the adverse interfacial reactions are suppressed through P 2 O 5 substitution. This work suggests that P 2 O 5 substitution is an effective strategy for sulfide electrolyte toward high energy all-solid-state lithium batteries.
研究领域:
材料科学
·
电化学
·
能源存储
·
固态离子学
·
电池技术
✓ 已验证
DOI
高影响因子
BIOMASS & BIOENERGY
·
2022
·
IF 5.774
Jie Zhang,Danyang Cao,Shanshan Wang,Xin Feng,Jiahua Zhu,Xiaohua Lu,Liwen Mu
In this study, heteroelement-rich groups (N and B elements, tris (2-hydrazinylethyl) borate) were successfully synthesised on lignin by microwave amination. The reaction between lignin and heteroelement-rich groups was confirmed using several characterization techniques, including fourier transform infrared (FT-IR) spectroscopy, thermogravimetric (TG) analysis, and X-ray photoelectron spectroscopy (XPS). A lignin model compound (2-phenoxyacetophenone (L-M)) was used to study the bond-breaking mechanism of lignin depolymerization , and the amine group, which acted as a nucleophile , attacked the C–C bond to form an amide bond with the lignin. As an effective additive, modified lignin can increase the viscosity of poly (ethylene glycol) 200 (PEG200), reducing the wear volume and friction coefficient in the friction test. Theoretical calculations showed that the polarity of the modified lignin increased, which allowed the modified lignin to form a strong physical adsorption on the metal surface. In addition, the reciprocal hydrogen bonding between the modified lignin and PEG200 contributes synergistically to the enhanced lubrication film strength , and thus, the better tribological properties of these new lubricants.
研究领域:
高分子化学
·
材料科学
·
绿色化学
·
表面工程
·
能源材料
·
可持续技术
✓ 已验证
DOI
高影响因子
ELECTROCHIMICA ACTA
·
2017
·
IF 4.798
Shaopei Jia,Yanhui Wang,Pengfei Tian,Shuyu Zhou,Haixia Cai,Hongwei Gao,Jianbing Zang
Nitrogen-doped mesoporous carbon (NMC) was synthesized via pyrolysis of cobalt-containing casein obtained by extraction from pure milk with the auxiliary of cobalt ions. The cobalt element in casein promoted specific surface area and N element doping amount of casein-derived porous carbon. The N-doped porous carbon obtained by carbonization at 800 °C (NPC-800) possessed a specific surface area of ∼886.7 m 2 g −1 , and the mesoporous size was centered at 2.7 and 7 nm. X-ray photoelectron spectroscopy analysis showed that the nitrogen content of NPC-800 was 3.29 at%. The NPC-800 was explored as a symmetric supercapacitor, which exhibited specific capacity of 380 F g −1 at a current density of 0.5 A g −1 , 218 F g −1 at a current density of 20 A g −1 , and high capacitance retention of 91.3% after charging/discharging 5,000 cycles.
研究领域:
材料科学
·
电化学
·
纳米材料
·
能源存储
·
功能材料
·
碳材料
✓ 已验证
DOI
高影响因子
JOURNAL OF MATERIALS SCIENCE
·
2017
·Vol. 52
·期 19
·11569-11579
·
IF 2.599
Lan Jin-Le,Ma Wenqiang,Deng Chengjie,Ren Guang-Kun,Lin Yuan-Hua,Yang Xiaoping
A series of K-doped Bi 1− x
K
x
CuSeO (0 ≤ x ≤ 0.10) compounds were prepared by combustion synthesis combined with spark plasma sintering method. Phase composition and microstructure analysis indicate almost single BiCuSeO phase in low doping level, while phase separation appears in heavy doping level. The thermoelectric properties of the Bi 1− x
K
x
CuSeO compounds have been measured in the temperature range of 323–823 K. The electrical conductivity is greatly enhanced by almost three times from 8.70 to 26.2 S/cm at 323 K by the substitution of Bi with K due to the large decrease of the activation energy. The overall thermal conductivity decreases significantly due to the strong point defect scattering by K doping and possibly enhanced interface scattering on the secondary phase. The maximum ZT reaches 0.6 at 823 K for the sample of x = 0.02, which is about 50% higher than that of the pristine sample. Our work offers a fast and more efficient approach for the fabrication of BiCuSeO-based materials.
研究领域:
材料科学
·
无机非金属材料
·
热电材料
·
固态化学
·
纳米复合材料
✓ 已验证
DOI
高影响因子
JOURNAL OF ALLOYS AND COMPOUNDS
·
2019
·
IF 4.175
Liang Zheng,Wenjie Zhang,Qi Wang,Hong Zhang,Zhou Yu,Cuihua Cheng,Yong Zhang,Ming Lei,Yong Zhao
MgB 2 bulks with NaCl doping amount ranging from 0–30 at% have been prepared by hot pressed sintering process . With the increase of NaCl doping amount, the c axis lattice parameter of MgB 2 monotonously increases, indicating the substitution of Mg atoms by larger Na atoms. Meanwhile, the intensity of diffraction peaks of both NaCl and impurity phase of MgO increases. More compact morphology was found in the NaCl doped MgB 2 samples. The critical transition temperature ( T c ) decreases from 38.2 K to 36.8 K with the increase of NaCl doping amount from 0 to 30 at%, and the corresponding transition width of T c (Δ T c ) increases from 0.5 K to 1.8 K. When the doping amount of NaCl is not exceeding 10 at%, the J c value is about 10 6 A/cm 2 at 4.2 K, 3 T, and 5 × 10 5 A/cm 2 at 10 K, 3T. J c performance of the 5 at% NaCl doped MgB 2 sample (NC05) reaches 6.8 × 10 5 A/cm 2 at 20 K, 2T, which improves approximately 20% compared to the pure one, attributing to the better grain connectivity of MgB 2 and enhancement of flux pinning force by NaCl doping.
研究领域:
凝聚态物理
·
材料科学
·
超导材料
·
无机固体化学
·
功能陶瓷
✓ 已验证
DOI
高影响因子