JOURNAL OF MATERIALS CHEMISTRY
·
2012
·Vol. 22
·期 15
·7291-7299
·
IF 5.968
Jungang Hou,Zheng Wang,Wenbin Kan,Shuqiang Jiao,Hongmin Zhu,R. V. Kumar
Large-scale hydrogen production through water splitting using photocatalysts with solar energy can potentially produce clean fuel from renewable resources. In this work, photocatalytic evolution of H2 with a high efficiency was achieved using graphene oxide (GO) nanosheets decorated with CdS sensitized TaON core–shell composites (GO–CdS@TaON). The CdS@TaON core–shell nanocomposites were prepared by an ion-exchange route with assistance from a hydrothermal process on GO as the support. The TaON core–shell composites containing 1 wt% CdS nanocrystals showed a high rate of H2-production at 306 μmol h−1 with an apparent quantum efficiency (QE) of 15% under 420 nm monochromatic light. The rate of hydrogen formation was 68 times faster in comparison with the rate observed on pure TaON. The rate was further increased to 633 μmol h−1 with a high quantum efficiency of 31% when the GO–CdS@TaON hybrid composite was coupled with 1 wt% of graphene oxide and 0.4 wt% of Pt (about 141 times higher than that of the pristine TaON). This high photocatalytic H2-production activity is ascribed firstly to the presence of CdS nanocrystals that alter the energy levels of the conduction and valence bands in the coupled semiconductor system; secondly to the involvement of graphene oxide that serves as an electron collector and transporter to efficiently lengthen the lifetime of the photogenerated charge carriers from CdS@TaON composites. This investigation can open up new possibilities for the development of highly efficient TaON-based photocatalysts that utilize visible light as an energy source.
研究领域:
材料化学
·
光催化
·
能源科学
·
纳米材料
·
半导体物理
·
可再生能源
✓ 已验证
DOI
高影响因子
JOURNAL OF MAGNETISM AND MAGNETIC MATERIALS
·
2024
·
IF 2.5
Jitao Zhang,Xingkui Mu,Qingfang Zhang,Natallia Poddubnaya,Dmitry Filippov,Jiagui Tao,Fang Wang,Liying Jiang,Lingzhi Cao
Development of high-quality ferrites behaved enhanced properties via inclusion of ions in 3d n and 4f n series are desirable for efficient power conversion solid-state devices. Nevertheless, inadequate microscopic behaviors with complex chemistry in materials enables researchers to design and produce the macroscopic target device that remained rudimentary and mindless. In this work, the microscopic properties in nickel-zinc spinel ferrite series of Ni 0.8 Zn 0.2 Sm x Fe 2- x O 4 ( x = 0, 0.02, 0.04, 0.06, 0.08) encompassing XRD, SEM, EDS, VSM, FTIR and ESR were systemically characterized, and the evolutionary mechanism of the corresponding structural, micro-structure, elemental composition and distribution, magnetic, cations exchange, and micro-magnetic behavior was profoundly revealed. Under microscopic examinations, the optimum composition at x = 0.02 with well-arranged spinel structure, dense texture with expected elemental composition, favorable soft magnetic properties and micro-magnetic behaviors is evident. Fortunately, this optimum is in coincidence with the achievable maximum magneto-mechanical coefficient, even the macroscopic electric properties with stronger magnetoelectric (ME) interactions and higher power conversion efficiency (PE) in tri-layered ME samples as expected. Experimental results show that the eventual PE reaches its maximum of 75.67 % under R opt = 33kΩ for samples at x = 0.02, and exhibit a 2.24 times higher PE than that of sample without samarium substitution. These findings provide a holographic perspective to connect the microscopic beneficial effects of materials to bulk device that are promising for efficient power conversion solid-state electronics.
研究领域:
材料科学
·
磁性材料
·
固态电子学
·
功能陶瓷
·
能源转换技术
✓ 已验证
DOI
高影响因子
PHYSICA STATUS SOLIDI A-APPLICATIONS AND MATERIALS SCIENCE
·
2016
·Vol. 213
·期 5
·1324-1328
·
IF 1.648
Yongzheng Zhang,Yuxiu Sun,Hao Wang,Hui Yan
Cu 2 ZnSnSe 4 (CZTSe) solar cell with a facile superstrate structure of carbon/CZTSe/CdS/ITO was fabricated entirely by non-vacuum processes. The influence of selenization temperature on the composition of CZTSe layer was briefly investigated. Compared with current superstrate-type CZTS(e) solar cells, the present CZTSe superstrate solar cell exhibited a higher power conversion efficiency of 2.44%.
研究领域:
材料科学
·
光伏技术
·
无机半导体
·
能源材料
·
薄膜器件
✓ 已验证
DOI
高影响因子
ELECTROCHIMICA ACTA
·
2013
·
IF 3.777
Lili Chai,Qunting Qu,Longfei Zhang,Ming Shen,Li Zhang,Honghe Zheng
Chitosan was applied as the electrode binder material for a spherical graphite anode in lithium-ion batteries. Compared to using poly (vinylidene fluoride) (PVDF) binder, the graphite anode using chitosan exhibited enhanced electrochemical performances in terms of the first Columbic efficiency, rate capability and cycling behavior. With similar specific capacity, the first Columbic efficiency of the chitosan-based anode is 95.4% compared to 89.3% of the PVDF-based anode. After 200 charge–discharge cycles at 0.5 C , the capacity retention of the chitosan-based electrode showed to be significantly higher than that of the PVDF-based electrode. Electrochemical impedance spectroscopy (EIS) and scanning electron microscopy (SEM) measurements were carried out to investigate the formation and evolution of the solid electrolyte interphase (SEI) formed on the graphite electrodes. The results show that a thin, homogenous and stable SEI layer is formed on the graphite electrode surface with chitosan binder compared with that using the conventional PVDF binder
研究领域:
电化学
·
材料科学
·
能源存储
·
电池技术
·
纳米材料
·
界面化学
✓ 已验证
DOI
高影响因子
Laser & Photonics Reviews
·
2023
·Vol. 17
·期 10
·2300158
·
IF 11
Gangyi Zhang,Deyin Wang,Jiejun Ren,Xiaopeng Zhou,Yuhua Wang
Luminescent metal halides have attracted increasing attention because of their tunable emission and superior photoelectric properties. However, it is still challenging to achieve near-infrared (NIR) emission from metal halides, which is important in applications such as food quality analysis and night vision. In this work, the broadband NIR emission is achieved by alloying Sn 2+ into zero-dimensional (0D) Cs 2 ZnBr 4 . The incorporating of Sn 2+ cations enables the originally weakly luminescent Cs 2 ZnBr 4 to exhibit an efficient broadband NIR emission. Upon photoexication, the optimized Sn 2+ alloyed Cs 2 ZnBr 4 (Cs 2 Zn 0.875 Sn 0.125 Br 4 ) exhibits a highly efficient broadband NIR emission peaked around 700 nm, with a large Stokes shift of 323 nm, a full width at maximum of 177 nm, and a high quantum efficiency of around 41%. Spectroscopic and theoretical calculations unveil that the efficient NIR emission originates from the self-trapping emission introduced by the Sn alloying. In addition to the high efficient broadband emission, the Sn 2+ alloyed Cs 2 ZnBr 4 also exhibits high thermal stability, retaining 78% of its initial intensity at 150 °C. The night vision application is demonstrated by using a light source fabricated by combining Sn 2+ alloyed Cs 2 ZnBr 4 phosphor with a 365 nm LED chip in the dark.
研究领域:
材料科学
·
光电子学
·
无机化学
·
固态物理
·
光学材料
✓ 已验证
DOI
高影响因子
FLAVOUR AND FRAGRANCE JOURNAL
·
2012
·Vol. 27
·期 5
·378-385
·
IF 1.424
Zhangfu Zeng,Yanxiong Fang,Hongbing Ji
The reason for low encapsulation efficiency of vanillin compared to p -hydroxybenzaldehyde within β -cyclodextrin was investigated. Fourier transform infrared spectra proved intermolecular interaction between guest and β -cyclodextrin. UV–visible studies indicated that vanillin and p -hydroxybenzaldehyde form 1:1 inclusion complexes with β -cyclodextrin. Nuclear magnetic resonance and quantum computational methods gave the most favourable orientation in which the guest molecule (vanillin or p -hydroxybenzaldehyde) is totally sequestered in the hydrophobic cavity of the cyclodextrin with the phenolic end located near the primary hydroxyls of the β -cyclodextrin and the aldehyde group near the secondary hydroxyls with hydrogen bonding formation. Encapsulation efficiency of the β -cyclodextrin inclusion with vanillin is about 29% lower than that with p -hydroxybenzaldehyde. This result could be attributable to the effect that the side chain methoxy group weakened the guest/host non-covalent intermolecular interaction, specifically, hydrogen bond interaction. Copyright © 2012 John Wiley & Sons, Ltd.
研究领域:
药物化学
·
超分子化学
·
分析化学
·
药剂学
·
分子识别
·
计算化学
✓ 已验证
DOI
高影响因子
RSC Advances
·
2016
·Vol. 6
·期 16
·13384-13391
·
IF 3.289
Bin Lu,Renzong Hu,Jiangwen Liu,Jun Liu,Hui Wang,Min Zhu
To improve the coulombic efficiency (CE) and cycle life of SnO2 anode in lithium ion batteries, SnO2–Cu–graphite composites with dual scale embedding structure are synthesized by ball milling. The SnO2–Cu composite, in which SnO2 nanoparticles with grain size less than 10 nm are uniformly dispersed in inactive nanocrystalline Cu matrix, is firstly obtained by milling the mixture of SnO2 and Cu nanopowders (molar ratio 1 : 2), and then further milling with graphite (C) to obtain SnO2–Cu–C composite with microsized graphite sheets as matrix of SnO2–Cu composite. The 50 h-milled SnO2–Cu composite exhibits higher initial CE (76.0 ± 1.5%) and subsequent CE than 50 h-milled SnO2. Furthermore, the SnO2–Cu–C composite anode is capable of retaining a maximum charge capacity of 450.8 mA h g−1 at 100 mA g−1 after 80 cycles with a capacity retention ratio of 74.4%, displaying superior cyclic stability to as-milled SnO2, SnO2–Cu and SnO2–C composites. The improved CE and cycleability are attributed to the unique dual scale embedding structure that offers good conductivity of electron and lithium ion as well as the nanostructure stability of active materials. This unique composite structure might be extended to other high-capacity anode materials, to achieve high performance lithium ion batteries.
研究领域:
材料科学
·
电化学
·
纳米材料
·
能源存储
·
锂离子电池
✓ 已验证
DOI
高影响因子
INTERNATIONAL JOURNAL OF HYDROGEN ENERGY
·
2011
·Vol. 36
·期 13
·7374-7380
·
IF 4.057
Wei Wang,Qiang Zhao,Jinxiang Dong,Jinping Li
A novel silver oxides oxygen evolving catalyst (Ag-OEC) for hydrogen production by water splitting was formed in situ on an indium tin oxide anode, in a near-neutral potassium tetraborate (K 2 B 4 O 7 ) electrolyte. The catalyst exhibited high activity and low overpotential for O 2 evolution under mild conditions. The main functional composition of the catalyst was a redox couple of Ag 2 O/AgO. Catalytic activity during oxygen evolution was evaluated by cyclic voltammetry and Tafel plot. The effects of the concentration, temperature, and pH of K 2 B 4 O 7 solution on the catalyst, and the Faradaic efficiency of the oxygen evolving reaction were examined. The results show that the Ag-OEC exhibits excellent oxygen evolution properties, with an oxygen evolving overpotential of 318 mV at a current density of 1 mA/cm 2 .
研究领域:
电催化
·
能源化学
·
材料科学
·
物理化学
·
可持续能源
✓ 已验证
DOI
高影响因子
Laser & Photonics Reviews
·
2023
·Vol. 18
·期 1
·2300732
·
IF 11
Zhuowei Li,Ge Zhu,Shanshan Li,Wen Xu,Qingfeng Bian,Yan Cong,Ming He,Xixian Luo,Shuangyu Xin,Bin Dong
The burgeoning phosphor-converted near-infrared light-emitting diodes (pc-NIR LEDs) have important applications in special illumination and spectroscopy analysis. However, the development of efficient NIR-emitting phosphors with high performance is still a challenge. In this work, a chemical unit co-substitution strategy is proposed to realize the excitation transition regulation and successfully achieve high-performance NIR luminescence in Ca 3- y Na y Mg 1- y Sb 2- x Al 2+ y O 12 : x Cr 3+ (0 ≤ x ≤ 0.05, 0 ≤ y ≤ 1) garnet-type solid solution phosphors. Through the excitation transition modulation from the 4 A 2 ground state to the 4 T 1 ( 4 P) and 4 T 1 ( 4 F) excitation state, the excitation intensity at the blue light region is largely enhanced by 25.6 times. Moreover, the NIR-emitting efficiency and thermal stability are improved, with the optimal luminescence internal quantum efficiency of 90.6% and thermal stability of 97%@423 K, without any flux-assisted sintering or reduction atmosphere protection. The structure regulation induced small Stokes shift, weak electron-phonon coupling effect, and decreased non-radiative transition are responsible for the excellent NIR-emitting performance. Finally, the NIR pc-LED is fabricated with photoelectric efficiencies of 18.7%@100 mA and NIR output powers of 63 mW@100 mA, presenting potential applications in nondestructive internal defect detection, veins imaging, and night vision surveillance.
研究领域:
材料科学
·
光学工程
·
固体化学
·
发光材料
·
半导体器件
✓ 已验证
DOI
高影响因子
CERAMICS INTERNATIONAL
·
2014
·Vol. 40
·期 9
·15199-15206
·
IF 2.086
Yanbo Yang,Xiao Peng,Si Chen,Liping Lin,Bao Zhang,Yaqing Feng
The novel hierarchical compact layer involving ZnO and TiO 2 blocking films is used to improve the overall performance of dye-sensitized solar cells. The ZnO compact films are fabricated as a bottom layer to block the electrons injection to the conductive glass and improve the open-circuit voltage. The TiO 2 compact layer is employed to suppress back electron transfer and avoid ZnO contacting the acid dyes directly. The short-circuit current density of the DSSC containing the hierarchical compact layer is improved by 30% compared to that of one with only ZnO as the compact layer. The open-circuit voltage is increased by 4% after introducing the additional TiO 2 blocking layer between the ZnO compact layer and mesoporous TiO 2 layer. Overall, the short-circuit current density, open-circuit voltage and solar energy conversion efficiency are enhanced by 15.3%, 3.7% and 29.6%, respectively, relative to the traditional DSSC without any blocking layers. The ZnO–TiO 2 blocking layer has been characterized by electrochemical impedance spectroscopy , open-circuit voltage decay and dark current measurement to reveal the mechanism of short-circuit current density and open-circuit voltage improvement.
研究领域:
材料科学
·
纳米科技
·
能源化学
·
光伏技术
·
表面科学
✓ 已验证
DOI
高影响因子
CHINESE JOURNAL OF CATALYSIS
·
2018
·Vol. 38
·期 12
·2132-2140
·
IF 3.525
Lingfeng Li,Xiaolong Zhao,Donglai Pan,Guisheng Li
Photoactive WO 3 is attractive as a photocatalyst for green energy evolution through water splitting. In the present work, an electrochemical anodic oxidation method was used to fabricate a photo-responsive nanotube array-like WO 3 /W (NA-WO 3 /W) photoanode from W foil as a precursor. Compared with a reference commercial WO 3 /W electrode, the NA-WO 3 /W photoanode exhibited enhanced and stable photoelectrocatalytic (PEC) activity for visible-light-driven water splitting with a typical H 2 /O 2 stoichiometric ratio of 2:1 and quantum efficiency of approximately 5.23% under visible-light irradiation from a light-emitting diode ( λ = 420 nm, 15 mW/cm 2 ). The greatly enhanced PEC performance of the NA-WO 3 /Wphotoanode was attributed to its fast electron–hole separation rate, which resulted from the one-dimensional nanotube array-like structure, high crystallinity of monoclinic WO 3 , and strong interaction between WO 3 and W foil. This work paves the way to a facile route to prepare highly active photoelectrodes for solar light transfer to chemical energy .
研究领域:
材料科学
·
物理化学
·
能源化学
·
纳米科技
·
光催化
·
电化学
·
可再生能源
✓ 已验证
DOI
高影响因子
IONICS
·
2024
·Vol. 30
·期 6
·3111-3119
·
IF 2.4
Teng Zeyu,Wang Zhilong,Li Zhongcheng,Chen Kanghua
Silicon is a strong competitor for the anode of the next generation of lithium-ion batteries, and ball-milled silicon has broad prospects as a low-cost method for preparing nano silicon. In order to match ball-milled silicon, it is imperative to develop better bonding agents with lower costs. Through adding amino silane coupling agent, the performance of ball-milling silicon anode is enhanced. This study explored the network structure formed by amino silane coupling agent with different chain lengths and polyacrylic acids. Herein, the crosslinked network prepared with 3-[2-(2-aminoethyl amino) ethyl amino] propyl-trimethoxysilane as coupling agent had the best performance, and the initial discharge capacity of the silicon anode prepared by this binder reached 3297.4 mAh·g −1 at a constant current density of 0.5A·g −1 , the initial Coulomb efficiency reached 92.25%. After 100 cycles, the discharge capacity of anode was still maintained at 2229.5 mAh·g −1 with excellent charge/discharge performance.
研究领域:
材料科学
·
电化学
·
纳米材料
·
能源存储
·
高分子化学
·
表面改性
✓ 已验证
DOI
高影响因子