分类: 物理学 >> 交叉学科物理及相关领域的科学与技术 提交时间: 2018-03-30
摘要: Co-Ni layered double hydroxides (LDHs), as promising supercapacitor electrode materials with high specific capacity, have suffered poor rate property and cycle stability. By doping and topochemical oxidation of Ni ions is considered as efficivent rout to overcome these drawbacks. In this work, Ni3+ doped cobalt-nickel layered double hydroxides (Co-Ni-LDHs) were synthesized by pluse laser ablation of Ni taget in CoCl2 aqeous solution. The existence of Ni3+ ions doped in Co-Ni-LDHs decline the conductive resistance, and increase the mobility of surface charge and transfer rate of electrolyte. As a results, the Ni3+ doped Co-Ni-LDHs display a maximum specific capacitance of 2275 F/g and 1450 F/g at the current density of 1 A/g and 20 A/g, respectivly, indicating a high rate specific capacitance. Moreover, the capacitance retention is to be 80% after 1800 cycles at the current density of 6 A/g, manifesting good cycling stability of Ni3+ doped Co-Ni-LDHs.
分类: 材料科学 >> 材料化学 提交时间: 2017-11-01
摘要: Doping additional ions into semiconductor is a potential strategy to modify the electronic structure of semiconductor materials. By using a highly reactive colloidal Cu clusters as doping precursor, we present here the successful doping of Cu ions into TiO2 nanocrystalline that simultaneously transformed from amorphous anodic TiO2 nanotubes during a dissolution and recrystallization process. The Cu-doped TiO2 nanoparticles (Cu-TNPs) film was characterized by X-ray diffraction, scanning and transmission electron microscopy and Raman spectroscopy. The Cu-TNPs show a rugby-like shape with exposed active {101}, {001} facets and the long-axis parallel to [001] lattice direction. The substitutional Cu2+ ions dopants in TiO2 nanocrystals caused the swelling of the crystalline unit cell. Such efficient doping design facilitate the improvement of nanostructured TiO2 as a potential biosensor for glucose molecules.
分类: 材料科学 >> 材料化学 提交时间: 2017-11-01
摘要: Morphology control and impurity doping are two widely applied strategies to improve the electrochemical performance of nanomaterials. Herein, we report an environmentally friendly approach to obtain Co-doped Ni(OH)2 nanosheet networks using a laser-induced cobalt colloid as a doping precursor followed by an aging treatment in a hybrid medium of nickel ions. The shape and specific surface area of the doped Ni(OH)2 can be successfully adjusted by changing the concentration of sodium thiosulfate. Furthermore, a Co-doped Ni(OH)2 nanosheet network was further converted into Co-doped NiO with its pristine morphology retained via facile thermal decomposition in air. The structure and electrochemical performance of the as-prepared samples are investigated with scanning and transmission electron microscopy, energy dispersive x-ray analysis, x-ray diffraction, Fourier transform infrared spectroscopy, the nitrogen adsorption-desorption isotherm technique, and electrochemical measurements. The Co-doped Ni(OH)2 electrode shows an ultrahigh specific capacitance of 1421 F/g at a current density of 6 A/g, and a good retention level of 76% after 1000 cycles, in sharp contrast with only a 47% retention level of the pure Ni(OH)2 electrode at the same current density. In addition, the Co-doped NiO electrode exhibits a capacitance of 720 F/g at 6 A/g and 92% retention after 1000 cycles, which is also superior to those values for relevant pure NiO electrodes. The Co2+ partially substitutes for Ni2+ in the metal hydroxide and oxide, resulting in an increase of free holes in the valence band, and, therefore, enhancement of the p-type conductivity of Ni(OH)2 and NiO. Moreover, such novel mesoporous nanosheet network structures are also able to enlarge the electrode-electrolyte contact area and shorten the path length for ion transport. The synergetic effect of these two results is responsible for the observed ultrahigh pseudocapacitor performance.
分类: 材料科学 >> 材料化学 提交时间: 2017-10-31
摘要: Incorporating noble metal nanoparticles on the surface or inner side of semiconductors to form a hybrid nanostructure is an effective route to improve the gas sensing performance of these semiconductors. In this study, we present novel Au-decorated ZnO nanospheres (Au-ZnO NSs) obtained by laser irradiation of liquids. Structural characterization indicated that the Au-ZnO NSs consisted of single crystalline ZnO NSs with few Au nanoparticles decorated on their surfaces and abundant encapsulated Au nanoparticles with relatively small sizes. Laser irradiation-induced heating–melting–evaporating processes are responsible for the formation of unique Au-ZnO NSs. Gas sensing properties of the Au-ZnO NSs, as gas sensing materials, were investigated and compared with those of pure ZnO NSs. The former showed lower working temperature, higher sensitivity, better selectivity, and good reproducibility. The response values of Au-ZnO NSs and pure ZnO NSs sensors to ethanol of 100 ppm were 252 and 75 at working temperature of 320 °C and 360 °C, respectively. The significant enhancements in gas sensing performance should be attributed to the electronic sensitization induced by the depleted layers between encapsulated Au nanoparticles and ZnO and chemical sensitization originating from the catalytic effects of Au nanoparticles decorated on the surfaces that dissociated molecular oxygen.
分类: 物理学 >> 交叉学科物理及相关领域的科学与技术 提交时间: 2018-03-30
摘要: Agglomeration-triggered deactivation of supported platinum electrocatalysts markedly hinders their application in methanol oxidation reaction (MOR). In this study, graphene-supported nickel–iron layered double hydroxide (NiFe–LDH/rGO), in which Fe3+ was introduced to replace Ni2+ partially in the Ni(OH)2 lattice to provide stronger metal–support bonding sites, was utilized to immobilize Pt nanoparticles (NPs). Given the optimized metal–support interfacial contact (Fe3+–O(H)–Pt) between Pt NPs and NiFe–LDH/rGO nanosheets for Pt/NiFe–LDH/rGO electrocatalysts, the Pt/NiFe–LDH/rGO electrocatalysts displayed dramatically enhanced durability than that of Pt/Ni(OH)2/rGO counterpart as well as commercial Pt/C, and 86.5% of its initial catalytic activity can be maintained even after 1200 cycles of cyclic voltammetry (CV) tests during MOR. First-principle calculations toward the resultant M–O(H)–Pt (M = Fe3+, Ni2+) interfacial structure further corroborates that the NiFe–LDH nanosheets can provide stronger bonding sites (via the Fe3+–O(H)–Pt bonds) to immobilize Pt NPs than those of Ni(OH)2 nanosheets (via the Ni2+–O(H)–Pt bonds).
分类: 材料科学 >> 材料化学 提交时间: 2017-11-01
摘要: We report a simple and environment-friendly route to prepare platinum/reduced graphene oxide (Pt/rGO) nanocomposites (NCs) with highly reactive MnOx colloids as reducing agents and sacrificial templates. The colloids are obtained by laser ablation of a metallic Mn target in graphene oxide (GO)-containing solution. Structural and morphological investigations of the as-prepared NCs revealed that ultrafine Pt nanoparticles (NPs) with an average size of 1.8 (± 0.6) nm are uniformly dispersed on the surfaces of rGO nanosheets. Compared with commercial Pt/C catalysts, Pt/rGO NCs with highly electrochemically active surface areas show remarkably improved catalytic activity and durability toward methanol oxidation. All of these superior characteristics can be attributed to the small particle size and uniform distribution of the Pt NPs, as well as the excellent electrical conductivity and stability of the rGO catalyst support. These findings suggest that Pt/rGO electrocatalysts are promising candidate materials for practical use in fuel cells.