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1.
《International Journal of Hydrogen Energy》2022,47(64):27516-27526
It is extremely desirable to develop high hydrogen evolution activity and stable visible-light-driven photocatalysts. The sluggish oxidation process and holes accumulation are the main obstacles to high catalysis activity and photo-stability. An efficient γ-NiOOH/ZnCdS photocatalyst was prepared by in-situ hydrothermal method. The γ-NiOOH nanosheets distribute on ZnCdS nanospheres surface and accelerate holes transfer. The hydrogen evolution rate is up to 48.60 mmol g?1 h?1 under visible-light illumination (λ = 400–780 nm), about 10.8 times of pure ZnCdS (4.50 mmol g?1 h?1) and 1.8 times of general β-NiOOH modified ZnCdS (27.40 mmol g?1 h?1). And apparent quantum yield of γ-NiOOH/ZCS-100 is up to 18.23% (400 nm). The carrier lifetime extends from 5.50 ns (ZnCdS) to 6.10 ns (γ-NiOOH/ZCS), examined by steady photoluminescence and time-resolved photoluminescence. Moreover, the γ-NiOOH/ZCS photocatalyst has exhibited excellent photo-stability even after one-year of storage. The γ-NiOOH nanosheets can be an excellent co-catalyst on accelerating both holes transfer and oxidation process for high photo-stability and photo-activity. 相似文献
2.
《International Journal of Hydrogen Energy》2022,47(26):12903-12913
Oxygen evolution reaction (OER) plays a decisive role in electrolytic water splitting. However, it is still challengeable to develop low-cost and efficient OER electrocatalysts. Herein, we present a combination strategy via heteroatom doping, hetero-interface engineering and introducing conductive skeleton to synthesize a hybrid OER catalyst of CNT-interconnected iron-doped NiP2/Ni2P (Fe-(NiP2/Ni2P)@CNT) heterostructural nanoflowers by a simple hydrothermal reaction and subsequent phosphorization process. The optimized Fe-(NiP2/Ni2P)@CNT catalyst delivers an ultralow Tafel slope of 46.1 mV dec?1 and overpotential of 254 mV to obtain 10 mA cm?2, which are even better than those of commercial OER catalyst RuO2. The excellent OER performance is mainly attributed to its unique nanoarchitecture and the synergistic effects: the nanoflowers constructed by a 2D-like nanosheets guarantee large specific area and abundant active sites; the highly conductive CNT skeleton and the electronic modulation by the heterostructural NiP2/Ni2P interface and the hetero-atom doping can improve the catalytic activity; porous nanostructure benefits electrolyte penetration and gas release; most importantly, the rough surface and rich defects caused by phosphorization process can further enhance the OER performance. This work provides a deep insight to boost catalytic performance by heteroatom doping and interface engineering for water splitting. 相似文献
3.
《International Journal of Hydrogen Energy》2022,47(93):39486-39498
Adjusting the band gap of organic-inorganic composites by chemical bonding can effectively construct Step-scheme (S-scheme) heterojunctions, featuring properties of fast photogenerated charge migration and excellent photocatalytic performance. In this work, a novel perylene-3, 4, 9, 10-tetracarboxylicdiimide (PDI)-titanium dioxide (TiO2) heterojunction is elaborately synthesized through simple solvent compounding method. The monodispersed spherical TiO2 nanoparticles was prepared with the capping agents of oleylamine and oleic acid, and suffered by a ligand exchange process with nitrosonium tetrafluoroborate (NOBF4) to remove oleylamine and oleic acid. The NOBF4 ligands were further replaced by PDI super molecular nanosheets to obtain two dimensional (2D)-zero dimensional (0D) PDI-TiO2 composites. TiO2 nanoparticles are evenly anchored on the surface of PDI nanosheets with intimate contact. The PDI-TiO2 composites has emerged considerably superior activity in hydrogen evolution. The highest hydrogen evolution rate for PDI-TiO2composites with the PDI weight percentage of 2.4% was 9766 μmol h?1 g?1 under solar light irradiation, which is 2.56 times of TiO2-NOBF4 catalyst. Moreover, PDI-TiO2 composites possess stoichiometric overall water splitting performance with H2 and O2 release rates of 238.20 and 114.18 μmol h?1 g?1. The superior photocatalytic performance of PDI-TiO2 composites can be attributed to the dramatic increase in visible and NIR light absorption caused by π-π stacking structure of PDI, the prevented charge recombination by the S-scheme heterojunction, and the enhanced oxygen evolution by the stronger oxidation capability of PDI. PDI supramolecular nanosheets may work as a novel functional support for many types of semiconductor nanomaterials as graphene, which will display a wide range of application prospects in the energy and environmental fields. 相似文献
4.
5.
Guandong Liang Guoxun Sun Jianqiang Bi Weili Wang Xiangning Yang Yonghan Li 《Ceramics International》2021,47(2):2058-2067
Uniformly dispersed boron nitride nanosheets (BNNSs) reinforced silicon nitride (Si3N4) composites were prepared by surface modification assisted flocculation combined with SPS sintering. In order to improve the dispersibility of the BNNSs in the composites, the liquid phase stripped BNNSs are surface functionalized by a two-step covalently modification. The amino-modified BNNSs (NH2-BNNSs) and Si3N4 powders have opposite surface potential, mixed evenly by electrostatic interaction during flocculation. The results showed that mechanical properties of Si3N4 composites were obviously enhanced by adding NH2-BNNSs. The fracture toughness and bending strength of Si3N4 composites added 0.75 wt% NH2-BNNSs were increased by 34% and 28%, respectively, compared with monolithic Si3N4. Toughening mechanisms are synergistic action of the torn, pull-out or bridging of BNNSs and crack deflection mechanisms with microstructural analyzes. The dielectric properties of the Si3N4 ceramics are also improved after the addition of NH2-BNNSs. 相似文献
6.
Keun-Young Shin Sung Gook Jin Bong June Sung 《Nanoscale and Microscale Thermophysical Engineering》2018,22(1):39-51
Preparation of three-dimensional (3D) networks has received significant attention as an effective approach for applications involving transport phenomena, such as thermal management materials, and several nanomaterials have been examined as potential building blocks of 3D networks for the improvement of heat conduction in polymer nanocomposites. For that purpose, nanocarbons such as graphene and graphite nanoplatelets have been spotlighted as suitable filler materials because of their excellent thermal conductivities (ca. 102–103 W·(m·K)?1 along their lateral axes) and morphological merits. However, the implications of morphological features such as the lateral length and thickness of graphene or graphene-like materials have not yet been identified. In this study, a controlled dissociation of bulk graphite to graphite nanosheets (GNSs) using a low-cost, ecofriendly bead mill process was extensively examined and, when configured in a 3D framework architecture formation, the size-controlled GNSs demonstrated that the thermal conductivities of a 3D interconnected framework of GNSs and the corresponding polymer nanocomposite were intimately correlated with the size of the GNSs, thus demonstrating the successful preparation of an efficient thermal management material without highly sophisticated efforts. The capability of controlling the lateral size and thickness of the GNSs as well as the use of a 3D interconnected framework architecture should greatly assist the commercialization of high-quality graphene-based thermal management materials in a scalable production process. 相似文献
7.
《International Journal of Hydrogen Energy》2021,46(80):39645-39657
This article reported a series of g–C3N4–CNS (g-C3N4 and carbon nanosheets) composite carriers formed by the hydrothermal method, and then the ethylene glycol reduction method was used to anchor Pt nanoparticles on the g–C3N4–CNS carrier to form the Pt/g–C3N4–CNS catalysts. The electrochemical test for the electrocatalytic oxidation of methanol (MOR) shown that the Pt/20%g–C3N4–CNS catalyst has the best catalytic performance and stability. These Pt/g–C3N4–CNS catalysts were analyzed by TEM, XRD, XPS, and BET characterization. It is discovered that the amount of g-C3N4 greatly influenced the structure and chemical properties of Pt/CNS precursor. As the content of g-C3N4 increases, the content of pyridine nitrogen and pyrrole nitrogen also increases, and N species can enhance the interaction between Pt nanoparticles and CNS, promote Pt dispersion, and increase the specific surface area of the catalyst. Similarly, an excessive addition of g-C3N4 will cause a sharp decline in the conductivity of the catalyst, and then led to the decline of MOR activity. 相似文献
8.
Wenqian Han Zihan Liu Yanbo Pan Guannan Guo Jinxiang Zou Yan Xia Zhenmeng Peng Wei Li Angang Dong 《Advanced materials (Deerfield Beach, Fla.)》2020,32(28):2002584
Fine-tuning strain and vacancies in 2H-phase transition-metal dichalcogenides, although extremely challenging, is crucial for activating the inert basal plane for boosting the hydrogen evolution reaction (HER). Here, atomically curved 2H-WS2 nanosheets with precisely tunable strain and sulfur vacancies (S-vacancies) along with rich edge sites are synthesized via a one-step approach by harnessing geometric constraints. The approach is based on the confined epitaxy growth of WS2 in ordered mesoporous graphene derived from nanocrystal superlattices. The spherical curvature imposed by the graphitic mesopores enables the generation of uniform strain and S-vacancies in the as-grown WS2 nanosheets, and simultaneous manipulation of these two key parameters can be realized by simply adjusting the pore size. In addition, the formation of unique mesoporous WS2@graphene van der Waals heterostructures ensures the ready access of active sites. Fine-tuning the WS2 layer number, strain, and S-vacancies enables arguably the best-performing HER 2H-WS2 electrocatalysts ever reported. Density functional theory calculations indicate that compared with strain, S-vacancies play a more critical role in enhancing the HER activity. 相似文献
9.
Ruizhi Hu Chen Dai Chunmei Wang Jie Lin Hui Hu Zhifang Li Han Lin Li Ding Yu Chen Bo Zhang 《Advanced functional materials》2021,31(25):2101660
As an anticancer drugs, arsenic trioxide (ATO) has been certified to efficiently treat refractory acute promyelocytic leukemia (APL). Unfortunately it suffers from limited therapeutic potency for solid tumors due to its in vivo restricted administration dose and rapid renal clearance. Herein, distinct 2D arsenic-phosphorus (AsP) nanosheets are engineered by adopting an alloy strategy followed by exfoliation, which can confine toxic arsenic into AsP crystals, thus significantly improving the biosafety and biocompatibility of arsenic-based chemotherapeutic drugs. Of particular note, the high light absorption and strong photothermal-conversion efficiency (37.6%) in the second near infrared biowindow (NIR-II) of AsP nanosheets not only endow them with desirable contrast-enhanced photoacoustic imaging properties, but also achieve efficient local tumor hyperthermia, which further synergistically triggers the in-situ transformation from low toxic/nontoxic AsP crystals into highly toxic arsenic species, exerting a strong arsenic-mediated antineoplastic effect. Both in vitro and in vivo data verify the synergy between photonic therapy in NIR-II and enhanced chemotherapy as enabled by AsP nanosheets, paving the way for efficient nanomedicine-enabled arsenic-based chemotherapeutic tumor treatment. 相似文献
10.
《International Journal of Hydrogen Energy》2020,45(35):17782-17794
Phosphotungstic acid (HPW) has a good potential as nanofillers in nanocomposite proton exchange membrane with the prerequisite of solving the leakage issue. It is immobilized onto mesoporous graphitic carbon nitride (mg-C3N4) nanosheets surface, and then incorporated into sulfonated poly (aryl ether sulfone) (SPAES) membrane. Structures of the HPW/mg-C3N4 nanocomposites and corresponding SPAES/HPW/mg-C3N4 membranes are characterized by spectroscopic techniques. Fundamental properties and fuel cell performance of the fabricated nanocomposite membranes, and the leakage of HPW are investigated. Along with the highly suppressed HPW leakage, the SPAES/HPW/mg-C3N4 membranes show improved dimensional stability, water affinity and physicochemical stability, as well as better proton conductivity and fuel cell performance. At 80 °C and 60–100% RH, the SPAES/HPW/mg–C3N4–1.5 membrane exhibits 2–3.6 times peak power densities (354.9–584.2 mW/cm2) of the pristine SPAES membrane, and proton conductivity of 203 mS/cm, dimensional change less than 7.5% and weight loss of 1.4% in Fenton oxidation test at 80 °C. 相似文献