Nanogap Engineered Plasmon‐Enhancement in Photocatalytic Solar Hydrogen Conversion

Graphitic carbon nitride modified with plasmonic Ag@SiO₂ core–shell nanoparticles (g‐C₃N₄/Ag@SiO₂) are proposed for enhanced photocatalytic solar hydrogen evolution under visible light. Nanosized gaps between the plasmonic Ag nanoparticles (NPs) and g‐C₃N₄ are created and precisely modulated to be 8, 12, 17, and 21 nm by coating SiO₂ shells on the Ag NPs. The optimized photocatalytic hydrogen production activity for g‐C₃N₄/Ag@SiO₂ is achieved with a nanogap of 12 nm (11.4 μmol h⁻¹) to be more than twice as high as that of pure g‐C₃N₄ (5.6 μmol h⁻¹). The plasmon resonance energy transfer (PRET) effect of Ag NPs is innovatively proved from a physical view on polymer semiconductors for photoredox catalysis. The PRET effect favors the charge carrier separation by inducing electron–hole pairs efficiently formed in the near‐surface region of g‐C₃N₄. Furthermore, via engineering the width of the nanogap, the PRET and energy‐loss Förster resonance energy transfer processes are perfectly balanced, resulting in considerable enhancement of photocatalytic hydrogen production activity over the g‐C₃N₄/Ag@SiO₂ plasmonic photocatalyst.     

Gold/WO<Subscript>3</Subscript> nanocomposite photoanodes for plasmonic solar water splitting

A facile electron-charging and reducing method was developed to prepare Au/WO₃ nanocomposites for plasmonic solar water splitting. The preparation method involved a charging step in which electrons were charged into WO₃ under negative bias, and a subsequent reducing step in which the stored electrons were used to reductively deposit Au on the surface of WO₃. The electron-charged WO₃ (c-WO₃) exhibited tunable reducibility that could be easily controlled by varying the charging parameters, and this property makes this method a universal strategy to prepare metal/WO₃ composites. The obtained Au/WO₃ nanocomposite showed greatly improved photoactivity toward the oxygen evolution reaction (OER) when compared with WO₃. After Au decoration, the OER photocurrent was improved by a percentage of over 80% at low potentials (<0.6 V vs. SCE), and by a percentage of over 30% at high potentials (>1.0 V vs. SCE). Oxygen evolution measurements were performed to quantitatively determine the Faraday efficiency for OER, which reflected the amount of photocurrent consumed by water splitting. The Faraday efficiency for OER was improved from 74% at the WO₃ photoanode to 94% at the Au-8/WO₃ composite photoanode, and this is the first direct evidence that the Au decoration significantly restrained the anodic side reactions and enhanced the photoelectrochemical (PEC) OER efficiency. The high photoactivity of the composite photoanode toward OER was ascribed to the plasmon resonance energy transfer (PRET) enhancement and the catalytic enhancement of Au nanoparticles (NPs).

Open image in new window

     

Interfacing BiVO4 with Reduced Graphene Oxide for Enhanced Photoactivity: A Tale of Facet Dependence of Electron Shuttling

Efficient interfacial charge transfer is essential in graphene‐based semiconductors to realize their superior photoactivity. However, little is known about the factors (for example, semiconductor morphology) governing the charge interaction. Here, it is demonstrated that the electron transfer efficacy in reduced graphene oxide‐bismuth oxide (RGO/BiVO₄) composite is improved as the relative exposure extent of {010}/{110} facets on BiVO₄ increases, indicated by the greater extent of photocurrent enhancement. The dependence of charge transfer ability on the exposure degree of {010} relative to {110} is revealed to arise due to the difference in electronic structures of the graphene/BiVO₄{010} and graphene/BiVO₄{110} interfaces, as evidenced by the density functional theory calculations. The former interface is found to be metallic with higher binding energy and smaller Schottky barrier than that of the latter semiconducting interface. The facet‐dependent charge interaction elucidated in this study provides new aspect for design of graphene‐based semiconductor photocatalyst useful in manifold applications.     

Multichannel Charge Transfer and Mechanistic Insight in Metal Decorated 2D–2D Bi2WO6–TiO2 Cascade with Enhanced Photocatalytic Performance

Promising semiconductor‐based photocatalysis toward achieving efficient solar‐to‐chemical energy conversion is an ideal strategy in response to the growing worldwide energy crisis, which however is often practically limited by the insufficient photoinduced charge‐carrier separation. Here, a rational cascade engineering of Au nanoparticles (NPs) decorated 2D/2D Bi₂WO₆–TiO₂ (B–T) binanosheets to foster the photocatalytic efficiency through the manipulated flow of multichannel‐enhanced charge‐carrier separation and transfer is reported. Mechanistic characterizations and control experiments, in combination with comparative studies over plasmonic Au/Ag NPs and nonplasmonic Pt NPs decorated 2D/2D B–T composites, together demonstrate the cooperative synergy effect of multiple charge‐carrier transfer channels in such binanosheets‐based ternary composites, including Z‐scheme charge transfer, “electron sink,” and surface plasmon resonance effect, which integratively leads to the boosted photocatalytic performance.     

Hierarchical Metal/Semiconductor Nanostructure for Efficient Water Splitting

A hierarchically patterned metal/semiconductor (gold nanoparticles/ZnO nanowires) nanostructure with maximized photon trapping effects is fabricated via interference lithography (IL) for plasmon enhanced photo‐electrochemical water splitting in the visible region of light. Compared with unpatterned (plain) gold nanoparticles‐coated ZnO NWs (Au NPs/ZnO NWs), the hierarchically patterned Au NPs/ZnO NWs hybrid structures demonstrate higher and wider absorption bands of light leading to increased surface enhanced Raman scattering due to the light trapping effects achieved by the combination of two different nanostructure dimensions; furthermore, pronounced plasmonic enhancement of water splitting is verified in the hierarchically patterned Au NPs/ZnO NWs structures in the visible region. The excellent performance of the hierarchically patterned Au NPs/ZnO NWs indicates that the combination of pre‐determined two different dimensions has great potential for application in solar energy conversion, light emitting diodes, as well as SERS substrates and photoelectrodes for water splitting.     

Yolk–Shell Nanostructure: An Ideal Architecture to Achieve Harmonious Integration of Magnetic–Plasmonic Hybrid Theranostic Platform

Magnetic–plasmonic hybrid nanoparticles (MPHNs) have attracted great interest in cancer theranostics. However, the relaxivity of the magnetic component is typically reduced by the plasmonic component in conventional core–shell structured MPHNs, due to the presence of a water‐impenetrable coating which severely restricts the proximity of protons to the magnetic portion. To circumvent this issue, yolk–shell structured MPHNs comprising a Fe₃O₄ core within a hollow cavity encircled by a porous Au outer shell are designed. As expected, the introduction of hollow cavity between the magnetic and plasmonic portions significantly prevents the decline in relaxivity of the Fe₃O₄ core caused by the Au layer. Moreover, in addition to conferring high near‐infrared absorption to plasmonic component, the hollow cavity and the pores in the outer shell can also provide a large storage space and release channels for anticancer drugs. Furthermore, the multicomponent nanoparticles (NPs) still have a compact size of less than 100 nm to ensure efficient tumor accumulation. Taken together, the yolk–shell Fe₃O₄@Au NPs can be regarded as an ideal magnetic–plasmonic theranostic platform for magnetic resonance/photoacoustic/positron emission tomography multimodal imaging and light‐activated chemothermal synergistic therapy.     

Plasmon Modes Induced by Anisotropic Gap Opening in Au@Cu2O Nanorods

Integration of semiconductors with noble metals to form heteronanostructures can give rise to many interesting plasmonic and electronic properties. A number of such heteronanostructures have been demonstrated comprising noble metals and n‐type semiconductors, such as TiO₂, ZnO, SnO₂, Fe₃O₄, and CuO. In contrast, reports on heteronanostructures made of noble metals and p‐type semiconductors are scarce. Cu₂O is an unintentional p‐type semiconductor with unique properties. Here, the uniform coating of Cu₂O on two types of Au nanorods and systematic studies of the plasmonic properties of the resultant core–shell heteronanostructures are reported. One type of Au nanorods is prepared by seed‐mediated growth, and the other is obtained by oxidation of the as‐prepared Au nanorods. The (Au nanorod)@Cu₂O nanostructures produced from the as‐prepared nanorods exhibit two transverse plasmon peaks, whereas those derived from the oxidized nanorods display only one transverse plasmon peak. Through electrodynamic simulations the additional transverse plasmon peak is found to originate from a discontinuous gap formed at the side of the as‐prepared nanorods. The existence of the gap is verified and its formation mechanism is unraveled with additional experiments. The results will be useful for designing metal–semiconductor heteronanostructures with desired plasmonic properties and therefore also for exploring plasmon‐enhanced applications in photocatalysis, solar‐energy harvesting, and biotechnologies.     

Plasmonic Enhancement in BiVO4 Photonic Crystals for Efficient Water Splitting

Photo‐electrochemical water splitting is a very promising and environmentally friendly route for the conversion of solar energy into hydrogen. However, the solar‐to‐H₂ conversion efficiency is still very low due to rapid bulk recombination of charge carriers. Here, a photonic nano‐architecture is developed to improve charge carrier generation and separation by manipulating and confining light absorption in a visible‐light‐active photoanode constructed from BiVO₄ photonic crystal and plasmonic nanostructures. Synergistic effects of photonic crystal stop bands and plasmonic absorption are observed to operate in this photonic nanostructure. Within the scaffold of an inverse opal photonic crystal, the surface plasmon resonance is significantly enhanced by the photonic Bragg resonance. Nanophotonic photoanodes show AM 1.5 photocurrent densities of 3.1 ± 0.1 mA cm^?2 at 1.23 V versus RHE, which is among the highest for oxide‐based photoanodes and over 4 times higher than the unstructured planar photoanode.     

A facile synthesis of monodisperse Au nanoparticles and their catalysis of CO oxidation

Monodisperse Au nanoparticles (NPs) have been synthesized at room temperature via a burst nucleation of Au upon injection of the reducing agent t-butylamine-borane complex into a 1, 2, 3, 4-tetrahydronaphthalene solution of HAuCl₄·3H₂O in the presence of oleylamine. The as-synthesized Au NPs show size-dependent surface plasmonic properties between 520 and 530 nm. They adopt an icosahedral shape and are polycrystalline with multiple-twinned structures. When deposited on a graphitized porous carbon support, the NPs are highly active for CO oxidation, showing 100% CO conversion at −45 °C. This article is published with open access at Springerlink.com     

Self‐Assembled Au/CdSe Nanocrystal Clusters for Plasmon‐Mediated Photocatalytic Hydrogen Evolution

Plasmon‐mediated photocatalytic systems generally suffer from poor efficiency due to weak absorption overlap and thus limited energy transfer between the plasmonic metal and the semiconductor. Herein, a near‐ideal plasmon‐mediated photocatalyst system is developed. Au/CdSe nanocrystal clusters (NCs) are successfully fabricated through a facile emulsion‐based self‐assembly approach, containing Au nanoparticles (NPs) of size 2.8, 4.6, 7.2, or 9.0 nm and CdSe quantum dots (QDs) of size ≈3.3 nm. Under visible‐light irradiation, the Au/CdSe NCs with 7.2 nm Au NPs afford very stable operation and a remarkable H₂‐evolution rate of (10× higher than bare CdSe NCs). Plasmon resonance energy transfer from the Au NPs to the CdSe QDs, which enhances charge‐carrier generation in the semiconductor and suppresses bulk recombination, is responsible for the outstanding photocatalytic performance. The approach used here to fabricate the Au/CdSe NCs is suitable for the construction of other plasmon‐mediated photocatalysts.     

TiO2 ALD decorated CuO/BiVO4 p-n heterojunction for improved photoelectrochemical water splitting

Bismuth vanadate (BiVO₄) is a promising photoanode material owing to the narrow bandgap, appropriate band position, and excellent resistance against photocorrosion, however, the performance of photoelectrochemical (PEC) water splitting is largely limited by the poor carrier separation and transport ability. To address these issues, for the first time, we fabricate BiVO₄ film/CuO nanocone p-n junctions as photoanodes by combing a facile spin-coating process and water bath reaction. This structure strengthens the light harvesting and promotes the charge separation and transport ability. The surface defects states are passivated by coating conformally ultrathin TiO₂ onto CuO surface through atomic layer deposition (ALD) technique. Benefiting from the favorable morphology, energy band, and surface treatment, the BiVO₄/CuO/TiO₂ heterojunction generates an improved photocurrent that is much higher than pure BiVO₄. The detailed mechanism investigations indicate that the synergetic optimization of charge separation and injection efficiency in the bulk and surface of photoelectrodes can significantly improve the performance of PEC cells.     

Binary Nanoparticle Superlattices for Plasmonically Modulating Upconversion Luminescence

Engineering a facile and controllable approach to modulate the spectral properties of lanthanide‐doped upconversion nanoparticles (UCNPs) is always an ongoing challenge. Herein, long‐range ordered, distinct two‐dimensional (2D) binary nanoparticle superlattices (BNSLs) composed of NaREF₄:Yb/Er (RE = Y and Gd) UCNPs and plasmonic metallic nanoparticles (Au NPs), including AB, AB₃, and AB₁₃ lattices, are fabricated via a slow evaporation‐driven self‐assembly to achieve plasmonic modulation of upconversion luminescence (UCL). Optical measurements reveal that typical red–green UCL from UCNPs can be effectively modulated into reddish output in BNSLs, with a drastically shortened lifetime. Notably, for AB₃‐ and AB₁₃‐type BNSLs with more proximal Au NPs around each UCNP, modified UCL with fine‐structured spectral lineshape is observed. These differences could be interpreted by the interplay of collective plasmon resonance introduced by 2D periodic Au arrays and spectrally selective energy transfer between UCNPs and Au. Thus, fabricating UCNP‐Au BNSLs with desired lattice parameters and NP configurations could be a promising way to tailor the UCL through controlled plasmonic modulation.     

Au–ZnO Nanocomposite Films for Plasmonic Photocatalysis

Nanocomposites based on plasmonic nanoparticles and metal‐oxide semiconductors are emerging as promising materials for conversion of solar energy into chemical energy. In this work, a Au–ZnO nanocomposite film with notably enhanced photocatalytic activity is successfully prepared by a single‐step process. Both ZnO and Au nanoparticles are synthesized in situ during baking of the film spin‐coated from a solution of Zn(CH₃COO)₂ and HAuCl₄. Furthermore, it is shown that this precursor solution can be formulated as a nanoink for the generation of micropatterns by microplotter printing, opening the way for the miniaturization of devices with enhanced properties for photocatalysis, optoelectronics, and sensing. The study demonstrates that Au–ZnO films exhibit 4.5‐fold enhanced photocatalytic properties for the decomposition of methyl orange upon sunlight exposure in comparison with ZnO films. Au nanoparticles improve significantly the photocatalytic activity of ZnO because they act as photosensitizers, absorbing photons at the localized surface plasmon resonance range (500–600 nm) and transferring electrons to the nearby ZnO semiconductor. XPS analysis of the Au–ZnO nanocomposite supports this explanation, indicating strong interactions between Au and ZnO.     

Facet‐Dependent Optical Properties Revealed through Investigation of Polyhedral Au–Cu2O and Bimetallic Core–Shell Nanocrystals

The ability to prepare Au–Cu₂O core–shell nanocrystals with precise control over particle size and shape has led to the discovery of facet‐dependent optical properties in cuprous oxide crystals. The use of Au cores not only allows the successful formation of Au–Cu₂O core–shell nanocrystals with tunable sizes, but also enables the observation of facet‐dependent optical properties in these crystals through the Au localized surface plasmon resonance (LSPR) absorption band. By tuning the Cu₂O shell morphology from rhombic dodecahedral to octahedral and cubic structures, and thus the exposed facets, the Au LSPR band position can be widely tuned. Such facet‐dependent optical effects are not observed in bimetallic Au–Ag and Au–Pd core–shell nanocrystals with the same precisely tuned particle sizes and shapes. It is believed that similar facet‐dependent optical properties could be observed in other ionic solids and other metal–metal oxide systems. The unusually large degree of plasmonic band tuning covering from the visible to the near‐infrared region in this type of nanostructure should be quite useful for a range of plasmonic applications.     

Plasmonic Metal Mediated Charge Transfer in Stacked Core–Shell Semiconductor Heterojunction for Significantly Enhanced CO2 Photoreduction

Construction of core–shell semiconductor heterojunctions and plasmonic metal/semiconductor heterostructures represents two promising routes to improved light harvesting and promoted charge separation, but their photocatalytic activities are respectively limited by sluggish consumption of charge carriers confined in the cores, and contradictory migration directions of plasmon-induced hot electrons and semiconductor-generated electrons. Herein, a semiconductor/metal/semiconductor stacked core–shell design is demonstrated to overcome these limitations and significantly boost the photoactivity in CO₂ reduction. In this smart design, sandwiched Au serves as a “stone”, which “kills two birds” by inducing localized surface plasmon resonance for hot electron generation and mediating unidirectional transmission of conduction band electrons and hot electrons from TiO₂ core to MoS₂ shell. Meanwhile, upward band bending of TiO₂ drives core-to-shell migration of holes through TiO₂–MoS₂ interface. The co-existence of TiO₂ → Au → MoS₂ electron flow and TiO₂ → MoS₂ hole flow contributes to spatial charge separation on different locations of MoS₂ outer layer for overall redox reactions. Additionally, reduction potential of photoelectrons participating in the CO₂ reduction is elaborately adjusted by tuning the thickness of MoS₂ shell, and thus the product selectivity is delicately regulated. This work provides fresh hints for rationally controlling the charge transfer pathways toward high-efficiency CO₂ photoreduction.     

Avalanche Carrier Multiplication in Multilayer Black Phosphorus and Avalanche Photodetector

A highly sensitive avalanche photodetector (APD) is fabricated by utilizing the avalanche multiplication mechanism in black phosphorus (BP), where a strong avalanche multiplication of electron–hole pairs is observed. Owing to the small bandgap (0.33 eV) of the multilayer BP, the carrier multiplication occurs at a significantly lower electric field than those of other 2D semiconductor materials. In order to further enhance the quantum efficiency and increase the signal‐to‐noise (S/N) ratio, Au nanoparticles (NPs) are integrated on the BP surface, which improves the light absorption by plasmonic effects. The BP–Au‐NPs structure effectively reduces both dark current (≈10 times lower) and onset of avalanche electric field, leading to higher carrier multiplication, photogain, quantum efficiency, and S/N ratio. For the BP–Au‐NPs APD, it is obtained that the external quantum efficiency (EQE) is 382 and the responsivity is 160 A W^‐1 at an electric field of 5 kV cm^‐1 (V_d ≈ 3.5 V, note that for the BP APD, EQE = 4.77 and responsivity = 2 A W^‐1 obtained at the same electric field). The significantly increased performance of the BP APD is promising for low‐power‐consumption, high‐sensitivity, and low‐noise photodevice applications, which can enable high‐performance optical communication and imaging systems.     

Periodical 2D Photonic–Plasmonic Au/TiOx Nanocavity Resonators for Photoelectrochemical Applications

Effective light trapping at the nanoscale is vital for efficient photoelectrochemical (PEC) applications. Photonic and plasmonic resonators are the two most promising approaches for this purpose, and the synergetic combination of these two resonators will tail the propagation lengths of incident light along with field enhancements, and thus presents further enhanced light‐trapping activity. Herein, a new hybrid photonic–plasmonic resonator is proposed through sputtering plasmonic Au nanoparticles (NPs) into the 2D photonic TiO_x nanocavity. Through facile control of the size of Au NPs, the matching of resonant wavelength of plasmonic Au NPs and photonic nanocavities maximize the light‐trapping intensity and thus further improve the PEC performance. Furthermore, for expanding the PEC applications, after functionalization of Au NPs with aptamer as a biomolecular recognition unit, a PEC aptasensor is also proposed and presents the highest sensitivity for antibiotic detection.     

Au NPs@MoS2 Sub‐Micrometer Sphere‐ZnO Nanorod Hybrid Structures for Efficient Photocatalytic Hydrogen Evolution with Excellent Stability

MoS₂ shows promising applications in photocatalytic water splitting, owing to its uniquely optical and electric properties. However, the insufficient light absorption and lack of performance stability are two crucial issues for efficient application of MoS₂ nanomaterials. Here, Au nanoparticles (NPs)@MoS₂ sub‐micrometer sphere‐ZnO nanorod (Au NPs@MoS₂‐ZnO) hybrid photocatalysts have been successfully synthesized by a facile process combining the hydrothermal method and seed‐growth method. Such photocatalysts exhibit high efficiency and excellent stability for hydrogen production via multiple optical‐electrical effects. The introduction of Au NPs to MoS₂ sub‐micrometer spheres forming a core–shell structure demonstrates strong plasmonic absorption enhancement and facilitates exciton separation. The incorporation of ZnO nanorods to the Au NPs@MoS₂ hybrids further extends the light absorption to a broader wavelength region and enhances the exciton dissociation. In addition, mutual contacts between Au NPs (or ZnO nanorods) and the MoS₂ spheres effectively protect the MoS₂ nanosheets from peeling off from the spheres. More importantly, efficiently multiple exciton separations help to restrain the MoS₂ nanomaterials from photocorrosion. As a result, the Au@MoS₂‐ZnO hybrid structures exhibit an excellent hydrogen gas evolution (3737.4 μmol g^?1) with improved stability (91.9% of activity remaining) after a long‐time test (32 h), which is one of the highest photocatalytic activities to date among the MoS₂ based photocatalysts.     

New BiVO4 Dual Photoanodes with Enriched Oxygen Vacancies for Efficient Solar‐Driven Water Splitting

Bismuth vanadate (BiVO₄) is a promising photoanode material for photoelectrochemical (PEC) water splitting. However, owing to the short carrier diffusion length, the trade‐off between sufficient light absorption and efficient charge separation often leads to poor PEC performance. Herein, a new electrodeposition process is developed to prepare bismuth oxide precursor films, which can be converted to transparent BiVO₄ films with well‐controlled oxygen vacancies via a mild thermal treatment process. The optimized BiVO₄ film exhibits an excellent back illumination charge separation efficiency mainly due to the presence of enriched oxygen vacancies which act as shallow donors. By loading FeOOH/NiOOH as the cocatalysts, the BiVO₄ dual photoanodes exhibit a remarkable and highly stable photocurrent density of 5.87 mA cm^?2 at 1.23 V versus the reversible hydrogen electrode under AM 1.5 G illumination. An artificial leaf composed of the BiVO₄/FeOOH/NiOOH dual photoanodes and a single sealed perovskite solar cell delivers a solar‐to‐hydrogen conversion efficiency as high as 6.5% for unbiased water splitting.     

Recent progress in oxynitride photocatalysts for visible-light-driven water splitting

Abstract

Photocatalytic water splitting into hydrogen and oxygen is a method to directly convert light energy into storable chemical energy, and has received considerable attention for use in large-scale solar energy utilization. Particulate semiconductors are generally used as photocatalysts, and semiconductor properties such as bandgap, band positions, and photocarrier mobility can heavily impact photocatalytic performance. The design of active photocatalysts has been performed with the consideration of such semiconductor properties. Photocatalysts have a catalytic aspect in addition to a semiconductor one. The ability to control surface redox reactions in order to efficiently produce targeted reactants is also important for photocatalysts. Over the past few decades, various photocatalysts for water splitting have been developed, and a recent main concern has been the development of visible-light sensitive photocatalysts for water splitting. This review introduces the study of water-splitting photocatalysts, with a focus on recent progress in visible-light induced overall water splitting on oxynitride photocatalysts. Various strategies for designing efficient photocatalysts for water splitting are also discussed herein.