Rising atmospheric levels of carbon dioxide and the depletion of fossil fuel reserves raise serious concerns about the ensuing effects on the global climate and future energy supply. Utilizing the abundant solar energy to convert CO2 into fuels such as methane or methanol could address both problems simultaneously as well as provide a convenient means of energy storage. In this Review, current approaches for the heterogeneous photocatalytic reduction of CO2 on TiO2 and other metal oxide, oxynitride, sulfide, and phosphide semiconductors are presented. Research in this field is focused primarily on the development of novel nanostructured photocatalytic materials and on the investigation of the mechanism of the process, from light absorption through charge separation and transport to CO2 reduction pathways. The measures used to quantify the efficiency of the process are also discussed in detail.

Photocatalytic reduction of CO2 on TiO2 and other semiconductors.

Lignocellulosic biomass: a sustainable platform for the production of bio-based chemicals and polymers

Titanium dioxide (TiO2), as an important semiconductor metal oxide, has been widely investigated in the field of photocatalysis. The properties of TiO2, including its light absorption, charge transport and surface adsorption, are closely related to its defect disorder, which in turn plays a significant role in the photocatalytic performance of TiO2. Among all the defects identified in TiO2, oxygen vacancy is one of the most important and is supposed to be the prevalent defect in many metal oxides, which has been widely investigated both by theoretical calculations and experimental characterizations. Here, we give a short review on the existing strategies for the synthesis of defective TiO2 with oxygen vacancies, and the defect related properties of TiO2 including structural, electronic, optical, dissociative adsorption and reductive properties, which are intimately related to the photocatalytic performance of TiO2. In particular, photocatalytic applications with regard to defective TiO2 are outlined. In addition, we offer some perspectives on the challenge and new direction for future research in this field. We hope that this tutorial minireview would provide some useful contribution to the future design and fabrication of defective semiconductor-based nanomaterials for diverse photocatalytic applications.

Defective TiO2 with oxygen vacancies: synthesis, properties and photocatalytic applications

Photoreduction of CO2 into sustainable and green solar fuels is generally believed to be an appealing solution to simultaneously overcome both environmental problems and energy crisis. The low selectivity of challenging multi-electron CO2 photoreduction reactions makes it one of the holy grails in heterogeneous photocatalysis. This Review highlights the important roles of cocatalysts in selective photocatalytic CO2 reduction into solar fuels using semiconductor catalysts. A special emphasis in this review is placed on the key role, design considerations and modification strategies of cocatalysts for CO2 photoreduction. Various cocatalysts, such as the biomimetic, metal-based, metal-free, and multifunctional ones, and their selectivity for CO2 photoreduction are summarized and discussed, along with the recent advances in this area. This Review provides useful information for the design of highly selective cocatalysts for photo(electro)reduction and electroreduction of CO2 and complements the existing reviews on various semiconductor photocatalysts.

Cocatalysts for Selective Photoreduction of CO2 into Solar Fuels.

Large amounts of anthropogenic CO2 emissions associated with increased fossil fuel consumption have led to global warming and an energy crisis. The photocatalytic reduction of CO2 into solar fuels such as methane or methanol is believed to be one of the best methods to address these two problems. In addition to light harvesting and charge separation, the adsorption/activation and reduction of CO2 on the surface of heterogeneous catalysts remain a scientifically critical challenge, which greatly limits the overall photoconversion efficiency and selectivity of CO2 reduction. This review describes recent advances in the fundamental understanding of CO2 photoreduction on the surface of heterogeneous catalysts and particularly provides an overview of enhancing the adsorption/activation of CO2 molecules. The reaction mechanism and pathways of CO2 reduction as well as their dependent factors are also analyzed and discussed, which is expected to enable an increase in the overall efficiency of CO2 reduction through minimizing the reaction barriers and controlling the selectivity towards the desired products. The challenges and perspectives of CO2 photoreduction over heterogeneous catalysts are presented as well.

CO2 photo-reduction: insights into CO2 activation and reaction on surfaces of photocatalysts

Inorganic nanowires with ultrathin diameters below the magic size (i.e., less than 2 nm) and even one unit cell size, have attracted much research attention in the past few years owing to their unique chemical and physical properties. As an important semiconductor material, tungsten oxide (WO3 x) nanowires and nanorods have attracted considerable attention because of their wide applications in gas sensors, electrochromic windows, optical devices, and photocatalysts. In particular, monoclinic W18O49 is of great interest owing to its unusual defect structure and promising properties in the nanometer regime. Early on, Park and co-workers reported the synthesis of W18O49 nanorods with a diameter of 4 nm by decomposing [W(CO)6] in Me3NO2·2 H2O and oleylamine. [16] Subsequently, Niederberger and co-workers synthesized hybrid W18O49/ organic nanowires with a very thin diameter of 1.3 nm by a bioligand-assisted method. Recently, Tremel and coworkers prepared W18O49 nanorods with a diameter of 2 nm by decomposing tungsten ethoxide in a mixture of oleic acid and trioctyl amine. Although good control over nanocrystal dimensions can be realized in these methods, removal of the surfactants or organic residues from the nanowire surface requires multiple washing steps. For fundamental investigations on the ultrathin oxide nanowire itself, as well as for technological applications (such as sensing and catalysis), the presence of residues on the nanowire surface from the synthesis may be a significant drawback. Herein, we report the preparation of ultrathin W18O49 nanowires that are efficient in the photochemical reduction of carbon dioxide by visible light. The ultrathin W18O49 nanowires were prepared by a very simple one-pot solution-phase method (see the experimental section in the Supporting Information). In a typical procedure, WCl6 was dissolved in ethanol, and the clear yellow solution was transferred to a teflon-lined stainless-steel autoclave and heated at 180 8C for 24 h. A blue flocculent precipitate was collected, washed, dried in air, and obtained in a yield of approximately 100 %. The product is insoluble in water and in acid (HCl, pH 0), and has a high specific surface area. W18O49 is a monoclinic structure type (P2 m) with lattice parameters of a = 18.318, b = 3.782, and c = 14.028 . Monoclinic W18O49 has a distorted ReO3 structure in which cornersharing distorted and tilt WO6 octahedra are connected in the a-, b-, and c-direction, thereby forming a three-dimensional structure (inset in Figure 1a). The X-ray diffraction (XRD) pattern of our sample demonstrates that the sample consists of monoclinic-phase W18O49 (Figure 1 a). The narrow (010) and (020) peaks strongly suggest that the possible crystal growth direction of the sample is [010], since the close-packed planes of the monoclinic W18O49 crystal are {010}, which will be further demonstrated by the direct observation of the highresolution transmission electron microscopy (HRTEM) image (see below). Energy-dispersive X-ray spectroscopy (EDS) confirms that the sample only contains W and O elements (Figure 1b). Furthermore, the Fourier transform infrared (FTIR) spectrum exhibits the clear surface of our sample (Figure S1 in the Supporting Information). Scanning electron microscopy (SEM) and transmission electron microscopy (TEM) images show that the as-synthesized sample is composed of nanowires with large aspect ratio and lengths of up to several micrometers (Figure 1c, d). Interestingly, higher-magnification TEM images (Figure 1e and Figures S2 and S3 in the Supporting Information) clearly reveal that the nanowires shown in Figure 1d are composed of a lot of individual, thinner nanowires. The diameter of the thinner nanowires is only about 0.9 nm. The HRTEM image and corresponding fast Fourier transform (FFT) pattern demonstrate that the ultrathin nanowires are crystalline and grow along [010] direction (Figure 1 f and Figure S4 in the Supporting Information). A comparison of the unit cell of W18O49 projected along the [010] direction with the typical diameter of the nanowires of 0.9 nm (red circle) allows [*] Dr. G. C. Xi, Dr. S. X. Ouyang, P. Li, Prof. J. H. Ye International Center for Materials Nanoarchitectonics (WPIMANA), and Environmental Remediation Materials Unit National Institute for Materials Science (NIMS) 1-2-1 Sengen, Tsukuba, Ibaraki 305-0047 (Japan) E-mail: jinhua.ye@nims.go.jp

Ultrathin W18O49 nanowires with diameters below 1 nm: synthesis, near-infrared absorption, photoluminescence, and photochemical reduction of carbon dioxide.

Metal/semiconductor hybrid materials of various sizes and morphologies have many applications in areas such as catalysis and sensing. Various organic agents are necessary to stabilize metal nanoparticles during synthesis, which leads to a layer of organic compounds present at the interfaces between the metal particles and the semiconductor supports. Generally, high-temperature oxidative treatment is used to remove the organics, which can extensively change the size and morphology of the particles, in turn altering their activity. Here we report a facile method for direct growth of noble-metal particles on WO3 through an in situ redox reaction between weakly reductive WO2.72 and oxidative metal salts in aqueous solution. This synthetic strategy has the advantages that it takes place in one step and requires no foreign reducing agents, stabilizing agents, or pretreatment of the precursors, making it a practical method for the controlled synthesis of metal/semiconductor hybrid nanomaterials. This synthetic m...

In Situ Growth of Metal Particles on 3D Urchin-like WO3 Nanostructures

Compared with noble metals, semiconductors with surface plasmon resonance effect are another type of SERS substrate materials. The main obstacles so far are that the semiconducting materials are often unstable and easy to be further oxidized or decomposed by laser irradiating or contacting with corrosive substances. Here, we report that metallic MoO2 can be used as a SERS substrate to detect trace amounts of highly risk chemicals including bisphenol A (BPA), dichloropheno (DCP), pentachlorophenol (PCP) and so on. The minimum detectable concentration was 10−7 M and the maximum enhancement factor is up to 3.75 × 106. To the best of our knowledge, it may be the best among the metal oxides and even reaches or approaches to Au/Ag. The MoO2 shows an unexpected high oxidation resistance, which can even withstand 300 °C in air without further oxidation. The MoO2 material also can resist long etching of strong acid and alkali. Semiconducting materials are potential SERS substrates as alternatives to noble metals, but often suffer from poor stabilities and sensitivities. Here, the authors use molybdenum dioxide as a SERS material, showing high enhancement factors and stability to oxidation even at high temperatures.

Hua Bai

Papers

Ultrathin W18O49 nanowires with diameters below 1 nm: synthesis, near-infrared absorption, photoluminescence, and photochemical reduction of carbon dioxide.

In Situ Growth of Metal Particles on 3D Urchin-like WO3 Nanostructures

A metallic molybdenum dioxide with high stability for surface enhanced Raman spectroscopy.

Screening melamine adulterant in milk powder with laser Raman spectrometry

Disposable paper-based electrochemical sensor based on stacked gold nanoparticles supported carbon nanotubes for the determination of bisphenol A