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.

Increasing the sensitivity of non-noble metal surface-enhanced Raman spectroscopy (SERS) is an urgent issue that needs to be solved at present. Herein, metallic WO nanowires with a strong localized surface plasmon resonance (LSPR) effect are prepared. Interestingly, the LSPR peaks of these nanowires would undergo a strong blue shift from near-infrared (NIR) to visible light regions as the aggregation degree of the nanowires increases. By narrowing the gap between the LSPR absorption peak and the Raman excitation wavelength (532 nm), the oriented WO bundles with a LSPR peak centered at 561 nm have greatly improved SERS sensitivity compared with that of the dispersed nanowires with a LSPR peak centered at 1025 nm. Enhancement mechanism investigation shows that the high sensitivity can be attributed to the synergistic effect of LSPR coupling among the oriented ultrathin nanowires and oxygen vacancy (V)-assisted charge transfer.

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Semiconductor-based surface-enhanced Raman spectroscopy is getting more and more attention because of its great price advantage. One of the biggest obstacles to the large-scale application of it is the poor stability. Here, we report that plasmonic MoO nanospheres can be used as a highly sensitive and stable semiconducting-substrate material for surface-enhanced Raman scattering (SERS). By using the MoO nanospheres as Raman substrates, a series of typical compounds with high attention can be accurately detected. This new non-noble metal substrate material shows a very high detection limit of 10 M, and exhibits great near-field enhancement with one of the highest enhancement factor of 4.8 × 10 reported to date. More importantly, the oxide with intermediate valence displays unexpected ultrahigh stability, which can withstand the corrosion of strong acid and strong alkali as well as 150 °C high temperature oxidation in air. Moreover, the accurate detection of multicomponent samples was also successful on this substrate. These results show that some simple metal oxides with intermediate valence may become sensitive and stable SERS substrate materials due to their abundant free electrons and structure that easily causes hot spots.

Cucumber mosaic virus (CMV) infection could induce mosaic symptoms on a wide-range of host plants. However, there is still limited information regarding the molecular mechanism underlying the development of the symptoms. In this study, the coat protein (CP) was confirmed as the symptom determinant by exchanging the CP between a chlorosis inducing CMV-M strain and a green-mosaic inducing CMV-Q strain. A yeast two-hybrid analysis and bimolecular fluorescence complementation revealed that the chloroplast ferredoxin I (Fd I) protein interacted with the CP of CMV-M both in vitro and in vivo, but not with the CP of CMV-Q. The severity of chlorosis was directly related to the expression of Fd1, that was down-regulated in CMV-M but not in CMV-Q. Moreover, the silencing of Fd I induced chlorosis symptoms that were similar to those elicited by CMV-M. Subsequent analyses indicated that the CP of CMV-M interacted with the precursor of Fd I in the cytoplasm and disrupted the transport of Fd I into chloroplasts, leading to the suppression of Fd I functions during a viral infection. Collectively, our findings accentuate that the interaction between the CP of CMV and Fd I is the primary determinant for the induction of chlorosis in tobacco.