Chun-Fu Lu

Conjugated Polymer/Nanoparticles Nanocomposites for High Efficient and Real-Time Volatile Organic Compounds Sensors

The present work demonstrates a high efficient and low cost volatile organic compounds (VOCs) sensor. Nowadays, VOCs, which are typically toxic, explosive, flammable, and an environmental hazard, are extensively used in R&D laboratories and industrial productions. Real-time and accurately monitoring the presence of harmful VOC during the usage, storage, or transport of VOCs is extremely important which protects humans and the environment from exposure in case of an accident and leakage of VOCs. The present work utilizes conducting polymer/nanoparticles blends to sense various VOCs by detecting the variation of optical properties. The novel sensor features high sensitivity, high accuracy, quick response, and very low cost. Furthermore, it is easy to fabricate into a sensing chip and can be equipped anywhere such as a laboratory or a factory where the VOCs are either used or produced and on each joint between transporting pipes or each switch of VOC storage tanks. Real-time sensing is achievable on the basis of the instant response to VOC concentrations of explosive limits. Therefore, an alarm can be delivered within a few minutes for in time remedies. This research starts from investigating fundamental properties, processing adjustments, and a performance test and finally extends to real device fabrication that practically performs the sensing capability. The demonstrated results significantly advance the current sensor technology and are promising in commercial validity in the near future for human and environmental safety concerns against hazardous VOCs.

Improved Solar-Driven Photocatalytic Performance of Highly Crystalline Hydrogenated TiO 2 Nanofibers with Core-Shell Structure

Hydrogenated titanium dioxide has attracted intensive research interests in pollutant removal applications due to its high photocatalytic activity. Herein, we demonstrate hydrogenated TiO2 nanofibers (H:TiO2 NFs) with a core-shell structure prepared by the hydrothermal synthesis and subsequent heat treatment in hydrogen flow. H:TiO2 NFs has excellent solar light absorption and photogenerated charge formation behavior as confirmed by optical absorbance, photo-Kelvin force probe microscopy and photoinduced charge carrier dynamics analyses. Photodegradation of various organic dyes such as methyl orange, rhodamine 6G and brilliant green is shown to take place with significantly higher rates on our novel catalyst than on pristine TiO2 nanofibers and commercial nanoparticle based photocatalytic materials, which is attributed to surface defects (oxygen vacancy and Ti3+ interstitial defect) on the hydrogen treated surface. We propose three properties/mechanisms responsible for the enhanced photocatalytic activity, which are: (1) improved absorbance allowing for increased exciton generation, (2) highly crystalline anatase TiO2 that promotes fast charge transport rate, and (3) decreased charge recombination caused by the nanoscopic Schottky junctions at the interface of pristine core and hydrogenated shell thus promoting long-life surface charges. The developed H:TiO2 NFs can be helpful for future high performance photocatalysts in environmental applications.

Light induced electrostatic force spectroscopy: Application to local electronic transitions in InN epifilms

A technique based on electrostatic force microscopy in which light is used to change the charge states of the local region in a solid is introduced and demonstrated. This technique provides a unique feature that it can be used to probe local electronic transitions of a solid in a submicron scale. As an illustration, it has been applied to study local electronic structure in InN epifilms. Combining with atomic force microscopy, it is found that surface state density in the dale region is larger than that in the pinnacle region and an electron accumulation layer does exist on the surface. In addition, the magnitude of the surface band bending obtained for the regions with different surface states is consistent with the result measured by other techniques. We point out that light induced scanning electrostatic force spectroscopy is a very useful tool to probe the local electronic transitions of a solid in a submicron scale with high sensitivity.

Low temperature and rapid formation of high quality metal oxide thin film via a hydroxide-assisted energy conservation strategy

Metal oxide thin films made from a sol–gel solution process are promising candidates for stable, low cost, and high performance electronic devices. Reducing the thermal budget required for their crystallization process can relax the fabrication limitation and expand their possible applications. We show that with the addition of an adequate amount of tetramethylammonium hydroxide (TMAOH) in the precursor solution, the activation energy of the sol–gel reaction can be reduced by about 50%. Using this strategy, not only can the required thermal treatment time and temperature of the sol–gel reaction be significantly reduced but also the quality of the film can be improved. The enhanced reaction rate can be ascribed to the presence of hydroxyl anions, which facilitate the formation of the metal hydroxide and the subsequent metal oxide. Additionally, the strategy developed here can be applied to multiple kinds of metal oxides. By this method, the processing temperature can be lowered by at least 50 °C and the time can be shortened by half for the fabrication of electronic devices such as thin film transistors and photovoltaics. Our results open up a new paradigm to fabricate highly crystalline metal oxide thin films quickly at an energy saving low temperature using the solution process.