Ultraviolet (UV) photodetectors have drawn extensive attention owing to their applications in industrial, environmental and even biological fields. Compared to UV-enhanced Si photodetectors, a new generation of wide bandgap semiconductors, such as (Al, In) GaN, diamond, and SiC, have the advantages of high responsivity, high thermal stability, robust radiation hardness and high response speed. On the other hand, one-dimensional (1D) nanostructure semiconductors with a wide bandgap, such as β-Ga2O3, GaN, ZnO, or other metal-oxide nanostructures, also show their potential for high-efficiency UV photodetection. In some cases such as flame detection, high-temperature thermally stable detectors with high performance are required. This article provides a comprehensive review on the state-of-the-art research activities in the UV photodetection field, including not only semiconductor thin films, but also 1D nanostructured materials, which are attracting more and more attention in the detection field. A special focus is given on the thermal stability of the developed devices, which is one of the key characteristics for the real applications.
Etching characteristics of nondoped GaN films with the polar surface in KOH solution have been investigated. It is confirmed that the continuous etching in KOH solution takes place only for the GaN films with N-face (Ϫc) polarity independent of the deposition method and growth condition. It is found by x-ray photoelectron spectroscopy ͑XPS͒ analysis for the Ga face (ϩc) and N-face (Ϫc) GaN films that the atomic composition of the ϩc surface is not changed before and after dipping in KOH solution and that on the other hand, the amount of oxygen ͑oxide͒ on the Ϫc surface is significantly decreased by the etching. It is also found that the band bending increases by Ϫ0.4Ϯ0.2 and 0.6Ϯ0.2 eV for the ϩc and Ϫc surfaces after etching, respectively. This is discussed in terms of the surface chemistry. Based on the XPS result, the selective etching of the GaN polar surface is pointed out to originate from bonding configuration of nitrogen at the surface.
Defects in GaN grown using metalorganic chemical vapor deposition were studied through the use of monoenergetic positron beams. For Mg-doped GaN, no large change in the diffusion length of positrons was observed before and after activation of Mg. This was attributed to the scattering of positrons by potentials caused by electric dipoles of Mg–hydrogen pairs. For Si-doped GaN, the line-shape parameter S increased as carrier density increased, suggesting an introduction of Ga vacancy due to the Fermi level effect. Based on these results, we discuss the effects of the growth polar direction of GaN on optical properties in this article. Although the optical properties of a GaN film grown toward the Ga face direction exhibited excitonic features, a film grown toward the N face (−c) direction exhibited broadened photoluminescence and transmittance spectra, and a Stokes shift of about 20 meV was observed. This difference was attributed to extended band-tail states introduced by high concentrations of donors and acceptor-type defects in −c GaN.
We have investigated the dependence of impurity incorporation on the polar direction of GaN growth by using secondary ion mass spectroscopy (SIMS). GaN films were deposited under conditions used for growing device-quality materials on sapphire substrates while controlling their polar direction. It was found that the polarity of the GaN film influences the incorporation of impurities. SIMS analysis has revealed that the impurities related to carbon, oxygen, and aluminum are more readily incorporated into N-face GaN films.
Polarity issues affecting III-V nitride semiconductors are reviewed with respect to their determination and control. A set of conditions crucial to the polarity control of GaN is provided for each of the following growth techniques; molecular beam epitaxy (MBE), pulsed laser deposition (PLD) and hydride vapor phase epitaxy (HVPE). Although GaN films might have been deposited by identical growth methods using the same buffer layer technologies, there is often a conflict between the resulting polarities achieved by different research groups. In this paper, we present the implications of the conditions used in each of the processes used for two-step metalorganic chemical vapor deposition (MOCVD), demonstrating systematic control of the polarity of GaN films on sapphire substrates. The potential for confusion in polarity control will be explained, taking into account the implications clarified in our studies. The correlation between the polarity and the growth conditions will be discussed in order to provide a mechanism for the determination and control of the crystal polarity during the growth of GaN films.
Growth and characterization of N-polar GaN films on SiC by metal organic chemical vapor deposition J. Appl. Phys.Nondestructive determination of the polarity of GaN has been achieved by the use of coaxial impact-collision ion scattering spectroscopy analysis. The polarity of a GaN film with a smooth surface on non-nitrided c-plane sapphire was identified ͑0001͒ ͑Ga face; ϩc͒. GaN films with a 20 nm buffer layer on nitrided sapphire had (0001 ) ͑N face; Ϫc͒ polarity and a hexagonal faceted surface. The influence of both the buffer layer and of substrate nitridation on the polarity of wurtzite ͕0001͖ GaN films deposited by two-step metal organic chemical vapor deposition ͑MOCVD͒ has been investigated. The polarity of the buffer layer on a nitrided sapphire substrate was altered by varying its thickness or the annealing time. It was found that the polarity of the GaN film is determined by the polarity of the annealed buffer layer; MOCVD-GaN films on buffer layers with ϩc and Ϫc polarity have either ϩc ͑smooth surface͒ or Ϫc ͑hexagonal facet͒ polarity, respectively.
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