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Naofumi Nishikawa

Publications and source records attributed to Naofumi Nishikawa.

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Boron-Doping Effects on Local Structures of Semiconducting Ultrananocrystalline Diamond/Hydrogenated Amorphous Carbon Composite Thin Films Fabricated via Coaxial Arc Plasma: an X-ray Absorption Spectroscopic Study

Ultrananocrystalline diamond/hydrogenated amorphous carbon composite thin films synthesized via coaxial arc plasma possess a marked structural feature of diamond grains embedded in an amorphous carbon and a hydrogenated amorphous carbon matrix which are the largest constituents of the films. Since the amorphous nature yields much larger light absorption coefficients as well as a generation source of photo-induced carriers with UV rays, these films can be potential candidates for deep-UV photodetector applications. From some previous studies p-type conduction of the films has been realized by doping boron in experimental conditions. In addition, their optical and electrical characteristics were investigated previously. However, the bonding structures which largely affect the physical properties of the devices have not been investigated. In this work, near-edge X-ray absorption fine structure spectroscopy characterizations are carried out. The result reveals that a bonding state σ* C-B of diamond surfaces is formed preferentially and structural distortion is caused at an early stage of boron-doping. Further doping into the films lessens the amount of unsaturated bonds such as π* C=-C, which may be a cause of the device performance degradations. Our work suggests a fundamental case model of boron-doping effects on a local structure of the film.

cond-mat.mtrl-sci

Evidence of hydrogen termination at grain boundaries in ultrananocrystalline diamond/hydrogenated amorphous carbon composite thin films synthesized via coaxial arc plasma

Ultranonocrystalline diamond/hydrogenated amorphous carbon composite thin films consist of three different components; ultrananocrystalline diamond crystallites, hydrogenated amorphous carbon, and grain boundaries between them. Since grain boundaries contain a lot of dangling bonds and unsaturated bonds, they would be a cause of carrier trap center degrading device performance in possible applications such as UV photo-detectors. We experimentally demonstrate hydrogen atoms preferentially incorporate at grain boundaries and terminate dangling bonds by means of several spectroscopic techniques. XPS measurements cannot detect quantitative transitions of sp^2- and sp^3-hybridized carbons in the films, resulting in 55-59 % of sp^3 contents. On the other hand, FT-IR and NEXAFS exhibit some variations of the amounts of certain carbon hybridization for sure. The former confirms the transformation from sp^2 to sp^3 hydrocarbons by ~10 % by additional hydrogenation, and the latter represents chemical configuration changes from π* C{\equiv}C and π* C=C to σ* C-H. These results can be an evidence of localized hydrogen at grain boundaries, which plays a part in terminating dangling bonds and unsaturated bonds, and they are correlated with the optical and electrical properties of the films investigated in some previous research. Our spectroscopic studies on the hydrogenation effects combined with the discussion on the optical and electrical characteristics confirm that the hydrogenation can be an effective tool of an enhancement of photovoltaic performance in the above sensing applications.

cond-mat.mtrl-sci