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Keita Nishioka

Publications and source records attributed to Keita Nishioka.

4 recordsLinked to original sources

A Rotation-Compensated Smartphone Accelerometer Application for Undergraduate Mechanics Experiments

Smartphones equipped with sensors such as accelerometers, gyroscopes, and magnetometers offer valuable opportunities for physics education, allowing students to measure motion using their own devices. However, commonly used applications provide acceleration only in the device-fixed coordinate system, which makes it difficult to analyze two- or three-dimensional motion when the device rotates. To address this limitation, we developed a web-based accelerometer application that can provide acceleration in a stationary global coordinate system. This is achieved by simultaneously recording acceleration in the device-fixed coordinate system and Euler angles, and converting them to rotation-compensated acceleration in real time. We also built a companion web application for numerical integration, noise reduction, and visualization of the measured data. Both applications are installation-free and can be accessed directly through a smartphone browser. We demonstrate the capabilities of the newly developed system through several representative types of motion, including sliding motion, projectile motion, and circular motion, by showing that rotation-compensated acceleration enables accurate reconstruction of velocity, displacement, and trajectories even when the smartphone changes its orientation. The applications were implemented in undergraduate mechanics classes, where students used them in group-based experiments. Classroom observations suggested that the use of these tools facilitated a deeper understanding of the relationships among acceleration, velocity, and position. These results suggest that rotation-compensated smartphone measurements provide a practical and effective tool for physics education.

physics.ed-ph↗

Negative-Temperature State Formed and Interactions Inverted by Symmetric Monocycle Optical Pulse Excitation

The excited state dynamics of correlated electron and electron-phonon systems triggered by an oscillating electric-field pulse of large amplitude are theoretically investigated. A "negative-temperature" state and inversion of electron-electron and electron-phonon interactions are induced even by a symmetric monocycle pulse. This fact is numerically demonstrated, using the exact diagonalization method, in a band-insulator phase of one-dimensional three-quarter-filled strongly dimerized extended Peierls-Hubbard and Holstein models. When the total-energy increment is maximized as a function of the electric field amplitude, the occupancy of the bonding and antibonding orbitals is inverted to produce a negative-temperature state. Around this state, the dependences of time-averaged electron-electron and electron-phonon correlation functions on interaction parameters are opposite to those in the ground state.

cond-mat.str-el↗

Proposal of Two-Pulse Excitation to Efficiently Photoinduced Novel $sp^3$ Nano Domain with Frozen Shear in Graphite Crystal

We propose a two-pulse excitation to efficiently photoinduced a novel $sp^3$-bonded nano-domain with a frozen shear in a graphite crystal. This $sp^3$ structure is known to be well stabilized by shear displacement between neighboring two graphite layers. This shear motion is generated only as a transient and unfrozen one by the first visible laser pulse, shone over the graphite crystal. While, the second pulse is proved to freeze it before it disappears, resulting in an efficient interlayer $σ$ ($sp^3$) bond formation.

cond-mat.mtrl-sci↗

Cooperative domain type interlayer $sp^3$-bond formation in graphite

Using the classical molecular dynamics and the semiempirical Brenner's potential, we theoretically study the interlayer sigma bond formation, as cooperative and nonlinear phenomena induced by visible light excitations of a graphite crystal. We have found several cases, wherein the excitations of certain lattice sites result in new interlayer bonds even at non-excited sites. We have also found that, a new interlayer bond is easier to be formed around a bond, if it is already existing. As many more sites are going to be excited, the number of interlayer bonds increases nonlinearly with the number of excited sites. This nonlinearity shows 1.7 power of the total number of excited sites, corresponding to about three- or four-photon process.

cond-mat.mtrl-sci↗