Reversal of Band-Ordering Leads to High Hole Mobility in Strained p-type Scandium Nitride.

Low hole mobility of nitride semiconductors is a significant impediment to realizing their high-efficiency device applications. Scandium nitride (ScN), an emerging rocksalt indirect band gap semiconductor, suffers from low hole mobility. Utilizing the ab initio Boltzmann transport formalism including spin-orbit coupling, here we show the dominating role of ionized impurity scattering in reducing the hole mobility in ScN thin films. We suggest a route to increase the hole mobility by reversing band ordering through strain engineering. Our calculation shows that the biaxial tensile strain in ScN lifts the split-off hole band above the heavy hole and light hole bands, leading to a lower hole-effective mass and increasing mobility. Along with the impurity scattering, the Fröhlich interaction also plays a vital role in the carrier scattering mechanism due to the polar nature of ScN. Increased hole mobility in ScN will lead to higher efficiencies in thermoelectric, plasmonics, and neuromorphic computing devices.

Polar Semiconducting Scandium Nitride as an Infrared Plasmon and Phonon-Polaritonic Material.

The interaction of light with collective charge oscillations, called plasmon-polariton, and with polar lattice vibrations, called phonon-polariton, are essential for confining light at deep subwavelength dimensions and achieving strong resonances. Traditionally, doped-semiconductors and conducting metal oxides (CMO) are used to achieve plasmon-polaritons in the near-to-mid infrared (IR), while polar dielectrics are utilized for realizing phonon-polaritons in the long-wavelength IR (LWIR) spectral regions. However, demonstrating low-loss plasmon- and phonon-polaritons in one host material will make it attractive for practical applications. Here, we demonstrate high-quality tunable short-wavelength IR (SWIR) plasmon-polariton and LWIR phonon-polariton in complementary metal-oxide-semiconductor compatible group III-V polar semiconducting scandium nitride (ScN) thin films. We achieve both resonances by utilizing n-type (oxygen) and p-type (magnesium) doping in ScN that allows modulation of carrier concentration from 5 × 1018 to 1.6 × 1021 cm-3. Our work enables infrared nanophotonics with an epitaxial group III semiconducting nitride, opening the possibility for practical applications.

A photonic artificial synapse with a reversible multifaceted photochromic compound.

Modern computational technology based on the von Neumann architecture physically partitions memory and the central processing unit, resulting in fundamental speed limitations and high energy consumption. On the other hand, the human brain is an extraordinary multifunctional organ composed of more than a billion neurons capable of simultaneously thinking, processing, and storing information. Neurons are interconnected with synapses that control information flow from pre-synaptic-to-post-synaptic neurons. Therefore, emulating synaptic functionalities and developing neuromorphic computational architecture has recently attracted much interest. Due to their high-speed, large bandwidth, and no interconnect-related power loss, photonic (all-optical) synapses can overcome the existing hurdles with electronic synapses. Here, we show an artificial photonic synapse by utilizing the well-established reversible, high-contrast photochromic organic compound, spiropyran, stimulated by optical pulses. Optical transmission of spiropyran significantly changes during spiropyran-merocyanine isomerization driven by UV-visible optical pulses. Such changes are equivalent to the biological synapses' inhibitory and excitatory synaptic actions. The slow relaxation to the initial state is considered as synaptic plasticity responsible for learning and memory formation. Short-term memory (STM), long-term memory (LTM), and transition from the STM to the LTM are demonstrated in all-optical synapses by modulating the stimuli's strength. The solvatochromic properties of spiropyran are further utilized to augment memory in synapses. Our work shows that photochromic organic compounds are excellent hosts for artificial photonic synapses and can be implemented in neuromorphic applications.

Charge Transfer in the Heterostructure of CsPbBr3 Nanocrystals with Nitrogen-Doped Carbon Dots.

Heterostructures of inorganic halide perovskites with mixed-dimensional inorganic nanomaterials have shown great potential not only in the field of optoelectronic energy devices and photocatalysis but also for improving our fundamental understanding of the charge transfer across the heterostructure interface. Herein, we present for the first time the heterostructure integration of the CsPbBr3 nanocrystal with an N-doped carbon dot. We explore the photoluminescence (PL) and photoconductivity of the heterostructure of CsPbBr3 nanocrystals and N-doped carbon dots. PL quenching of CsPbBr3 nanocrystals with the addition of N-doped carbon dots was observed. The photoexcited electrons from the conduction band of CsPbBr3 are trapped in the N-acceptor state of N-doped carbon dots, and the charge transfer occurs via quasi type II-like electronic band alignment. The charge transfer in the halide perovskite-based heterostructure should motivate further research into the new heterostructure synthesis with perovskites and the fundamental understanding of the mechanism of charge/energy transfer across the heterostructure interface.