Inorganic semiconductors are vital for a number of critical applications but are almost universally brittle. Here, we report the superplastic deformability of indium selenide (InSe). Bulk single-crystalline InSe can be compressed by orders of magnitude and morphed into a Möbius strip or a simple origami at room temperature. The exceptional plasticity of this two-dimensional van der Waals inorganic semiconductor is attributed to the interlayer gliding and cross-layer dislocation slip that are mediated by the long-range In-Se Coulomb interaction across the van der Waals gap and soft intralayer In-Se bonding. We propose a combinatory deformability indicator (Ξ) to prescreen candidate bulk semiconductors for use in next-generation deformable or flexible electronics.

We report herein the preparation and UV-stimulated wettability conversion of superhydrophobic TiO2 surfaces, as well as the preparation of superhydrophilic−superhydrophobic patterns by use of UV irradiation through a photomask. A CF4 plasma was used to roughen smooth TiO2 sol−gel films to produce a nanocolumnar morphology, and subsequent hydrophobic modification with octadecylphosphonic acid (ODP) rendered the roughened surfaces superhydrophobic. The superhydrophobic properties of these surfaces were evaluated by both static and dynamic water contact angle (CA) measurements. It was found that the surface morphology of the TiO2 film, which was dependent on the etching time, has a great influence on the observed superhydrophobic properties. The nanocolumnar surface morphology exhibited large water CA and small contact angle hysteresis (CAH); this is discussed in terms of the Wenzel equation and the Cassie−Baxter equation. Under low-intensity UV illumination (1 mW cm-2), the superhydrophobic TiO2 surface underwent a gradual decrease of water CA and finally became superhydrophilic, due to photocatalytic decomposition of the ODP monolayer. Readsorption of ODP molecules led to the recovery of the superhydrophobic state. This UV-stimulated wettability conversion was employed to prepare superhydrophilic stripes (50 and 500 μm wide) on a superhydrophobic TiO2 surface. The pattern was able to guide water condensation, as well as the evaporation of a polystyrene microsphere suspension, due to the extremely large wettability contrast between superhydrophobic and superhydrophilic areas.

Single crystalline tin selenide (SnSe) recently emerged as a very promising thermoelectric material for waste heat harvesting and thermoelectric cooling, due to its record high figure of merit ZT in mediate temperature range. The most striking feature of SnSe lies in its extremely low lattice thermal conductivity as ascribed to the anisotropic and highly distorted Sn-Se bonds as well as the giant bond anharmonicity by previous studies, yet no theoretical models so far can give a quantitative explanation to such low a lattice thermal conductivity. In this work, we presented direct observation of an astonishingly vast number of off-stoichiometric Sn vacancies and Se interstitials, using sophisticated aberration corrected scanning transmission electron microscope; and credited the previously reported ultralow thermal conductivity of the SnSe single crystalline samples partly to their off-stoichiometric feature. To further validate the conclusion, we also synthesized stoichiometric SnSe single crystalline samples, and illustrated that the lattice thermal conductivity is deed much higher as compared with the off-stoichiometric single crystals.

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SnSe single crystals have drawn extensive attention for their ultralow thermal conductivity and outstanding thermoelectric performance. Here, we report super large Sn 1−x Se single crystals with excellent thermoelectric properties, fabricated via an advanced horizontal Bridgman technique with great yield and high reproducibility. The obtained single crystals have a super large size of ∼70 × 50 × 15 mm with a considerable weight of 148 g, which leads to a record-high mass density of >6.1 g cm −3 . Extensive chemical characterization demonstrates that ∼0.3% Sn vacancies are present, which results in a large concentration of holes, ∼1.2 × 10 19 cm −3 , and an enhanced power factor of ∼6.1 μW cm −1 K −2 at 793 K. Simultaneously, the Sn-vacancy-induced lattice distortions result in a low thermal conductivity of ∼0.39 W m −1 K −1 at 793 K, leading to a competitive ZT of ∼1.24. This work demonstrates that large-size off-stoichiometric SnSe single crystals hold promise to achieve high thermoelectric performance.

By increasing the carrier concentration and the DOS effective mass, a ZT of 0.54 was achieved at 793 K.

SnSe has attracted increasing attention as a promising thermoelectric material. In this work, a horizontal vapor transfer method was developed to synthesize high-quality, fully dense, and stoichiometric SnSe single crystals, which enables an evaluation of the transport properties inherent to SnSe along the bc-plane. The electronic transport properties can be well-understood by a single parabolic band model with acoustic phonon scattering, enabling insights into the fundamental material parameters determining the electronic properties. The lattice thermal conductivity (κ l ) decreases from 2.0 W m −1 K −1 at 300 K to 0.55 W m −1 K −1 at 773 K. It is revealed that an increase in hole concentration, an involvement of low-lying bands for transport, and a further reduction in κ l would all enable p-type SnSe to be a promising eco-friendly thermoelectric material. This work not only provides a fundamental understanding of the charge transport but also guides the further improvement of thermoelectric SnSe.

This study investigated the complementary and competitive effects of a resonant level and band convergence in In–Cd codoped SnTe.