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Abstract Tightly bound electron-hole pairs (excitons) hosted in atomically-thin semiconductors have emerged as prospective elements in optoelectronic devices for ultrafast and secured information transfer. The controlled exciton transport in such excitonic devices requires manipulating potential energy gradient of charge-neutral excitons, while electrical gating or nanoscale straining have shown limited efficiency of exciton transport at room temperature. Here, we report strain gradient induced exciton transport in monolayer tungsten diselenide (WSe₂) across microns at room temperature via steady-state pump-probe measurement. Wrinkle architecture enabled optically-resolvable local strain (2.4%) and energy gradient (49 meV/μm) to WSe₂. We observed strain gradient induced flux of high-energy excitons and emission of funneled, low-energy excitons at the 2.5 μm-away pump point with nearly 45% of relative emission intensity compared to that of excited excitons. Our results strongly support the strain-driven manipulation of exciton funneling in two-dimensional semiconductors at room temperature, opening up future opportunities of 2D straintronic exciton devices. 

Abstract The emergence of two-dimensional (2D) materials as functional surfaces for sensing, electronics, mechanics, and other myriad applications underscores the importance of understanding 2D material–liquid interactions. The thinness and environmental sensitivity of 2D materials induce novel surface forces that drive liquid interactions. This complexity makes fundamental 2D material–liquid interactions variable. In this review, we discuss the (1) wettability, (2) electrical double layer (EDL) structure, and (3) frictional interactions originating from 2D material–liquid interactions. While many 2D materials are inherently hydrophilic, their wettability is perturbed by their substrate and contaminants, which can shift the contact angle. This modulation of the wetting behavior enables templating, filtration, and actuation. Similarly, the inherent EDL at 2D material–liquid interfaces is easily perturbed. This EDL modulation partially explains the wettability modulation and enables distinctive electrofluidic systems, including supercapacitors, energy harvesters, microfluidic sensors, and nanojunction gating devices. Furthermore, nanoconfinement of liquid molecules at 2D material surfaces arising from a perturbed liquid structure results in distinctive hydrofrictional behavior, influencing the use of 2D materials in microchannels. We expect 2D material–liquid interactions to inform future fields of study, including modulation of the chemical reactivity of 2D materials via tuning 2D material–liquid interactions. Overall, 2D material–liquid interactions are a rich area for research that enables the unique tuning of surface properties, electrical and mechanical interactions, and chemistry. 

Abstract Flexible, architectured, photonic nanostructures such as colloidal photonic crystals (CPCs) can serve as colorimetric strain sensors, where external applied strain leads to a noticeable color change. However, CPCs' response to strain is difficult to quantify without the use of optical spectroscopy. Integration of flexible electrical readout of CPCs' color change is a challenge due to a lack of flexible/stretchable electrical transducers. This work details a colorimetric strain sensor with optoelectrical quantification based on an integrated system of CPCs over a crumpled graphene phototransducer, which optoelectrically quantifies CPCs, response to strain. The hybrid system enables direct visual perception of strain, while strain quantification via electrical measurement of the hybrid system outperforms that of crumpled graphene strain sensors by more than 100 times. The unique combination of a photonic sensing element with a deformable transducer will allow for the development of novel, electrically quantifiable colorimetric sensors with high sensitivity. 

Abstract Boron nitride nanotubes (BNNT) uniformly dispersed in stretchable materials, such as poly(dimethylsiloxane) (PDMS), could create the next generation of composites with augmented mechanical, thermal, and piezoelectric characteristics. This work reports tunable piezoelectricity of multifunctional BNNT/PDMS stretchable composites prepared via co‐solvent blending with tetrahydrofuran (THF) to disperse BNNTs in PDMS while avoiding sonication or functionalization. The resultant stretchable BNNT/PDMS composites demonstrate augmented Young's modulus (200% increase at 9 wt% BNNT) and thermal conductivity (120% increase at 9 wt% BNNT) without losing stretchability. Furthermore, BNNT/PDMS composites demonstrate piezoelectric responses that are linearly proportional to BNNT wt%, achieving a piezoelectric constant (|d₃₃|) of 18 pmV⁻¹at 9 wt% BNNT without poling, which is competitive with commercial piezoelectric polymers. Uniquely, BNNT/PDMS accommodates tensile strains up to 60% without plastic deformation by aligning BNNTs, which enhances the composites’ piezoelectric response approximately five times. Finally, the combined stretchable and piezoelectric nature of the composite was exploited to produce a vibration sensor sensitive to low‐frequency (≈1 kHz) excitation. This is the first demonstration of multifunctional, stretchable BNNT/PDMS composites with enhanced mechanical strength and thermal conductivity and furthermore tunable piezoelectric response by varying BNNT wt% and applied strain, permitting applications in soft actuators and vibration sensors.