The development of methods to synthesize and physically manipulate extremely thin, single-crystalline inorganic semiconductor materials, so-called nanomembranes, has led to an almost explosive growth of research worldwide into uniquely enabled opportunities for their use in new "soft" and other unconventional form factors for high-performance electronics. The unique properties that nanomembranes afford, such as their flexibility and lightweight characteristics, allow them to be integrated into electronic and optoelectronic devices that, in turn, adopt these unique attributes. For example, nanomembrane devices are able to make conformal contact to curvilinear surfaces and manipulate strain to induce the self-assembly of various 3D nano/micro device architectures. Further, thin semiconductor materials (e.g., Si-nanomembranes, transition metal dichalcogenides, and phosphorene) are subject to the impacts of quantum and other size-dependent effects that in turn enable the manipulation of their bandgaps and the properties of electronic and optoelectronic devices fabricated from them. In this Perspective, nanomembrane synthesis techniques and exemplary applications of their use are examined. We specifically describe nanomembrane chemistry exploiting high-performance materials, along with precise/high-throughput techniques for their manipulation that exemplify their growing capacities to shape outcomes in technology. Prominent challenges in the chemistry of these materials are presented along with future directions that might guide the development of next generation nanomembrane-based devices.

Commercial smart window technologies for dynamic light and heat management in building and automotive environments traditionally rely on electrochromic (EC) materials powered by an external source. This design complicates building-scale installation requirements and substantially increases costs for applications in retrofit construction. Self-powered photoelectrochromic (PEC) windows are an intuitive alternative wherein a photovoltaic (PV) material is used to power the electrochromic device, which modulates the transmission of the incident solar flux. The PV component in this application must be sufficiently transparent and produce enough power to efficiently modulate the EC device transmission. Here, we propose Si solar microcells (μ-cells) that are i) small enough to be visually transparent to the eye, and ii) thin enough to enable flexible PEC devices. Visual transparency is achieved when Si μ-cells are arranged in high pitch (i.e. low-integration density) form factors while maintaining the advantages of a single-crystalline PV material (i.e., long lifetime and high performance).Additionally, the thin dimensions of these Si μ-cells enable fabrication on flexible substrates to realize these flexible PEC devices. The current work demonstrates this concept using WO 3 as the EC material and V 2 O 5 as the ion storage layer, where each component is fabricated via sol-gel methods that afford improved prospects for scalability and tunability in comparison to thermal evaporation methods. The EC devices display fast switching times, as low as 8 seconds, with a modulation in transmission as high as 33%. Integration with two Si μ-cells in series (affording a 1.12 V output) demonstrates an integrated PEC module design with switching times of less than 3 minutes, and a modulation in transmission of 32% with an unprecedented EC:PV areal ratio.

Ultrathin silicon solar microcells (μ‐cells) afford a means to reduce semiconductor material consumption and can be integrated with concentration optics to improve their power density. A μ‐cell design is described that optimizes electron and photon collection with enhanced efficiency for solar concentration applications. An interdigitated back contact (IBC) design improves carrier collection partially due to larger contact coverage while further enabling optimization of the μ‐cell front surface. To do so, a silicon nitride antireflection thin film coating is utilized to enhance photon absorption and improve surface passivation. Performance of IBC μ‐cells is compared to an optimized top contact design and improves μ‐cell conversion efficiencies from 9.9 to 13.7%. Improvements at 1 Sun are amplified under concentration and increase power densities at 20 Suns to 346 from 192 mW cm−2 due to minimized series resistance. Benefits afforded by IBC μ‐cells are exemplified following their integration into a dual concentrator system, affording photon collection capacities for direct and diffuse irradiance. A traditional lens concentrates direct light while a luminescent solar concentrator (LSC) collects diffuse photons otherwise not utilized by passive optics. Addition of the LSC increases maximum power densities on clear and cloudy days, providing concentration for the latter and further increasing the power density.

A key display characteristic is its efficiency (emitted light power divided by input power). While display efficiencies are being improved through emissive (e.g., quantum dot and organic light emitting display (OLED) designs1,2, which remove the highly inefficient color filters found in traditional liquid crystal displays (LCDs)3,4, polarization filters, which block about 50% of the light, remain required to inhibit ambient light reflection. We introduce a luminescent cavity design to replace both the color and polarization filters. Narrow-band, large Stokes shift, CdSe/CdS quantum dot emitters are embedded in a reflective cavity pixel element with a small top aperture. The remainder of the top surface is coated black reducing ambient light reflection. A single pixel demonstrates an extraction efficiency of 40.9% from a cavity with an 11% aperture opening. A simple proof-of-concept multi-pixel array is demonstrated.