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Solar steam water purification and fog collection are two independent processes that could enable abundant fresh water generation. We developed a hydrogel membrane that contains hierarchical three-dimensional microstructures with high surface area that combines both functions and serves as an all-day fresh water harvester. At night, the hydrogel membrane efficiently captures fog droplets and directionally transports them to a storage vessel. During the daytime, it acts as an interfacial solar steam generator and achieves a high evaporation rate of 3.64 kg m −2 h −1 under 1 sun enabled by improved thermal/vapor flow management. With a homemade rooftop water harvesting system, this hydrogel membrane can produce fresh water with a daily yield of ~34 L m −2 in an outdoor test, which demonstrates its potential for global water scarcity relief. Solar steam water purification and fog collection are two independent processes that could enable abundant fresh water generation. Here, the authors develop a hydrogel membrane that contains microstructures and combines both functions and serves as an all-day fresh water harvester.

Light is a powerful tool to manipulate matter, but existing approaches often necessitate focused, high-intensity light that limits the manipulated object’s shape, material and size. Here, we report that self-stabilizing optical manipulation of macroscopic—millimetre-, centimetre- and even metre-scale—objects could be achieved by controlling the anisotropy of light scattering along the object’s surface. In a scalable design that features silicon resonators on silica substrate, we identify nanophotonic structures that can self-stabilize when rotated and/or translated relative to the optical axis. Nanoscale control of scattering across a large area creates restoring behaviour by engineering the scattered phase, without needing to focus incident light or excessively constrain the shape, size or material composition of the object. Our findings may lead to platforms for manipulating macroscopic objects, with applications ranging from contactless wafer-scale fabrication and assembly, to trajectory control for ultra-light spacecraft and even laser-propelled light sails for space exploration.Mechanical stability of macroscopic structures on the millimetre-, centimetre- and even metre-scale could be realized by tailoring the anisotropy of light scattering along the object’s surface, without needing to focus incident light or excessively constrain the shape, size or material composition of the object.

This review article surveys the potential of using plasmonic nanostructures to enhance the absorption of photovoltaic devices. As a result, the physical thickness of solar cells can be reduced, leading to new photovoltaic-device designs. The emerging field of plasmonics has yielded methods for guiding and localizing light at the nanoscale, well below the scale of the wavelength of light in free space. Now plasmonics researchers are turning their attention to photovoltaics, where design approaches based on plasmonics can be used to improve absorption in photovoltaic devices, permitting a considerable reduction in the physical thickness of solar photovoltaic absorber layers, and yielding new options for solar-cell design. In this review, we survey recent advances at the intersection of plasmonics and photovoltaics and offer an outlook on the future of solar cells based on these principles.

New materials are being developed that meet the requirements for nanoscale photonics. Metamaterials (MMs) are artificial, engineered materials with rationally designed compositions and arrangements of nanostructured building blocks. These materials can be tailored for almost any application because of their extraordinary response to electromagnetic, acoustic, and thermal waves that transcends the properties of natural materials ( 1 – 3 ). The astonishing MM-based designs and demonstrations range from a negative index of refraction, focusing and imaging with sub-wavelength resolution, invisibility cloaks, and optical black holes to nanoscale optics, data processing, and quantum information applications ( 3 ). Metals have traditionally been the material of choice for the building blocks, but they suffer from high resistive losses—even metals with the highest conductivities, silver and gold, exhibit excessive losses at optical frequencies that restrict the development of devices in this frequency range. The development of new materials for low-loss MM components and telecommunication devices is therefore required.

For decades, solar-cell efficiencies have remained below the thermodynamic limits. However, new approaches to light management that systematically minimize thermodynamic losses will enable ultrahigh efficiencies previously considered impossible.

Theoretical limiting efficiencies have a critical role in determining technological viability and expectations for device prototypes, as evidenced by the photovoltaics community’s focus on detailed balance. However, due to their multicomponent nature, photoelectrochemical devices do not have an equivalent analogue to detailed balance, and reported theoretical efficiency limits vary depending on the assumptions made. Here we introduce a unified framework for photoelectrochemical device performance through which all previous limiting efficiencies can be understood and contextualized. Ideal and experimentally realistic limiting efficiencies are presented, and then generalized using five representative parameters—semiconductor absorption fraction, external radiative efficiency, series resistance, shunt resistance and catalytic exchange current density—to account for imperfect light absorption, charge transport and catalysis. Finally, we discuss the origin of deviations between the limits discussed herein and reported water-splitting efficiencies. This analysis provides insight into the primary factors that determine device performance and a powerful handle to improve device efficiency. Theoretical limiting efficiencies play a critical role in determining technological viability and expectations for device prototypes. Here, the authors present a unified framework for photoelectrochemical device performance through which previous limiting efficiencies can be understood and contextualized.

Thermal emission—the process through which all objects with a finite temperature radiate electromagnetic energy—has generally been thought to obey reciprocity, where the absorbed and emitted radiation from a body are equal for a given wavelength and angular channel. This equality, formalized by Gustav Kirchhoff in 1860, is known as Kirchhoff’s law of thermal radiation and has long guided designs to control the emitted radiation. Removing the constraint of Kirchhoff’s law unlocks a multitude of applications and designs for thermal emitters. Decoupling the absorptivity and emissivity relationship can be leveraged to achieve novel functions, ranging from reducing re-emission losses to the Sun in the context of solar energy harvesting systems to radiative camouflage. Here we report the direct measurements of an inequality between the spectral directional emissivity and absorptivity for a photonic design that supports a guided-mode resonance coupled to a magneto-optic material. This inequality occurs under the application of an in-plane magnetic field that modifies the normally diagonal permittivity tensor to a non-diagonal tensor in magneto-optic InAs, resulting in an antisymmetric relationship where the magnetic tuning of enhanced emissivity for a given angle correlates with decreased absorptivity for the same angle.An inequality is shown to exist between the spectral directional emissivity and absorptivity in a structure supporting a guided-mode resonance coupled to a magneto-optic material. This finding provides the direct observation of the violation of Kirchhoff’s law of thermal radiation.

In the late nineteenth century, Heinrich Hertz demonstrated that the electromagnetic properties of materials are intimately related to their structure at the subwavelength scale by using wire grids with centimetre spacing to manipulate metre-long radio waves. More recently, the availability of nanometre-scale fabrication techniques has inspired scientists to investigate subwavelength-structured metamaterials with engineered optical properties at much shorter wavelengths, in the infrared and visible regions of the spectrum. Here we review how optical metamaterials are expected to enhance the performance of the next generation of integrated photonic devices, and explore some of the challenges encountered in the transition from concept demonstration to viable technology.

Tunable metasurfaces enable dynamical control of the key constitutive properties of light at a subwavelength scale. To date, electrically tunable metasurfaces at near-infrared wavelengths have been realized using free carrier modulation, and switching of thermo-optical, liquid crystal and phase change media. However, the highest performance and lowest loss discrete optoelectronic modulators exploit the electro-optic effect in multiple-quantum-well heterostructures. Here, we report an all-dielectric active metasurface based on electro-optically tunable III–V multiple-quantum-wells patterned into subwavelength elements that each supports a hybrid Mie-guided mode resonance. The quantum-confined Stark effect actively modulates this volumetric hybrid resonance, and we observe a relative reflectance modulation of 270% and a phase shift from 0° to ~70°. Additionally, we demonstrate beam steering by applying an electrical bias to each element to actively change the metasurface period, an approach that can also realize tunable metalenses, active polarizers, and flat spatial light modulators. Here, the authors demonstrate an electrically tunable metasurface with III–V semiconducting MQW structures as resonant metasurface elements. The amplitude and phase of the light reflected from the metasurface can be continuously tuned by applying DC electric field across the MQW metasurface elements.

Capture and conversion of CO 2 from oceanwater can lead to net-negative emissions and can provide carbon source for synthetic fuels and chemical feedstocks at the gigaton per year scale. Here, we report a direct coupled, proof-of-concept electrochemical system that uses a bipolar membrane electrodialysis (BPMED) cell and a vapor-fed CO 2 reduction (CO 2 R) cell to capture and convert CO 2 from oceanwater. The BPMED cell replaces the commonly used water-splitting reaction with one-electron, reversible redox couples at the electrodes and demonstrates the ability to capture CO 2 at an electrochemical energy consumption of 155.4 kJ mol −1 or 0.98 kWh kg −1 of CO 2 and a CO 2 capture efficiency of 71%. The direct coupled, vapor-fed CO 2 R cell yields a total Faradaic efficiency of up to 95% for electrochemical CO 2 reduction to CO. The proof-of-concept system provides a unique technological pathway for CO 2 capture and conversion from oceanwater with only electrochemical processes. Isolating CO 2 to use in electrochemical CO 2 reduction systems is an ongoing issue. Here, the authors present a proof-of-concept integrated system combining a bipolar membrane electrodialysis cell with a vapor-fed CO 2 reduction cell for capture and conversion of CO 2 from oceanwater.