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Conventional photoluminescence (PL) yields at most one emitted photon for each absorption event. Downconversion (or quantum cutting) materials can yield more than one photon by virtue of energy transfer processes between luminescent centers. In this work, we introduce Gd₂O₂S:Tm³⁺ as a multi-photon quantum cutter. It can convert near-infrared, visible, or ultraviolet photons into two, three, or four infrared photons of ∼1800 nm, respectively. The cross-relaxation steps between Tm³⁺ ions that lead to quantum cutting are identified from (time-resolved) PL as a function of the Tm³⁺ concentration in the crystal. A model is presented that reproduces the way in which the Tm³⁺ concentration affects both the relative intensities of the various emission lines and the excited state dynamics and providing insight in the quantum cutting efficiency. Finally, we discuss the potential application of Gd₂O₂S:Tm³⁺ for spectral conversion to improve the efficiency of next-generation photovoltaics.

The present study assessed the ability of optogenetics techniques to provide a better understanding of the control of insulin secretion, particularly regarding pancreatic β-cell function in homeostasis and pathological conditions such as diabetes mellitus (DM). We used optogenetics to investigate whether insulin secretion and blood glucose homeostasis could be controlled by regulating intracellular calcium ion concentrations ([Ca²⁺]i) in a mouse pancreatic β-cell line (MIN6) transfected with the optogenetic protein channelrhodopsin-2 (ChR2). The ChR2-transfected MIN6 (ChR2-MIN6) cells secreted insulin following irradiation with a laser (470 nm). The increase in [Ca²⁺]i was accompanied by elevated levels of messenger RNAs that encode calcium/calmodulin-dependent protein kinase II delta and adenylate cyclase 1. ChR2-MIN6 cells suspended in matrigel were inoculated into streptozotocin-induced diabetic mice that were then subjected to a glucose tolerance test. Laser irradiation of these mice caused a significant decrease in blood glucose, and the irradiated implanted cells expressed insulin. These findings demonstrate the power of optogenetics to precisely and efficiently controlled insulin secretion by pancreatic β-cells ‘on demand', in contrast to techniques using growth factors or chemical inducers. Optogenetic technology shows great promise for understanding the mechanisms of glucose homeostasis and for developing treatments for metabolic diseases such as DM.

Organic photodetectors are interesting for low cost, large area optical sensing applications. Combining organic semiconductors with discrete absorption bands outside the visible wavelength range with transparent and conductive electrodes allows for the fabrication of visibly transparent photodetectors. Visibly transparent photodetectors can have far reaching impact in a number of areas including smart displays, window-integrated electronic circuits and sensors. Here, we demonstrate a near-infrared sensitive, visibly transparent organic photodetector with a very high average visible transmittance of 68.9%. The transmitted light of the photodetector under solar irradiation exhibits excellent transparency colour perception and rendering capabilities. At a wavelength of 850 nm and at −1 V bias, the photoconversion efficiency is 17% and the specific detectivity is 10¹² Jones. Large area photodetectors with an area of 1.6 cm² are demonstrated.

Interfaces between organic electron-donating (D) and electron-accepting (A) materials have the ability to generate charge carriers on illumination. Efficient organic solar cells require a high yield for this process, combined with a minimum of energy losses. Here, we investigate the role of the lowest energy emissive interfacial charge-transfer state (CT₁) in the charge generation process. We measure the quantum yield and the electric field dependence of charge generation on excitation of the charge-transfer (CT) state manifold via weakly allowed, low-energy optical transitions. For a wide range of photovoltaic devices based on polymer:fullerene, small-molecule:C₆₀ and polymer:polymer blends, our study reveals that the internal quantum efficiency (IQE) is essentially independent of whether or not D, A or CT states with an energy higher than that of CT₁ are excited. The best materials systems show an IQE higher than 90% without the need for excess electronic or vibrational energy.

Perovskite solar cells with submicrometre-thick CH₃NH₃PbI₃ or CH₃NH₃PbI_3–xCl_x active layers show a power conversion efficiency as high as 15%. However, compared to the best-performing device, the average efficiency was as low as 12%, with a large standard deviation (s.d.). Here, we report perovskite solar cells with an average efficiency exceeding 16% and best efficiency of 17%. This was enabled by the growth of CH₃NH₃PbI₃ cuboids with a controlled size via a two-step spin-coating procedure. Spin-coating of a solution of CH₃NH₃I with different concentrations follows the spin-coating of PbI₂, and the cuboid size of CH₃NH₃PbI₃ is found to strongly depend on the concentration of CH₃NH₃I. Light-harvesting efficiency and charge-carrier extraction are significantly affected by the cuboid size. Under simulated one-sun illumination, average efficiencies of 16.4% (s.d. ± 0.35), 16.3% (s.d. ± 0.44) and 13.5% (s.d. ± 0.34) are obtained from solutions of CH₃NH₃I with concentrations of 0.038 M, 0.050 M and 0.063 M, respectively. By controlling the size of the cuboids of CH₃NH₃PbI₃ during their growth, we achieved the best efficiency of 17.01% with a photocurrent density of 21.64 mA cm^–2, open-circuit photovoltage of 1.056 V and fill factor of 0.741.

Luminescence upconversion nanocrystals capable of converting two low-energy photons into a single photon at a higher energy are sought-after for a variety of applications, including bioimaging and photovoltaic light harvesting. Currently available systems, based on rare-earth-doped dielectrics, are limited in both tunability and absorption cross-section. Here we present colloidal double quantum dots as an alternative nanocrystalline upconversion system, combining the stability of an inorganic crystalline structure with the spectral tunability afforded by quantum confinement. By tailoring its composition and morphology, we form a semiconducting nanostructure in which excited electrons are delocalized over the entire structure, but a double potential well is formed for holes. Upconversion occurs by excitation of an electron in the lower energy transition, followed by intraband absorption of the hole, allowing it to cross the barrier to a higher energy state. An overall conversion efficiency of 0.1% per double excitation event is achieved.

Dye-sensitized solar cells are a promising alternative to traditional inorganic semiconductor-based solar cells. Here we report an open-circuit voltage of over 1,000 mV in mesoscopic dye-sensitized solar cells incorporating a molecularly engineered cobalt complex as redox mediator. Cobalt complexes have negligible absorption in the visible region of the solar spectrum, and their redox properties can be tuned in a controlled fashion by selecting suitable donor/acceptor substituents on the ligand. This approach offers an attractive alternate to the traditional I₃⁻/I⁻ redox shuttle used in dye-sensitized solar cells. A cobalt complex using tridendate ligands [Co(bpy-pz)₂]^3+/2+(PF₆)_3/2 as redox mediator in combination with a cyclopentadithiophene-bridged donor-acceptor dye (Y123), adsorbed on TiO₂, yielded a power conversion efficiency of over 10% at 100 mW cm⁻². This result indicates that the molecularly engineered cobalt redox shuttle is a legitimate alternative to the commonly used I₃⁻/I⁻ redox shuttle.

The Pan-STARRS1 survey is collecting multi-epoch, multi-color observations of the sky north of declination −30° to unprecedented depths. These data are being photometrically and astrometrically calibrated and will serve as a reference for many other purposes. In this paper, we present our determination of the Pan-STARRS1 photometric system: g_P1, r_P1, i_P1, z_P1, y_P1, and w_P1. The Pan-STARRS1 photometric system is fundamentally based on the Hubble Space Telescope Calspec spectrophotometric observations, which in turn are fundamentally based on models of white dwarf atmospheres. We define the Pan-STARRS1 magnitude system and describe in detail our measurement of the system passbands, including both the instrumental sensitivity and atmospheric transmission functions. By-products, including transformations to other photometric systems, Galactic extinction, and stellar locus, are also provided. We close with a discussion of remaining systematic errors.

Multi-photon ionization (MPI) spectroscopy of solid surfaces under ambient conditions and in nitrogen has been established and exemplified for a variety of materials. This was accomplished using a dedicated experimental setup that monitors the photoelectron yield as a function of the laser wavelength. The MPI spectra resemble the absorption characteristics, however, possess more peaks and are more detailed. This demonstrated the possibility to apply MPI spectroscopy for fast analysis of solids. The dependence of the signals upon the laser flux implies that the ionization mechanism depends on the examined molecule and in many cases it is a two-step process, via a long-living intermediate energy state. The method provides quantification in the pmole range and allows for surface imaging.