Half of the sun's power lies in the infrared. As a result, the optimal bandgaps for solar cells in both the single-junction and even the tandem architectures lie beyond 850 nm. However, progress in low-cost, large-area, physically flexible solar cells has instead been made in organic and polymer materials possessing absorption onsets in the visible. Recent advances have been achieved in solution-cast infrared photovoltaics through the use of colloidal quantum dots. Here we report stable solution-processed photovoltaic devices having 3.6% power conversion efficiency in the infrared. The use of a strongly bound bidentate linker, benzenedithiol, ensures device stability over weeks. The devices reach external quantum efficiencies of 46% in the infrared and 70% across the visible. We investigate in detail the physical mechanisms underlying the operation of this class of device. In contrast with drift-dominated behavior in recent reports of PbS quantum dot photovoltaics, we find that diffusion of electrons and holes over hundreds of nanometers through our PbSe colloidal quantum dot solid is chiefly responsible for the high external quantum efficiencies obtained in this new class of devices.

Planar Schottky photovoltaic devices were prepared from solution-processed PbS nanocrystal quantum dot films with aluminum and indium tin oxide contacts. These devices exhibited up to 4.2% infrared power conversion efficiency, which is a threefold improvement over previous results. Solar power conversion efficiency reached 1.8%. The simple, optimized architecture allows for direct implementation in multijunction photovoltaic device configurations.

PbS colloidal quantum dot photovoltaic devices in a Schottky architecture have demonstrated an infrared power conversion efficiency of 4.2%. Here, we elucidate the internal mechanisms leading to this efficiency. At relevant intensities, the drift length is 10 m for holes and 1 m for electrons. Transport within the 150 nm wide depletion region is therefore highly efficient. The electron diffusion length of 0.1 m is comparable to neutral region width. We quantitatively account for the observed 37% external quantum efficiency, showing that it results from the large depletion width and long carrier lifetime combined.

Photodetection in semiconductors enables digital imaging, spectroscopy, and optical communications. Integration of solution-processed light-sensing materials with a range of substrates offers access to new spectral regimes, the prospect of enhanced sensitivity, and compatibility with flexible electronics. Photoconductive photodetectors based on solution-cast nanocrystals have shown tremendous progress in recent years; however, high-performance reports to date have employed Pb- and Cd-containing materials. Here we report a high-sensitivity (photon-to-electron gain >40), high-speed (video-frame-rate-compatible) photoconductive photodetector based on In(2)S(3). Only by decreasing the energetic depth of hole traps associated with intrinsic vacancies in beta-phase In(2)S(3) were we able to achieve this needed combination of sensitivity and speed. Our incorporation of Cu(+) cations into beta-In(2)S(3)'s spinel vacancies that led to acceptable temporal response in the devices showcases the practicality of incorporating dopants into nanoparticles. The devices are stable in air and under heating to 215 degrees C, advantages rooted in the reliance on the stable inclusion of dopants into available sites instead of surface oxide species.

We report PbS quantum dot lumophores emitting in the near-infrared. The lumophores are stable for at least 5 days stored in physiologically relevant pH 6−8 buffer, have sub-10 nm hydrodynamic diameter, and exhibit 26% quantum yield.