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Narrow bandgap quantum dots (QDs) are an important class of materials for near‐infrared (NIR) optoelectronic devices owing to their size‐tunable bandgap and chemical root processing. In photovoltaic applications, NIR QDs could be particularly useful to complement the sub‐bandgap transmission loss of NIR solar radiation from perovskite and c‐Si solar cells. However, insufficient carrier extraction thickness associated with the narrow NIR excitonic bandwidth of QDs limits the conversion efficacy of the broad NIR solar spectrum. Here, we utilize a multi‐bandgap QD ensemble which widens the NIR absorption bandwidth to mimic the broad solar spectrum. A solution‐phase ligand passivation strategy is used to control doping properties and energy level alignment of multi‐bandgap QDs. We successfully developed bulk‐heterojunction solar cells using the multi‐bandgap QD ensemble, which yields higher carrier extraction thickness and broader NIR absorption. The gain from NIR absorption and carrier transport resulted in higher short‐circuit current generation and power conversion efficiency (PCE) in solar cell devices. The champion device shows 8.73% PCE under 1.5 AM solar illumination and 7.44% and 5.05% PCE for the NIR photons transmitted from perovskite and c‐Si layers. [ABSTRACT FROM AUTHOR]

Progress in device engineering and surface passivation strategies has led to steady progress in colloidal quantum dot (QD) solar cells. Bulk homojunction (BHJ) device architecture has several advantages over the conventional planar junction in developing QD solar cells. Herein, surface ligand chemistry is utilized to control the doping type and dispersibility of oppositely doped PbS QDs to develop BHJ solar cells. Thiocyanate and thiol ligand combination is introduced to develop p‐PbS QD ink, which is blended with halide‐passivated n‐PbS QDs to build BHJ solar cells. It is shown that BHJ solar cells are benefited from high energy offset and higher hole mobility. This leads to the superior carrier extraction from a thicker active layer without compromising fill factor and open circuit voltage. Power conversion efficiency has reached 10.7% in 530 nm‐thick BHJ solar cells, a 24% improvement over the best performing planar solar cells. With the help of the 1D solar cell capacitance simulator, it is shown that a 15% efficient QD solar cell can be realized by further improving the hole mobility above 0.1 cm2 V−1 s−1. [ABSTRACT FROM AUTHOR]

In the fabrication of III-V semiconductor nanostructures for electronic and optoelectronic devices, techniques that are capable of removing material with monolayer precision are as important as material growth to achieve best device performances. A robust chemical treatment is demonstrated using sulfur (S)-oleylamine (OA) solution, which etches layer by layer in an inverse epitaxial fashion and simultaneously passivates the surface. The application of this process to push the limits of top-down nanofabrication is demonstrated by the realization of InP-based high optical quality nanowire arrays, with aspect ratios more than 50, and nanostructures with new topologies. The findings are relevant for other III-V semiconductors and have potential applications in III-V device technologies. [ABSTRACT FROM AUTHOR]

Colloidal PbS quantum dots (QDs) have provoked a revolution in the field of optoelectronic devices owing to their low‐cost fabrication processing and excellent physical properties. Recently, the fabrication of nanostructured PbS QD photovoltaic (PV) devices based on zinc oxide (ZnO) nanowire array appears as an effective strategy for improving the overall device performance. Despite its potentially strong impact on the device performance, the role of nanowire areal density on photon absorption and exciton dynamics has not yet been studied and still remains unexplored. Here, for the first time, the areal density of ZnO nanowires is tuned through controlling the precursor concentration and its impact on PbS QD PV performance is studied. It is found that the device with optimized ZnO nanowire areal density yields significantly increased power conversion efficiency (PCE) (10.1% vs 8.5% of control nanowire‐based device) due to improved antireflection effect and reduced surface recombination states. To further improve the photovoltaic performance, the ZnO nanowire surface is treated with hydrogen plasma. Transient photovoltage (TPV) measurement reveals that this passivation process noticeably reduces the nonradiative charge recombination yielding a champion device with a remarkable PCE of 10.8%. [ABSTRACT FROM AUTHOR]