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Solar cells based on a mesoporous structure of TiO2 and the polysulfide redox electrolyte were prepared by direct adsorption of colloidal CdSe quantum dot light absorbers onto the oxide without any particular linker. Several factors cooperate to improve the performance of quantum-dot-sensitized solar cells: an open structure of the wide bandgap electron collector, which facilitates a higher covering of the internal surface with the sensitizer, a surface passivation of TiO2 to reduce recombination and improved counter electrode materials. As a result, solar cells of 1.83% efficiency under full 1 sun illumination intensity have been obtained. Despite a relatively large short circuit current (J(sc) = 7.13 mA cm(-2)) and open circuit voltage (V(oc) = 0.53 V), the colloidal quantum dot solar cell performance is still limited by a low fill factor of 0.50, which is believed to arise from charge transfer of photogenerated electrons to the aqueous electrolyte.

Delafossite CuFeO2 is a promising material for solar hydrogen production, but is limited by poor photocurrent. Strategies are demonstrated herein to improve the performance of CuFeO2 electrodes prepared directly on transparent conductive substrates by using a simple sol-gel technique. Optimizing the delafossite layer thickness and increasing the majority carrier concentration (through the thermal intercalation of oxygen) give insights into the limitations of photogenerated charge extraction and enable performance improvements. In oxygen-saturated electrolyte, (sacrificial) photocurrents (1 sun illumination) up to 1.51 mA cm(-2) at +0.35 V versus a reversible hydrogen electrode (RHE) are observed. Water photoreduction with bare delafossite is limited by poor hydrogen evolution catalysis, but employing methyl viologen as an electron acceptor verifies that photogenerated electrons can be extracted from the conduction band before recombination into mid-gap trap states identified by electrochemical impedance spectroscopy. Through the use of suitable oxide overlayers and a platinum catalyst, sustained solar hydrogen production photocurrents of 0.4 mA cm(-2) at 0 V versus RHE (0.8 mA cm(-2) at -0.2 V) are demonstrated. Importantly, bare CuFeO2 is highly stable at potentials at which photocurrent is generated. No degradation is observed after 40 h under operating conditions in oxygen-saturated electrolyte.

WSe2—a layered semiconductor that can be exfoliated into atomically thin two-dimensional sheets—offers promising characteristics for application in solar energy conversion. However, the lack of controllable, cost-effective methods to scalably fabricate homogeneous thin films currently limits practical application. Here we present a technique to prepare controlled thin films of 2D WSe2 from dispersions of solvent-exfoliated few-layer flakes. Flake self-assembly at a liquid/liquid interface (formed exceptionally from two non-solvents for WSe2) followed by substrate transfer affords large-area thin films with superior 2D flake alignment compared with traditional (liquid/air) self-assembly techniques. We further demonstrate, for the first time, solar-to-hydrogen conversion from solution-processed WSe2 thin films. Bare photoelectrodes with a thickness of ca. 25 nm exhibit sustained p-type photocurrent under simulated solar illumination, and up to 1.0 mA cm–2 at 0 V versus reversible hydrogen electrode with an added water reduction catalyst (Pt). The importance of the self-assembled morphology is established by photoelectrochemical and conductivity measurements.

The electrochemical nitrate reduction reaction (NITRR) provides a promising solution for restoring the imbalance in the global nitrogen cycle while enabling a sustainable and decentralized route to source ammonia. Here, we demonstrate a novel electrocatalyst for NITRR consisting of Rh clusters and single‐atoms dispersed onto Cu nanowires (NWs), which delivers a partial current density of 162 mA cm−2 for NH3 production and a Faradaic efficiency (FE) of 93 % at −0.2 V vs. RHE. The highest ammonia yield rate reached a record value of 1.27 mmol h−1 cm−2. Detailed investigations by electron paramagnetic resonance, in situ infrared spectroscopy, differential electrochemical mass spectrometry and density functional theory modeling suggest that the high activity originates from the synergistic catalytic cooperation between Rh and Cu sites, whereby adsorbed hydrogen on Rh site transfers to vicinal *NO intermediate species adsorbed on Cu promoting the hydrogenation and ammonia formation.