Search

Abstract Electrochemical carbon dioxide (CO2) conversion to hydrocarbon fuels, such as methane (CH4), offers a promising solution for the long-term and large-scale storage of renewable electricity. To enable this technology, CO2-to-CH4 conversion must achieve high selectivity and energy efficiency at high currents. Here, we report an electrochemical conversion system that features proton-bicarbonate-CO2 mass transport management coupled with an in-situ copper (Cu) activation strategy to achieve high CH4 selectivity at high currents. We find that open matrix Cu electrodes sustain sufficient local CO2 concentration by combining both dissolved CO2 and in-situ generated CO2 from the bicarbonate. In-situ Cu activation through alternating current operation renders and maintains the catalyst highly selective towards CH4. The combination of these strategies leads to CH4 Faradaic efficiencies of over 70% in a wide current density range (100 – 750 mA cm-2) that is stable for at least 12 h at a current density of 500 mA cm-2. The system also delivers a CH4 concentration of 23.5% in the gas product stream.

While water electrolysis devices represent a technology for renewable energy, there are few stable catalysts that survive the acidic conditions. Here, authors enhance acidic oxygen evolution by introducing strong Brønsted acid sites into RuO2 to accelerate bridging-oxygen-assisted deprotonation.

The realisation of film made up of different compositions using colloidal QD inks remains a challenge because of redispersing of underlying films by polar solvents. Here, the authors introduce aromatic ligands to achieve QD inks in weakly-polar solvents that enable fabrication of multi-compositional films.

Metal-halide perovskite based tandem solar cells are appealing but making a high efficiency device is not trivial. Here Chen et al. increase the carrier collection in the perovskite layer and largely enhance the efficiency in tandem cells when combined with colloidal quantum dot or silicon layers.

Reduced-dimensional halide perovskites are promising for light-emitting diodes but suffer from photo-degradation. Here Quan et al. identify the edge of the perovskite nanoplatelets as the degradation channels and use phosphine oxides to passivate the edges and boost device performance and lifetime.

It is challenging to realize doping and surface passivation simultaneously in colloidal quantum dot inks. Here Choi et al. employ a cascade surface modification approach to solve the problem and obtain record high efficiency of 13.3% for bulk homojunction solar cells based on these inks.

Efficient harvest of solar energy beyond the silicon absorption edge of 1100 nm by semiconductor solar cells remains a challenge. Here Sun et al. mix high multi-bandgap lead sulfide colloidal quantum dot ensembles to further increase both short circuit current and open circuit voltage.

Solution processed colloidal quantum dots are emerging photovoltaic materials with tuneable infrared bandgaps. Here, Yang et al. create a class of quantum dot bulk heterojunction solar cell via ligand design, enabling longer photocarrier diffusion lengths for greater photocurrent and performance.

Efficient implementation of quantum dot and well architectures are restricted to costly vacuum-epitaxially-grown semiconductors. The authors use quantum dots in perovskite to build field-emission photodiodes that are sensitive across the visible and into the short-wavelength infrared.