BACKGROUND: As the world continues to transition toward carbon emissions–free energy technologies, there remains a need to also reduce the carbon emissions of the chemical production industry. Today many of the world’s chemicals are produced from fossil fuel–derived feedstocks. Electrochemical conversion of carbon dioxide (CO ₂ ) into chemical feedstocks offers a way to turn waste emissions into valuable products, closing the carbon loop. When coupled to renewable sources of electricity, these products can be made with a net negative carbon emissions footprint, helping to sequester CO ₂ into usable goods. Research and development into electrocatalytic materials for CO ₂ reduction has intensified in recent years, with advances in selectivity, efficiency, and reaction rate progressing toward practical implementation. A variety of chemical products can be made from CO ₂ , such as alcohols, oxygenates, synthesis gas (syngas), and olefins—staples in the global chemical industry. Because these products are produced at substantial scale, a switch to renewably powered production could result in a substantial carbon emissions reduction impact. The advancement of electrochemical technology to convert electrons generated from renewable power into stable chemical form also represents one avenue to long-term (e.g., seasonal) storage of energy. ADVANCES: The science of electrocatalytic CO ₂ reduction continues to progress, with priority given to the need to pinpoint more accurately the targets for practical application, the economics of chemical products, and barriers to market entry. It will be important to scale CO ₂ electrolyzers and increase the stability of these catalysts to thousands of hours of continuous operation. Product separation and efficient recycling of CO ₂ and electrolyte also need to be managed. The petrochemical industry operates at a massive scale with a complicated global supply chain and heavy capital costs. Commodity chemical markets are difficult to penetrate and are priced on feedstock, which is currently inexpensive as a result of the shale gas boom. CO ₂ capture costs from the flue or direct air and product separation from unreacted CO ₂ are also important to consider. Assuming that the advancement of electrocatalytic technologies continues apace, what will it take to disrupt the chemical production sector, and what will society gain by doing so? This review presents a technoeconomic and carbon emissions assessment of CO ₂ products such as ethylene, ethanol, and carbon monoxide, offering target figures of merit for practical application. The price of electricity is by far the largest cost driver. Electrochemical production costs begin to match those of traditional fossil fuel–derived processes when electricity prices fall below 4 cents per kWh and energy conversion efficiencies reach at least 60%. When powered by renewable electricity, these products can be made with a net negative carbon emissions footprint. A comparative analysis of electrocatalytic, biocatalytic, and fossil fuel–derived chemical production shows that electrocatalytic production has the potential to yield the greatest reduction in carbon emissions, provided that a steady supply of clean electricity is available. Additionally, opportunities exist to combine electrochemical conversion of CO ₂ with a range of other thermo- and biocatalytic processes to slowly electrify the existing petrochemical supply chain and further upgrade CO ₂ into more useful chemicals. Technical challenges such as operating lifetime, energy efficiency, and product separation are discussed. Supply chain management of products and entrenched industrial petrochemical competition are also considered. OUTLOOK: There exists increasingly widespread recognition of the need to transition to carbon emissions–free means of chemical production. CO ₂ pricing mechanisms are being developed and are seeing increased governmental support. The nascent carbon utilization economy is gaining traction, with startup companies, global prizes, and industrial research efforts all pursuing new carbon conversion technologies. Recent advances in electrochemical CO ₂ reduction through the use of gas diffusion electrodes are pushing current densities and selectivities into a realm of industrial use. Despite this progress, there remain technical challenges that must be overcome for commercial application. Additionally, market barriers and cost economics will ultimately decide whether this technology experiences widespread implementation. Electrochemical CO ₂ conversion.: Reduction of CO ₂ using renewably sourced electricity could transform waste CO ₂ emissions into commodity chemical feedstocks or fuels.

A very basic pathway from CO ₂ to ethylene: Ethylene is an important commodity chemical for plastics. It is considered a tractable target for synthesizing renewably from carbon dioxide (CO ₂ ). The challenge is that the performance of the copper electrocatalysts used for this conversion under the required basic reaction conditions suffers from the competing reaction of CO ₂ with the base to form bicarbonate. Dinh et al. designed an electrode that tolerates the base by optimizing CO ₂ diffusion to the catalytic sites (see the Perspective by Ager and Lapkin). This catalyst design delivers 70% efficiency for 150 hours. Science , this issue p. 783 ; see also p. 707

Modulating metal oxides: The more difficult step in fuel cells and water electrolysis is the oxygen evolution reaction. The search for earth-abundant materials to replace noble metals for this reaction often turns to oxides of three-dimensional metals such as iron. Zhang et al. show that the applied voltages needed to drive this reaction are reduced for iron-cobalt oxides by the addition of tungsten. The addition of tungsten favorably modulates the electronic structure of the oxyhydroxide. A key development is to keep the metals well mixed and avoid the formation of separate phases. Science , this issue p. 333

Passivating traps in perovskites: Low-temperature processing of planar organic-inorganic perovskite solar cells made through solution processing would allow for simpler manufacturing and the use of flexible substrates. However, materials currently in use form interfaces with charge carrier trap states that limit performance. Tan et al. used chlorine-capped TiO ₂ colloidal nanocrystal films as an electron-selective layer, which limited interface recombination in solution-processed solar cells. Such cells achieved certified efficiencies of 19.5% for active areas of 1.1 cm ² . Science , this issue p. 722

The road ahead for perovskites: The high power conversion efficiencies of small-area perovskite solar cells (PSCs) have driven interest in the development of commercial devices. Rong et al. review recent progress in addressing stability, how to allow mass production, and how to maintain uniformity of large-area films. They note that lifetimes exceeding 10,000 hours under 1 sun (1 kW/m ² ) illumination have been reported for printable triple mesoscopic PSCs. Science , this issue p. eaat8235