A highly selective and durable electrocatalyst for carbon dioxide (CO2) conversion to formate is developed, consisting of tin (Sn) nanosheets decorated with bismuth (Bi) nanoparticles. Owing to the formation of active sites through favorable orbital interactions at the Sn‐Bi interface, the Bi‐Sn bimetallic catalyst converts CO2 to formate with a remarkably high Faradaic efficiency (96%) and production rate (0.74 mmol h−1 cm−2) at −1.1 V versus reversible hydrogen electrode. Additionally, the catalyst maintains its initial efficiency over an unprecedented 100 h of operation. Density functional theory reveals that the addition of Bi nanoparticles upshifts the electron states of Sn away from the Fermi level, allowing the HCOO* intermediate to favorably adsorb onto the Bi‐Sn interface compared to a pure Sn surface. This effectively facilitates the flow of electrons to promote selective and durable conversion of CO2 to formate. This study provides sub‐atomic level insights and a general methodology for bimetallic catalyst developments and surface engineering for highly selective CO2 electroreduction.

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The theoretical yield of charcoal from biomass lies in the range 50−80% on a dry weight basis. In spite of the fact that mankind has been manufacturing charcoal for about 6000 years, traditional methods for charcoal production in developing countries realize yields of 20% or less, and modern industrial technology offers yields of only 25−37%. Moreover, reaction times for the batch process in an industrial kiln are typically 8 days. In this article we describe a practical method for manufacturing high-quality charcoal from biomass that realizes near-theoretical yields of 42−62% with a reaction time of about 15 min to 2 h, depending on the moisture content of the feed. Because of its high efficiency, this technology can help to reduce worldwide deforestation and pollution, while providing greater amounts of a desirable, renewable fuel and chemical resource to mankind.

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