Electrocatalytic reduction of carbon monoxide into fuels or chemicals with two or more carbons is very attractive due to their high energy density and economic value. Herein we demonstrate the synthesis of a hydrophobic Cu/Cu2O sheet catalyst with hydrophobic n-butylamine layer and its application in CO electroreduction. The CO reduction on this catalyst produces two or more carbon products with a Faradaic efficiency of 93.5% and partial current density of 151 mA cm−2 at the potential of −0.70 V versus a reversible hydrogen electrode. A Faradaic efficiency of 68.8% and partial current density of 111 mA cm−2 for ethanol were reached, which is very high in comparison to all previous reports of CO2/CO electroreduction with a total current density higher than 10 mA cm−2. The as-prepared catalyst also showed impressive stability that the activity and selectivity for two or more carbon products could remain even after 100 operating hours. This work opens a way for efficient electrocatalytic conversion of CO2/CO to liquid fuels.

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Sodium metal batteries (NMBs) have attracted increasing attention as next‐generation rechargeable batteries. How to improve their cycling stability and safety under limited sodium excess conditions, ideally zero sodium excess (i.e., anode‐free architecture), is highly desired yet remains challenging. Herein, it is demonstrated that sodium formate (HCOONa), one component of the solid electrolyte interphase (SEI) naturally formed on sodium metal anode, is a promising candidate for designing high‐performance artificial SEI layers, which can suppress the sodium dendrite formation and reduce the side reactions between sodium and the electrolyte. Profiting from the HCOONa interface, the Na|Na3V2(PO4)3 battery with a high mass loading of Na3V2(PO4)3 (10 mg cm−2) exhibits a superior cycling stability with an ultralow decay rate of 0.004% per cycle over 800 cycles. More impressively, a single molecular layer of HCOONa in situ formed on commercial copper current collector helps to extend the lifespan of the anode‐free Cu|Na3V2(PO4)3 battery to 400 cycles with 88.2% capacity relation, representing the longest cycle lifetime reported in anode‐free NMBs.

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