Electrochemical reduction of carbon dioxide (CO 2 ) into value-added chemicals is ap romising strategy to reduce CO 2 emission and mitigate climate change.O ne of the most serious problems in electrocatalytic CO 2 reduction (CO 2 R) is the lows olubility of CO 2 in an aqueous electrolyte,w hich significantly limits the cathodic reaction rate.T his paper proposes af acile method of catholyte-free electrocatalytic CO 2 reduction to avoid the solubility limitation using commercial tin nanoparticles as acathode catalyst. Interestingly,as the reaction temperature rises from 303 Kto363 K, the partial current density (PCD) of formate improves more than two times with 52.9 mA cm À2 ,despite the decrease in CO 2 solubility. Furthermore,asignificantly high formate concentration of 41.5 gL À1 is obtained as aone-path product at 343 Kwith high PCD (51.7 mA cm À2 )and high Faradaic efficiency (93.3 %) via continuous operation in afull flowcell at alow cell voltage of 2.2 V.The electrocatalytic CO 2 reduction (CO 2 R) into useful chemicals or fuels has attracted significant interest for renewable energy storage and environmental sustainability. [1][2][3][4] There are several electrochemical pathways to convert CO 2 into valuable products, [1,5,6] among which formic acid or formate has received particular attention over the past few years because the CO 2 Ri nto formic acid is regarded as as uitable reaction for industrial scale production. [7][8][9] However,there still remain some problems to be solved, including alarge overpotential, low Faradaic efficiency(FE), and poor stability of electrocatalysts.Inparticular, the low solubility of CO 2 in the catholyte significantly limits the reaction rate,thus greatly hindering the large-scale application of the CO 2 R. [1] Furthermore,t he liquid electrolytes dilute the reduction products,w hich increases the separation costs for product recovery.Some efforts have been reported to overcome the solubility limitation and enhance the current density of formate production, including development of ah ighly porous structure of SnO 2 ,t unable alloys,a nd ionic liquids (ILs). [2,[10][11][12][13] Despite these significant results,t heir kinetics of CO 2 Rconversion into formate is still limited by the low CO 2 concentration in electrolytes.I nr ecent years,s ome research groups reported remarkable improvement in the current density of CO 2 Rt of ormate using gas diffusion electrodes (GDEs) with metal nanoparticles. [5,[14][15][16][17][18][19] This type of electrode provides at hree-phase interface of gas/ electrolyte/ catalyst, in which the CO 2 molecules only have to diffuse through av ery thin liquid layer of electrolyte to reach the catalyst surface. [19] Castillo et al. [5] achieved ah igh formate concentration of 2.5 gL À1 via continuous operation of a10cm 2 filterpress cell using Sn-GDEs under galvanostatic condition of 150 mA cm À2 .A lthough they obtained an enhanced performance over previous results,their method still suffered from ahigh cell voltage of 3.7 V, alow FE of 70 %, and t...