Synthesis and Optimization of Ti/Li/Al Ternary Layered Double Hydroxides for Efficient Photocatalytic Reduction of CO2 to CH4

Abstract

Abstract A series of Ti/Li/Al ternary layered double hydroxides (TiLiAl-LDHs) with different Ti:Li:Al molar ratios were prepared by a coprecipitation method for photocatalytic CO 2 reduction. It was demonstrated that the contents of anions between the layers of Ti/Li/Al-LDHs greatly determined the photocatalytic activity for CO 2 reduction. With Ti:Li:Al molar ratios optimized to be 1:3:2, the largest contents of $${{\bf{CO}}}_{{\bf{3}}}^{{\bf{2}}}$$ <mml:math xmlns:mml="http://www.w3.org/1998/Math/MathML"> <mml:msubsup> <mml:mrow> <mml:mi>CO</mml:mi> </mml:mrow> <mml:mrow> <mml:mn>3</mml:mn> </mml:mrow> <mml:mrow> <mml:mn>2</mml:mn> </mml:mrow> </mml:msubsup> </mml:math> − anion and hydroxyl group were obtained for the Ti 1 Li 3 Al 2 -LDHs sample, which exhibited the highest photocatalytic activity for CO 2 reduction, with CH 4 production rate achieving 1.33 mmol h −1 g −1 . Moreover, the theoretical calculations show that Ti 1 Li 3 Al 2 -LDHs is a p-type semiconductor with the narrowest band gap among all the obtained TiLiAl-LDHs. After calcined at high temperatures such as 700 °C, and the obtained TiLiAl-700 sample showed much increased photocatalytic activity for CO 2 reduction, with CH 4 production rate reaching about 1.59 mmol h −1 g −1 . This calcination induced photocatalytic enhancement should be related to the cystal structure transformation from hydrotalcite to mixed oxides containing high reactive oxygen species for more efficient CO 2 reduction.