Ye Minheng, Wang Xin, Liu Enzuo, Ye Jinhua, Wang Defa
TJU-NIMS International Collaboration Laboratory, Key Laboratory of Advanced Ceramics and Machining Technology (Ministry of Education, China), Tianjin Key Laboratory of Composite and Functional Materials, School of Materials Science and Engineering, Tianjin University, 92 Weijin Road, Tianjin, 300072, P.R. China.
Collaborative Innovation Center of Chemical Science and Engineering, 92 Weijin Road, Tianjin, 300072, P.R. China.
ChemSusChem. 2018 May 25;11(10):1606-1611. doi: 10.1002/cssc.201800083. Epub 2018 Mar 23.
Although they are widely used as cocatalysts in promoting photocatalysis, practical application of noble metals is limited by their high cost and rarity. Development of noble-metal-free cocatalysts is thus highly demanded. Herein titanium carbide (Ti C ) MXene is shown to be a highly efficient noble-metal-free cocatalyst with commercial titania (P25) for photocatalytic CO reduction. Surface alkalinization of Ti C dramatically enhances the activity; the evolution rates of CO (11.74 μmol g h ) and CH (16.61 μmol g h ) are 3- and 277-times higher than those of bare P25, respectively. The significantly enhanced activity is attributed to the superior electrical conductivity and charge-carrier separation ability, as well as the abundant CO adsorption and activation sites of surface-alkalinized Ti C MXene, indicating its promise as a highly-active noble-metal-free cocatalysts for photocatalytic CO reduction.
尽管它们作为助催化剂在促进光催化方面被广泛使用,但贵金属的实际应用受到其高成本和稀有性的限制。因此,对无贵金属助催化剂的开发有很高的需求。在此,碳化钛(TiC)MXene被证明是一种与商业二氧化钛(P25)用于光催化CO还原的高效无贵金属助催化剂。TiC的表面碱化显著提高了活性;CO(11.74 μmol g h)和CH(16.61 μmol g h)的析出速率分别比裸P25高3倍和277倍。活性的显著提高归因于优异的电导率和电荷载流子分离能力,以及表面碱化的TiC MXene丰富的CO吸附和活化位点,表明其有望成为用于光催化CO还原的高活性无贵金属助催化剂。