Deciphering the role of amine in amino silane-functionalized Pd/rGO catalyst for formic acid decomposition at room temperature
Source abstract
Abstract
Additive free, selective decomposition of formic acid to hydrogen and carbon dioxide at room temperature is still a challenging catalytic process which often requires noble metal catalyst (Pd, AuPd, AuPt) and sodium formate as an additive. Till date, catalyst design is targeted towards minimum noble metal usage along with incorporation of basic functionalities to produce in situ formate ion (key intermediate for dehydrogenation) from formic acid. In this work, we have studied the catalytic behaviour of amino silane-functionalized graphene oxide (GO) containing palladium nanoparticles for formic acid decomposition in ambient condition. By varying amine functionalization on GO and palladium content, the best performing catalyst was obtained with 5 wt% palladium loading. Additionally, it was observed for the first time that along with stability of a catalyst in reaction medium, its interaction with decomposed products, i.e., carbon dioxide with amine functional groups plays a crucial role in recyclability of a catalyst.
Source: openaire · Quality: candidate unverified · Source record ↗
Research context
OpenAlex topics: Carbon dioxide utilization in catalysis · Metal-Organic Frameworks: Synthesis and Applications · Catalytic Processes in Materials Science
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
References (42)
Show source-provided references
1. Jacobson M Z, Colella W and Golden D 2005 Science 308 190110.1126/science.1109157 ↗
2. Aceves S M, Martinez-Frias J and Garcia-Villazana O 2000 Int. J. Hydrog. Energy 25 107510.1016/S0360-3199(00)00016-1 ↗
3. Orimo S-I, Nakamori Y, Eliseo J R, Züttel A and Jensen C M 2007 Chem. Rev. 107 411110.1021/cr0501846 ↗
4. Furukawa H, Ko N, Go Y B, Aratani N, Choi S B, Choi E et al 2010 Science 329 42410.1126/science.1192160 ↗
5. Yang S J, Kim T, Im J H, Kim Y S, Lee K, Jung H et al 2012 Chem. Mater. 24 46410.1021/cm202554j ↗
6. Hodoshima S, Takaiwa S, Shono A, Satoh K and Saito Y 2005 Appl. Catal. A: Gen. 283 23510.1016/j.apcata.2005.01.010 ↗
7. Kariya N, Fukuoka A and Ichikawa M 2002 Appl. Catal. A: Gen. 233 9110.1016/S0926-860X(02)00139-4 ↗
8. Preuster P, Papp C and Wasserscheid P 2016 Acc. Chem. Res. 50 7410.1021/acs.accounts.6b00474 ↗
9. Tingelöf T, Hedström L, Holmström N, Alvfors P and Lindbergh G 2008 Int. J. Hydrog. Energy 33 206410.1016/j.ijhydene.2008.02.002 ↗
10. Loges B, Boddien A, Gärtner F, Junge H and Beller M 2010 Top. Catal. 53 90210.1007/s11244-010-9522-8 ↗
11. Johnson T C, Morris D J and Wills M 2010 Chem. Soc. Rev. 39 8110.1039/B904495G ↗
12. Fellay C, Dyson P J and Laurenczy G 2008 Angew. Chem. Int. Ed. 47 396610.1002/anie.200800320 ↗
13. Grasemann M and Laurenczy G 2012 Energy Environ. Sci. 5 969810.1039/c2ee21928j ↗
14. Kiss F E, Jovanović M and Bošković G C 2010 Fuel Process. Technol. 91 131610.1016/j.fuproc.2010.05.001 ↗
15. Liu H, Huang B, Zhou J, Wang K, Yu Y, Yang W et al 2018 J. Mater. Chem. A 6 197910.1039/C7TA10963F ↗
16. Fukuda K, Noto Y, Onishi T and Tamaru K 1967 T. Faraday Soc. 63 307210.1039/tf9676303072 ↗
17. Gazsi A, Bánsági T and Solymosi F 2011 J. Phys. Chem. C 115 1545910.1021/jp203751w ↗
18. Solymosi F, Koós Á, Liliom N and Ugrai I 2011 J. Catal. 279 21310.1016/j.jcat.2011.01.023 ↗
19. Zhu Q-L, Tsumori N and Xu Q 2014 Chem. Sci. 5 19510.1039/C3SC52448E ↗
20. Wang Z-L, Yan J-M, Wang H-L, Ping Y and Jiang Q 2012 Sci. Rep. 2 59810.1038/srep00598 ↗
21. Wan C, Yao F, Li X, Hu K, Ye M, Xu L et al 2016 Chem. Select. 1 6907
22. Outka D A and Madix R 1987 Surf. Sci. 179 36110.1016/0039-6028(87)90063-X ↗
23. Bi Q-Y, Du X L, Liu Y-M, Cao Y, He H-Y and Fan K-N 2012 J. Am. Chem. Soc. 134 892610.1021/ja301696e ↗
24. Navlani-García M, Mori K, Salinas-Torres D, Kuwahara Y and Yamashita H 2019 Front. Mater. 6 221310.3389/fmats.2019.00044 ↗
25. Wang X, Meng Q, Gao L, Jin Z, Ge J, Liu C et al 2018 Int. J. Hydrog. Energy 43 705510.1016/j.ijhydene.2018.02.146 ↗
26. Shih C-J, Lin S, Sharma R, Strano M S and Blankschtein D 2012 Langmuir 28 23510.1021/la203607w ↗
27. Abbas S S, Rees G J, Kelly N L, Dancer C E J, Hanna J V and McNally T 2018 Nanoscale 10 1623110.1039/C8NR04781B ↗
28. Wang Z, Hao X, Hu D, Li L, Song X, Zhang W et al 2017 Catal. Sci. Technol. 7 2213
29. Wang Z-L, Yan J-M, Wang H-L, Ping Y and Jiang Q 2013 J. Mater. Chem. A 1 1272110.1039/c3ta12531a ↗
30. Hosseini H, Mahyari M, Bagheri A and Shaabani A 2014 J. Power Sources 247 7010.1016/j.jpowsour.2013.08.061 ↗
31. Song F-Z, Zhu Q-L, Tsumori N and Xu Q 2015 ACS Catal. 5 514110.1021/acscatal.5b01411 ↗
32. Yan J M, Li S J, Yi S S, Wulan B R, Zheng W T and Jiang Q 2018 Adv. Mater. 30 170303810.1002/adma.201703038 ↗
33. Hummers W S Jr and Offeman R E 1958 J. Am. Chem. Soc. 80 133910.1021/ja01539a017 ↗
34. Serna-Guerrero R, Da’na E and Sayari A 2008 Ind. Eng. Chem. Res. 47 940610.1021/ie801186g ↗
35. Krishna K S, Sandeep C S, Philip R and Eswaramoorthy M 2010 ACS Nano 4 268110.1021/nn100320s ↗
36. Hou S, Su S, Kasner M L, Shah P, Patel K and Madarang C J 2010 Chem. Phys. Lett. 501 6810.1016/j.cplett.2010.10.051 ↗
37. Sun S-W, Lin Y-C, Weng Y-M and Chen M-J 2006 J. Food Compos. Anal. 19 11210.1016/j.jfca.2005.04.006 ↗
38. Achari A, Datta K, De M, Dravid V P and Eswaramoorthy M 2013 Nanoscale 5 531610.1039/c3nr01108a ↗
39. Croft G and Fuller M 1977 Nature 269 58510.1038/269585a0 ↗
40. Jiang K, Xu K, Zou S and Cai W-B 2014 J. Am. Chem. Soc. 136 486110.1021/ja5008917 ↗
41. Böttinger W, Maiwald M and Hasse H 2008 Fluid Phase Equilib. 263 13110.1016/j.fluid.2007.09.017 ↗
42. Moreno M, Ibañez F J, Jasinski J B and Zamborini F P 2011 J. Am. Chem. Soc. 133 438910.1021/ja108378x ↗