Rationally Designed Semiconducting 2D Surface-Confined Metal–Organic Network
Source abstract
Abstract
Two-dimensional (2D) surface-confined metal-organic networks (SMONs) are metal-doped self-assembled monolayers of molecules on solid surfaces. We report the formation of uniform large-area solution-processed semiconducting SMONs of Pd and Zn with mellitic acid (MA) on a highly oriented pyrolytic graphite (HOPG) surface under ambient conditions. The microscopic structure is determined using scanning tunneling microscopy (STM), atomic force microscopy (AFM), and X-ray photoelectron spectroscopy (XPS). Using tunneling spectroscopy, we observed a reduction in the band gap of ≈900 and ≈300 meV for MA-Pd and MA-Zn SMONs, respectively, compared to the pure MA assembly. Concomitant density functional theory (DFT) calculations reveal that the coordination geometry and microscopic arrangement give rise to the observed reduction in the band gap. The dispersion of the frontier bands and their delocalization due to strong electronic coupling (between MA and metal) suggest that the MA-Pd SMON could potentially be a 2D electronic material.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Surface Chemistry and Catalysis · Graphene research and applications · Surface and Thin Film Phenomena
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Chemistry, Indian Institute of Technology Kanpur, Kanpur 208016, India
Department of Chemical Engineering, Indian Institute of Technology Kanpur, Kanpur 208016, India
Funding
Council of Scientific and Industrial Research · Ministry of Electronics and Information technology · Indian Institute of Technology Kanpur · Science and Engineering Research Board
References (66)
Show source-provided references
1. 10.1039/C0NR00323A10.1039/C0NR00323A ↗
2. 10.1126/science.107082110.1126/science.1070821 ↗
3. 10.1002/1438-5171(200204)3:1<25::AID-SIMO25>3.0.CO;2-K10.1002/1438-5171(200204)3:1<25::AID-SIMO25>3.0.CO;2-K ↗
4. 10.1016/j.susc.2018.10.00810.1016/j.susc.2018.10.008 ↗
5. 10.1006/jmbi.1998.244110.1006/jmbi.1998.2441 ↗
6. 10.1038/3509805910.1038/35098059 ↗
7. 10.1103/PhysRevLett.83.32410.1103/PhysRevLett.83.324 ↗
8. 10.1002/adma.20060092910.1002/adma.200600929 ↗
9. 10.1002/(SICI)1521-3773(19990517)38:10<1393::AID-ANIE1393>3.0.CO;2-H10.1002/(SICI)1521-3773(19990517)38:10<1393::AID-ANIE1393>3.0.CO;2-H ↗
10. 10.1021/cr800422910.1021/cr8004229 ↗
11. 10.1039/c2nj40348j10.1039/c2nj40348j ↗
12. 10.1021/ja039529x10.1021/ja039529x ↗
13. Werner, A. Coordination chemistry Z. Anorg. Chem. 1893.
14. 10.1039/C1CS15092H10.1039/C1CS15092H ↗
15. 10.1039/c2sc00029f10.1039/c2sc00029f ↗
16. 10.1021/acs.jpclett.7b0213810.1021/acs.jpclett.7b02138 ↗
17. 10.1002/admi.20150073810.1002/admi.201500738 ↗
18. 10.1021/nn100303z10.1021/nn100303z ↗
19. 10.1088/0957-4484/21/30/30570310.1088/0957-4484/21/30/305703 ↗
20. 10.1039/c1cc12519b10.1039/c1cc12519b ↗
21. 10.1038/ncomms194210.1038/ncomms1942 ↗
22. 10.1103/PhysRevB.90.12540810.1103/PhysRevB.90.125408 ↗
23. 10.1021/jp510380310.1021/jp5103803 ↗
24. 10.1002/chem.20130185210.1002/chem.201301852 ↗
25. 10.1002/anie.20140652810.1002/anie.201406528 ↗
26. 10.1021/ja511611r10.1021/ja511611r ↗
27. 10.1021/acs.jpcc.9b0032610.1021/acs.jpcc.9b00326 ↗
28. 10.1021/jp104954w10.1021/jp104954w ↗
29. 10.1002/chem.20030542410.1002/chem.200305424 ↗
30. 10.1039/B616601F10.1039/B616601F ↗
31. 10.1021/acs.jpcc.6b0343410.1021/acs.jpcc.6b03434 ↗
32. 10.1021/acs.jpcc.9b0490810.1021/acs.jpcc.9b04908 ↗
33. 10.1063/1.243241010.1063/1.2432410 ↗
34. 10.1002/asia.20190058610.1002/asia.201900586 ↗
35. 10.1088/0953-8984/21/39/39550210.1088/0953-8984/21/39/395502 ↗
36. 10.1103/PhysRevLett.78.139610.1103/PhysRevLett.78.1396 ↗
37. 10.1103/PhysRevB.46.667110.1103/PhysRevB.46.6671 ↗
38. 10.1103/PhysRevB.13.518810.1103/PhysRevB.13.5188 ↗
39. 10.1063/1.338234410.1063/1.3382344 ↗
40. 10.1140/epjb/e2013-31162-910.1140/epjb/e2013-31162-9 ↗
41. 10.1038/srep4090710.1038/srep40907 ↗
42. Mesh average: This procedure averages over equivalent parts obtained from an image with periodic contrast. The parts are generated by a 2D FFT of the original image.
43. 10.1016/j.susc.2012.08.00810.1016/j.susc.2012.08.008 ↗
44. 10.1016/j.susc.2010.03.02310.1016/j.susc.2010.03.023 ↗
45. 10.1002/1521-3773(20020104)41:1<48::AID-ANIE48>3.0.CO;2-U10.1002/1521-3773(20020104)41:1<48::AID-ANIE48>3.0.CO;2-U ↗
46. 10.1038/185756a010.1038/185756a0 ↗
47. 10.1021/la046764010.1021/la0467640 ↗
48. 10.1103/PhysRevB.93.19520810.1103/PhysRevB.93.195208 ↗
49. 10.1063/1.497484410.1063/1.4974844 ↗
50. 10.1021/jp077156710.1021/jp0771567 ↗
51. 10.1002/ejic.20200052710.1002/ejic.202000527 ↗
52. 10.1039/c2970000658b10.1039/c2970000658b ↗
53. 10.1039/jr965000363210.1039/jr9650003632 ↗
54. 10.1039/b502122g10.1039/b502122g ↗
55. 10.1107/S160053680503069210.1107/S1600536805030692 ↗
56. 10.1107/S0365110X5300201510.1107/S0365110X53002015 ↗
57. 10.1107/S010827018609087X10.1107/S010827018609087X ↗
58. 10.1002/anie.20046139010.1002/anie.200461390 ↗
59. 10.1007/s10973-016-5521-810.1007/s10973-016-5521-8 ↗
60. 10.1016/j.molcata.2014.11.00810.1016/j.molcata.2014.11.008 ↗
61. 10.1039/DT989000071910.1039/DT9890000719 ↗
62. 10.1039/b515699h10.1039/b515699h ↗
63. 10.1021/ic00035a00810.1021/ic00035a008 ↗
64. 10.1016/0167-6989(88)90250-410.1016/0167-6989(88)90250-4 ↗
65. 10.1021/ic50128a05910.1021/ic50128a059 ↗
66. Sharma, A.; Singh, B. P.; Dhar, S. In Origin of the Green Luminescence Band in ZnO Nanoparticles Synthesized by Sol-Gel Route, 2011 11th IEEE International Conference on Nanotechnology, 2011; pp 662–665.10.1109/NANO.2011.6144396 ↗