Nonprecious Metal Catalysts for Tuning Discharge Product Distribution at Solid–Solid Interfaces of Aprotic Li–O2 Batteries
Source abstract
Abstract
Tuning catalysis at solid–solid interfaces is critical for the development of next-generation energy storage devices such as Li–O2 batteries, where solid lithium–oxygen species are formed and dissociated on a solid catalyst. Herein, atomically controlled synthesis is combined with theoretical calculations, electrochemical studies, and detailed characterization measurements to show that the interface between an oxide catalyst and the solid products is key to selectively control discharge product distribution, consequently affecting charge overpotentials. A surface structure-dependent electrochemical performance for nonprecious metal-containing, nanostructured lanthanum nickelate oxide (La2NiO4+δ, LNO) electrocatalysts is demonstrated. LNO nanostructures with (001) NiO-terminated surfaces exhibit lower charge overpotentials, as opposed to irregularly terminated polyhedral-shaped oxides of the same composition. It is found that these LNO nanostructures, with controlled surface structure, enhance the performance by providing a platform for stabilization of Li-deficient oxide species during discharge, consequently lowering overpotential losses associated with their oxidation during charge. Periodic density functional theory modeling of the solid–solid interface between the oxide catalyst and the lithium-discharge products suggests that stabilization of the Li-deficient products is due to the formation of a lithiated oxide surface, which is in turn facilitated by an electron transfer from the near surface Li to the surface lattice oxygen atoms. The potential-dependent stability of these lithium–oxygen species on LNO is predicted and confirmed experimentally. These results provide a framework for probing and engineering catalysis at solid–solid interfaces, and strategies for improving the efficiency of next-generation energy storage systems using nonprecious, nanostructured mixed metal oxide catalysts.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Advancements in Battery Materials · Advanced Battery Materials and Technologies · Supercapacitor Materials and Fabrication
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Chemical Engineering and Material Science, Wayne State University, Detroit, Michigan 48202, United States
Davidson School of Chemical Engineering, Purdue University, West Lafayette, Indiana 47907, United States
Toyota Research Institute—North America, Ann Arbor, Michigan 48105, United States
Funding
Basic Energy Sciences
References (53)
Show source-provided references
1. 10.1038/nenergy.2016.12810.1038/nenergy.2016.128 ↗
2. 10.1021/cr400573b10.1021/cr400573b ↗
3. 10.1038/nmat319110.1038/nmat3191 ↗
4. 10.1039/c5ee00838g10.1039/c5ee00838g ↗
5. 10.1039/c7sc02519j10.1039/c7sc02519j ↗
6. 10.1039/c6cs00929h10.1039/c6cs00929h ↗
7. 10.1021/am504900k10.1021/am504900k ↗
8. 10.1038/nnano.2017.2710.1038/nnano.2017.27 ↗
9. 10.1149/08513.0303ecst10.1149/08513.0303ecst ↗
10. 10.1038/nchem.210110.1038/nchem.2101 ↗
11. 10.1038/nchem.213210.1038/nchem.2132 ↗
12. 10.1149/2.118309jes10.1149/2.118309jes ↗
13. 10.1021/jp102019y10.1021/jp102019y ↗
14. 10.1038/nmat462910.1038/nmat4629 ↗
15. 10.1126/science.aas934310.1126/science.aas9343 ↗
16. 10.1038/nature1648410.1038/nature16484 ↗
17. 10.1021/ja103657210.1021/ja1036572 ↗
18. 10.1021/acs.jpcc.6b1295010.1021/acs.jpcc.6b12950 ↗
19. 10.1149/2.0111613jes10.1149/2.0111613jes ↗
20. 10.1021/acscatal.8b0223610.1021/acscatal.8b02236 ↗
21. 10.1063/1.344738110.1063/1.3447381 ↗
22. 10.1021/jacs.7b1113810.1021/jacs.7b11138 ↗
23. 10.1021/acs.chemmater.8b0069410.1021/acs.chemmater.8b00694 ↗
24. 10.1021/acscatal.5b0075610.1021/acscatal.5b00756 ↗
25. 10.1007/s11244-015-0395-810.1007/s11244-015-0395-8 ↗
26. 10.1039/c4cc07364a10.1039/c4cc07364a ↗
27. 10.1039/c3ee40697k10.1039/c3ee40697k ↗
28. 10.1002/anie.20121005710.1002/anie.201210057 ↗
29. 10.1021/jz501323n10.1021/jz501323n ↗
30. 10.1021/acs.nanolett.5b0351010.1021/acs.nanolett.5b03510 ↗
31. 10.1016/j.jelechem.2018.12.02310.1016/j.jelechem.2018.12.023 ↗
32. 10.1103/physrevb.54.1116910.1103/physrevb.54.11169 ↗
33. 10.1103/physrevlett.77.386510.1103/physrevlett.77.3865 ↗
34. 10.1103/physrevb.73.19510710.1103/physrevb.73.195107 ↗
35. 10.1021/acs.jpcc.5b0316910.1021/acs.jpcc.5b03169 ↗
36. 10.1002/anie.20180824610.1002/anie.201808246 ↗
37. 10.1038/nenergy.2017.7010.1038/nenergy.2017.70 ↗
38. 10.1038/nenergy.2017.7010.1038/nenergy.2017.70 ↗
39. 10.1038/nchem.149910.1038/nchem.1499 ↗
40. 10.1002/anie.20130797610.1002/anie.201307976 ↗
41. 10.1002/aenm.20120001810.1002/aenm.201200018 ↗
42. 10.1039/c2jm33440b10.1039/c2jm33440b ↗
43. 10.1021/ja508794r10.1021/ja508794r ↗
44. 10.1002/celc.20150021810.1002/celc.201500218 ↗
45. 10.1021/acs.jpclett.7b0004010.1021/acs.jpclett.7b00040 ↗
46. 10.1039/c0cs00145g10.1039/c0cs00145g ↗
47. 10.1021/acsenergylett.7b0111110.1021/acsenergylett.7b01111 ↗
48. 10.1021/acscatal.8b0518210.1021/acscatal.8b05182 ↗
49. 10.1021/jz300142y10.1021/jz300142y ↗
50. 10.1021/jacs.5b0779210.1021/jacs.5b07792 ↗
51. 10.1021/cs501444210.1021/cs5014442 ↗
52. 10.1021/acs.chemmater.6b0502210.1021/acs.chemmater.6b05022 ↗
53. 10.1038/ncomms338310.1038/ncomms3383 ↗