Dual-Responsive Self-Propulsion Smart Device Steadily Driven by CO2 and H2O2
Source abstract
Abstract
In this paper, we introduce a kind of tertiary amine-based CO 2 -responsive material combining with the H 2 O 2 -responsive material to develop a dual-responsive self-propulsion smart device which can convert the chemical energy of H 2 O 2 into mechanical energy steadily through diving–surfacing cycles. In this dual-responsive device, the CO 2 -responsive material is designed as a wettability conversion species, which is wrapped with a strip of platinum to catalyze the decomposition of H 2 O 2 to generate gaseous O 2 to realize surfacing. In deionized water, the device floats on the surface of the water initially and can perform a diving–surfacing cycle when CO 2 and H 2 O 2 stimuli are alternately applied to the aqueous solution. The cyclic movement of the device can be realized by the generation and release of the inner gas through the hydrophobic cover, leading to a new controllable transition of different kinds of energy.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Catalytic Processes in Materials Science · Electrohydrodynamics and Fluid Dynamics · Advanced Sensor and Energy Harvesting Materials
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Key Laboratory of Superlight Materials and Surface Technology of Ministry of Education, College of Materials Science and Chemical Engineering, Harbin Engineering University, Harbin 150001, China
School of Materials Science and Engineering, University of Science and Technology Beijing, Beijing 100083, China
Funding
Ministry of Education of the People's Republic of China · National Natural Science Foundation of China
References (39)
Show source-provided references
1. 10.1038/nmat289110.1038/nmat2891 ↗
2. 10.1126/science.288.5471.162410.1126/science.288.5471.1624 ↗
3. 10.1039/c1cc12644j10.1039/c1cc12644j ↗
4. 10.1126/science.107893310.1126/science.1078933 ↗
5. 10.1039/c2py20089a10.1039/c2py20089a ↗
6. 10.1002/(sici)1097-4660(199708)69:4<421::aid-jctb730>3.0.co;2-310.1002/(sici)1097-4660(199708)69:4<421::aid-jctb730>3.0.co;2-3 ↗
7. 10.1126/science.285.5431.124610.1126/science.285.5431.1246 ↗
8. 10.1021/ja807087z10.1021/ja807087z ↗
9. 10.1021/am100139j10.1021/am100139j ↗
10. 10.1021/ma301572810.1021/ma3015728 ↗
11. 10.1002/anie.20110070810.1002/anie.201100708 ↗
12. 10.1126/science.112814210.1126/science.1128142 ↗
13. 10.1002/adma.20050177210.1002/adma.200501772 ↗
14. 10.1016/s0040-4039(03)00424-610.1016/s0040-4039(03)00424-6 ↗
15. 10.1039/c1jm11412c10.1039/c1jm11412c ↗
16. 10.1002/marc.20130028810.1002/marc.201300288 ↗
17. 10.1038/4361102a10.1038/4361102a ↗
18. 10.1039/c0gc00806k10.1039/c0gc00806k ↗
19. 10.1021/mz200017510.1021/mz2000175 ↗
20. 10.1021/ja408655n10.1021/ja408655n ↗
21. 10.1002/anie.20150103410.1002/anie.201501034 ↗
22. 10.1021/bm100545410.1021/bm1005454 ↗
23. 10.1039/c2cc35784d10.1039/c2cc35784d ↗
24. 10.1002/adma.20120299110.1002/adma.201202991 ↗
25. 10.1021/ja400518c10.1021/ja400518c ↗
26. 10.1039/c4cc03156c10.1039/c4cc03156c ↗
27. 10.1021/ma500140410.1021/ma5001404 ↗
28. 10.1021/acs.langmuir.5b0175610.1021/acs.langmuir.5b01756 ↗
29. 10.1021/acs.langmuir.6b0318910.1021/acs.langmuir.6b03189 ↗
30. 10.1002/adma.20100157710.1002/adma.201001577 ↗
31. 10.1002/adma.20140223710.1002/adma.201402237 ↗
32. 10.1021/la061546n10.1021/la061546n ↗
33. 10.1021/ma001152h10.1021/ma001152h ↗
34. 10.1002/1521-3773(20020215)41:4<652::aid-anie652>3.0.co;2-u10.1002/1521-3773(20020215)41:4<652::aid-anie652>3.0.co;2-u ↗
35. 10.1021/ja203773g10.1021/ja203773g ↗
36. 10.1021/nn304335x10.1021/nn304335x ↗
37. 10.1063/1.482614110.1063/1.4826141 ↗
38. 10.1039/c4nr02393e10.1039/c4nr02393e ↗
39. 10.1016/j.nanoen.2015.11.03710.1016/j.nanoen.2015.11.037 ↗