journal article·2023-03-08

Regulating Hollow Carbon Cage Supported NiCo Alloy Nanoparticles for Efficient Electrocatalytic Hydrogen Evolution Reaction

Bo Qi, Wen Chang, Qixin Xu, Luran Jiang, Sai An, Jin-Feng Chu, Yu-Fei Song

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Abstract

The NiCo alloy is one of the most promising alternatives to the noble-metal electrocatalysts for the hydrogen evolution reaction (HER); however, its performance is largely restricted by insufficient active sites and low surface area. Here, we fabricated a hierarchical hollow carbon cage supported NiCo alloy (denoted as HC NiCo/C) and a bulk NiCo alloy (denoted as NiCo) by reduction of a partially ZIF-67 etched ZIF-67@NiCo-LDH (LDH = layered double hydroxide) precursor and a fully ZIF-67 etched NiCo-LDH precursor, respectively. The as-prepared HC NiCo/C, in which the Ni 29 Co 71 alloy nanocrystals with an average 6 nm size were encapsulated in graphitic carbon layers, provided a vastly increased electrochemically active surface area ( ca . 13 times than the NiCo) and abundant catalytic active sites, which resulted in a higher HER performance with an overpotential of 99 mV than the 198 mV for NiCo at 10 mA cm –2 . Detailed experimental results suggested that only the HC NiCo/C possessed the active alloy surface composed of unsaturated Ni 0 and Co 0 atoms, and both the metal–support interaction and alloying effect influenced the electronic structure of Co and Ni in HC NiCo/C, whereas the NiCo exhibited pure Ni surface. Theoretical calculations further revealed the Ni 29 Co 71 alloy surface in HC NiCo/C possessed the appropriate adsorption energy of the intermediate state (adsorbed H*). This work provided new insight into the construction of the stable small-sized bimetallic alloy nanocatalysts by regulating the reduction precursors.
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Research context

OpenAlex topics: Electrocatalysts for Energy Conversion · Advanced battery technologies research · Supercapacitor Materials and Fabrication

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

State Key Laboratory of Chemical Resource Engineering, Beijing University of Chemical Technology, Beijing 100029, P. R. China

Funding

Central University Basic Research Fund of China · National Natural Science Foundation of China

References (33)

Show source-provided references
1. 10.1126/science.aad499810.1126/science.aad4998 ↗
2. 10.1126/science.aaw877510.1126/science.aaw8775 ↗
3. 10.1002/anie.20211033510.1002/anie.202110335 ↗
4. 10.1038/nnano.2016.30410.1038/nnano.2016.304 ↗
5. 10.1016/j.nanoen.2017.01.00310.1016/j.nanoen.2017.01.003 ↗
6. 10.1002/advs.20190011610.1002/advs.201900116 ↗
7. 10.1016/j.nanoen.2022.10698910.1016/j.nanoen.2022.106989 ↗
8. 10.1021/acscatal.9b0040710.1021/acscatal.9b00407 ↗
9. 10.1021/acs.chemrev.7b0068910.1021/acs.chemrev.7b00689 ↗
10. 10.1002/anie.20220251810.1002/anie.202202518 ↗
11. 10.1021/acsnano.2c0106410.1021/acsnano.2c01064 ↗
12. 10.1016/j.cej.2021.12951210.1016/j.cej.2021.129512 ↗
13. 10.1038/s41467-020-19277-910.1038/s41467-020-19277-9 ↗
14. 10.1021/acscatal.8b0481410.1021/acscatal.8b04814 ↗
15. 10.1038/s41467-020-17188-310.1038/s41467-020-17188-3 ↗
16. 10.1039/D2NR00053A10.1039/D2NR00053A ↗
17. 10.1002/aic.1797310.1002/aic.17973 ↗
18. 10.1002/anie.20211366410.1002/anie.202113664 ↗
19. 10.1016/j.renene.2021.03.10010.1016/j.renene.2021.03.100 ↗
20. 10.1039/C5CS00268K10.1039/C5CS00268K ↗
21. 10.1039/C4CS00160E10.1039/C4CS00160E ↗
22. 10.1021/jacs.5b0246510.1021/jacs.5b02465 ↗
23. 10.1039/D0QI01259A10.1039/D0QI01259A ↗
24. 10.1021/acsami.2c0288810.1021/acsami.2c02888 ↗
25. 10.1039/c3nr03829g10.1039/c3nr03829g ↗
26. 10.1002/adma.20190562210.1002/adma.201905622 ↗
27. 10.1002/adma.20160408010.1002/adma.201604080 ↗
28. 10.1021/jacs.0c1028510.1021/jacs.0c10285 ↗
29. 10.1103/PhysRevLett.77.386510.1103/PhysRevLett.77.3865 ↗
30. 10.1103/PhysRevB.54.1116910.1103/PhysRevB.54.11169 ↗
31. 10.1103/PhysRevB.47.55810.1103/PhysRevB.47.558 ↗
32. 10.1149/1.185698810.1149/1.1856988 ↗
33. 10.1016/j.commatsci.2005.04.01010.1016/j.commatsci.2005.04.010 ↗