2021
DOI: 10.1016/j.cej.2021.129842
|View full text |Cite
|
Sign up to set email alerts
|

Synergistic balancing hydrogen and hydroxyl adsorption/desorption of nickel sulfide via cation and anion dual-doping for boosting alkaline hydrogen evolution

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
2
1

Citation Types

1
25
0

Year Published

2022
2022
2024
2024

Publication Types

Select...
9

Relationship

2
7

Authors

Journals

citations
Cited by 45 publications
(26 citation statements)
references
References 54 publications
1
25
0
Order By: Relevance
“…The electron interaction between *OH and FeS 2 is presumed to be the coupling between O 2p and the highest occupied d‐states ( E d ), which has been proposed in previous reports 43,44 . The higher energy of E d compared with E f results in a slighter filling of the antibonding states and the more forceful adsorption *OH 43,45,46 . Thus Ni doping can enhance *OH adsorption due to the slighter filling of antibonding states, which is demonstrated by the distribution of crystal orbital Hamilton populations (COHP) of Fe‐O bonds (Figure 4E).…”
Section: Resultsmentioning
confidence: 68%
See 1 more Smart Citation
“…The electron interaction between *OH and FeS 2 is presumed to be the coupling between O 2p and the highest occupied d‐states ( E d ), which has been proposed in previous reports 43,44 . The higher energy of E d compared with E f results in a slighter filling of the antibonding states and the more forceful adsorption *OH 43,45,46 . Thus Ni doping can enhance *OH adsorption due to the slighter filling of antibonding states, which is demonstrated by the distribution of crystal orbital Hamilton populations (COHP) of Fe‐O bonds (Figure 4E).…”
Section: Resultsmentioning
confidence: 68%
“…43,44 The higher energy of E d compared with E f results in a slighter filling of the antibonding states and the more forceful adsorption *OH. 43,45,46 Thus Ni doping can enhance *OH adsorption due to the slighter filling of antibonding states, which is demonstrated by the distribution of crystal orbital Hamilton populations (COHP) of Fe-O bonds (Figure 4E). The stronger *OH adsorption can decrease the deprotonation energy, as shown in Figure 4F.…”
Section: Resultsmentioning
confidence: 93%
“…Numerous studies revealed that the adsorption energy of intermediates has scale relation, such as ΔG(*OOH) = ΔG(*OH)+3.2, the ΔG *OOH can be restricted by ΔG *OH , which limit a minimum theoretical overpotential of about 0.37 V, and the adsorption energy of intermediates cannot be optimized independently on a catalyst composed of a single type of site. So the synergistic effect of multi-site was put forward to break or overcome the adsorption-energy scaling relations ( Song et al, 2021 ). Du et al design the NiO/NiFe LDH interface to introduce additional active sites, and the intermediates can be adsorbed by the interfacial dual-site, so the adsorption energy of each intermediate can be adjusted independently to decrease the overpotential into 0.2 V ( Figure 1D ) ( Gao et al, 2019 ).…”
Section: Regulation Of Active Site For Promoting Oermentioning
confidence: 99%
“…Therefore, it is urgent to realize alternative media in this eld to meet the growing demand for hydrogen. [23][24][25][26][27][28][29] Considering that seawater occupies about 96.5% of the total water reserves, along with the removal of complex desalination and purication technologies, direct water electrolysis in raw seawater is also highly favored in the industry. 30 The water electrolysis in freshwater will lay a foundation for seawater electrolysis.…”
Section: Introductionmentioning
confidence: 99%