2021
DOI: 10.1038/s41929-021-00618-w
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Analysis of the limitations in the oxygen reduction activity of transition metal oxide surfaces

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Cited by 203 publications
(240 citation statements)
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References 65 publications
(50 reference statements)
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“…The model only analyzes and discusses the dual winding motor and energy source system, without considering the whole vehicle power transmission system, ignoring the energy loss and transmission efficiency in the process of mechanical transmission. In addition, Li et al [27] pointed that the oxygen reduction (ORR) is the key bottleneck in the performance of fuel cells, and identified two reasons why it is difficult to find transition metal oxides (TMOs) with a high ORR activity, which is also of great significance to realize the operation stability of fuel cells. With such knowledge, an improved dual winding motor drive technology could be possible, which could ensure the durability and cost necessary for achieving commercial success.…”
Section: Discussionmentioning
confidence: 99%
“…The model only analyzes and discusses the dual winding motor and energy source system, without considering the whole vehicle power transmission system, ignoring the energy loss and transmission efficiency in the process of mechanical transmission. In addition, Li et al [27] pointed that the oxygen reduction (ORR) is the key bottleneck in the performance of fuel cells, and identified two reasons why it is difficult to find transition metal oxides (TMOs) with a high ORR activity, which is also of great significance to realize the operation stability of fuel cells. With such knowledge, an improved dual winding motor drive technology could be possible, which could ensure the durability and cost necessary for achieving commercial success.…”
Section: Discussionmentioning
confidence: 99%
“…These results indicate that the formation of oxygen vacancy during synthesis leads to a significant change in the electronic properties of NiO, creating active sites for the reaction. Due to the weak-binding nature of metal-atop site over metal oxide surfaces (with details shown by a recent study [53] ), oxygen vacancy (e. g., the four-fold Ni-site analyzed in Figure 7) is expected to be the active site because it leads to a stronger bonding to the adsorbate which helps activate the NÀ N bond during the reaction. [54]…”
Section: Theoretical Analysismentioning
confidence: 96%
“…In theory, electroactivity depends on the reaction mechanism. 27 The Tafel slopes and electron transfer numbers (n) are calculated to explain the possible synergistic effect of K + cations and defects on the reaction mechanism. According to Fig.…”
Section: Electrocatalytic Performancementioning
confidence: 99%