2020
DOI: 10.1002/adfm.202070136
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Bimetal Catalysts: Bimetal Schottky Heterojunction Boosting Energy‐Saving Hydrogen Production from Alkaline Water via Urea Electrocatalysis (Adv. Funct. Mater. 21/2020)

Abstract: In article number 2000556, Chenglin Yan, Guozhen Shen, Xianfu Wang, and co‐workers present a bimetal Schottky heterojunction using an in‐situ electrochemical turning strategy. With the self‐driven charge transfer and redistribution at the interface, the developed catalyst with its built‐in electric field demonstrates excellent bifunctional catalysis for both urea oxidation and hydrogen evolution in alkaline systems.

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Cited by 35 publications
(49 citation statements)
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“…As a result, our catalyst possesses electrophilic Ni domain and nucleophilic NiO domain, respectively. Therefore, electron‐donating amino group and electron‐withdrawing carbonyl group in urea molecules can be selectively adsorbed on the above electrophilic and nucleophilic domains in Figure d . As a result, the C−N bond cleavage became favorable, and urea oxidation could proceed at lower potential.…”
Section: Resultsmentioning
confidence: 99%
See 1 more Smart Citation
“…As a result, our catalyst possesses electrophilic Ni domain and nucleophilic NiO domain, respectively. Therefore, electron‐donating amino group and electron‐withdrawing carbonyl group in urea molecules can be selectively adsorbed on the above electrophilic and nucleophilic domains in Figure d . As a result, the C−N bond cleavage became favorable, and urea oxidation could proceed at lower potential.…”
Section: Resultsmentioning
confidence: 99%
“…found that CoS 2 /MoS 2 Schottky heterojunctions was able to yield the current density of 10 mA/cm 2 at 1.29 V for UOR . Wang's group developed a bimetal Schottky heterostructure CoMn/CoMn 2 O 4 , which possessed self‐driven charge transfer at the heterointerface, and exhibited potential of 1.32 V to reach 10 mA/cm 2 for UOR . In brief, the existence of the Schottky heterointerface will effectively modulate the electronic structure of materials, favoring the UOR process.…”
Section: Introductionmentioning
confidence: 99%
“…[ 34–36 ] More particularly, the integration of metal and semiconductor with different energy structures such as Mott–Schottky heterojunctions could spontaneously drive electrons to flow across the metal–semiconductor heterointerfaces until the work functions on both sides reach equilibrium, generating an oriented built‐in electric field and quite stable local nucleophilic/electrophilic regions. [ 37,38 ] As a result, the redistributed electron cloud density may significantly enhance the electric conductivity and alter the chemisorption behaviors of the reaction intermediates, ultimately leading to substantially boosted reactivity and selectivity as compared with the physical mixture and individual counterparts. [ 39,40 ] As well known, cerium oxide (CeO 2 ), benefitting from its remarkable oxygen‐storage capacity, reversible conversion between Ce 3+ and Ce 4+ oxidation states, intrinsically outstanding ionic conductivity, and rich oxygen vacancies, has recently attracted enormous attention as a promising auxiliary promoter in electrocatalysis field to improve activity and stability.…”
Section: Introductionmentioning
confidence: 99%
“…Therefore, UOR is a favorable substitution for sluggish OER for energy‐saving hydrogen generation, accompanying by simultaneous urea‐containing wastewater remediation with non‐toxic oxidized products of CO 2 and N 2 [7] . Nevertheless, the bottleneck of UOR is its inherent sluggish six‐electron transfer process, which makes overall urea electrolysis still face low activity and high potential [8] . Thus, it demands highly active and earth‐abundant electrocatalysts to reduce the potential of UOR.…”
Section: Introductionmentioning
confidence: 99%