Low‐Spin Fe3+ Evoked by Multiple Defects with Optimal Intermediate Adsorption Attaining Unparalleled Performance in Water Oxidation DOI Open Access
Yihao Wang, Shanqing Li, Xu Hou

et al.

Advanced Materials, Journal Year: 2024, Volume and Issue: unknown

Published: Nov. 14, 2024

Abstract Electrocatalytic water splitting is long constrained by the sluggish kinetics of anodic oxygen evolution reaction (OER), and rational spin‐state manipulation holds great promise to break through this bottleneck. Low‐spin Fe 3+ (LS, t 2g 5 e g 0 ) species are identified as highly active sites for OER in theory, whereas it still a formidable challenge construct experimentally. Herein, new strategy demonstrated effective construction LS NiFe‐layered double hydroxide (NiFe‐LDH) introducing multiple defects, which induce coordination unsaturation over thus enlarge their d orbital energy. The as‐obtained catalyst exhibits extraordinary performance with an ultra‐low overpotential 244 mV at industrially required current density 500 mA cm −2 , 110 lower than that conventional NiFe‐LDH high‐spin (HS, 3 2 superior most previously reported NiFe‐based catalysts. Comprehensive experimental theoretical studies reveal configuration effectively reduces adsorption strength O* intermediate compared HS case, thereby altering rate‐determining step from (O* → OOH*) (OH* O*) lowering its energy barrier. This work paves avenue developing efficient spin‐dependent electrocatalysts beyond.

Language: Английский

A critical review on correlating active sites, oxidative species and degradation routes with persulfate-based antibiotics oxidation DOI
Ning Li, Jingya Ye,

Haoxi Dai

et al.

Water Research, Journal Year: 2023, Volume and Issue: 235, P. 119926 - 119926

Published: March 27, 2023

Language: Английский

Citations

187

High-spin Co3+ in cobalt oxyhydroxide for efficient water oxidation DOI Creative Commons
Xin Zhang, Haoyin Zhong, Qi Zhang

et al.

Nature Communications, Journal Year: 2024, Volume and Issue: 15(1)

Published: Feb. 15, 2024

Abstract Cobalt oxyhydroxide (CoOOH) is a promising catalytic material for oxygen evolution reaction (OER). In the traditional CoOOH structure, Co 3+ exhibits low-spin state configuration ( $${t}_{2{{{{{\rm{g}}}}}}}^{6}{e}_{{{{{{\rm{g}}}}}}}^{0}$$ t 2 g 6 e 0 ), with electron transfer occurring in face-to-face $${t}_{2{{{{{\rm{g}}}}}}}^{*}$$ * orbitals. this work, we report successful synthesis of high-spin by introducing coordinatively unsaturated atoms. As compared to CoOOH, occurs apex-to-apex $${e}_{{{{{{\rm{g}}}}}}}^{*}$$ orbitals, which faster ability. result, performs superior OER activity an overpotential 226 mV at 10 mA cm −2 , 148 lower than that CoOOH. This work emphasizes effect spin on based electrocatalysts water splitting, and thus provides new strategy designing highly efficient electrocatalysts.

Language: Английский

Citations

63

Dual-site segmentally synergistic catalysis mechanism: boosting CoFeSx nanocluster for sustainable water oxidation DOI Creative Commons

Siran Xu,

Sihua Feng,

Yue Yu

et al.

Nature Communications, Journal Year: 2024, Volume and Issue: 15(1)

Published: Feb. 26, 2024

Abstract Efficient oxygen evolution reaction electrocatalysts are essential for sustainable clean energy conversion. However, catalytic materials followed the conventional adsorbate mechanism (AEM) with inherent scaling relationship between key intermediates *OOH and *OH, or lattice-oxygen-mediated (LOM) possible lattice migration structural reconstruction, which not favorable to balance high activity stability. Herein, we propose an unconventional Co-Fe dual-site segmentally synergistic (DSSM) single-domain ferromagnetic catalyst CoFeS x nanoclusters on carbon nanotubes (CNT) (CFS-ACs/CNT), can effectively break without sacrificing Co 3+ (L.S, t 2g 6 e g 0 ) supplies strongest OH* adsorption energy, while Fe (M.S, 4 1 exposes strong O* adsorption. These dual-sites synergistically produce of Co-O-O-Fe intermediates, thereby accelerating release triplet-state ( ↑ O = ). As predicted, prepared CFS-ACs/CNT exhibits less overpotential than that commercial IrO 2 , as well approximately 633 h stability significant potential loss.

Language: Английский

Citations

58

Unveiling the Electrolyte Cations Dependent Kinetics on CoOOH‐Catalyzed Oxygen Evolution Reaction DOI

Hongnan Jia,

Na Yao, Can Yu

et al.

Angewandte Chemie International Edition, Journal Year: 2023, Volume and Issue: 62(49)

Published: Oct. 21, 2023

The electrolyte cations-dependent kinetics have been widely observed in many fields of electrocatalysis, however, the exact mechanism influence on catalytic performance is still a controversial topic considerable discussion. Herein, combined with operando X-ray diffraction (XRD) and high-resolution transmission electron microscopy (HRTEM), we verify that cations could intercalate into layer pristine CoOOH catalyst during oxygen evolution reaction (OER) process, while bigger lead to enlarged interlayer spacing increased OER activity, following order Cs+ >K+ >Na+ >Li+ . absorption spectroscopy (XAS), situ Raman, Ultraviolet-visible (UV/Vis) spectroscopy, XAS cyclic voltammetry (CV), theoretical calculations reveal intercalation efficiently modify oxidation states Co by enlarging Co-O bonds, which turn enhance d-band center Co, optimize adsorption strength intermediates, facilitate formation active Co(IV) species, reduce energy barrier rate-determing step (RDS), thereby enhancing activity. This work not only provides an informative picture understand complicated dependence cations, but also sheds light understanding other cation-targeted electrocatalysis.

Language: Английский

Citations

56

Advanced Architectures of Air Electrodes in Zinc–Air Batteries and Hydrogen Fuel Cells DOI Open Access

Longbin Li,

Xiannong Tang,

Bing Wu

et al.

Advanced Materials, Journal Year: 2023, Volume and Issue: 36(13)

Published: Oct. 12, 2023

The air electrode is an essential component of air-demanding energy storage/conversion devices, such as zinc-air batteries (ZABs) and hydrogen fuel cells (HFCs), which determines the output power stability devices. Despite atom-level modulation in catalyst design being recently achieved, electrodes have received much less attention, causing a stagnation development equipment. Herein, evolution for ZABs HFCs from early stages to current requirements reviewed. In addition, operation mechanism corresponding electrocatalytic mechanisms are summarized. particular, by clarifying interfaces at different scales, several approaches improve rechargeable reviewed, including innovative structures bifunctional oxygen catalysts. Afterward, operating proton-exchange-membrane (PEMFCs) anion-exchange-membrane (AEMFCs) explained. Subsequently, strategies employed enhance efficiency membrane assembly (MEA) PEMFCs AEMFCs, respectively, highlighted discussed detail. Last, prospects considered discussing main challenges. aim this review facilitate industrialization HFCs.

Language: Английский

Citations

44

Electronic structure regulation of the Fe-based single-atom catalysts for oxygen electrocatalysis DOI
Xiaochen Wang,

Zhiwen Kang,

Dan Wang

et al.

Nano Energy, Journal Year: 2024, Volume and Issue: 121, P. 109268 - 109268

Published: Jan. 9, 2024

Language: Английский

Citations

40

Ambient Electrochemical Ammonia Synthesis: From Theoretical Guidance to Catalyst Design DOI Creative Commons

Jianjia Mu,

Xuan‐Wen Gao,

Tong Yu

et al.

Advanced Science, Journal Year: 2024, Volume and Issue: 11(15)

Published: Feb. 12, 2024

Abstract Ammonia, a vital component in the synthesis of fertilizers, plastics, and explosives, is traditionally produced via energy‐intensive environmentally detrimental Haber–Bosch process. Given its considerable energy consumption significant greenhouse gas emissions, there growing shift toward electrocatalytic ammonia as an eco‐friendly alternative. However, developing efficient electrocatalysts capable achieving high selectivity, Faraday efficiency, yield under ambient conditions remains challenge. This review delves into decades‐long research synthesis, highlighting evolution fundamental principles, theoretical descriptors, reaction mechanisms. An in‐depth analysis nitrogen reduction (NRR) nitrate (NitRR) provided, with focus on their electrocatalysts. Additionally, theories behind electrocatalyst design for are examined, including Gibbs free approach, Sabatier principle, d ‐band center theory, orbital spin states. The culminates comprehensive overview current challenges prospective future directions development NRR NitRR, paving way more sustainable methods production.

Language: Английский

Citations

32

Spin states of metal centers in electrocatalysis DOI Creative Commons
Yuwei Zhang, Qian Wu, Justin Zhu Yeow Seow

et al.

Chemical Society Reviews, Journal Year: 2024, Volume and Issue: 53(16), P. 8123 - 8136

Published: Jan. 1, 2024

This tutorial review provides a comprehensive introduction to the spin state of metal centers and its role in electrocatalysis.

Language: Английский

Citations

27

Synergistic promotion of electrocatalytic activities and multilevel descriptors in nitrogen-doped graphene supported dual-atom catalysts for lithium-sulfur batteries DOI

Xingjia Chen,

Haifeng Lv, Xiaojun Wu

et al.

Energy storage materials, Journal Year: 2024, Volume and Issue: 65, P. 103187 - 103187

Published: Jan. 10, 2024

Language: Английский

Citations

20

Optimizing photocatalysis via electron spin control DOI Creative Commons
Shaoxiong He, Yanxi Chen, Jingyun Fang

et al.

Chemical Society Reviews, Journal Year: 2025, Volume and Issue: unknown

Published: Jan. 1, 2025

This review systematically summarizes recent advanced strategies for manipulating electron spin to optimize photocatalysis. It provides valuable insights guide future research on control enhancing photocatalytic applications.

Language: Английский

Citations

4