Approaching a high-rate and sustainable production of hydrogen peroxide: oxygen reduction on Co–N–C single-atom electrocatalysts in simulated seawater DOI
Qinglan Zhao, Yian Wang, Wei‐Hong Lai

et al.

Energy & Environmental Science, Journal Year: 2021, Volume and Issue: 14(10), P. 5444 - 5456

Published: Jan. 1, 2021

Sustainable production of H 2 O is boosted by oxygen reduction reaction on Co–N 5 sites in a flow cell simulated seawater.

Language: Английский

Intrinsic Electrocatalytic Activity Regulation of M–N–C Single‐Atom Catalysts for the Oxygen Reduction Reaction DOI
Zhao Chang-xin, Bo‐Quan Li, Jia‐Ning Liu

et al.

Angewandte Chemie International Edition, Journal Year: 2020, Volume and Issue: 60(9), P. 4448 - 4463

Published: April 21, 2020

Abstract Single‐atom catalysts (SACs) with highly active sites atomically dispersed on substrates exhibit unique advantages regarding maximum atomic efficiency, abundant chemical structures, and extraordinary catalytic performances for multiple important reactions. In particular, M–N–C SACs (M=transition metal atom) demonstrate optimal electrocatalytic activity the oxygen reduction reaction (ORR) have attracted extensive attention recently. Despite substantial efforts in fabricating various SACs, principles regulating intrinsic of their not been sufficiently studied. this Review, we summarize regulation strategies promoting ORR by modulation center atoms, coordinated environmental guest groups. Theoretical calculations experimental investigations are both included to afford a comprehensive understanding structure–performance relationship. Finally, future directions developing advanced other analogous reactions proposed.

Language: Английский

Citations

589

Simultaneously Achieving High Activity and Selectivity toward Two-Electron O2 Electroreduction: The Power of Single-Atom Catalysts DOI
Xiangyu Guo, Shiru Lin, Jinxing Gu

et al.

ACS Catalysis, Journal Year: 2019, Volume and Issue: 9(12), P. 11042 - 11054

Published: Sept. 23, 2019

On-site production of hydrogen peroxide (H2O2) using electrochemical methods could be more efficient than the current industrial process. However, due to existence scaling relations for adsorption reaction intermediates, there is a long established trade-off between activity and selectivity catalysts, as enhancement catalytic typically accompanied by four-electron O2 reduction (ORR), leading reduced H2O2 production. Herein, means density functional theory (DFT) computations, we reported feasibility several classes important representative experimentally achievable single-atom catalysts (SACs) toward two-electron ORR, paying attention their stability, selectivity, at acidic medium. Starting from 210 two-dimensional (2D) SACs, demonstrated that 31 SACs have potential break metal-based simultaneously achieve high screened out 7 with higher PtHg4 in media. Especially, noble metal-free SAC, namely, single Zn atom centered phthalocyanine (Zn@Pc-N4), has remarkable improvement small overpotential 0.15 V. Moreover, multivariable analysis machine-learning techniques, provided comprehensive understanding underlying origin unveiled intrinsic correlations structure performance. This work may pave way design discovery promising materials

Language: Английский

Citations

432

Tailoring Selectivity of Electrochemical Hydrogen Peroxide Generation by Tunable Pyrrolic‐Nitrogen‐Carbon DOI
Laiquan Li, Cheng Tang, Yao Zheng

et al.

Advanced Energy Materials, Journal Year: 2020, Volume and Issue: 10(21)

Published: April 17, 2020

Abstract The electrochemical reduction of O 2 via a two‐electron reaction pathway to H provides possibility for replacing the current anthraquinone process, enabling sustainable and decentralized production. Here, nitrogen‐rich few‐layered graphene (N‐FLG) with tunable nitrogen configuration is developed generation. A positive correlation between content pyrrolic‐N selectivity experimentally observed. critical role elucidated by variable intermediate adsorption profiles as well dependent negative shifts peak on X‐ray near edge structure spectra. By virtue optimized N doping unique porous structure, as‐fabricated N‐FLG electrocatalyst exhibits high toward synthesis superior long‐term stability. To achieve high‐value products both anode cathode energy efficiency, practical device coupling generation furfural oxidation assembled, simultaneously yield rate at (9.66 mol h −1 g cat ) 2‐furoic acid (2.076 m −2 under small cell voltage 1.8 V.

Language: Английский

Citations

403

Theory-oriented screening and discovery of advanced energy transformation materials in electrocatalysis DOI Creative Commons
Hongyu Jing, Peng Zhu, Xiaobo Zheng

et al.

Advanced Powder Materials, Journal Year: 2021, Volume and Issue: 1(1), P. 100013 - 100013

Published: Nov. 15, 2021

Various metal-based electrocatalysts from nanocrystals, to clusters and single-atoms, have been well-discovered towards high-efficient power devices electrocatalytic conversion. To accelerate energy transformation materials discovery, developing high-throughput DFT calculations machine-learning techniques is of great necessity. This review comprehensively outlines the latest progress theory-guided design advanced materials. Especially, we focus on study single atoms in various devices, such as fuel cell (oxygen reduction reaction, ORR; acid oxidation reaction; alcohol reaction), other reactions for energy-related conversion small molecules, H2O2 evolution (2e− ORR), water splitting (H2 reaction/O2 HER/OER), N2 reaction (NRR), CO2 (CO2RR). Firstly, electronic structure, interaction mechanism, activation path are discussed provide an overall blueprint electrocatalysis batteries mentioned above. Thereafter, experimental synthesis strategies, structural recognition, performance figured out. Finally, some viewpoints into current issues future concept provided.

Language: Английский

Citations

376

A Review on Challenges and Successes in Atomic-Scale Design of Catalysts for Electrochemical Synthesis of Hydrogen Peroxide DOI

Samira Siahrostami,

Santiago Jimenez-Villegas,

Amir Hassan Bagherzadeh Mostaghimi

et al.

ACS Catalysis, Journal Year: 2020, Volume and Issue: 10(14), P. 7495 - 7511

Published: June 10, 2020

Hydrogen peroxide is a valuable chemical oxidant with wide range of applications in variety industrial processes, especially water sanitization. Electrochemical synthesis hydrogen (H2O2) through two-electron oxygen reduction reaction (2e-ORR) or oxidation (2e-WOR) has emerged as an appealing process for onsite production this chemically oxidant. On-site produced H2O2 can be applied wastewater treatment remote locations any where needed oxidizing agent. This Review studies the theoretical efforts understanding challenges catalysis electrochemical well providing design principles more efficient catalyst materials.

Language: Английский

Citations

374

Confined local oxygen gas promotes electrochemical water oxidation to hydrogen peroxide DOI
Chuan Xia, Seoin Back, Stefan Ringe

et al.

Nature Catalysis, Journal Year: 2020, Volume and Issue: 3(2), P. 125 - 134

Published: Jan. 6, 2020

Language: Английский

Citations

358

Highly active and selective oxygen reduction to H2O2 on boron-doped carbon for high production rates DOI Creative Commons
Xia Yang, Xunhua Zhao, Chuan Xia

et al.

Nature Communications, Journal Year: 2021, Volume and Issue: 12(1)

Published: July 9, 2021

Abstract Oxygen reduction reaction towards hydrogen peroxide (H 2 O ) provides a green alternative route for H production, but it lacks efficient catalysts to achieve high selectivity and activity simultaneously under industrial-relevant production rates. Here we report boron-doped carbon (B-C) catalyst which can overcome this activity-selectivity dilemma. Compared the state-of-the-art oxidized catalyst, B-C presents enhanced (saving more than 210 mV overpotential) currents (up 300 mA cm −2 while maintaining (85–90%). Density-functional theory calculations reveal that boron dopant site is responsible due low thermodynamic kinetic barriers. Employed in our porous solid electrolyte reactor, demonstrates direct continuous generation of pure solutions with 95%) partial ~400 ), illustrating catalyst’s great potential practical applications future.

Language: Английский

Citations

352

High-Concentration Single Atomic Pt Sites on Hollow CuSx for Selective O2 Reduction to H2O2 in Acid Solution DOI Creative Commons

Rongan Shen,

Wenxing Chen, Qing Peng

et al.

Chem, Journal Year: 2019, Volume and Issue: 5(8), P. 2099 - 2110

Published: May 23, 2019

Language: Английский

Citations

347

Recent Progress of Electrochemical Production of Hydrogen Peroxide by Two‐Electron Oxygen Reduction Reaction DOI Creative Commons
Nan Wang,

Shaobo Ma,

Pengjian Zuo

et al.

Advanced Science, Journal Year: 2021, Volume and Issue: 8(15)

Published: May 27, 2021

Shifting electrochemical oxygen reduction reaction (ORR) via two-electron pathway becomes increasingly crucial as an alternative/green method for hydrogen peroxide (H2 O2 ) generation. Here, the development of 2e- ORR catalysts in recent years is reviewed, aspects mechanism exploration, types high-performance catalysts, factors to influence catalytic performance, and potential applications ORR. Based on previous theoretical experimental studies, underlying firstly unveiled, aspect pathway, thermodynamic free energy diagram, limiting potential, volcano plots. Then, various efficient producing H2 are summarized. Additionally, active sites catalysts' such electronic structure, carbon defect, functional groups (O, N, B, S, F etc.), synergistic effect, others (pH, pore steric hindrance etc.) discussed. The electrogeneration also has wastewater treatment, disinfection, organics degradation, storage. Finally, future directions prospects electrochemically examined. These insights may help develop highly active/selective shape application this method.

Language: Английский

Citations

327

Promoting H2O2 production via 2-electron oxygen reduction by coordinating partially oxidized Pd with defect carbon DOI Creative Commons
Qiaowan Chang, Pu Zhang,

Amir Hassan Bagherzadeh Mostaghimi

et al.

Nature Communications, Journal Year: 2020, Volume and Issue: 11(1)

Published: May 1, 2020

Abstract Electrochemical synthesis of H 2 O through a selective two-electron (2e − ) oxygen reduction reaction (ORR) is an attractive alternative to the industrial anthraquinone oxidation method, as it allows decentralized production. Herein, we report that synergistic interaction between partially oxidized palladium (Pd δ+ and oxygen-functionalized carbon can promote 2e ORR in acidic electrolytes. An electrocatalyst synthesized by solution deposition amorphous Pd clusters 3 4 onto mildly nanotubes -OCNT) shows nearly 100% selectivity toward positive shift onset potential ~320 mV compared with OCNT substrate. A high mass activity (1.946 mg −1 at 0.45 V) -OCNT achieved. Extended X-ray absorption fine structure characterization density functional theory calculations suggest nearby oxygen-containing groups key for ORR.

Language: Английский

Citations

310