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光催化H2O2生成
CHEMICAL ENGINEERING JOURNAL · 2023 · IF 15.1

Dual P-doped-site modified porous g-C3N4 achieves high dissociation and mobility efficiency for photocatalytic H2O2 production

Guiyang Yu,Ke Gong,Chuanwang Xing,Lan Hu,Haibin Huang,Lejie Gao,Debao Wang,Xiyou Li

Organic semiconductor under photoexcitation could generate abundant strong-binding Frenkel excitons and inevitably suffer from low dissociation efficiency (<1%) and poor mobility ability, which severely suppresses the efficient utilization of photogenerated charges and corresponding activity. Herein, a dual P-doping strategy is proposed in bay and corner sites implanted polymeric carbon nitride (PCN-D) for visible-driven H 2 O 2 production. The dual P doping breaks localized electron state around original symmetric heptazine units and weakens the binding energy between electrons and holes, increasing dissociation efficiency to reach 11.9% with 20-fold improvement. In addition, the conductivity ability of PCN-D, including formed carrier charge concentration and mobility, achieves 13-fold and 7-fold improvement, which facilitates the charge transfer and separation. The proposed dual doped-P-site strategy, with the blessing of porous structure, provides plentiful active center for effective adsorption and activation of O 2 molecule, further accelerating reaction progress and achieving six-times increase of photocatalytic H 2 O 2 production rate. This work provides in-depth insight into the importance of dual P-doping to optimize kinetic behavior of photogenerated charges and opens an avenue to the multiscale doping-modulation of semiconductor with high efficiency solar energy conversion.

研究领域: 材料科学 · 化学 · 光化学 · 催化
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ADVANCED FUNCTIONAL MATERIALS · 2025 · IF 19

Pyridine Heterocycle Driven Microenvironment Regulation of β-Ketoenamine COFs for Enhanced Photocatalytic H2O2 Production

Bihong Chen,Yuehua Pan,Yuxiang Deng,Yunhao Hou,Haixuan Liang,Nannan Wang,Jun Luo,Kai Chen,Xinpeng Wang

Pyridine heterocyclic covalent organic frameworks (COFs) have attracted widespread attention in the field of photo-driven hydrogen peroxide (H 2 O 2 ) synthesis due to their unique optoelectronic properties and excellent electron affinity. In this study, the microenvironment change of COFs is achieved through the system regulation of pyridine content in its skeleton. Among these COFs, the bipyridine-structured TpDaBp exhibits the best visible-light-driven H 2 O 2 evolution rate of 8156 µmol g −1 h −1 and reveals significant potential for photocatalytic uranium extraction, attributed to its enhanced π–π interactions, improved optoelectronic performance, and enlarged specific surface area. This work not only provided a new strategy for further designing novel pyridine N-heterocyclic-based COFs but also shows its novel advantages of application.

研究领域: 材料科学 · 光催化 · 有机化学 · 能源化学 · 环境修复
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JOURNAL OF PHOTOCHEMISTRY AND PHOTOBIOLOGY A-CHEMISTRY · 2025 · IF 4.7

Self-regenerative Co2+/Co3+ mediation in Co-doped CdIn2S4 superstructures enables efficient sacrificial-agent-free H2O2 photogeneration

Yun Deng,Shukui Shi,Di Zhao,Mohan Zu,Lu Pang,Xin Li,Zhihao Du,Xiaoli Jin,Zhengdao Li,Fengyun Su,Haiquan Xie

Photocatalytic H 2 O 2 production suffers from severe charge recombination and sacrificial agent dependency. Hydrangea-like Co-doped CdIn 2 S 4 superstructures (Co/CIS (HD)) synthesized via hydrothermal method exhibit hierarchical porous architecture that enhances light harvesting and reactant diffusion. Atomic Co doping introduces mixed-valence Co 2+ /Co 3+ species, reducing the work function from 6.287 to 5.896 eV and extending carrier lifetime. The dual-valent system establishes a self-regenerative redox cycle where Co 3+ mediates photogenerated electron transfer for O 2 activation while Co 2+ scavenges holes to suppress recombination and photocorrosion. Without sacrificial agents, the optimized 6.5-Co/CIS (HD) achieves an exceptional H 2 O 2 production rate of 1952 μmol g −1  h −1 under visible light, 6.33 times higher than pristine CdIn 2 S 4 . The catalyst maintains structural stability over five cycles due to dynamic Co 2+ /Co 3+ regeneration. This work provides a strategic design for efficient photocatalytic H 2 O 2 synthesis via synergistic morphological and electronic engineering.

研究领域: 材料科学 · 光催化 · 环境化学 · 能量转换 · 纳米材料
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INTERNATIONAL JOURNAL OF HYDROGEN ENERGY · 2024 · IF 8.1

Construction of visible-light-response K, Na doped g-C3N4/FeOCl photocatalysis-self-Fenton system for pollutants degradation in water

Lina Wang,Hanpei Yang,Qiangshun Wu,Rui Ma

Photocatalysis-self-Fenton system, integrating photocatalysis with Fenton technology, emerge as promising approaches for environmental remediation. In this study, we introduced K, Na doped g-C 3 N 4 /FeOCl (DCN/FeOCl) catalyst, where amino groups on the DCN surface interacted with unsaturated Fe on FeOCl, forming Fe–N bonds and a Z-scheme heterojunction . The resulting DCN/FeOCl demonstrated efficient H 2 O 2 production and rapid tetracycline (TC) degradation under visible light. The Z-scheme heterojunction and nitrogen vacancy enhanced electron-hole pair separation and O 2 adsorption. Additionally, we proposed a mechanism for dual-channel photocatalytic H 2 O 2 production. This work presents a novel strategy for in-situ H 2 O 2 production and activation, facilitating water decontamination .

CAS / MDL: 85721-33-1
研究领域: 环境科学 · 材料科学 · 化学工程
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JOURNAL OF HAZARDOUS MATERIALS · 2020 · IF 9.038

Carbon nitride-doped melamine-silver adsorbents with peroxidase-like catalysis and visible-light photocatalysis: Colorimetric detection and detoxification removal of total mercury

Mengyuan Yin,Yuqi Wan,Shuai Li,Xiaoting Zhao,Wenwen Zhang,Yun Zhang,Hua Wang

Mesoporous melamine-silver (MA-Ag) nanocomposites doped with carbon nitride quantum dots (CN QDs ) were fabricated simply by the controlled supramolecular self-assembly. It was discovered that the resulting nanoflower-like CN QDs @MA-Ag nanocomposites could exhibit the peroxidase-like catalysis, which could be specifically enhanced by Hg 2+ by forming [email protected] alloys. A double catalysis-based colorimetric method was thereby developed for the fast detecting of Hg 2+ and Hg 0 in wastewater samples, with the levels down to 0.050 nM and 18.3 nM, respectively. Moreover, strong visible-light-driven photocatalysis of the nanocomposites was demonstrated for oxidizing Hg 0 into Hg 2+ through photocatalytic H 2 O 2 production so as to realize the detoxification of Hg 0 in the environmental wastewater. Besides, the fabricated mesoporous CN QDs @MA-Ag nanocomposites with large specific surface areas might facilitate the high Hg adsorption through the powerful MA-Hg chelate interaction, showing the efficient adsorption and/or removal of total Hg. The catalysis-selective colorimetric analysis and photocatalysis-based detoxification removal of total mercury may promise for wide applications in the environmental monitoring and wastewater treatment of toxic heavy metals of mercury.

研究领域: 环境科学 · 纳米技术 · 分析化学 · 材料科学 · 废水处理
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