电子转移
异质结
人工光合作用
催化作用
质子耦合电子转移
光化学
化学
光催化
光合作用
制氢
纳米技术
分解水
析氧
电子
电子传输链
过氧化氢
可再生能源
电子供体
氧化还原
材料科学
质子
化学工程
降级(电信)
过程(计算)
光合反应中心
生产(经济)
反应机理
太阳能
超氧化物
电子空穴
能量转换
电化学
太阳能转换
作者
Zheng Wang,Guixiang Ding,Chunxue Li,Hongwei Huang,Yuwei Xiao,Zihe Chen,Juntao Zhang,Hang Xiao,Zheng Wang,Lihui Chen,Li Shuai,Yonghao Ni,Guangfu Liao
出处
期刊:eScience
[Elsevier BV]
日期:2026-03-01
卷期号:: 100562-100562
被引量:5
标识
DOI:10.1016/j.esci.2026.100562
摘要
Artificial photosynthesis offers a sustainable route for hydrogen peroxide (H 2 O 2 ) production, yet its practical efficacy is heavily constrained by two pivotal challenges: the photogenerated charges undergo rapid recombination and oxidation reaction (ORR) proceeds with sluggish kinetics. S-scheme heterojunctions address the first challenge by enhancing charge separation, but their H 2 O 2 production remains limited by inefficient proton transfer that restricts the critical proton-coupled electron transfer (PCET), process underlying ORR. To overcome this remaining limitation, the introduction of carboxyl-functionalized cellulose nanofibril (f-CNF), synergizes the intrinsic merits of biomass-derived materials with enhanced proton-donating capability and tailored interfacial interactions, thereby promoting PCET and resolving the inefficient proton supply of S-scheme heterojunctions. Herein, we exhibit a hydrogen-bonding network via engineering CdS/g-C 3 N 4 (CdS/PCN) S‐scheme heterojunction with f-CNF molecular for non-sacrificial H 2 O 2 production through accelerated PCET process. In pure water systems, the catalyst presents an exceptional photocatalytic activity of 2867 μmol L −1 h −1 , which is superior to state-of-the-art photocatalysts. The impressive performance is primarily ascribed to the synergistic effect arising from the CdS/PCN S-scheme mechanism and the molecular engineering of biomass-derived CNFs, which collectively boost the supplement and combination of electrons and protons, lower the reaction energy barrier of *OOH intermediate, and accelerate the conversion of superoxide conversion. This significantly accelerates the PCET process for further superior H 2 O 2 photosynthesis. This breakthrough supplies a perspective to markedly elevate photocatalytic performance and bears substantial implications for the sustainable, large-scale photosynthetic production of H 2 O 2 . • A hydrogen-bonding network was constructed by engineering CdS/PCN with f-CNF. • The catalyst exhibited a high photocatalytic activity of 2867 μmol L −1 h −1 in pure water. • The synergistic effect arises from the CdS/PCN S-scheme mechanism and molecular engineering of CNFs. • Synergistic effect accelerates PCET process, enabling superior H 2 O 2 photosynthesis.
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