Surface oxygenation of non-oxide boosts oxidation activity on polyoxometalate subunits: An enhanced Venus flytrap mechanism

催化作用 化学 多金属氧酸盐 吸附 光化学 电子转移 离子液体 氧化还原 X射线光电子能谱 部分 无机化学 化学工程 有机化学 工程类
作者
You-wei Sun,Wenyu Long,Jian Zhang,Yanjuan Wang,Shaozheng Hu,Yixin Lian,Weizhou Jiao,Ruixin Wang,Yazhou Zhang,Haiqiang Lin,Xinping Duan
出处
期刊:Chemical Engineering Journal [Elsevier]
卷期号:470: 144272-144272 被引量:8
标识
DOI:10.1016/j.cej.2023.144272
摘要

Typically, the interfacial wettability of catalysts, coupled with electronic modulation, is vitally controlled through surface treatments that boost catalytic performance. Simulation of the biomimetic catalytic process, for instance, a Venus Flytrap mechanism, is deemed as one of the most prospective but particularly challenging protocols to achieve efficient redox catalysis. Herein, a green oxidative desulfurization (ODS) system was readily fabricated, which constituted a modular moiety ionic liquid ([Bmim]Br) triggered PW12O40 (BHPW) anchored on oxygenated graphitic carbon nitride (o-CN). The BHPW/o-CN activates the reaction at 50 °C and is almost two times higher activity than that of BHPW/CN, combined ultrastability with handy synthetic availability for the deep oxidation of carbon–sulfur (C–S) bonds. Oxygen content serves as a descriptor for the catalytic performance. We demonstrate through mimicking CS2- and thiophene-TPD that the adsorption and pre-activation of C–S bonds on the hydrophilic CN surface are critically important for proceeding ODS reaction. Further, systematic characterization containing FT-IR, XPS, and UV–vis indicates the nature of the electron acceptor raised by the oxygen moieties for a plausible mechanism of C–S bonds and spilling to reactive centers. 1H NMR and H–D isotopic exchange analysis confirm the transfer of a proton from HPW to protonated [Bmim]– functional groups triggering the active sites for C–S bonds oxidation. Additionally, density functional calculation revealed the electronic modification of the CN properties shows conclusive activation and synergistic electron transfer mechanism for C–S. The catalyst realizes deep ODS of real diesel at 70 °C with negligible decay in successive cycles. Importantly, the extension of this protocol to other non-oxide (boron nitride) and active phases (molybdenum oxide and polyoxometalates) gives to the present widespread versatility and applicability.
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
1秒前
酷波er应助威武从霜采纳,获得10
2秒前
dodo完成签到 ,获得积分10
2秒前
5秒前
量子星尘发布了新的文献求助10
6秒前
6秒前
7秒前
叶成会完成签到 ,获得积分10
8秒前
陌陌发布了新的文献求助10
11秒前
shelly7788发布了新的文献求助10
11秒前
bzlish发布了新的文献求助10
12秒前
13秒前
科研通AI6应助承一采纳,获得10
13秒前
快乐的画笔完成签到 ,获得积分10
13秒前
南知完成签到,获得积分10
14秒前
科研通AI6应助bzlish采纳,获得10
16秒前
科研通AI6应助bzlish采纳,获得10
16秒前
小马甲应助bzlish采纳,获得10
16秒前
嗷呜完成签到,获得积分10
16秒前
heart完成签到,获得积分10
17秒前
安晓慧完成签到 ,获得积分10
18秒前
19秒前
Lucas应助陌陌采纳,获得10
20秒前
20秒前
我是老大应助万物可爱采纳,获得10
24秒前
领导范儿应助v小飞侠101采纳,获得30
24秒前
24秒前
sanmu发布了新的文献求助10
25秒前
Ty完成签到,获得积分10
27秒前
29秒前
隐形曼青应助zhaojian采纳,获得10
30秒前
懦弱的安珊完成签到,获得积分10
31秒前
sanlunainiu发布了新的文献求助10
31秒前
英姑应助嘻嘻采纳,获得10
32秒前
my完成签到,获得积分10
32秒前
欣慰的山竹完成签到,获得积分10
34秒前
条条大路完成签到,获得积分10
38秒前
dragon完成签到 ,获得积分10
38秒前
丿淘丶Tao丨完成签到,获得积分10
39秒前
41秒前
高分求助中
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
Encyclopedia of Reproduction Third Edition 3000
Comprehensive Methanol Science Production, Applications, and Emerging Technologies 2000
化妆品原料学 1000
Psychology of Self-Regulation 800
1st Edition Sports Rehabilitation and Training Multidisciplinary Perspectives By Richard Moss, Adam Gledhill 600
Red Book: 2024–2027 Report of the Committee on Infectious Diseases 500
热门求助领域 (近24小时)
化学 材料科学 生物 医学 工程类 计算机科学 有机化学 物理 生物化学 纳米技术 复合材料 内科学 化学工程 人工智能 催化作用 遗传学 数学 基因 量子力学 物理化学
热门帖子
关注 科研通微信公众号,转发送积分 5642700
求助须知:如何正确求助?哪些是违规求助? 4759529
关于积分的说明 15018532
捐赠科研通 4801206
什么是DOI,文献DOI怎么找? 2566533
邀请新用户注册赠送积分活动 1524546
关于科研通互助平台的介绍 1484071