Polar bonds induced strong Pd-support electronic interaction drives remarkably enhanced oxygen reduction activity and stability

催化作用 电子转移 电解质 金属 化学 纳米颗粒 化学极性 化学工程 耐久性 材料科学 光化学 纳米技术 分子 电极 有机化学 物理化学 复合材料 工程类
作者
Qiaoling Li,Xuewei Wang,Zhihui Xie,Xingkai Peng,Lingli Guo,Xiaofei Yu,Xiaojing Yang,Zunming Lu,Xinghua Zhang,Lanlan Li
出处
期刊:Applied Catalysis B-environmental [Elsevier BV]
卷期号:305: 121020-121020 被引量:59
标识
DOI:10.1016/j.apcatb.2021.121020
摘要

The strong metal-support interaction (SMSI) effect is attractive for improving the activity and durability of metal catalyst. Here, we uncovered that the strong polar bond in support can significantly boost the electrocatalytic oxygen reduction activity and durability of Pd nanoparticles (NPs). The mass-specific activity and surface-specific activity of optimized Pd/p-BNO at 0.90 V (vs.RHE) is almost 1.9 and 2.2 times higher than that of commercial Pt/C catalyst, respectively. By means of a joint experimental and computational study, the enhanced activity of Pd/p-BNO stems from the electron directly transfer through the strong polar O B bonds from support to Pd NPs leading to the electron-rich Pd surface. Moreover, the strong bonding effect of the caused by polarity bond effectively improves the stability of Pd/p-BNO. This progress demonstrates the vital role of polar chemical bonds in support on inducing SMSI effect, which might open up new opportunities in designing superior heterogeneous catalysts. In this paper, O B bonds with larger polarity were successfully introduced to porous boron nitride support (p-BNO) to realize the electron directional transfer from the support to Pd catalyst. Benefit from the constructed SMSI effect, Pd/p-BNO catalyst displays an enhanced activity and durability in both alkaline and acidic electrolyte. • A controllable route was proposed to introduce O−B bonds to the p-BNO. • p-BNO support offers stable anchoring sites for the formation and subsequent attachment of Pd NPs. • The electron transfers from p-BNO to Pd NPs lead to an electron-rich Pd surface. • The durability of Pd is greatly enhanced due to the strong (O−B)⋯Pd interaction.
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
CipherSage的应助被牛八先生采纳,获得10
1秒前
2秒前
NexusExplorer的应助被鱼鱼鱼采纳,获得10
2秒前
云起天山发布了新的文献求助10
2秒前
2秒前
钰c完成签到,获得积分20
2秒前
littleblack发布了新的文献求助10
3秒前
兴奋的高跟鞋完成签到,获得积分10
3秒前
何晨完成签到,获得积分10
4秒前
钰c发布了新的文献求助10
4秒前
深情安青的应助被www采纳,获得10
5秒前
小菠萝完成签到 ,获得积分10
5秒前
KX发布了新的文献求助30
6秒前
6秒前
Owen的应助被Ly采纳,获得10
6秒前
紧张的宛凝完成签到 ,获得积分10
6秒前
6秒前
科研通AI6.4的应助被大气世平采纳,获得10
7秒前
7秒前
wanghh发布了新的文献求助10
7秒前
fengzhigean发布了新的文献求助10
7秒前
8秒前
8秒前
完美世界的应助被震动的牛排采纳,获得10
8秒前
无花果的应助被梨花酒采纳,获得10
8秒前
9秒前
希望天下0贩的0的应助被why采纳,获得10
10秒前
辛夷发布了新的文献求助10
10秒前
一半发布了新的文献求助10
11秒前
MAJIALE发布了新的文献求助10
11秒前
醉熏的文轩完成签到,获得积分10
12秒前
顾以白发布了新的文献求助10
12秒前
12秒前
12秒前
13秒前
qr发布了新的文献求助10
13秒前
无花果的应助被初景采纳,获得100
13秒前
sakatagintoki发布了新的文献求助10
13秒前
shine发布了新的文献求助30
13秒前
13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
Performance standards for antimicrobial disk and dilution susceptibility tests for bacteria isolated from animals 888
Rosenblum, Global Change Biology 800
Holistic Discourse Analysis, Second Edition by Robert E. Longacre (2012-09-10) 666
Final Report for the 2-D Test of Model 901 Rotor and Wing Airfoils (BSWT 592) 528
Berberine regulates the TLR4 signaling pathway to suppress hypoxia-induced proliferation and migration of pulmonary arterial smooth muscle cells 520
Organizational Behavior 510
热门求助领域 (近24小时)
化学 材料科学 医学 生物 计算机科学 工程类 纳米技术 物理 有机化学 化学工程 内科学 生物化学 复合材料 催化作用 心理学 细胞生物学 无机化学 电极 光电子学 人工智能
热门帖子
关注 科研通微信公众号,转发送积分 7885636
求助须知:如何正确求助?哪些是违规求助? 9398154
关于积分的说明 20825204
捐赠科研通 7487845
什么是DOI,文献DOI怎么找? 3356255
关于科研通互助平台的介绍 2495066
邀请新用户注册赠送积分活动 2384111