Bifunctional hydroxyl group over polymeric carbon nitride to achieve photocatalytic H2O2 production in ethanol aqueous solution with an apparent quantum yield of 52.8% at 420 nm

2019 ◽  
Vol 55 (88) ◽  
pp. 13279-13282 ◽  
Author(s):  
Weishu Hou ◽  
Yunxiang Li ◽  
Shuxin Ouyang ◽  
Huayu Chen ◽  
Jinhua Ye ◽  
...  

Hydroxyl group modified polymeric carbon nitride achieves efficient photoreduction of O2 to H2O2 and highly selective photooxidization of C2H5OH simultaneously.

2015 ◽  
Vol 51 (65) ◽  
pp. 12935-12938 ◽  
Author(s):  
Yoshihisa Sakata ◽  
Takuya Hayashi ◽  
Ryō Yasunaga ◽  
Nobuyuki Yanaga ◽  
Hayao Imamura

Remarkably high photocatalytic activity for the overall H2O splitting was achieved by utilizing a Rh0.5Cr1.5O3(Rh; 0.5 wt%)/Zn(3 mol%)–Ga2O3 photocatalyst when Ga2O3 was prepared using dilute CaCl2 aqueous solution (0.001 mol l−1).


2021 ◽  
Vol 12 (1) ◽  
Author(s):  
Yubao Zhao ◽  
Peng Zhang ◽  
Zhenchun Yang ◽  
Lina Li ◽  
Jingyu Gao ◽  
...  

AbstractSolar-driven hydrogen peroxide (H2O2) production presents unique merits of sustainability and environmental friendliness. Herein, efficient solar-driven H2O2 production through dioxygen reduction is achieved by employing polymeric carbon nitride framework with sodium cyanaminate moiety, affording a H2O2 production rate of 18.7 μmol h −1 mg−1 and an apparent quantum yield of 27.6% at 380 nm. The overall photocatalytic transformation process is systematically analyzed, and some previously unknown structural features and interactions are substantiated via experimental and theoretical methods. The structural features of cyanamino group and pyridinic nitrogen-coordinated soidum in the framework promote photon absorption, alter the energy landscape of the framework and improve charge separation efficiency, enhance surface adsorption of dioxygen, and create selective 2e− oxygen reduction reaction surface-active sites. Particularly, an electronic coupling interaction between O2 and surface, which boosts the population and prolongs the lifetime of the active shallow-trapped electrons, is experimentally substantiated.


2020 ◽  
Author(s):  
Yubao Zhao ◽  
Jingyu Gao ◽  
Lina Li ◽  
Sheng Chen ◽  
Chun Hu ◽  
...  

Abstract Solar-driven hydrogen peroxide (H2O2) production presents unique merits of sustainability and environmental friendliness. Herein, highly efficient solar-driven H2O2 production through dioxygen reduction is achieved by employing polymeric carbon nitride (PCN) framework with sodium cyanaminate moiety (PCN-NaCA), affording a superior H2O2 production rate of 175 μmol/h on 10 mg photocatalyst and a notable apparent quantum yield of 27.6% at 380 nm. The overall photocatalytic transformation process is systematically analyzed using various steady-state/transient spectroscopic and computational methods. The presence of sodium cyanaminate moiety in PCN-NaCA induces the following multiple effects: enhancing photon absorption, creating the coexistence of p-type and n-type domains, strengthening surface adsorption of dioxygen, and favoring highly selective 2e− ORR. In particular, the adsorption of dioxygen on PCN-NaCA enhances the population and lifetime of trapped electrons in the ps-ns time regime, which should have a notable synergic effect on oxygen reduction process.


2019 ◽  
Vol 7 (13) ◽  
pp. 7373-7379 ◽  
Author(s):  
Xuezhong Gong ◽  
Sijia Yu ◽  
Meili Guan ◽  
Xianglin Zhu ◽  
Can Xue

Covalently grafting pyrene groups on polymeric carbon nitride enables photocatalytic CO2 reduction in aqueous solution with simultaneous alkene oxidation in organic phase.


2021 ◽  
Author(s):  
Linjuan Pei ◽  
Hao Tan ◽  
Meixian Liu ◽  
Ruiyi Wang ◽  
Xianmo Gu ◽  
...  

Regulating the surface properties of catalysts to control the selectivity of reaction is fascinating. The bulk polymeric carbon nitride exhibited poor N-phenylhydroxylamine yield in nitrobenzene reduction reaction mainly due to...


2018 ◽  
Author(s):  
Chaofeng Huang ◽  
Jing Wen ◽  
Yanfei Shen ◽  
Fei He ◽  
Li Mi ◽  
...  

<a></a><a>As a metal-free conjugated polymer, carbon nitride (CN) has attracted tremendous attention as heterogeneous (photo)catalysts. </a><a></a><a>By following prototype of enzymes, making all catalytic sites of accessible via homogeneous reactions is a promising approach toward maximizing CN activity, but hindered due to </a><a></a><a>the poor insolubility of CN</a>. Herein, we report the dissolution of CN in environment-friendly methane sulfonic acid and the homogeneous photocatalysis driven by CN for the first time with the activity boosted up to 10-times, comparing to the heterogeneous counterparts. Moreover, facile recycling and reusability, the <a>hallmark</a> of heterogeneous catalysts, were kept for the homogeneous CN photocatalyst via reversible precipitation using poor solvents. It opens new vista of CN in homogeneous catalysis and offers a successful example of polymeric catalysts in bridging gaps of homo/heterogeneous catalysis.


2019 ◽  
Author(s):  
Zhengyuan Jin ◽  
Xiantao Jiang ◽  
Qitao Zhang ◽  
Shaolong Huang ◽  
Luhong Zhang ◽  
...  

ChemSusChem ◽  
2020 ◽  
Vol 13 (14) ◽  
pp. 3605-3613 ◽  
Author(s):  
Qin Lei ◽  
Rongzhi Chen ◽  
Yurong Zhao ◽  
Huanyu Chen ◽  
Xinxin Long ◽  
...  

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