scispace - formally typeset
B

Baishu Zheng

Researcher at Hunan University of Science and Technology

Publications -  56
Citations -  2306

Baishu Zheng is an academic researcher from Hunan University of Science and Technology. The author has contributed to research in topics: Catalysis & Adsorption. The author has an hindex of 21, co-authored 50 publications receiving 1926 citations. Previous affiliations of Baishu Zheng include Nanjing University.

Papers
More filters
Journal ArticleDOI

Enhanced CO2 Binding Affinity of a High-Uptake rht-Type Metal-Organic Framework Decorated with Acylamide Groups

TL;DR: An rht-type metal-organic framework prepared from M(2)(carboxylate)(4) (M = Cu, Co) paddlewheel clusters and a flexible C(3)-symmetric hexacarboxylates ligand with acylamide groups exhibits larger CO(2) uptake, an enhanced heat of adsorption, and higher selectivity toward CO(1)/N(2).
Journal ArticleDOI

High and selective CO2 capture by two mesoporous acylamide-functionalized rht-type metal–organic frameworks

TL;DR: Two mesoporous and flexible acylamide-functionalized rht-type MOFs exhibit not only high excess unsaturation CO(2) uptake at 20 bar and 273 K, but also good selectivity of CO( 2)/CH(4) andCO(2)/N(2), confirmed by GCMC and first-principles calculations.
Journal ArticleDOI

Highly selective CO2 capture of an agw-type metal-organic framework with inserted amides: experimental and theoretical studies.

TL;DR: An amide-inserted metal-organic framework (NJU-Bai3) presents high storage and high selectivity toward CO(2) and combines these two interesting characters which strongly support the expectation that amide groups can significantly enhance the CO( 2) binding ability and selectivity of MOFs.
Journal ArticleDOI

Porous NbO-type metal–organic framework with inserted acylamide groups exhibiting highly selective CO2 capture

TL;DR: In this paper, a new expanded microporous NbO-type metal-organic framework with inserted acylamide groups was designed and synthesized, which showed both a large CO2-uptake capacity (156.4 cm3 g−1 at 1 bar) and a high selectivity for CO2 over N2 (39.8) and CH4 (7.2) at 273 K.
Journal ArticleDOI

Expanded porous MOF-505 analogue exhibiting large hydrogen storage capacity and selective carbon dioxide adsorption.

TL;DR: An expanded 4,4-paddlewheel-connected porous porous MOF-505-type metal-organic framework (MOF), [Cu2(PDEB)(H2O)2]·xS (NJU-Bai12) has been designed from a nanosized rectangular diisophthalate linker containing alkyne groups 5,5'-(1, 4-phenylenedi-2,1-ethynediyl)bis( 1,