arXiv subjects

Gui-Fang Huang

Publications and source records attributed to Gui-Fang Huang.

14 recordsLinked to original sources

arXiv2025

Breaking the Sabatier Principle by Dynamic Adsorption-Desorption Decoupling in Electrocatalytic Hydrogen Evolution

The Sabatier principle establishes a fundamental trade-off in heterogeneous electrocatalysis.In the hydrogen evolution reaction (HER), this trade-off is manifested by the coupling of Volmer step, which requires strong hydrogen adsorption, with the Heyrovsky/Tafel step, which favors facile desorption, thus giving rise to the classical volcano relationship and limiting activity even at $ΔG=0$. Here, we demonstrate a ferroelectric platform with dynamic tunability -- monolayer GeS$_2$ decorated with transition metal atoms as a proof-of-concept -- where polarization-driven surface electronic reconstruction enables real-time modulation of intermediate binding strength, thereby breaking the Sabatier constraint. Reversible control of hydrogen adsorption allows strong H binding to accelerate the Volmer step, followed by weakened adsorption to promote the Heyrovsky/Tafel step.This dynamic adsorption-desorption decoupling not only surpasses the volcano limit to achieve unprecedented HER activity, but also establishes a general paradigm for designing adaptive electrocatalysts capable of reconfiguring under operating conditions.

cond-mat.mtrl-sci↗

arXiv2025

Active-Spin-State-Derived Descriptor for Hydrogen Evolution Reaction Catalysis

Spin states are pivotal in modulating the electrocatalytic activity of transition-metal (TM)-based compounds, yet quantitatively evaluating the activity-spin state correlation remains a formidable challenge. Here, we propose an 'activity index n' as a descriptor, to assess the activity of the spin states for the hydrogen evolution reaction (HER). n descriptor integrates three key electronic parameters: the proportion (P), broadening range (R) and center cc of active spin state, which collectively account for the electronic structure modulation induced by both the intrinsic active site and its local coordination environment. Using 1T-phase ZrSe2-anchored TM atoms (TM=Sc to Ni) as prototypes, we reveal that the correlation between Gibbs free energy and the n value follows a linear relation, namely, the vGH reduces as the n decreases. Notably, ZrSe2-Mn exhibits the optimal n value (-0.56), corresponding the best HER activity with a vGH of 0.04 eV closer to the thermoneutral ideal value (0 eV) than even Pt (vGH = -0.09 eV). This relationship suggests that n is the effective descriptor of active spin state for HER of TM-based catalysts. Our study brings fundamental insights into the HER activity-spin state correlation, offering new strategies for HER catalyst design.

cond-mat.mtrl-sci↗

arXiv2025

Electronic origin of stability of 2D 1H-phase Janus transition metal dichalcogenides and beyond

Janus transition metal dichalcogenides (JTMDs) monolayers have emerged as a new paradigm to broaden the family of two-dimensional (2D) materials. Despite numerous theoretical predictions of JTMDs, their experimental realization remains scarce, most probably due to intrinsic structural fragility. We identify a dependence of the structural stability of 1H-phase JTMDs on the transition metal group, with Group-VIB-based monolayers exhibiting robust stability, as evidenced by the successful synthesized MoSSe and WSSe. The group-dependent stability arises from the competition between metal-ligand ionic bonding and ligand-ligand covalent bonding, as well as the high-energy d-electron orbital splitting. We propose an electron configuration that describes the interactions of electrons near the Fermi level to correlate the stability, and introduce an electron compensation strategy to stabilize certain unstable JTMDs systems. Guided by the electronic origin of stability, we predict a family of stable 2D Janus transition metal halides with intrinsic ferromagnetic valley properties. This work bridges the gap between electronic structure and stability predictions, and extends the design rules for synthesizing 2D Janus materials.

cond-mat.mtrl-sci↗

arXiv2024

Doping-free Janus homojunction solar cell with efficiency exceeding 23%

Photovoltaic solar cell is one of the main renewable energy sources, and its power conversion efficiency (PCE) is improved by employing doping or heterojunction to reduce the photogenerated carrier recombination. Here, we propose a doping-free homojunction solar cell utilizing two-dimensional Janus semiconductors to achieve high PCE. Thanks to the intrinsic dipole of Janus structure, doping-free Janus homojunction has naturally not only a type-II band alignment to promote the photoexciton dissociation, but also a smaller effective bandgap to enhance light absorption. More importantly, the intrinsic electric field across the Janus structure will drive photoinduced electron and hole transfer from the interface to the opposite transport layers respectively, significantly enhancing the efficiency of carrier separation and transport. We illustrate the concept in titanium-based Janus monolayer homojunction, where the theoretically observed PCE reaches 23.22% of TiSSe homojunction. Our work opens a novel avenue to design low-cost, high-efficiency solar cells.

physics.app-ph↗

arXiv2024

Symmetry-breaking-induced giant Stark effect in 2D Janus materials

Symmetry breaking generally induce exotic physical properties, particularly for low-dimensional materials. Herein we demonstrate that symmetry breaking induces a giant Stark effect in 2D Janus materials using group IV-V monolayers with a four-atom-layer structure as a model system, which are constructed by Ge and As element substitution of symmetrical SnSb monolayer. A linear giant Stark effect is found in Janus semiconductor monolayers, as verified by the band gap variation up to 134 meV of Sn2SbAs monolayer, which is 30 times larger than that of SnSb monolayer (4 meV) when the applied electric field is increased from -0.30 to 0.30 V/Å. By considering the induced electronic field, we propose a generalized and effective formula that efficiently determines the band gap variation owing to Stark effect. The calculated results from proposed formula are well agreement with those from DFT-HSE06 functional. The giant Stark effect is originated from the large spatial separation of centers of the conduction band minimum and valence band maximum states of Janus structure due to its intrinsic potential gradient. The wide-range tuning of band gap under electronic field shows potential applications of 2D Janus materials in optoelectronic devices.

physics.app-ph↗

arXiv2023

Correlation between spin state and activity for hydrogen evolution

Spin plays a key role in physical and chemical reactions, such as oxygen evolution and hydrogen evolution reactions (OER/HER); but the spin-activity correlation has remained unclear. Based on a transition metal (TM)-doped PtN2 monolayer model with a well-defined spin center as adsorption site, we here reveal that only active spin state can enhance the strength of hydrogen adsorption, while inert spin state offers very little influence. Specifically, the unpaired electron along the out-of-plane direction such as in dZ2 orbital, acting as an active spin state, will strongly hybridize with hydrogen, resulting in enhanced hydrogen binding energy because dZ2 orbital is just enough to accommodate two electrons to form a bonding orbital. While the in-plane unpaired electron such as in dX2-Y2 orbital, plays a negligible role in adsorbing hydrogen atom. This is verified by a series of single atom catalysts comprising of PtN2 monolayer by replacing Pt atom with a TM (Fe, Co, Ni, Ru, Rh, Pd, Os, or Ir) atom, or subsequent adsorbing a Cl atom. One of the most promising materials is Pd@PtN2-Cl that offers superior HER activity, even better than pure Pt. This work uncovers the nature of spin-activity correlation, thus paving the way for the design of high-performance catalysts through spin-engineering.

cond-mat.mtrl-sci↗

arXiv2022

Symmetry-breaking-induced multifunctionalities of two-dimensional chromium-based materials for nanoelectronics and clean energy conversion

Structural symmetry-breaking that could lead to exotic physical properties plays a crucial role in determining the functions of a system, especially for two-dimensional (2D) materials. Here we demonstrate that multiple functionalities of 2D chromium-based materials could be achieved by breaking inversion symmetry via replacing Y atoms in one face of pristine CrY (Y=P, As, Sb) monolayers with N atoms, i.e., forming Janus Cr2NY monolayers. The functionalities include spin-gapless, very low work function, inducing carrier doping and catalytic activity, which are predominately ascribed to the large intrinsic dipole of Janus Cr2NY monolayers, making them having great potentials in various applications. Specifically, Cr2NSb is found to be a spin-gapless semiconductor, Cr2NP and Cr2NHPF could simultaneously induce n- and p-type carrier doping for two graphene sheets with different concentrations (forming intrinsic p-n vertical junction), and Cr2NY exhibits excellent electrocatalytic hydrogen evolution activity, even superior to benchmark Pt. The results confirm that breaking symmetry is a promising approach for the rational design of multifunctional 2D materials.

physics.comp-ph↗

arXiv2020

Algorithm for generating irreducible site-occupancy configurations

Generating irreducible site-occupancy configurations by taking advantage of crystal symmetry is a ubiquitous method for accelerating of disordered structure prediction, which plays an important role in condensed matter physics and material science. Here, we present a new algorithm for generating irreducible site-occupancy configurations, that works for arbitrary parent cell with any supercell expansion matrix, and for any number of atom types with arbitrary stoichiometry. The new algorithm identifies the symmetrically equivalent configurations by searching the space group operations of underlying lattice and building the equivalent atomic matrix based on it. Importantly, an integer representation of configurations can greatly accelerate the speed of elimination of duplicate configurations, resulting into a linear scale of run time with the number of irreducible configurations that finally found. Moreover, based on our new algorithm, we write the corresponding code named as disorder in FORTRAN programming language, and the performance test results show that the time efficiency of our disorder code is superior to that of other related codes (supercell, enumlib and SOD).

physics.comp-ph↗

arXiv2018

Substrate-induced magnetism and topological phase transition in silicene

Silicene has shown great application potential as a versatile material for nanoelectronics, particularly promising as building block for spintronic applications. Unfortunately, despite its intriguing properties, such as relatively large spin-orbit interactions, one of the biggest hurdles for silicene to be useful as a host spintronic material is the lack of magnetism or the topological phase transition owing to the silicene-substrate interactions, which influence its fundamental properties and has yet to be fully explored. Here, we show that when silicene is grown on CeO2 substrate, an appreciable robust magnetic moment appears in silicene covalently bonded to CeO2 (111), while a topological phase transition to a band insulator occurs regardless of van der Waals (vdWs) interaction or covalent bonding interaction at interface. The induced magnetism of silicene is due to the breaking of Si-Si π-bonding, also resulting in trivial topological phase. The silicene-substrate interaction, even weak vdWs force (equivalent to an electric field), can destroy quantum spin Hall effect (QSHE) of silicene. We propose a viable strategy --- constructing inverse symmetrical sandwich structure (protective layer/silicene/substrate) --- to preserve quantum spin Hall (QSH) state of silicene in weak vdWs interaction system. This work takes a critical step towards fundamental physics and realistic applications of silicene-based spintronic devices.

cond-mat.mes-hall↗

arXiv2018

Can the quantum spin Hall state of silicene be preserved on substrate

The substrate-induced topological phase transition of silience is a formidable obstacle for developing silicene-based materials and devices for compatibility with current electronics by using its topologically protected dissipationless edge states. First-principles calculations indicate that the substrate will result in a phase transition from topological nontrivial phase to trivial phase of silicene, although its Dirac cone is still obvious. The substrate effect (equivalent to an electric field) annihilates its spin-orbit coupling effect, the reason why its quantum spin Hall effect (QSHE) of silicene has not been experimentally observed. Unfortunately, external electric field seems impossible to recover the QSHE due to the screen effect of substrate. We here first propose a viable strategy (constructing inverse symmetrical sandwich structure (protective layer/silicene/substrate)) to preserve quantum spin Hall (QSH) state of silicene, which is demonstrated by using two representatives (CeO2(111)/silicene/CeO2(111) and CaF2(111)/silicene/CaF2(111)) through the calculated edge states and Z2 invariant. This work takes a critical step towards fundamental physics and realistic applications of silicene-based nanoelectronic devices.

physics.comp-ph↗

arXiv2016

Origin of enhanced visible-light photocatalytic activity of transition metal (Fe, Cr and Co) doped CeO2: Effect of 3d-orbital splitting

Enhanced visible light photocatalytic activity of transition metal-doped ceria (CeO2) nanomaterials have experimentally been demonstrated, whereas there are very few reports mentioning the mechanism of this behavior. Here we use first-principles calculations to explore the origin of enhanced photocatalytic performance of CeO2 doped with transition metal impurities (Fe, Cr and Co). When a transition metal atom substitutes a Ce atom into CeO2, t2g and eg levels of 3d orbits appear in the middle of band gap owing to the effect of cubic ligand field, and the former is higher than latter. Interestingly, t2g subset of FeCe (CoCe and CrCe)-Vo-CeO2 is split into two parts: one merges into the conduction band, the other as well as eg will remain in the gap, because O vacancy defect adjacent to transition metal atom will break the symmetry of cubic ligand field. These eg and t2g levels in the band gap are beneficial for absorbing visible light and enhancing quantum efficiency because of forbidden transition, which is one key factor for enhanced visible light photocatalytic activity. The band gap narrowing also leads to a redshift of optical absorbance and high photoactivity. These findings can rationalize the available experimental results and provide some new insights for designing CeO2-based photocatalysts with high photocatalytic performance.

cond-mat.mtrl-sci↗

arXiv2016

Interfacial interaction in monolayer transition metal dichalcogenides (MX2)/metal oxide heterostructures and its effects on electronic and optical properties: The case of MX2/CeO2

Two-dimensional transition metal dichalcogenides (MX2)/metal oxide heterostructures have shown unique physical properties, making them promising materials for various applications ranging from photocatalysis to solar energy conversion. Understanding the interfacial interactions is highly desirable for designing these heterostructures having excellent performance. Here we systematically study the interfacial interaction in monolayer MX2 (M=Mo, W; X=S, Se)/CeO2 heterostructures and its effects on electronic and optical properties by density functional theory. It is found that the interfacial interaction in the MX2/CeO2 depends predominantly on the chalcogen (X) element. Particularly, the band gap variation and important electronic states at conduction band minimum or valence band maximum of the heterostructures are determined by the strength of interfacial interaction. The MX2/CeO2 heterostructures with the same chalcogen (X) element have similar absorption spectra from ultraviolet to near-infrared regions. These results suggest that the chalcogen (X) element is a key factor in tuning the properties of MX2/metal oxide heterostructures.

cond-mat.mtrl-sci↗

arXiv2016

2D MoS2-Graphene-based multilayer van der Waals heterostructures: Enhanced charge transfer and optical absorption, and electric-field tunable Dirac point and band gap

Multilayer van der Waals (vdWs) heterostructures assembled by diverse atomically thin layers have demonstrated a wide range of fascinating phenomena and novel applications. Understanding the interlayer coupling and its correlation effect is paramount for designing novel vdWs heterostructures with desirable physical properties. Using a detailed theoretical study of 2D MoS2-graphene (GR)-based heterostructures based on state-of-the-art hybrid density functional theory, we reveal that for 2D few-layer heterostructures, vdWs forces between neighboring layers depend on the number of layers. Compared to that in bilayer, the interlayer coupling in trilayer vdW heterostructures can significantly be enhanced by stacking the third layer, directly supported by short interlayer separations and more interfacial charge transfer. The trilayer shows strong light absorption over a wide range (<700 nm), making it very potential for solar energy harvesting and conversion. Moreover, the Dirac point of GR and band gaps of each layer and trilayer can be readily tuned by external electric field, verifying multilayer vdWs heterostructures with unqiue optoelectronic properties found by experiments. These results suggest that tuning the vdWs interaction, as a new design parameter, would be an effective strategy for devising particular 2D multilayer vdWs heterostructures to meet the demands in various applications.

cond-mat.mes-hall↗

arXiv2015

Tuning near-gap electronic structure, interface charge transfer and visible light response of hybrid doped graphene and Ag3PO4 composite: Dopant effects

The enhanced photocatalytic performance of doped graphene(GR)/semiconductor nanocomposites have recently been widely observed, but an understanding of the underlying mechanisms behind it is still out of reach. As a model system to study the effect of dopants, we investigate the electronic structures and optical properites of doped GR/Ag3PO4 nanocomposites using the first-principles calculations, demonstrating that the band gap, near-gap electronic structure and interface charge transfer of the doped GR/Ag3PO4(100) composite can be tuned by the dopants. Interestingly, the doping atom and C atoms bonded to dopant become active sites for photocatalysis because they are positively or negatively charged due to the charge redistribution caused by interaction. The dopants can enhance the visible light absorption and photoinduced electrons transfer. We propose that the N atom may be most appropriate doping for the GR/Ag3PO4 photocatalyst. This work can rationalize the available experimental results about N-doped GR-semiconductor composites, and enriches our understanding on the effect of dopants in the doped GR-based composites for developing high-performance photocatalysts.

physics.comp-ph↗